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21 pages, 8661 KiB  
Article
Assessing the Peripheral Levels of the Neurotransmitters Noradrenaline, Dopamine and Serotonin and the Oxidant/Antioxidant Equilibrium in Circus Horses
by Raffaella Cocco, Sara Sechi, Maria Rizzo, Federica Arrigo, Claudia Giannetto, Giuseppe Piccione and Francesca Arfuso
Animals 2024, 14(16), 2354; https://doi.org/10.3390/ani14162354 (registering DOI) - 14 Aug 2024
Abstract
Due to the paucity of information on circus management effects on the welfare of horses, this study investigated the plasma concentrations of noradrenaline, dopamine and serotonin, known to be indices of mental status, as well as the reactive oxygen metabolites (d-Roms) and the [...] Read more.
Due to the paucity of information on circus management effects on the welfare of horses, this study investigated the plasma concentrations of noradrenaline, dopamine and serotonin, known to be indices of mental status, as well as the reactive oxygen metabolites (d-Roms) and the biological antioxidant potential (BAP), likely to denote the oxidant/antioxidant equilibrium of organisms, in horses managed in different Italian circuses. For the study, 56 circus horses of different breeds and ages were enrolled and divided into six groups according to the horses’ management (circus management, groups G1–G5; classic riding management representing the control group, CG). From each horse, blood samples were collected in order to assess the concentration of selected parameters. One-way ANOVA showed no differences (p > 0.05) in serotonin, dopamine, noradrenaline, d-Roms and BAP values between circus and control horses. No differences related to the breed of the horses enrolled in the study were found in the values of all investigated parameters (p > 0.05). Furthermore, neurotransmitters showed overlapping levels between the different age classes of investigated horses (p > 0.05); contrariwise, the age of the horse displayed a significant effect on BAP values, with the oldest horses (16–21 age class) exhibiting lower BAP values compared to 4–5, 6–10 and 11–15 age classes (p < 0.05), whereas the d-Roms showed similar values in horses of different age classes (p > 0.05). The results gathered in the present study suggest that the mental status of horses under circus management was not compromised; however, better attention and care in the management of older horses is advocated, as they showed a lower biological antioxidant potential than younger horses; thus, they could be more susceptible to oxidative stress. Full article
(This article belongs to the Section Animal Physiology)
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Figure 1

Figure 1
<p>Normal quantile plot (Q-Q Plot) showing the normal distribution of serotonin, dopamine and noradrenaline values measured in investigated horses when analyzing the group’s effect (G1–G5 vs. CG).</p>
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<p>Normal quantile plot (Q-Q Plot) showing the normal distribution of serotonin, dopamine and noradrenaline values measured in investigated horses when analyzing the breed’s effect (Arabian, Andalusian, Friesian and Pony).</p>
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<p>Normal quantile plot (Q-Q Plot) showing the normal distribution of serotonin, dopamine and noradrenaline values measured in investigated horses when analyzing the effect of age class (4–5, 6–10, 11–15 and 16–21 years).</p>
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<p>Normal quantile plot (Q-Q Plot) showing the normal distribution of the reactive oxygen metabolites (d-Roms) and the biological antioxidant potential (BAP) values measured in investigated horses when analyzing the group’s effect (G1–G5 vs. CG).</p>
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<p>Normal quantile plot (Q-Q Plot) showing the normal distribution of the reactive oxygen metabolites (d-Roms) and the biological antioxidant potential (BAP) values measured in investigated horses when analyzing the breed’s effect (Arabian, Andalusian, Friesian and Pony).</p>
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<p>Normal quantile plot (Q-Q Plot) showing the normal distribution of the reactive oxygen metabolites (d-Roms) and the biological antioxidant potential (BAP) values measured in investigated horses when analyzing the effect of age class (4–5, 6–10, 11–15 and 16–21 years).</p>
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<p>Violin plot showing distributions of serotonin, dopamine and noradrenaline values measured in investigated horses together with the relative statistical significances when analyzing the group’s effect (G1–G5 vs. CG).</p>
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<p>Violin plot showing distributions of the reactive oxygen metabolites (d-Roms) and the biological antioxidant potential (BAP) values measured in investigated horses together with the relative statistical significances when analyzing the group’s effect (G1–G5 vs. CG).</p>
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<p>Mean values ± 95% confidence intervals of serotonin, dopamine and noradrenaline values measured in investigated horses together with the relative statistical significances when analyzing the breed’s effect (Arabian, Andalusian, Friesian and Pony).</p>
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<p>Mean values ± 95% confidence intervals of the reactive oxygen metabolites (d-Roms) and the biological antioxidant potential (BAP) values measured in investigated horses together with the relative statistical significances when analyzing the breed’s effect (Arabian, Andalusian, Friesian and Pony).</p>
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<p>Mean values ± 95% confidence intervals of serotonin, dopamine and noradrenaline values measured in investigated horses together with the relative statistical significances when analyzing the effect of age class (4–5, 6–10, 11–15 and 16–21 years).</p>
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<p>Mean values ± 95% confidence intervals of the reactive oxygen metabolites (d-Roms) and the biological antioxidant potential (BAP) values together with the relative statistical significances when analyzing the effect of age class (4–5, 6–10, 11–15 and 16–21 years).</p>
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12 pages, 1219 KiB  
Review
Nutritional Management of Patients with Fatty Acid Oxidation Disorders
by Luis Peña-Quintana and Patricia Correcher-Medina
Nutrients 2024, 16(16), 2707; https://doi.org/10.3390/nu16162707 (registering DOI) - 14 Aug 2024
Abstract
Treatment of fatty acid oxidation disorders is based on dietary, pharmacological and metabolic decompensation measures. It is essential to provide the patient with sufficient glucose to prevent lipolysis and to avoid the use of fatty acids as fuel as far as possible. Dietary [...] Read more.
Treatment of fatty acid oxidation disorders is based on dietary, pharmacological and metabolic decompensation measures. It is essential to provide the patient with sufficient glucose to prevent lipolysis and to avoid the use of fatty acids as fuel as far as possible. Dietary management consists of preventing periods of fasting and restricting fat intake by increasing carbohydrate intake, while maintaining an adequate and uninterrupted caloric intake. In long-chain deficits, long-chain triglyceride restriction should be 10% of total energy, with linoleic acid and linolenic acid intake of 3–4% and 0.5–1% (5/1–10/1 ratio), with medium-chain triglyceride supplementation at 10–25% of total energy (total MCT+LCT ratio = 20–35%). Trihepatnoin is a new therapeutic option with a good safety and efficacy profile. Patients at risk of rhabdomyolysis should ingest MCT or carbohydrates or a combination of both 20 min before exercise. In medium- and short-chain deficits, dietary modifications are not advised (except during exacerbations), with MCT contraindicated and slow sugars recommended 20 min before any significant physical exertion. Parents should be alerted to the need to increase the amount and frequency of carbohydrate intake in stressful situations. The main measure in emergency hospital treatment is the administration of IV glucose. The use of carnitine remains controversial and new therapeutic options are under investigation. Full article
(This article belongs to the Special Issue Nutritional Management of Patients with Inborn Errors of Metabolism)
16 pages, 4292 KiB  
Article
Recovery of Zinc and Rhenium for the Production of Zinc Perrhenates
by Katarzyna Leszczyńska-Sejda, Joanna Malarz, Dorota Kopyto, Karolina Goc, Alicja Grzybek, Mateusz Ciszewski, Arkadiusz Palmowski, Grzegorz Benke and Karolina Pianowska
Crystals 2024, 14(8), 725; https://doi.org/10.3390/cryst14080725 - 14 Aug 2024
Abstract
This study outlines findings from an investigation into the development of a hydrometallurgical process for manufacturing various forms of zinc perrhenate, entirely from waste from recycling and from the Zn–Pb industry. Scraps of Re-bearing Ni-based superalloys and acidic waste, circulating zinc solutions generated [...] Read more.
This study outlines findings from an investigation into the development of a hydrometallurgical process for manufacturing various forms of zinc perrhenate, entirely from waste from recycling and from the Zn–Pb industry. Scraps of Re-bearing Ni-based superalloys and acidic waste, circulating zinc solutions generated during the production of Zn by the electrolytic method and which contain >45 g/dm3 of Zn, Na, Mn, and Mg, were used in the research. In the publication, the conditions for the production of three types of zinc perrhenate, i.e., Zn(ReO4)2·4H2O, Zn(ReO4)2, and Zn(ReO4)2·2H2O, are presented. As a result of the analysis of the obtained results, it was concluded that to obtain the above-mentioned forms of zinc perrhenate, zinc carbonate can be used, precipitated from acidic, waste, and multi-component solutions after their prior neutralization to pH 4.0 and partial purification from Mn, Mg, and Na using metallurgical zinc oxide. Zinc carbonate should be precipitated using Na2CO3 at pH 6.3 and subsequently purified from other impurities, i.e., Mg, Na, and Mn, using aqueous ammonia solutions. As a result, zinc carbonate was obtained, which was used in a reaction with an aqueous solution of HReO4 to produce zinc perrhenate. The precipitated forms of Zn(ReO4)2 were obtained by appropriately drying the crude and hydrated Zn(ReO4)2 to obtain its tetrahydrate, dihydrate, and anhydrous forms, respectively, using drying temperatures of 55, 135, and 185 °C. The developed technology has been submitted for a patent and is an example of a technology founded on the principles of sustainable development, with a particular emphasis on the minimalization of loss of rhenium and zinc at all stages of its realization. Full article
(This article belongs to the Topic Advances in Inorganic Synthesis)
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Figure 1
<p>The influence of the excess precipitating agent (sodium carbonate) on the Zn precipitation efficiency.</p>
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<p>The influence of the excess precipitating agent (ammonium bicarbonate) on the Zn precipitation efficiency.</p>
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<p>SEM analysis of ZnCO<sub>3</sub>.</p>
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<p>EDS analysis of ZnCO<sub>3</sub>.</p>
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<p>DTA and TG analyses of ZnCO<sub>3</sub> with heating to 1200 °C. *: temperature at which TGA analysis was performed.</p>
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<p>The influence of Re concentration in HReO<sub>4</sub> on the Zn(ReO<sub>4</sub>)<sub>2</sub> precipitation efficiency.</p>
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<p>The influence of the pH on the Zn(ReO<sub>4</sub>)<sub>2</sub> precipitation efficiency.</p>
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<p>XRD patterns of zinc perrhenate produced entirely from waste, dried at 180 °C.</p>
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<p>Drying graphs for zinc perrhenate.</p>
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<p>Scheme of producing zinc perrhenate from zinc carbonate obtained from waste solutions from the Zn–Pb industry.</p>
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18 pages, 962 KiB  
Article
Nebivolol Polymeric Nanoparticles-Loaded In Situ Gel for Effective Treatment of Glaucoma: Optimization, Physicochemical Characterization, and Pharmacokinetic and Pharmacodynamic Evaluation
by Pradeep Singh Rawat, Punna Rao Ravi, Mohammed Shareef Khan, Radhika Rajiv Mahajan and Łukasz Szeleszczuk
Nanomaterials 2024, 14(16), 1347; https://doi.org/10.3390/nano14161347 - 14 Aug 2024
Abstract
Nebivolol hydrochloride (NEB), a 3rd-generation beta-blocker, was recently explored in managing open-angle glaucoma due to its mechanism of action involving nitric oxide release for the vasodilation. To overcome the issue of low ocular bioavailability and the systemic side effects associated with [...] Read more.
Nebivolol hydrochloride (NEB), a 3rd-generation beta-blocker, was recently explored in managing open-angle glaucoma due to its mechanism of action involving nitric oxide release for the vasodilation. To overcome the issue of low ocular bioavailability and the systemic side effects associated with conventional ocular formulation (aqueous suspension), we designed and optimized polycaprolactone polymeric nanoparticles (NEB-PNPs) by applying design of experiments (DoE). The particle size and drug loading of the optimized NEB-PNPs were 270.9 ± 6.3 nm and 28.8 ± 2.4%, respectively. The optimized NEB-PNPs were suspended in a dual-sensitive in situ gel prepared using a mixture of P407 + P188 (as a thermo-sensitive polymer) and κCRG (as an ion-sensitive polymer), reported previously by our group. The NEB-PNPs-loaded in situ gel (NEB-PNPs-ISG) formulation was characterized for its rheological behavior, physical and chemical stability, in vitro drug release, and in vivo efficacy. The NEB-PNPs-loaded in situ gel, in ocular pharmacokinetic studies, achieved higher aqueous humor exposure (AUC0–t = 329.2 ng × h/mL) and for longer duration (mean residence time = 9.7 h) than compared to the aqueous suspension of plain NEB (AUC0–t = 189 ng × h/mL and mean residence time = 6.1 h) reported from our previous work. The pharmacokinetic performance of NEB-PNPs-loaded in situ gel translated into a pharmacodynamic response with 5-fold increase in the overall percent reduction in intraocular pressure by the formulation compared to the aqueous suspension of plain NEB reported from our previous work. Further, the mean response time of NEB-PNPs-loaded in situ gel (12.4 ± 0.6 h) was three times higher than aqueous suspension of plain NEB (4.06 ± 0.3 h). Full article
(This article belongs to the Topic Advances in Controlled Release and Targeting of Drugs)
24 pages, 665 KiB  
Review
Adsorption of Polycyclic Aromatic Hydrocarbons from Wastewater Using Iron Oxide Nanomaterials Recovered from Acid Mine Water: A Review
by Tumelo M. Mogashane, Johannes P. Maree and Lebohang Mokoena
Minerals 2024, 14(8), 826; https://doi.org/10.3390/min14080826 - 14 Aug 2024
Abstract
Polycyclic aromatic hydrocarbons (PAHs) are a group of organic pollutants known for their persistence and potential carcinogenicity. Effective removal techniques are required since their presence in wastewater poses serious threats to human health and the environment. In this review study, iron oxide nanomaterials [...] Read more.
Polycyclic aromatic hydrocarbons (PAHs) are a group of organic pollutants known for their persistence and potential carcinogenicity. Effective removal techniques are required since their presence in wastewater poses serious threats to human health and the environment. In this review study, iron oxide nanomaterials (IONs), a by-product of mining operations, recovered from acid mine water are used to investigate the adsorption of PAHs from wastewater. The mechanisms of PAH adsorption onto IONs are investigated, with a focus on the effects of concentration, temperature, and pH on adsorption efficiency. The better performance, affordability, and reusable nature of IONs are demonstrated by comparative studies with alternative adsorbents such as activated carbon. Economic and environmental ramifications highlight the benefits of employing recovered materials, while case studies and real-world applications show how effective IONs are in removing PAHs in the real world. This review concludes by discussing potential future developments in synthesis processes, areas for more research, and emerging trends in nanomaterial-based adsorption. This research intends to contribute to the development of more effective and sustainable wastewater treatment technologies by offering a thorough assessment of the present and future potential of employing IONs for PAH removal from wastewater. Full article
(This article belongs to the Special Issue Acid Mine Drainage: A Challenge or an Opportunity?)
24 pages, 1043 KiB  
Review
Breath and Sputum Analyses in Asthmatic Patients: An Overview
by Piera Soccio, Carla Maria Irene Quarato, Pasquale Tondo, Donato Lacedonia, Anela Hoxhallari, Maria Pia Foschino Barbaro and Giulia Scioscia
Cells 2024, 13(16), 1355; https://doi.org/10.3390/cells13161355 - 14 Aug 2024
Abstract
Recent advancements in asthma management include non-invasive methodologies such as sputum analysis, exhaled breath condensate (EBC), and fractional exhaled nitric oxide (FeNO). These techniques offer a means to assess airway inflammation, a critical feature of asthma, without invasive procedures. Sputum analysis provides detailed [...] Read more.
Recent advancements in asthma management include non-invasive methodologies such as sputum analysis, exhaled breath condensate (EBC), and fractional exhaled nitric oxide (FeNO). These techniques offer a means to assess airway inflammation, a critical feature of asthma, without invasive procedures. Sputum analysis provides detailed insights into airway inflammation patterns and cellular composition, guiding personalized treatment strategies. EBC collection, reflecting bronchoalveolar lining fluid composition, provides a non-invasive window into airway physiology. FeNO emerges as a pivotal biomarker, offering insights into eosinophilic airway inflammation and aiding in asthma diagnosis, treatment monitoring, and the prediction of exacerbation risks. Despite inherent limitations, each method offers valuable tools for a more comprehensive assessment of asthma. Combining these techniques with traditional methods like spirometry may lead to more personalized treatment plans and improved patient outcomes. Future research is crucial to refine protocols, validate biomarkers, and establish comprehensive guidelines in order to enhance asthma management with tailored therapeutic strategies and improved patient outcomes. Full article
(This article belongs to the Special Issue Cell Biology: State-of-the-Art and Perspectives in Italy 2024)
32 pages, 44965 KiB  
Article
Hybrid Cellulosic Substrates Impregnated with Meta-PBI-Stabilized Carbon Nanotubes/Plant Extract-Synthesized Zinc Oxide—Antibacterial and Photocatalytic Dye Degradation Study
by Hristo Penchev, Katerina Zaharieva, Silvia Dimova, Georgy Grancharov, Petar D. Petrov, Maria Shipochka, Ognian Dimitrov, Irina Lazarkevich, Stephan Engibarov and Rumyana Eneva
Nanomaterials 2024, 14(16), 1346; https://doi.org/10.3390/nano14161346 - 14 Aug 2024
Abstract
Novel fibrous cellulosic substrates impregnated with meta-polybenzimidazole (PBI)-stabilized carbon nanotubes/zinc oxide with different weight content of ZnO and with the use of dimethylacetamide as dispersant media. The pristine ZnO nanoparticle powder was prepared by plant extract-mediated synthesis using Vaccinium vitis-idaea L. The green [...] Read more.
Novel fibrous cellulosic substrates impregnated with meta-polybenzimidazole (PBI)-stabilized carbon nanotubes/zinc oxide with different weight content of ZnO and with the use of dimethylacetamide as dispersant media. The pristine ZnO nanoparticle powder was prepared by plant extract-mediated synthesis using Vaccinium vitis-idaea L. The green synthesized ZnO possesses an average crystallite size of 15 nm. The formation of agglomerates from ZnO NPs with size 250 nm–350 nm in the m-PBI@CNTs/ZnO was determined. The prepared materials were investigated by PXRD analysis, XPS, SEM, EDS, AFM, and TEM in order to establish the phase and surface composition, structure, and morphology of the hybrids. The potential of the synthesized hybrid composites to degrade methylene blue (MB) dye as a model contaminant in aqueous solutions under UV illumination was studied. The photocatalytic results show that in the course of the photocatalytic reaction, the m-PBI@CNTs/ZnO 1:3 photocatalyst leads to the highest degree of degradation of the methylene blue dye (67%) in comparison with the other two studied m-PBI@CNTs/ZnO 1:1 and 1:2 composites (48% and 41%). The antibacterial activity of ZnO nanoparticles and the hybrid CNT materials was evaluated by the RMDA and the dynamic contact method, respectively. The profound antibacterial effect of the m-PBI@CNTs/ZnO hybrids was monitored for 120 h of exposition in dark and UV illumination regimes. The photocatalytic property of ZnO nanoparticles significantly shortens the time for bactericidal action of the composites in both regimes. The m-PBI@CNTs/ZnO 1:2 combination achieved complete elimination of 5.105 CFU/mL E. coli cells after 10 min of UV irradiation. Full article
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Figure 1
<p>Schematic representation of m-PBI surface wrapping stabilization of MWCNTs. Pictures of the hybrid dispersions from left to right: pristine ZnO NPs dispersed in DMAc; m-PBI@ZnO; m-PBI@CNTs; m-PBI@CNTs/ZnO 1:1 and m-PBI@CNTs/ZnO 3:1 (<b>A</b>); time stability comparison of the bare plant extract ZnO NPs and m-PBI@ZnO dispersions in DMAc before (left) and after 60 min stay (right) (<b>B</b>).</p>
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<p>Size distribution plot of PBI-modified MWCNTs dispersions in DMAc (<b>A</b>). Size distribution plots of PBI-modified MWCNTs/ZnO dispersions in DMAA at different CNTs/ZnO mass ratios (<b>B</b>).</p>
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<p>Digital pictures of 1 mL free drop spread of m-PBI@CNT and m-PBI@CNTs/ZnO 1:1 suspensions (<b>top</b>) and light microscopy pictures of these two dispersions after 1 mL deposition onto cellulose filter substrate (<b>bottom</b>).</p>
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<p>PXRD patterns of green synthesized ZnO, m-PBI/CNTs, and m-PBI@CNTs/ZnO 1:3.</p>
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<p>Deconvoluted photoelectron spectra of C1s, O1s, and N1s and core level spectra of Zn2p and ZnLMM of m-PBI/ZnO; m-PBI/CNTs; m-PBI@CNTs/ZnO 1:1; and m-PBI@CNTs/ZnO 1:3.</p>
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<p>SEM images of microfibrous cellulose substrates impregnated with (<b>A</b>) m-PBI@CNTs; (<b>B</b>) m-PBI@CNTs/ZnO 1:1; (<b>C</b>) m-PBI@CNTs/ZnO 1:2; and (<b>D</b>) m-PBI@CNTs/ZnO 1:3.</p>
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<p>EDS mapping of cellulose substrate impregnated with m-PBI@CNTs/ZnO 1:1 (<b>A</b>); m-PBI@CNTs/ZnO 1:2 (<b>B</b>); and m-PBI@CNTs/ZnO 1:3 (<b>C</b>).</p>
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<p>EDS mapping of cellulose substrate impregnated with m-PBI@CNTs/ZnO 1:1 (<b>A</b>); m-PBI@CNTs/ZnO 1:2 (<b>B</b>); and m-PBI@CNTs/ZnO 1:3 (<b>C</b>).</p>
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<p>EDS spectra of m-PBI/CNTs, m-PBI@CNTs/ZnO 1:1, PBI@CNTs/ZnO 1:2, and m-PBI@CNTs/ZnO 1:3.</p>
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<p>(<b>A</b>) AFM 2D image of CNTs; (<b>B</b>) AFM 3D image of CNTs; (<b>C</b>) AFM 2D image of green synthesized ZnO nanoparticles; (<b>D</b>) AFM 3D image of green synthesized ZnO nanoparticles; (<b>E</b>) AFM 2D image of m-PBI/ZnO; (<b>F</b>) AFM 3D image of m-PBI/ZnO; (<b>G</b>) AFM 2D image of m-PBI@CNTs/ZnO; (<b>H</b>) AFM 3D image of m-CNTs/ZnO.</p>
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<p>TEM images of (<b>A</b>) green synthesized ZnO nanoparticles; (<b>B</b>) m-PBI/ZnO; (<b>C</b>) m-PBI/CNTs; (<b>D</b>) m-PBI@CNTs/ZnO 1:1; and (<b>E</b>) m-PBI@CNTs/ZnO 1:3.</p>
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<p>HR TEM images of images of green synthesized ZnO nanoparticles (<b>A</b>). m-PBI@CNTs hybrid (<b>B</b>).</p>
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<p>HR TEM images of images of green synthesized ZnO nanoparticles (<b>A</b>). m-PBI@CNTs hybrid (<b>B</b>).</p>
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<p>Digital pictures of preliminary experiment for 15 min UV light illumination of hybrid catalytic m-PBI@CNT/ZnO 1:1 cellulose substrate in contact with diluted MB solution.</p>
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<p>(<b>a</b>) The concentration ratio C/C<sub>0</sub> and (<b>b</b>) degree of degradation of Methylene Blue dye with time of UV illumination using prepared hybrid materials as photocatalysts.</p>
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<p>(<b>a</b>) The concentration ratio C/C<sub>0</sub> and (<b>b</b>) degree of degradation of Methylene Blue dye with time of UV illumination using m-PBI/ZnO and bare green synthesized ZnO as photocatalysts.</p>
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<p>(<b>a</b>) The concentration ratio C/C<sub>0</sub> and (<b>b</b>) degree of degradation of Methylene Blue dye with time of UV illumination using prepared hybrid materials as photocatalysts in the presence of H<sub>2</sub>O<sub>2</sub>.</p>
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<p>Degree of degradation of MB dye after 180 min under UV light using (<b>a</b>) m-PBI@CNTs/ZnO 1:2; (<b>b</b>) m-PBI@CNTs/ZnO 1:1; and (<b>c</b>) m-PBI@CNTs/ZnO 1:3 photocatalysts in three photocatalytic runs.</p>
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<p>RMDA method for evaluation of MIC in 96-well plate. Wells in the rectangles are inoculated with a bacterial culture of 5 × 10<sup>5</sup> CFU/mL. (<b>a</b>) MIC of MWCNTs, lines A, B: a sector from 96-well plate kept in static condition. Lines F–H: a sector from another 96-well plate incubated on a wrist shaker. Legend between B and F lines shows the concentration of MWCNTs in each column of wells. Well G12—positive control. (<b>b</b>) MIC of ZnO nanoparticles, column 6: positive control, column 10: control wells of resazurin dye for each ZnO concentration.</p>
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<p>ASTM Standard Test Method E 2149–10. Data are presented as lg of the CFU/mL. (<b>a</b>,<b>b</b>) Antibacterial effect of the tested hybrid materials, their constituents, and combinations of constituents tested on <span class="html-italic">E. coli</span>. © Effect of the combination of cellulose and PBIs, tested on <span class="html-italic">B. subtilis</span>.</p>
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<p>(<b>a</b>). Effect of UV irradiation on standard <span class="html-italic">E. coli</span> suspension with 0.5 mg/mL ZnO NPs. Samples were taken before the 15′ incubation in the dark, at the start of UV irradiation, and at 10′, 20′, and 30′: (1) a beaker irradiated with UV light; (2) a beaker kept in the dark throughout the whole experiment; (<b>b</b>) effect of the tested hybrid materials: left—without irradiation; right—after UV irradiation; K—control, 1—Cell/PBI, 2—Cell/PBI/ZnO, 3—Cell/PBI@CNT, 4—Cell/PBI@CNT/ZnO 1:1, 5—Cell/PBI@CNT/ZnO 1:2, 6—Cell/PBI@CNT/ZnO 1:3. Sample 5 displays bactericidal effect.</p>
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<p>SEM images of the hybrid material Cell/PBI@CNT incubated with <span class="html-italic">E. coli</span> suspension overnight. Putative effusions of cell contents are indicated by arrows. Areas marked in rectangles were observed at higher magnification and shown below: (<b>a</b>) a specimen kept in the dark; (<b>b</b>) a specimen irradiated by UV light.</p>
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16 pages, 4502 KiB  
Article
Effects of Cryoprotectant Concentration and Exposure Time during Vitrification of Immature Pre-Pubertal Lamb Cumulus–Oocyte Complexes on Nuclear and Cytoplasmic Maturation
by Letizia Temerario, Nicola Antonio Martino, Monika Bennink, Agnes de Wit, Sipke Joost Hiemstra, Maria Elena Dell’Aquila and Julie Lamy
Animals 2024, 14(16), 2351; https://doi.org/10.3390/ani14162351 - 14 Aug 2024
Abstract
Oocyte vitrification allows for the storing of endangered breed female gametes. Cryoprotectant (CPA) concentration and exposure time should ensure cell protection with minimal toxicity. In the present study, a high concentration-rapid exposure (HC-RE) and a low concentration-slow exposure (LC-SE) vitrification protocol, using dimethyl [...] Read more.
Oocyte vitrification allows for the storing of endangered breed female gametes. Cryoprotectant (CPA) concentration and exposure time should ensure cell protection with minimal toxicity. In the present study, a high concentration-rapid exposure (HC-RE) and a low concentration-slow exposure (LC-SE) vitrification protocol, using dimethyl sulfoxide (DMSO) and ethylene glycol (EG) as permeating CPAs, were evaluated on meiotic competence and bioenergetic-oxidative status of pre-pubertal lamb immature COCs after in vitro maturation (IVM). For each protocol, COCs vitrified through a traditional protocol and fresh ones were used as controls. Both protocols allowed COC morphology preservation after vitrification-warming (V-W) and cumulus expansion after IVM. The maturation rate (7% and 14%) was comparable to the vitrified control (13% and 21%) but not satisfactory compared to fresh ones (58% and 64%; p < 0.001). The rate of mature oocytes displaying a perinuclear/subcortical (P/S) mitochondrial distribution pattern, an index of cytoplasmic maturity, was comparable between vitrified and fresh oocytes. The LC-SE vitrification protocol did not affect quantitative bioenergetic-oxidative parameters compared to both controls whereas HC-RE protocol significantly reduced intracellular reactive oxygen species (ROS) levels, indicating cell viability loss. In conclusion, to improve pre-pubertal lamb immature COC vitrification, the combination of low CPA concentrations with prolonged exposure time could be more promising to investigate further. Full article
(This article belongs to the Special Issue Advances in Animal Fertility Preservation—Second Edition)
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<p>Schematic representation of the experimental design described in the present study. Pre-pubertal lamb immature COCs were vitrified through a high concentration-rapid exposure (HC-RE) or low concentration-slow exposure (LC-SE) vitrification protocol, using DMSO and EG as permeating CPAs. After warming, COCs underwent IVM. Immature COCs cryopreserved through a traditional vitrification protocol and fresh COCs directly subjected to IVM after selection were used as controls. COC = cumulus–oocyte complex; CPA = cryoprotectant; DMSO = dimethyl sulfoxide; EG = ethylene glycol; IVM = in vitro maturation.</p>
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<p>Effect of HC-RE vitrification protocol in pre-pubertal lamb COCs on (<b>1</b>) COC preserved morphology rate after vitrification and warming. A total of 75–89 COCs were evaluated per condition in 4 replicates. Each bar represents mean + SEM, (<b>2</b>) cumulus expansion rate after IVM. A total of 75–89 COCs were evaluated per condition in 4 replicates. Each bar represents mean + SEM, (<b>3</b>) nuclear chromatin configuration rate after IVM. A total of 70–84 oocytes were evaluated per condition in 4 replicates. Each bar represents mean + SEM and (<b>4</b>) qualitative (perinuclear/subcortical P/S mitochondrial distribution pattern) and quantitative (mitochondrial membrane potential, intracellular reactive oxygen species ROS levels and mitochondria/ROS colocalization) bioenergetic/oxidative parameters in MII oocytes obtained in HC-RE vitrified, vitrified and fresh ctrl (5, 10 and 49 oocytes, respectively). For quantitative parameters, each bar represents mean presented as a percentage of the signal of fresh ctrl + SEM. One-way analysis of variance ANOVA followed by Tukey’s multiple comparison test: * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effects of HC-RE vitrification protocol in pre-pubertal lamb COCs: (<b>1</b>) pre-pubertal lamb COCs in HC-RE vitrified, vitrified ctrl and fresh ctrl, as observed before IVM. Scale bars represent 120 µm. (<b>2</b>) Pre-pubertal lamb COCs in HC-RE vitrified, vitrified ctrl and fresh ctrl, as observed after IVM. Scale bars represent 120 µm. (<b>3</b>) Photomicrographs showing representative images of one MII oocyte obtained in HC-RE vitrified, vitrified ctrl and fresh ctrl after IVM. Corresponding epifluorescence images showing (<b>Ia</b>–<b>IIIa</b>) nuclear chromatin configuration (Hoechst 33258) and confocal images showing (<b>Ib</b>–<b>IIIb</b>) mitochondrial distribution pattern and activity (MitoTracker Orange), (<b>Ic</b>–<b>IIIc</b>) intracellular ROS localization and levels (DCF) and (<b>Id</b>–<b>IIId</b>) mitochondria/ROS colocalization (Merge). Confocal images were taken at the oocyte equatorial plane. Scale bars represent 40 µm.</p>
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<p>Effect of LC-SE vitrification protocol in pre-pubertal lamb COCs on (<b>1</b>) COC preserved morphology rate after vitrification and warming. A total of 75–82 COCs were evaluated per condition in 4 replicates. Each bar represents mean + SEM, (<b>2</b>) cumulus expansion rate after IVM. A total of 75–82 COCs were evaluated per condition in 4 replicates. Each bar represents mean + SEM, (<b>3</b>) nuclear chromatin configuration rate after IVM. A total of 72–77 oocytes were evaluated per condition in 4 replicates. Each bar represents mean + SEM and (<b>4</b>) qualitative (perinuclear/subcortical P/S mitochondrial distribution pattern) and quantitative (mitochondrial membrane potential, intracellular reactive oxygen species ROS levels and mitochondria/ROS colocalization) bioenergetic/oxidative parameters in MII oocytes obtained in LC-SE vitrified, vitrified and fresh ctrl (10, 16 and 48 oocytes, respectively). For quantitative parameters, each bar represents mean presented as a percentage of the signal of fresh ctrl + SEM. One-way analysis of variance ANOVA followed by Tukey’s multiple comparison test: * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effect of LC-SE vitrification protocol in pre-pubertal lamb COCs on (<b>1</b>) COC preserved morphology rate after vitrification and warming. A total of 75–82 COCs were evaluated per condition in 4 replicates. Each bar represents mean + SEM, (<b>2</b>) cumulus expansion rate after IVM. A total of 75–82 COCs were evaluated per condition in 4 replicates. Each bar represents mean + SEM, (<b>3</b>) nuclear chromatin configuration rate after IVM. A total of 72–77 oocytes were evaluated per condition in 4 replicates. Each bar represents mean + SEM and (<b>4</b>) qualitative (perinuclear/subcortical P/S mitochondrial distribution pattern) and quantitative (mitochondrial membrane potential, intracellular reactive oxygen species ROS levels and mitochondria/ROS colocalization) bioenergetic/oxidative parameters in MII oocytes obtained in LC-SE vitrified, vitrified and fresh ctrl (10, 16 and 48 oocytes, respectively). For quantitative parameters, each bar represents mean presented as a percentage of the signal of fresh ctrl + SEM. One-way analysis of variance ANOVA followed by Tukey’s multiple comparison test: * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Effects of LC-SE vitrification protocol in pre-pubertal lamb COCs: (<b>1</b>) pre-pubertal lamb COCs in LC-SE vitrified, vitrified ctrl and fresh ctrl, as observed before IVM. Scale bars represent 120 µm. (<b>2</b>) Pre-pubertal lamb COCs in LC-SE vitrified, vitrified ctrl and fresh ctrl, as observed after IVM. Scale bars represent 120 µm. (<b>3</b>) Photomicrographs showing representative images of one MII oocyte obtained in LC-SE vitrified, vitrified ctrl and fresh ctrl after IVM. Corresponding epifluorescence images showing (<b>Ia</b>–<b>IIIa</b>) nuclear chromatin configuration (Hoechst 33258) and confocal images showing (<b>Ib</b>–<b>IIIb</b>) mitochondrial distribution pattern and activity (MitoTracker Orange), (<b>Ic</b>–<b>IIIc</b>) intracellular ROS localization and levels (DCF) and (<b>Id</b>–<b>IIId</b>) mitochondria/ROS colocalization (Merge). Confocal images were taken at the oocyte equatorial plane. Scale bars represent 40 µm.</p>
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18 pages, 1548 KiB  
Article
An Optical Device Based on a Chemical Chip and Surface Plasmon Platform for 2-Furaldehyde Detection in Insulating Oil
by Letizia De Maria, Francesco Arcadio, Giuseppe Gabetta, Daniele Merli, Giancarla Alberti, Luigi Zeni, Nunzio Cennamo and Maria Pesavento
Sensors 2024, 24(16), 5261; https://doi.org/10.3390/s24165261 - 14 Aug 2024
Abstract
2-Furaldehyde (2-FAL) is one of the main by-products of the degradation of hemicellulose, which is the solid material of the oil–paper insulating system of oil-filled transformers. For this reason, it has been suggested as a marker of the degradation of the insulating system; [...] Read more.
2-Furaldehyde (2-FAL) is one of the main by-products of the degradation of hemicellulose, which is the solid material of the oil–paper insulating system of oil-filled transformers. For this reason, it has been suggested as a marker of the degradation of the insulating system; sensing devices for 2-FAL analysis in a wide concentration range are of high interest in these systems. An optical sensor system is proposed; this consists of a chemical chip, able to capture 2-FAL from the insulating oil, coupled with a surface plasmon resonance (SPR) probe, both realized on multimode plastic optical fibers (POFs). The SPR platform exploits gold nanofilm or, alternatively, a double layer of gold and silicon oxide to modulate the sensor sensitivity. The capturing chip is always based on the same molecularly imprinted polymer (MIP) as a receptor specific for 2-FAL. The system with the SPR probe based on a gold nanolayer had a higher sensitivity and a lower detection limit of fractions of μg L−1. Instead, the SPR probe, based on a double layer (gold and silicon oxide), has a lower sensitivity with a worse detection limit, and it is suitable for the detection of 2-FAL at concentrations of 0.01 mg L−1–1 mg L−1. Full article
15 pages, 1723 KiB  
Article
The Role of the Gut Microbiota in Sanfilippo Syndrome’s Physiopathology: An Approach in Two Affected Siblings
by Raquel Barbero-Herranz, María Garriga-García, Ana Moreno-Blanco, Esther Palacios, Pedro Ruiz-Sala, Saioa Vicente-Santamaría, Sinziana Stanescu, Amaya Belanger-Quintana, Guillem Pintos-Morell, Beatriz Arconada, Rosa del Campo and José Avendaño-Ortiz
Int. J. Mol. Sci. 2024, 25(16), 8856; https://doi.org/10.3390/ijms25168856 - 14 Aug 2024
Abstract
Sanfilippo syndrome, or mucopolysaccharidosis type III (MPS III), is a rare lysosomal disease caused by congenital enzymatic deficiencies in heparan sulfate (HS) degradation, leading to organ dysfunction. The most severe hallmark of MPS III comprises neurological alterations, although gastrointestinal symptoms (GISs) have also [...] Read more.
Sanfilippo syndrome, or mucopolysaccharidosis type III (MPS III), is a rare lysosomal disease caused by congenital enzymatic deficiencies in heparan sulfate (HS) degradation, leading to organ dysfunction. The most severe hallmark of MPS III comprises neurological alterations, although gastrointestinal symptoms (GISs) have also been shown to be relevant in many patients. Here, we explored the contribution of the gut microbiota to MPS III GISs. We analyzed the composition and functionality of the gut microbiota in two MPS III siblings with the same mutation (c.544C > T, c.1080delC, in the SGSH gene) and the same diet, but with differences in their GISs, including recurrent diarrhea in one of them. Using 16S sequencing, we observed that the MPS III patients exhibited decreased alpha diversity and a lower abundance of Lachnospiraceae and Bifidobacteriaceae accompanied by a higher abundance of the Ruminococcaceae and Rikenellaceae families than the healthy control subjects. Comparing siblings, we found an increased abundance of Bacteroidaceae and a lower abundance of Ruminococcaceae and Akkermansiaceae in the GIS-free patient. This patient also had a higher relative abundance of Sus genes (SusA, SusB, SusE, and SusG) involved in glycosaminoglycan metabolism. We found higher HS levels in the stool of the two MPS III patients than in healthy volunteers, particularly in the patient with GISs. Functionally, whole fecal metabolites from the patient with GISs induced oxidative stress in vitro in healthy monocytes. Finally, the Bacteroides thetaiotaomicron strain isolated from MPS III stool samples exhibited HS degradation ability. Overall, our results reveal different microbiota compositions and functionalities in MPS III siblings, who exhibited differential gastrointestinal symptomatology. Our study may serve as a gateway to explore the impact of the gut microbiota and its potential to enhance the quality of life in Sanfilippo syndrome patients. Full article
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<p>Analysis of gut microbiota in <span class="underline">h</span>ealthy <span class="underline">v</span>olunteers (HVs) and patients with Sanfilippo syndrome (MPS III). (<b>A</b>) The alpha diversity, Chao1, Shannon, and Faith PD indexes and the principal coordinates analysis (PCoA) plot of Bray−Curtis beta diversity are shown. Microbial composition was analyzed by 16S rRNA amplicon sequencing of feces from 4 HVs and the MPS III siblings included in the study. Relative abundance of families (<b>B</b>) and the 20 most abundant genera (<b>C</b>). f__, family; GIS, gastrointestinal symptoms; g__, genus.</p>
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<p>Relative abundance of PUL (<span class="html-italic">SusA</span>, <span class="html-italic">SusB</span>, <span class="html-italic">SusE</span>, <span class="html-italic">and SusG</span>) genes assessed by qPCR from stool samples of MPS III siblings and healthy volunteers. GIS, gastrointestinal symptoms; HV, healthy volunteers; MPS III, Sanfilippo syndrome siblings. Each dot represents the average of 3 technical replicates and bars are expressed as mean ± SD. HV, <span class="html-italic">n</span> = 4 stool samples from 4 different healthy volunteers; GIS+, <span class="html-italic">n</span> = 2 two different day samples from the GIS+ MPS III patient.; GIS−, <span class="html-italic">n</span> = 2 two different day stool samples from the GIS+ MPS III patient.</p>
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<p>Fecal levels of heparan sulfate (HS) (<b>A</b>), acetate (<b>B</b>), propionate (<b>C</b>), and butyrate (<b>D</b>) were determined by ELISA and gas chromatography coupled with mass spectrometry (GC-MS), respectively. Each dot represents the average of 3 technical replicates and bars are expressed as mean ± SD. HV, <span class="html-italic">n</span> = 4 stool samples from 4 different healthy volunteers; GIS+, <span class="html-italic">n</span> = 2 two different day samples from the GIS+ MPS III patient.; GIS−, <span class="html-italic">n</span> = 2 two different day stool samples from the GIS+ MPS III patient. GIS, gastrointestinal symptoms; HV, healthy volunteers; MPS III, Sanfilippo syndrome siblings.</p>
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<p>Effects of MPS III fecal metabolites on healthy monocytes. Monocytes from 5 healthy volunteers’ peripheral blood were isolated and stimulated for 24 h with fecal metabolites from patients with MPS III. (<b>A</b>) Oxidative stress in gated monocytes established by Green CellROX staining was analyzed by means of flow cytometry. Levels of IL-1β (<b>B</b>), IL-6 (<b>C</b>), and TNF-α (<b>D</b>) in monocyte culture supernatant are shown. Each dot represents the average from experiments with 5 independent human healthy monocytes and bars are expressed as mean ± SD. HV, <span class="html-italic">n</span> = 4 stool samples from 4 different healthy volunteers; GIS+, <span class="html-italic">n</span> = 2 two different day stool samples from the GIS+ MPS III patient.; GIS−, <span class="html-italic">n</span> = 2 two different day samples from the GIS+ MPS III patient. Unst, unstimulated.</p>
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<p>HS degradation activity of bacteria isolated from the stool of MPS III patients. <span class="html-italic">Bacteroides</span> spp. strains were isolated from stool samples of the two MPS III siblings included in this study. Bacteria were cultured in the presence of 75 µg/mL of HS at 37 °C under anaerobic conditions for 48 h. (<b>A</b>) Total GAG in the culture supernatant determined using the 1,9-dimethylmethylene blue procedure is shown. (<b>B</b>) Percentage of total GAG normalized to the PBS control. Bf, <span class="html-italic">Bacteroides fragilis</span>; Bt, <span class="html-italic">Bacteroides thetaiotaomicron</span>; n.d., not detected. KW, Kruskal–Wallis statistic; * <span class="html-italic">p</span>-value &lt; 0.05 and *** <span class="html-italic">p</span>-value &lt; 0.001 analyzed using the Kruskal–Wallis ANOVA test followed by Dunn’s multiple comparisons test. Data are expressed as mean ± SD from <span class="html-italic">n</span> = 4 independent experiments.</p>
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17 pages, 9350 KiB  
Article
The Utilization of Rice Husk as Both the Silicon Source and Mesoporous Template for the Green Preparation of Mesoporous TiO2/SiO2 and Its Excellent Catalytic Performance in Oxidative Desulfurization
by Xiaoxue Liu, Lanfen Zhang, Jian Hu, Wei Zhang, Xiaorong Xiang, Huiqing Cheng, Li Qin and Hao Li
Molecules 2024, 29(16), 3856; https://doi.org/10.3390/molecules29163856 - 14 Aug 2024
Abstract
In recent years, TiO2-based catalysts have received extensive attention from researchers for their excellent oxidative desulfurization (ODS) performances. In this paper, a series of mesoporous TiO2/SiO2 catalysts with different TiO2 loadings are prepared, using an incipient wetness [...] Read more.
In recent years, TiO2-based catalysts have received extensive attention from researchers for their excellent oxidative desulfurization (ODS) performances. In this paper, a series of mesoporous TiO2/SiO2 catalysts with different TiO2 loadings are prepared, using an incipient wetness impregnation method with agricultural waste rice husk as both the silicon source and mesoporous template and tetrabutyl titanate as the titanium source. The effect of different TiO2 loadings on the ODS performance of the samples is investigated, and the appropriate TiO2 loading is 2.5%. Compared with pure TiO2, the 2.5%TiO2/SiO2 sample exhibits high catalytic activity for oxidative desulfurization. This is, on the one hand, due to the high specific surface area and mesopore volume of the 2.5%TiO2/SiO2 sample. On the other hand, it is due to the uniform dispersion of TiO2 grains with an average diameter of 6.1 nm on the surface of the mesoporous SiO2 carrier, which greatly increases the active sites of the 2.5%TiO2/SiO2 sample, thus improving the catalytic activity of the sample. The recycling performances of the 2.5%TiO2/SiO2 sample are further investigated. The results show that, after fifteen cycles, the 2.5%TiO2/SiO2 sample still maintains high conversions of dibenzothiophene (99.8%) and 4,6-dimethyldibenzothiophene (99.7%) without deactivation. In addition, the 2.5%TiO2/SiO2 sample treated with TBHP aqueous solution is characterized by the technique of UV-Vis, and the Ti-peroxo (Ti-OOtBu) species, the active intermediate for the ODS of bulky organic sulfides, is successfully captured. Finally, a possible reaction mechanism for the ODS process over the 2.5%TiO2/SiO2 sample is proposed. Full article
(This article belongs to the Special Issue Functional Nanomaterials in Green Chemistry, 2nd Edition)
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<p>The XRD patterns of the SiO<sub>2</sub>-RH, pure TiO<sub>2</sub>, and TS-RH-x samples (<b>a</b>), and the fresh and regenerated TS-RH-2.5 samples (<b>b</b>): (1) SiO<sub>2</sub>-RH, (2) TS-RH-0.5, (3) TS-RH-1.0, (4) TS-RH-2.5, (5) TS-RH-5.0, (6) TS-RH-10, (7) pure TiO<sub>2</sub>, (8) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (9) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>UV-Vis spectra of the pure TiO<sub>2</sub>, and TS-RH-x samples (<b>a</b>), and the fresh and regenerated TS-RH-2.5 samples, and oxidation products of DBT and 4,6-DMDBT (<b>b</b>): (1) TS-RH-0.5, (2) TS-RH-1.0, (3) TS-RH-2.5, (4) TS-RH-5.0, (5) TS-RH-10, (6) pure TiO<sub>2</sub>, (7) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, (8) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT, (9) oxidation product of DBT, and (10) oxidation product of 4,6-DMDBT.</p>
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<p>N<sub>2</sub> adsorption–desorption isotherms (<b>a</b>,<b>c</b>) and pore size distribution curves (<b>b</b>,<b>d</b>) of the samples: (1) SiO<sub>2</sub>-RH, (2) TS-RH-0.5, (3) TS-RH-1.0, (4) TS-RH-2.5, (5) TS-RH-5.0, (6) TS-RH-10, (7) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (8) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>N<sub>2</sub> adsorption–desorption isotherms (<b>a</b>,<b>c</b>) and pore size distribution curves (<b>b</b>,<b>d</b>) of the samples: (1) SiO<sub>2</sub>-RH, (2) TS-RH-0.5, (3) TS-RH-1.0, (4) TS-RH-2.5, (5) TS-RH-5.0, (6) TS-RH-10, (7) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (8) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>SEM images of the samples: (<b>a</b>) TiO<sub>2</sub>, (<b>b</b>) SiO<sub>2</sub>-RH, (<b>c</b>) TS-RH-2.5, (<b>d</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (<b>e</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>EDS elemental mappings of the samples: (<b>a</b>) TS-RH-2.5, (<b>b</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (<b>c</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>EDS elemental mappings of the samples: (<b>a</b>) TS-RH-2.5, (<b>b</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (<b>c</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>TEM images of the samples: (<b>a</b>) SiO<sub>2</sub>-RH, (<b>b</b>) TS-RH-2.5, (<b>c</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (<b>d</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>Particle size distribution histograms of the samples: (<b>a</b>) TS-RH-2.5, (<b>b</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, and (<b>c</b>) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT.</p>
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<p>Effect of reaction time on the ODS of DBT and 4,6-DMDBT model oils catalyzed by the TS-RH-2.5 sample. Reaction conditions: model oils, 10 mL; catalyst to oil ratio, 10.0 g/L; TBHP/S molar ratio, 2.1; and temperature, 333 K.</p>
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<p>FT-IR spectra of the reactants and their corresponding products: (<b>a</b>) DBT and its oxidation product and (<b>b</b>) 4,6-DMDBT and its oxidation product.</p>
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<p>LC-MS spectra of the oxidation products of DBT (<b>a</b>) and 4,6-DMDBT (<b>b</b>).</p>
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<p>Recycle tests for the ODS of DBT and 4,6-DMDBT model oils over the TS-RH-2.5c samples.</p>
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<p>UV-Vis spectra of fresh TS-RH-2.5 and TS-RH-2.5c samples: (1) fresh TS-RH-2.5, (2) fresh TS-RH-2.5 treated with TBHP, (3) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT, (4) TS-RH-2.5c regenerated from the 15th ODS reaction of DBT and treated with TBHP, (5) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT, and (6) TS-RH-2.5c regenerated from the 15th ODS reaction of 4,6-DMDBT and treated with TBHP.</p>
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<p>The standard curves of DBT (<b>a</b>) and 4,6-DMDBT (<b>b</b>) model oils.</p>
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<p>The absorption spectra of DBT (<b>a</b>) and 4,6-DMDBT (<b>b</b>) model oils before and after the ODS reaction catalyzed by the TS-RH-2.5 sample: (1) DBT model oil before the reaction diluted 2000 times, (2) DBT model oil after the reaction diluted 2000 times, (3), 4,6-DMDBT model oil before the reaction diluted 2000 times, and (4) 4,6-DMDBT model oil after the reaction diluted 2000 times.</p>
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<p>Schematic representation of the reaction mechanism and process flow for the oxidative removal of DBT and 4,6-DMDBT in the TS-RH-2.5 and TBHP catalytic system (R represents H or CH<sub>3</sub>).</p>
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19 pages, 1864 KiB  
Article
Effects of Pulsed Electromagnetic Field Treatment on Skeletal Muscle Tissue Recovery in a Rat Model of Collagenase-Induced Tendinopathy: Results from a Proteome Analysis
by Enrica Torretta, Manuela Moriggi, Daniele Capitanio, Carlotta Perucca Orfei, Vincenzo Raffo, Stefania Setti, Ruggero Cadossi, Laura de Girolamo and Cecilia Gelfi
Int. J. Mol. Sci. 2024, 25(16), 8852; https://doi.org/10.3390/ijms25168852 - 14 Aug 2024
Abstract
Tendon disorders often result in decreased muscle function and atrophy. Pulsed Electromagnetic Fields (PEMFs) have shown potential in improving tendon fiber structure and muscle recovery. However, the molecular effects of PEMF therapy on skeletal muscle, beyond conventional metrics like MRI or markers of [...] Read more.
Tendon disorders often result in decreased muscle function and atrophy. Pulsed Electromagnetic Fields (PEMFs) have shown potential in improving tendon fiber structure and muscle recovery. However, the molecular effects of PEMF therapy on skeletal muscle, beyond conventional metrics like MRI or markers of muscle decline, remain largely unexplored. This study investigates the metabolic and structural changes in PEMF-treated muscle tissue using proteomics in a rat model of Achilles tendinopathy induced by collagenase. Sprague Dawley rats were unilaterally induced for tendinopathy with type I collagenase injection and exposed to PEMFs for 8 h/day. Gastrocnemius extracts from untreated or PEMF-treated rats were analyzed with LC-MS/MS, and proteomics differential analysis was conducted through label-free quantitation. PEMF-treated animals exhibited decreased glycolysis and increased LDHB expression, enhancing NAD signaling and ATP production, which boosted respiratory chain activity and fatty acid beta-oxidation. Antioxidant protein levels increased, controlling ROS production. PEMF therapy restored PGC1alpha and YAP levels, decreased by tendinopathy. Additionally, myosins regulating slow-twitch fibers and proteins involved in fiber alignment and force transmission increased, supporting muscle recovery and contractile function. Our findings show that PEMF treatment modulates NAD signaling and oxidative phosphorylation, aiding muscle recovery through the upregulation of YAP and PGC1alpha and increasing slow myosin isoforms, thus speeding up physiological recovery. Full article
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<p>Experimental design and label-free LC–ESI–MS/MS results. (<b>A</b>) Untreated rats. Type I collagenase was injected into the right limbs (COL), while PBS was injected into their left counterparts (PBS). Animals were sacrificed on day 21, 30, and 45 after the injection. Based on this, right muscles (COL) were named COL21, COL30, and COL45, while left muscles (PBS) were named PBS21, PBS30, and PBS45. (<b>B</b>) PEMF-treated rats. Animals were treated with PEMFs (1.5 mT SD 0.2; 75 Hz) for eight hours/day. Right muscles (COL + PEMF) were named COL + PEMF21, COL + PEMF30, and COL + PEMF45. (<b>C</b>) Venn diagram. Comparisons of shared and distinct significantly changed proteins in COL vs. PBS (dusty blue circles) and in COL + PEMF and COL (pink circles). Data resulted from label-free quantitation after LC–ESI–MS/MS analysis (ANOVA followed by Tukey’s multiple comparison test, <span class="html-italic">p</span>-value &lt; 0.05). The graphical illustration was generated using BioRender (version 4).</p>
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<p>Glucose and stress metabolism. (<b>A</b>) Summary of changed metabolic enzymes in glucose metabolism in muscles attached to inflamed tendons, both without (COL) and with PEMF treatment (PEMF). (<b>B</b>) Heatmap illustrating the expression profile of significantly increased (in red) or decreased (in green) enzymes (ANOVA and Tukey’s test, <span class="html-italic">p</span>-value &lt; 0.05) involved in glucose metabolism and stress response pathways. The graphical illustration was generated using BioRender (version 4).</p>
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<p>TCA cycle, fatty acid oxidation, and oxidative phosphorylation pathways. (<b>A</b>,<b>B</b>) Heatmaps illustrating the expression profile of significantly increased (in red) or decreased (in green) enzymes (ANOVA and Tukey’s test, <span class="html-italic">p</span>-value &lt; 0.05) involved in TCA cycle, fatty acid oxidation (<b>A</b>), and oxidative phosphorylation (<b>B</b>) pathways. (<b>C</b>) Graphical representation of metabolic canonical pathways: activated (z-score &gt; 2; orange arrows) or inhibited (z-blue &lt; 2; blue arrows) in muscles attached to inflamed tendons, without (COL) and with PEMF treatment (PEMF). (<b>D</b>) Heatmap displaying the expression profile of enzymes involved in the NAD signaling pathway. (<b>E</b>) Heatmap presenting the most significant upstream regulators. Orange- and blue-colored rectangles indicate predicted regulator activation or inhibition, respectively, via the z-score statistic. (<b>F</b>,<b>G</b>) Bar graphs depicting the expression of Yes-Associated Protein (YAP) (<b>F</b>) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1alpha) (<b>G</b>) in the <span class="html-italic">gastrocnemius</span> muscle from PBS, COL, and COL + PEMF groups (mean ± SD; * = significant difference, ANOVA and Tukey’s test, <span class="html-italic">n</span> = 2, * <span class="html-italic">p</span>-value &lt; 0.05; ** <span class="html-italic">p</span>-value &lt; 0.01; *** <span class="html-italic">p</span>-value &lt; 0.001). Full-length images are available in <a href="#app1-ijms-25-08852" class="html-app">Supplementary Figure S1</a>. The graphical illustration was generated using BioRender (version 4).</p>
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<p>Muscle fiber characterization and contractile proteins. (<b>A</b>–<b>C</b>) Bar graphs showing the distribution of myosin heavy chain (MyHC) isoforms in untreated and PEMF-treated animals sacrificed at 21 days (<b>A</b>), 30 days (<b>B</b>), and 45 days (<b>C</b>) after collagenase injection. ANOVA and Tukey’s test, <span class="html-italic">n</span> = 3, * <span class="html-italic">p</span>-value &lt; 0.05; ** <span class="html-italic">p</span>-value &lt; 0.01; *** <span class="html-italic">p</span>-value &lt; 0.001. Representative gel images are displayed. (<b>D</b>–<b>G</b>) Heatmaps illustrating the expression profile and % fold changes in significantly increased (in red) or decreased (in green) proteins (ANOVA and Tukey’s test, <span class="html-italic">p</span>-value &lt; 0.05) in sarcomere structures: thin filaments (<b>D</b>), thick filaments (<b>E</b>), M line (<b>F</b>), and Z disk (<b>G</b>). Full-length images are available in <a href="#app1-ijms-25-08852" class="html-app">Supplementary Figure S2</a>. The graphical illustration was generated using BioRender (version 4).</p>
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15 pages, 1616 KiB  
Article
Changes in Lipid Metabolites and Enzyme Activities of Wheat Flour during Maturation
by Yanyan Chen, Yingtao Yu, Xin An, Huihui Zhang, Wei Gong, Ying Liang and Jinshui Wang
Foods 2024, 13(16), 2537; https://doi.org/10.3390/foods13162537 - 14 Aug 2024
Abstract
The maturation of wheat flour is a transformative process that elevates its processing and culinary attributes to their peak performance levels. Despite extensive research on starch and gluten protein modifications, the impact of lipid changes has been largely unexplored. This study addresses this [...] Read more.
The maturation of wheat flour is a transformative process that elevates its processing and culinary attributes to their peak performance levels. Despite extensive research on starch and gluten protein modifications, the impact of lipid changes has been largely unexplored. This study addresses this gap by examining the maturation of freshly milled wheat flour at 15 °C, 25 °C, and 40 °C over 60 days, focusing on enzymatic activities—lipase, lipoxidase, and catalase—and lipid metabolites, including free fatty acids, conjugated trienes, p-anisidine value, and total oxidation value. The results of this study showed that free fatty acids continued to increase at all temperatures, with the most significant increase of 50% at 15 °C. The p-anisidine value followed a pattern of initial increase followed by a decline, while conjugated trienes were markedly higher at 40 °C, suggesting temperature’s significant influence on lipid peroxidation. Notably, total oxidation values became erratic post 30 days, indicating a shift in oxidative dynamics. This study underscores the correlation between lipid metabolites and enzymatic activities, revealing the enzymes’ pivotal role in lipid oxidation. The interplay of temperature and time offers valuable insights for optimizing wheat flour maturation, ensuring superior quality for various applications. Full article
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<p>Change in free fatty acid content of wheat flour samples in the maturation process, the lowercase letters indicate significant differences in the same sample at different maturation times at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Changing the conjugated triene value of wheat flour samples during the maturation process, the lowercase letters denote significant differences between maturation times at the same maturation temperature at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Changing of <span class="html-italic">p</span>-anisidine value in wheat flour samples during the maturation process, the lowercase letters indicate significant differences between maturation times at the same maturation temperature, and uppercase letters indicate significant differences between maturation temperatures at the same maturation time (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changing of total oxidation value of wheat flour samples during the maturation process, the lowercase letters indicate significant differences between maturation times at the same maturation temperature, and uppercase letters indicate significant differences between maturation temperatures at the same maturation time (<span class="html-italic">p</span> &lt; 0.05).</p>
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<p>Changing pattern of endogenous lipase activity in wheat flour during maturation, the lowercase letters denote significant differences between maturation times at the same maturation temperature at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Changing pattern of endogenous lipoxygenase activity in wheat flour during maturation, the lowercase letters denote significant differences between maturation times at the same maturation temperature at <span class="html-italic">p</span> &lt; 0.05.</p>
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<p>Changing pattern of endogenous catalase activity in wheat flour during maturation, the lowercase letters indicate significant differences between maturation times at the same maturation temperature, and uppercase letters indicate significant differences between maturation temperatures at the same maturation time (<span class="html-italic">p</span> &lt; 0.05).</p>
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20 pages, 4448 KiB  
Article
Biogenic Synthesis Based on Cuprous Oxide Nanoparticles Using Eucalyptus globulus Extracts and Its Effectiveness for Removal of Recalcitrant Compounds
by Pablo Salgado, Katherine Márquez and Gladys Vidal
Catalysts 2024, 14(8), 525; https://doi.org/10.3390/catal14080525 - 14 Aug 2024
Abstract
Recalcitrant compounds resulting from anthropogenic activity are a significant environmental challenge, necessitating the development of advanced oxidation processes (AOPs) for effective remediation. This study explores the synthesis of cuprous oxide nanoparticles on cellulose-based paper (Cu2O@CBP) using Eucalyptus globulus leaf extracts, leveraging [...] Read more.
Recalcitrant compounds resulting from anthropogenic activity are a significant environmental challenge, necessitating the development of advanced oxidation processes (AOPs) for effective remediation. This study explores the synthesis of cuprous oxide nanoparticles on cellulose-based paper (Cu2O@CBP) using Eucalyptus globulus leaf extracts, leveraging green synthesis techniques. The scanning electron microscopy (SEM) analysis found the average particle size 64.90 ± 16.76 nm, X-ray diffraction (XRD) and Raman spectroscopy confirm the Cu2O structure in nanoparticles; Fourier-transform infrared spectroscopy (FTIR) suggests the reducing role of phenolic compounds; and ultraviolet–visible diffuse reflectance spectroscopy (UV-Vis DRS) allowed us to determine the band gap (2.73 eV), the energies of the valence band (2.19 eV), and the conduction band (−0.54 eV) of Cu2O@CBP. The synthesized Cu2O catalysts demonstrated efficient degradation of methylene blue (MB) used as a model as recalcitrant compounds under LED-driven visible light photocatalysis and heterogeneous Fenton-like reactions with hydrogen peroxide (H2O2) using the degradation percentage and the first-order apparent degradation rate constant (kapp). The degradation efficiency of MB was pH-dependent, with neutral pH favoring photocatalysis (kapp = 0.00718 min−1) due to enhanced hydroxyl (·OH) and superoxide radical (O2·) production, while acidic pH conditions improved Fenton-like reaction efficiency (kapp = 0.00812 min−1) via ·OH. The reusability of the photocatalysts was also evaluated, showing a decline in performance for Fenton-like reactions at acidic pH about 22.76% after five cycles, while for photocatalysis at neutral pH decline about 11.44% after five cycles. This research provides valuable insights into the catalytic mechanisms and supports the potential of eco-friendly Cu2O nanoparticles for sustainable wastewater treatment applications. Full article
(This article belongs to the Section Photocatalysis)
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<p>Photographic images of (<b>a</b>) pristine cellulose-based paper and (<b>b</b>) Cu<sub>2</sub>O@CBP for 4 × 4 cm pieces.</p>
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<p>SEM images of (<b>a</b>) pristine paper, (<b>b</b>) Cu<sub>2</sub>O@CBP, and (<b>c</b>) particle size distribution of Cu<sub>2</sub>O@CBP (The red line represents the best curve fitting using the Gaussian distribution function).</p>
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<p>(<b>a</b>) Raman spectra for Cu<sub>2</sub>O@CBP (red numbers for Cu<sub>2</sub>O nanoparticles, green numbers for phenolic compounds, and black numbers for cellulose), (<b>b</b>) XRD patterns of pristine cellulose-based paper and Cu<sub>2</sub>O@CBP.</p>
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<p>FTIR analyses for pristine cellulose-based paper and Cu<sub>2</sub>O@CBP.</p>
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<p>(<b>a</b>) Band gap energy (E<sub>g</sub>) determination from the Tauc plot (green line) for Cu<sub>2</sub>O@CBP. The linear part of the plot is extrapolated to the x-axis using a dotted line for E<sub>g</sub> determination. (inset graph: DRS spectra for Cu<sub>2</sub>O@CBP). (<b>b</b>) Potential band diagram for Cu<sub>2</sub>O@CBP.</p>
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<p>Analysis of (<b>a</b>) total phenolic compounds, (<b>b</b>) total reducing sugars, (<b>c</b>) total proteins, (<b>d</b>) FRAP, and (<b>e</b>) CUPRAC in <span class="html-italic">E. globulus</span> extract before and after the synthesis of Cu<sub>2</sub>O@CBP. Differences between groups were compared using ANOVA with Tukey post hoc analysis. **** <span class="html-italic">p</span> &lt; 0.0001, ns: no significant differences.</p>
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<p>FTIR spectra of <span class="html-italic">E. globulus</span> extract before (black spectra) and after synthesis (green spectra) of Cu<sub>2</sub>O@CBP.</p>
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<p>MB removal efficiency by (<b>a</b>) photocatalysis under LED visible light and (<b>b</b>) Fenton-like reaction catalyzed by Cu<sub>2</sub>O@CBP at pH 3.0 and 7.0 (inset: legend represents samples at different pH). (<b>c</b>) Photocatalytic and (<b>d</b>) Fenton-like calculated degradation rate constant (<span class="html-italic">k<sub>app</sub></span>) for Cu<sub>2</sub>O@CBP at pH 3.0 and 7.0 (inset: legend represents samples at different pH, <span class="html-italic">k<sub>app</sub></span>, and r<sup>2</sup> of a pseudo-first order model).</p>
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<p>Cycling performance of Cu<sub>2</sub>O@CBP for MB degradation by (<b>a</b>) photocatalysis under LED visible light at pH = 7.0 and (<b>b</b>) Fenton-like at pH = 3.0 under dark. The data obtained are presented as mean ± standard deviation.</p>
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<p>MB removal by Cu<sub>2</sub>O@CBP under influence of scavenging agents (<b>a</b>) Na<sub>2</sub>C<sub>2</sub>O<sub>4</sub>, CrO<sub>3</sub>, BQ, and IP on photocatalytic degradation under LED visible light, and (<b>b</b>) BQ and IP on Fenton-like under darkness. The data obtained are presented as mean ± standard deviation.</p>
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<p>Scheme of Fenton-like reaction at acidic pH under dark and photocatalysis at neutral pH under LED visible light to generate reactive species and MB degradation process.</p>
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<p>(<b>a</b>) Internal view and (<b>b</b>) view from above of the reactor used for photocatalysis and Fenton-like reaction degradation of MB by Cu<sub>2</sub>O@CBP.</p>
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15 pages, 1895 KiB  
Article
Fish Oil Containing Pro-Resolving Mediators Enhances the Antioxidant System and Ameliorates LPS-Induced Inflammation in Human Bronchial Epithelial Cells
by Alfio Distefano, Laura Orlando, Sebastiano Giallongo, Emanuela Tropea, Mariarita Spampinato, Annalisa Santisi, Lucia Longhitano, Giuseppe Parisi, Salvatore Leonardi, Arcangelo Russo, Massimo Caruso, Michelino Di Rosa, Daniele Tibullo, Maurizio Salamone, Giovanni Li Volti and Ignazio Alberto Barbagallo
Pharmaceuticals 2024, 17(8), 1066; https://doi.org/10.3390/ph17081066 - 14 Aug 2024
Abstract
Fish oil, renowned for its high content of omega-3 fatty acids, particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), has gained considerable attention for its potential health benefits. EPA and DHA exhibit anti-inflammatory effects by promoting the production of specialized pro-resolving mediators (SPMs), [...] Read more.
Fish oil, renowned for its high content of omega-3 fatty acids, particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), has gained considerable attention for its potential health benefits. EPA and DHA exhibit anti-inflammatory effects by promoting the production of specialized pro-resolving mediators (SPMs), such as resolvins and protectins. Fish oil has been studied for its potential to reduce bronchial inflammation, a key feature of respiratory conditions like asthma and COPD. This study investigates the cellular mechanisms of fish oil in an in vitro model of lung inflammation using lipopolysaccharide (LPS) on a healthy human bronchial epithelium cell line. LPS exposure for 24 h reduced cell viability, elevated reactive oxygen species (ROS), depleted glutathione (GSH), and induced mitochondrial depolarization, indicating oxidative stress and inflammation. Fish oil administration significantly mitigated ROS production, prevented GSH depletion, and reduced mitochondrial depolarization. This was associated with the upregulation of the endogenous antioxidant system, evidenced by restored GSH levels and the increased gene expression of glutathione peroxidase (GPX), catalase (CAT), superoxide dismutase 1 (SOD1), and superoxide dismutase 2 (SOD2). Fish oil also suppressed IL-6 and IL-1β expression and increased anti-inflammatory cytokine IL-10 expression. Furthermore, fish oil upregulated the expression of pro-resolving mediator receptors, suggesting a role in inflammation resolution. These findings highlight the potential of fish oil supplementation as a preventive measure against pulmonary diseases characterized by unresolved inflammation such as lung inflammation. Full article
(This article belongs to the Special Issue New Therapeutic Opportunities for Epigenetic Drugs)
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<p>Biosynthetic pathways of specialized pro-resolving mediators (SPMs). Lipoxins (LxA4 and LxB4) are produced from AA, E-series of resolvins (RvE1, RvE2, and RvE3) are produced from EPA, and D-series of resolvins (RvD1, RvD2, RvD3, RvD4, RvD5, and RvD6), protectins (PD1 and PDX), and maresins (MaR1 and MaR2) are produced from DHA. HpEPE: hydroperoxyeicosapentaenoic acid; HpDHA: hydroperoxydocosahexaenoic acid.</p>
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<p>FO and LPS impact on cell viability. (<b>A</b>) FO supplementation at 100 mg/mL decreases BEAS viability. MTT assay quantification detecting cell viability following FO treatment at 10, 50, and 100 μg/mL. BSA condition was included given its role as FO vehicle. (<b>B</b>) LPS supplementation hampers BEAS viability following 24 h treatment. Histograms are representative of MTT assay performed on BEAS treated with 1 and 10 μg/mL LPS at different timepoints. (<b>C</b>) FO supplementation recovers LPS-induced cell death. Quantification of MTT test assessing cell viability following FO 10 μg/mL, LPS 10 μg/mL single treatments, and their combination. Histograms are representative of 4 biological replicates. (* <span class="html-italic">p</span> ≤ 0.05; *** <span class="html-italic">p</span> ≤ 0.001; **** <span class="html-italic">p</span> ≤ 0.0001 compared to CTRL. #### <span class="html-italic">p</span> ≤ 0.0001 compared to LPS).</p>
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<p>FO supplementation recovers cells’ LPS-induced mitochondrial potential loss and oxidative stress. (<b>A</b>) FO supplementation prevents LPS-induced JC-1 signal decrease. Representative images showing JC-1 assay in BEAS, supplemented with FO, LPS, and their combination. (<b>B</b>) FO recovers LPS-induced mitochondrial depolarization. Quantification of JC-1 signal as in (<b>A</b>). Histogram showing JC-1 quantification following BEAS treatment with FO, LPS, and their combination. (<b>C</b>) FO restores LPS-induced oxidative stress. Histogram showing ROS quantification by fluoresceine fluorescence measurement following BEAS treatment with FO, LPS, and their combination. Histograms are representative of 4 biological replicates. (** <span class="html-italic">p</span> ≤ 0.01; **** <span class="html-italic">p</span> ≤ 0.0001 compared to CTRL; ## <span class="html-italic">p</span> ≤ 0.01; #### <span class="html-italic">p</span> ≤ 0.0001 compared to LPS).</p>
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<p>FO recovers cellular ROS scavenging ability. (<b>A</b>) FO supplementation implement GSH production upon LPS treatment. Histogram showing GSH quantification in BEAS following treatment with FO, LPS, and their combination. RT-PCR evaluating the expression GPX (<b>B</b>), CAT (<b>C</b>), SOD2 (<b>D</b>), IL-6 (<b>E</b>), IL-10 (<b>F</b>), and TNF- α (<b>G</b>) following treatment with FO, LPS, and their combination. Histograms are representative of 4 biological replicates. (* <span class="html-italic">p</span> ≤ 0.05; ** <span class="html-italic">p</span> ≤ 0.01; *** <span class="html-italic">p</span> ≤ 0.001; **** <span class="html-italic">p</span> ≤ 0.0001 compared to CTRL. # <span class="html-italic">p</span> ≤ 0.05; ## <span class="html-italic">p</span> ≤ 0.01; ### <span class="html-italic">p</span> ≤ 0.001; #### <span class="html-italic">p</span> ≤ 0.0001 compared to LPS).</p>
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<p>FO effect relies on resolvin-mediated inflammation resolution. RT- PCR analysis showing PTGS1 (<b>A</b>), ALOX15 (<b>B</b>), FPR2 (<b>C</b>), and GPR32 (<b>D</b>) expression following BEAS supplementation with FO, LPS, and their combination. Histograms are representative of 4 biological replicates. (* <span class="html-italic">p</span> ≤ 0.05; *** <span class="html-italic">p</span> ≤ 0.001; **** <span class="html-italic">p</span> ≤ 0.0001 compared to CTRL. ### <span class="html-italic">p</span> ≤ 0.001; #### <span class="html-italic">p</span> ≤ 0.0001 compared to LPS).</p>
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