JP2008214191A - Agent for suppressing accumulation of lipid in liver - Google Patents
Agent for suppressing accumulation of lipid in liver Download PDFInfo
- Publication number
- JP2008214191A JP2008214191A JP2005130514A JP2005130514A JP2008214191A JP 2008214191 A JP2008214191 A JP 2008214191A JP 2005130514 A JP2005130514 A JP 2005130514A JP 2005130514 A JP2005130514 A JP 2005130514A JP 2008214191 A JP2008214191 A JP 2008214191A
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- JP
- Japan
- Prior art keywords
- liver
- lipid
- kuzuka
- accumulation
- suppressing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/48—Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
- A61K36/488—Pueraria (kudzu)
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
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- Medicines Containing Plant Substances (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
本発明は、葛花処理物を有効成分とする肝中脂質蓄積抑制剤に関する。 The present invention relates to a hepatic lipid accumulation inhibitor comprising as an active ingredient a kuzu flower treatment product.
葛はマメ科の植物であり、古くから葛澱粉として和菓子の原料に用いられるほか、その根及び花はそれぞれ葛根、葛花と称して解熱、鎮痛、鎮痙、発汗等の症状に対する漢方薬の原料として配合されてきた。また、葛花は、他のマメ科植物とはことなり、肝障害改善や二日酔い予防効果、尿窒素代謝改善効果等の効果を有することが明らかとなってきている(特許文献1〜3)。
しかし、葛花は、フラボノイドをはじめとした様々な成分を含有しているが、ごく限られた機能しか明らかになっていないため、葛花の用途は狭小であるという問題点があった。 However, Kuzuka contains various components including flavonoids, but only a limited function has been clarified, so there was a problem that the uses of Kuzuka are narrow.
また、近年は食生活の変化により、脂肪や糖分、アルコールの過剰摂取が原因で、肝臓に脂肪(中性脂肪やコレステロール、リン脂質などのうち、特に中性脂肪)が蓄積されることによって引き起こされる脂肪肝が増加している。近年では、アルコールを過剰に摂取していなくとも発症する非アルコール性脂肪肝が増加しており、問題となっている。さらに、脂肪肝は、肝硬変、糖尿病、高脂血症、高血圧、動脈硬化のリスクを高めることも指摘されている。 In recent years, due to dietary changes, fat (sugar, sugar, alcohol, especially neutral fat) is accumulated in the liver due to excessive intake of fat, sugar and alcohol. There is an increase in fatty liver. In recent years, non-alcoholic fatty liver disease that develops even without excessive intake of alcohol has increased and has become a problem. Furthermore, it has been pointed out that fatty liver increases the risk of cirrhosis, diabetes, hyperlipidemia, hypertension and arteriosclerosis.
本発明は、上記問題点に鑑みてなされたものであって、その目的は、葛花の新たな機能を見出すことにより、葛花の用途拡大をはかり、また、肝臓中(以下、肝中ということがある)の脂質改善剤を提供することにある。 The present invention has been made in view of the above-mentioned problems, and its purpose is to find out a new function of Kuzuka, thereby expanding the use of Kuzuka, and in the liver (hereinafter referred to as liver). A lipid improving agent.
本発明者は、葛花の機能性を鋭意検討したところ、葛花処理物は、優れた肝中脂質改善効果を有することを見出し、本発明を完成させるに至った。 As a result of intensive studies on the functionality of Kuzuka, the present inventor has found that the Kuzuka treated product has an excellent liver lipid improving effect, and has completed the present invention.
すなわち、本発明は、葛花処理物を有効成分とする肝中脂質蓄積抑制剤に関する。 That is, this invention relates to the lipid accumulation inhibitor in a liver which uses a Kuzuka processed material as an active ingredient.
また、本発明は、前記の肝中脂質蓄積抑制剤を含有する、食品組成物もしくは医薬品組成物に関する。 The present invention also relates to a food composition or a pharmaceutical composition containing the liver lipid accumulation inhibitor.
本発明の葛花処理物を有効成分とする肝中脂質蓄積抑制剤は、優れた肝中脂質改善効果を有する。 The hepatic lipid accumulation inhibitor containing the processed kuzuhana product of the present invention as an active ingredient has an excellent liver lipid improving effect.
従って、葛花の肝中脂質改善作用という新たな機能により、葛花の用途を拡大することができるとともに、優れた肝中脂質蓄積抑制剤も提供できる。 Therefore, the new function of Kuzuka's liver lipid improving action can expand the uses of Kuzuka and provide an excellent inhibitor of hepatic lipid accumulation.
以下、本発明の実施形態について説明する。葛花処理物を有効成分とする、肝中脂質蓄積抑制剤(以下、本発明の肝中脂質蓄積抑制剤ということがある)に関する。また、本発明は肝中脂質蓄積抑制剤を含有する、食品(以下、本発明の食品ということがある)に関する。なお、本発明は、下記の実施形態で制限されない。つまり、特許請求の範囲に記載されている内容の範囲内において、本発明は変更が可能である。 Hereinafter, embodiments of the present invention will be described. The present invention relates to a hepatic lipid accumulation inhibitor (hereinafter, also referred to as a hepatic lipid accumulation inhibitor of the present invention) comprising a processed kuzuhana product as an active ingredient. The present invention also relates to a food (hereinafter sometimes referred to as the food of the present invention) containing a liver lipid accumulation inhibitor. In addition, this invention is not restrict | limited by the following embodiment. That is, the present invention can be modified within the scope of the contents described in the claims.
(葛花処理物)
本発明の葛花処理物を有効成分とする肝中脂質蓄積抑制剤は、葛花を用いている。まず、葛花について簡単に説明する。
(Katsuhana treatment product)
The hepatic lipid accumulation inhibitor containing the processed kuzuka product of the present invention as an active ingredient uses kuzuka. First, Katsuhana will be briefly explained.
(葛花)
葛花は、葛植物の花部であり、近年では、フラボノイドやサポニン、トリプトファン配糖体を含有していることが知られている。このような葛花は、好ましくは、花が全開する前の蕾の段階で採集される。
(Katsuhana)
Kuzuka is the flower part of the Kuzu plant, and in recent years, it is known to contain flavonoids, saponins, and tryptophan glycosides. Such Kuzuka is preferably collected at the stage of buds before the flowers are fully opened.
本発明の肝中脂質蓄積抑制剤に用いる葛花処理物としては、例えば、葛花乾燥物または葛花抽出物を用いることができる。 As the processed kuzuka product used for the liver lipid accumulation inhibitor of the present invention, for example, a dried kuzuka product or a kuzuka extract can be used.
なお、「葛花乾燥物」と記載した場合は、葛花抽出物などは含まずに、葛花を乾燥して得られた物、例えば、葛花そのものを乾燥後破砕して得られた乾燥粉末などのことを意味することとする。 In addition, when it is described as “dried kuzuka”, it does not include kuzuka extract, but is obtained by drying kuzuka, for example, dried by crushing katsuka itself and then crushing it. It means powder.
また、「葛花抽出物」と記載した場合は、葛花の搾汁、葛花と溶媒とを用いて抽出して得られた抽出液などを含むものとする。さらに、「葛花抽出物」には、それら搾汁または抽出液を濃縮した物、および、それら搾汁または抽出液を乾燥して得られた乾燥物(葛花抽出物の乾燥粉末)も含まれることとする。 In addition, the term “Kuzuka extract” includes kuzuka juice, an extract obtained by extraction using Kuzuka and a solvent, and the like. Furthermore, “Kuzuka extract” includes a product obtained by concentrating the juice or extract, and a dried product obtained by drying the juice or extract (dry powder of Kuzuka extract). Suppose that
なお、本発明で用いられる葛花は、いかなる開花の段階で採集された葛花であっても良いが、全開する前の蕾の段階で採集された葛花であることが好ましい。このことは、葛花乾燥物を得る場合および葛花抽出物を得る場合においても、同様である。 The kuzuka used in the present invention may be kuzuka collected at any stage of flowering, but is preferably katsuka collected at the stage of wrinkles before full opening. The same applies to the case of obtaining a dried kuzu flower and a kuzu flower extract.
葛花乾燥物は、例えば、全開する前の蕾の段階で採集された葛花を、日干しや熱風乾燥等により乾燥することにより得られる。乾燥は、好ましくは、水分含有量が10質量%となるまで、またはそれ以下となるまで行われるのが良い。また、必要に応じて、葛花乾燥物は、さらに粉砕されて、粉末としても良い。 The dried kuzu flower is obtained, for example, by drying kuzu flowers collected at the stage of cocoon before fully opening by sun drying or hot air drying. Drying is preferably performed until the water content becomes 10% by mass or less. If necessary, the dried kuzu flower product may be further pulverized into a powder.
葛花乾燥物の粉末を得る場合において、その粉末化の方法としては、例えば、当業者が通常用いる方法、ボールミルやハンマーミル、ローラーミル等により、乾燥後の葛花を粉砕・粉末化する方法が挙げられる。もちろん、乾燥前の葛花をマスコロイダーやスライサー、コミトロールで予め粉砕しておき、この粉砕物を乾燥するといった方法でも良い。 In the case of obtaining a dried kuzuka powder, examples of the powdering method thereof include a method commonly used by those skilled in the art, and a method of pulverizing and pulverizing katsukaka after drying by a ball mill, a hammer mill, a roller mill, or the like. Is mentioned. Of course, a method of previously pulverizing katsuhana before drying with a mass collider, slicer, or comitorol and drying the pulverized product may be used.
葛花抽出物は、葛花に溶媒を添加して、必要に応じて加温しつつ、抽出により得ることができる。もちろん、遠心分離またはろ過により抽出液を回収して、抽出物を得てもよい。なお、抽出物を得る場合に用いる葛花は、乾燥前の葛花であってもよいが、乾燥後の葛花(例えば葛花の乾燥粉末)であることが好ましい。 The kuzu flower extract can be obtained by extraction while adding a solvent to kuzu flower and heating as necessary. Of course, the extract may be obtained by collecting the extract by centrifugation or filtration. In addition, although the kuzuka used when obtaining an extract may be the kuzuka before drying, it is preferable that it is the kuzuka after drying (for example, dry powder of kuzuka).
葛花抽出物を得る場合において、用いることができる溶媒としては、例えば、水、有機溶媒、含水有機溶媒などが挙げられる。また、ここでいう有機溶媒としては、メタノール、エタノール、n−プロパノール、n−ブタノール、アセトン、ヘキサン、シクロヘキサン、プロピレングリコール、エチルメチルケトン、グリセリン、酢酸メチル、酢酸エチル、ジエチルエーテル、ジクロロメタン、食用油脂、1,1,1,2−テトラフルオロエタン、および1,1,2−トリクロロエテン等が挙げられる。そのうち、葛花の抽出液を得る場合において好ましい有機溶媒は、極性有機溶媒、より好ましくはエタノール、n−ブタノール、メタノール、アセトン、プロピレングリコール、酢酸エチルであり、最も好ましくはエタノールである。 Examples of the solvent that can be used in obtaining the kuzuhana extract include water, an organic solvent, a water-containing organic solvent, and the like. Moreover, as an organic solvent here, methanol, ethanol, n-propanol, n-butanol, acetone, hexane, cyclohexane, propylene glycol, ethyl methyl ketone, glycerin, methyl acetate, ethyl acetate, diethyl ether, dichloromethane, edible fats and oils 1,1,1,2-tetrafluoroethane, 1,1,2-trichloroethene and the like. Among them, a preferable organic solvent for obtaining an extract of Kuzuka is a polar organic solvent, more preferably ethanol, n-butanol, methanol, acetone, propylene glycol, and ethyl acetate, and most preferably ethanol.
加温して抽出する場合、その方法としては、例えば、加熱還流等の加温抽出法や超臨界抽出法等が挙げられ、場合によっては加圧して加温を行ってもよい。加温する場合、葛花に添加した溶媒が揮発するのを防ぐ必要があるが、その加温における温度の下限値は、50℃以上、好ましくは70℃以上であり、その加温における温度の上限値は、130℃以下、好ましくは100℃以下とするのがよい。 In the case of extraction by heating, examples of the method include a heating extraction method such as heating and reflux, a supercritical extraction method, and the like. In some cases, heating may be performed by applying pressure. When heating, it is necessary to prevent the solvent added to Kuzuhana from volatilizing, but the lower limit of the temperature in the heating is 50 ° C. or higher, preferably 70 ° C. or higher. The upper limit is 130 ° C. or lower, preferably 100 ° C. or lower.
抽出にかかる時間は、葛花から十分に可溶性成分が抽出される時間であればよく、好ましくは30分〜48時間である。なお、加温を行わない、すなわち50℃未満で抽出を行う場合は、6時間〜48時間浸漬することが好ましく、50℃以上で加温する場合は、30分〜24時間加温すればよい。 The time required for extraction may be a time during which a soluble component is sufficiently extracted from Kuzuka, and is preferably 30 minutes to 48 hours. In addition, when heating is not performed, that is, when extraction is performed at less than 50 ° C., it is preferable to immerse for 6 to 48 hours, and when heating is performed at 50 ° C. or more, heating may be performed for 30 minutes to 24 hours. .
また、例えば有機溶媒を除去するなど、必要に応じて、得られた抽出物(抽出液)を、減圧濃縮や凍結乾燥等によって、濃縮または乾燥してもよい。もちろん、そのような濃縮された抽出物や乾燥された抽出物を、本発明の葛花として利用してもよい。 Further, for example, the obtained extract (extract) may be concentrated or dried by vacuum concentration, lyophilization, or the like as necessary, for example, by removing an organic solvent. Of course, such a concentrated extract or a dried extract may be used as the kuzu flower of the present invention.
このようにして得られた葛花抽出物は、イソフラボン類やサポニンを含有し得る。葛花抽出物に含有されるイソフラボン類は、好ましくは抽出物の乾燥質量に対し、3質量%以上、より好ましくは5質量%〜90質量%である。また、含有されるサポニンは、好ましくは1質量%以上、より好ましくは2質量%〜50質量%である。 The kuzu flower extract thus obtained can contain isoflavones and saponins. The isoflavones contained in the Kuzuhana extract are preferably 3% by mass or more, more preferably 5% by mass to 90% by mass, based on the dry mass of the extract. The saponin contained is preferably 1% by mass or more, more preferably 2% by mass to 50% by mass.
(本発明の肝中脂質蓄積抑制剤)
本発明の肝中脂質蓄積抑制剤は、葛花処理物を含有する。これらの成分を含有することにより、優れた肝中脂質蓄積抑制効果を得られる。これによって、非アルコール性脂肪肝の予防もしくは治療もし得る。さらに、後述の脂質吸収抑制成分または脂質代謝促進成分を添加すれば、その成分との相乗的な効果が期待できる。つまり、単に糖や脂質の吸収抑制成分や代謝促進成分との組合せよりも、葛花の成分と脂質吸収抑制成分または脂質代謝促進成分との組合せは、優れた効果が期待できる。
(Liver lipid accumulation inhibitor of the present invention)
The hepatic lipid accumulation inhibitor of the present invention contains a processed kuzuka product. By containing these components, an excellent effect of suppressing lipid accumulation in the liver can be obtained. This can also prevent or treat non-alcoholic fatty liver. Furthermore, if a lipid absorption inhibiting component or a lipid metabolism promoting component described later is added, a synergistic effect with that component can be expected. That is, the combination of the Kuzuka component and the lipid absorption suppressing component or the lipid metabolism promoting component can be expected to have an excellent effect, rather than simply combining the sugar or lipid absorption suppressing component or the metabolism promoting component.
これらの各成分の配合量には特に制限はない。しかし、葛花抽出物(乾燥質量)の配合量については、成人一日あたりにおける葛花抽出物(乾燥質量)の摂取量の下限値が、10mg以上となるように配合されるのが良い。また、成人一日あたりにおける葛花抽出物(乾燥質量)の摂取量の上限値が、3000mg以下、好ましくは1000mg以下となるように配合されるのが良い。 There is no restriction | limiting in particular in the compounding quantity of these each component. However, the amount of kuzuhana extract (dry mass) is preferably blended so that the lower limit of the intake amount of kuzuka extract (dry mass) per adult day is 10 mg or more. Moreover, it is good to mix | blend so that the upper limit of the intake of the kuzu flower extract (dry mass) per adult day may be 3000 mg or less, Preferably it is 1000 mg or less.
なお、葛花乾燥物の場合は、成人一日あたりにおける葛花乾燥物の摂取量の下限値が、0.1g以上となるように配合されるのがよく、成人一日あたりにおける葛花乾燥物の摂取量の上限値が、30g以下、好ましくは10g以下となるように配合されるのが良い。 In the case of dried kuzuka, it is preferable that the lower limit of the intake of dried kuzuka per adult is 0.1 g or more. The upper limit of the amount of food intake should be 30 g or less, preferably 10 g or less.
(本発明の食品)
本発明の食品は、肝中脂質蓄積抑制剤を含有する。つまり、葛花処理物を含有している。
(Food of the present invention)
The food of the present invention contains a liver lipid accumulation inhibitor. That is, it contains the Kuzuhana processed product.
葛花処理物等の配合量は、その形態や剤形によって異なるため、適宜調整されればよい。例えば、葛花抽出物の場合、食品100質量部に対して、葛花抽出物(乾燥質量)の下限値は、0.0001質量部以上、好ましくは0.01質量部以上とするのがよく、葛花抽出物(乾燥質量)の上限値は、50質量部以下、好ましくは30質量部以下とするのがよい。葛花乾燥物の場合、食品100質量部に対して、葛花乾燥物の下限値は、0.01質量部以上、好ましくは0.1質量部以上とするのがよく、葛花乾燥物の上限値は、80質量部以下、好ましくは50質量部以下とするのがよい。 Since the compounding quantity of katsuhana processed material etc. changes with the forms and dosage forms, what is necessary is just to adjust suitably. For example, in the case of Kuzuka extract, the lower limit value of Kuzuka extract (dry mass) is 0.0001 parts by mass or more, preferably 0.01 parts by mass or more with respect to 100 parts by mass of food. The upper limit of the Kuzuhana extract (dry mass) is 50 parts by mass or less, preferably 30 parts by mass or less. In the case of dried kuzuhana, the lower limit value of dried kuzuka is 0.01 parts by mass or more, preferably 0.1 parts by mass or more, with respect to 100 parts by mass of food. The upper limit is 80 parts by mass or less, preferably 50 parts by mass or less.
なお、本発明の食品には、必要に応じて、賦形剤、増量剤、結合剤、増粘剤、乳化剤、着色料、香料、他の食品原料、調味料、医薬品原料などを添加してもよい。さらに、本発明の肝中脂質蓄積抑制剤を含有する食品は、用途に応じて、顆粒、錠剤などの形態に成形されてもよい。また、本発明の成分を添加した食品の剤形については、必要に応じてハードカプセル、ソフトカプセルなどのカプセル剤、錠剤、もしくは丸剤などに、あるいは粉末状、顆粒状、茶状、ティーバッグ状、もしくは飴状などの形態に成形したり、そのまま飲料として用いたりすることができる。これらの形状または好みに応じて、そのまま食してもよく、あるいは水、湯、牛乳などに溶いて飲んでも良い。また、粉末化してティーバッグ状などの場合、成分を浸出させてから飲んでも良い。 In addition, excipients, extenders, binders, thickeners, emulsifiers, colorants, fragrances, other food ingredients, seasonings, pharmaceutical ingredients, etc. may be added to the food of the present invention as necessary. Also good. Furthermore, the food containing the hepatic lipid accumulation inhibitor of the present invention may be formed into a form such as a granule or a tablet depending on the application. As for the dosage form of the food to which the ingredients of the present invention are added, capsules such as hard capsules and soft capsules, tablets or pills as necessary, or powder, granules, tea, tea bags, Or it can shape | mold into forms, such as a bowl shape, or can be used as it is as a drink. Depending on their shape or preference, they may be eaten as they are, or they may be dissolved in water, hot water, milk or the like. In the case of powdered tea bags, etc., the ingredients may be leached before drinking.
本発明の食品に添加可能な食品原料としては、例えば、ローヤルゼリー、プロポリス、ビタミン類(A、C、D、E、K、葉酸、パントテン酸、ビオチン、これらの誘導体等)、ミネラル(鉄、マグネシウム、カルシウム、亜鉛等)、セレン、α−リポ酸、レシチン、ポリフェノール(フラボノイド類、これらの誘導体等)、カロテノイド(リコピン、アスタキサンチン、ゼアキサンチン、ルテイン等)、キサンチン誘導体(カフェイン等)、脂肪酸、タンパク質(コラーゲン、エラスチン等)、ムコ多糖類(ヒアルロン酸など)、アミノ糖(グルコサミン、アセチルグルコサミン、ガラクトサミン、アセチルガラクトサミン、ノイラミン酸、アセチルノイラミン酸、ヘキソサミン、それらの塩等)、オリゴ糖(イソマルトオリゴ糖、環状オリゴ糖等)、スフィンゴ脂質やリン脂質及びその誘導体(フォスファチジルコリン、スフィンゴミエリン、セラミド等)、含硫化合物(アリイン、セパエン、タウリン、グルタチオン、メチルスルホニルメタン等)、糖アルコール、リグナン類(セサミン等)、これらを含有する動植物抽出物、根菜類(ウコン、ショウガ等)、麦若葉末等のイネ科植物の緑葉、ケール等のアブラナ科植物の緑葉などが挙げられる。 Examples of food materials that can be added to the food of the present invention include royal jelly, propolis, vitamins (A, C, D, E, K, folic acid, pantothenic acid, biotin, derivatives thereof, etc.), minerals (iron, magnesium) , Calcium, zinc, etc.), selenium, α-lipoic acid, lecithin, polyphenols (flavonoids, derivatives thereof, etc.), carotenoids (lycopene, astaxanthin, zeaxanthin, lutein, etc.), xanthine derivatives (caffeine, etc.), fatty acids, proteins (Collagen, elastin, etc.), mucopolysaccharide (hyaluronic acid, etc.), amino sugar (glucosamine, acetylglucosamine, galactosamine, acetylgalactosamine, neuraminic acid, acetylneuraminic acid, hexosamine, salts thereof, etc.), oligosaccharide (isomalto-oligo) Sugar, cyclic o Sugar beet, etc.), sphingolipids and phospholipids and derivatives thereof (phosphatidylcholine, sphingomyelin, ceramide, etc.), sulfur-containing compounds (such as alliin, sepaene, taurine, glutathione, methylsulfonylmethane), sugar alcohols, lignans ( Sesamin, etc.), animal and plant extracts containing these, root vegetables (turmeric, ginger, etc.), green leaves of gramineous plants such as wheat powder, green leaves of cruciferous plants such as kale.
特に本発明においては、上記葛花処理物だけでなく、脂質吸収抑制成分および脂質代謝促進成分の少なくともいずれかの成分を添加すれば、相乗的な脂質の蓄積抑制または体脂肪減少効果を得ることができる。その結果、例えば、抗糖尿病効果、肥満より生ずる様々な症状の予防効果などが期待できる。 In particular, in the present invention, if not only the processed Kuzuka product but also at least one of a lipid absorption suppressing component and a lipid metabolism promoting component is added, a synergistic lipid accumulation suppression or body fat reduction effect can be obtained. Can do. As a result, for example, an antidiabetic effect and a preventive effect for various symptoms caused by obesity can be expected.
ここでいう脂質吸収抑制成分としては、例えば、キトサンおよびその誘導体、サイリウム、プロアントシアニジンなどの胆汁酸を排泄する作用を有する成分、ガロタンニン、ビワ葉等およびその抽出物などのリパーゼ阻害作用を有する成分が挙げられる。なお、例えば、松樹皮抽出物といったプロアントシアニジンを多く含む植物抽出物を、プロアントシアニジンとして用いることも可能である。 Examples of the lipid absorption inhibitory component herein include components having an action of excreting bile acids such as chitosan and its derivatives, psyllium and proanthocyanidins, and components having a lipase inhibitory action such as gallotannins, loquat leaves and the like and extracts thereof. Is mentioned. In addition, for example, a plant extract containing a large amount of proanthocyanidins such as a pine bark extract can be used as the proanthocyanidins.
脂質代謝促進成分としては、リボフラビン類、茶カテキン類、異性化リノール酸、カフェイン、カプサイシン、カルニチン、コエンザイムQ10、大豆ペプチド、分岐アミノ酸、フォスファチジルコリン、アリルスルフィド化合物、フォルスコリン、ベルゲニン、ケルセチン、アスチルビン、ヒドロキシクエン酸、およびこれらの塩などが挙げられる。もちろん、これら脂質代謝促進成分を含有する植物抽出物、例えば、茶、コレウスフォコリ、アカショウマ、黄杞、大豆、唐辛子、ソバ、ニンニク、タマネギ、コーヒーなどの抽出物を、脂質代謝促進成分として用いることも可能である。 Lipid metabolism promoting components include riboflavins, tea catechins, isomerized linoleic acid, caffeine, capsaicin, carnitine, coenzyme Q10, soybean peptide, branched amino acid, phosphatidylcholine, allyl sulfide compound, forskolin, bergenin, quercetin , Astilbine, hydroxycitric acid, and salts thereof. Of course, plant extracts containing these lipid metabolism promoting components, for example, extracts of tea, coleus foli, red pepper, yellow potato, soybean, chili, buckwheat, garlic, onion, coffee, etc. are used as lipid metabolism promoting components. It is also possible.
上記脂質吸収抑制成分および脂質代謝促進成分は、目的に応じて適宜配合される。例えば、脂質吸収抑制成分および脂質代謝促進成分のいずれかの成分のみを添加してもよく、脂質吸収抑制成分および脂質代謝促進成分の両方を添加してもよい。もちろん、2種類以上の脂質吸収抑制成分を添加しても、2種類以上の脂質代謝促進成分を添加してもよい。 The lipid absorption suppressing component and the lipid metabolism promoting component are appropriately blended depending on the purpose. For example, only one of the lipid absorption suppressing component and the lipid metabolism promoting component may be added, or both the lipid absorption suppressing component and the lipid metabolism promoting component may be added. Of course, two or more lipid absorption inhibiting components may be added, or two or more lipid metabolism promoting components may be added.
とくに、近年健康のために飲食されている、麦若葉(例えば大麦若葉)、ケール、明日葉、桑葉などの緑葉を粉末化して、飲料として摂取する、いわゆる「青汁」として、葛花処理物を利用すると、水との相乗効果で、他の青汁よりも嗜好性のよい青汁とすることができ、さらには、摂取しにくい他の青汁原料と共に配合することで、他の青汁原料を摂取しやすくすることも可能である。さらに、上記食品原料を含む飲料、例えば、植物発酵ジュース、野菜ジュース(例えば、人参ジュース)、植物抽出物、果汁などにも利用され得、葛花処理物を含有させることにより、嗜好性を良くするだけでなく、機能性または栄養価の高い飲料とすることもできる。 In particular, as a so-called “green juice”, powdered green leaves such as young wheat leaves (eg, barley young leaves), kale, tomorrow leaves, and mulberry leaves, which have been eaten and eaten for health in recent years, are treated as kojika. By using the product, it can be made into a green juice with a better taste than other green juices due to a synergistic effect with water, and further, it can be mixed with other green juice ingredients that are difficult to ingest. It is also possible to make it easy to take the soup ingredients. Furthermore, it can be used for beverages containing the above food materials, for example, plant fermented juice, vegetable juice (for example, carrot juice), plant extract, fruit juice, etc. In addition, it can be a functional or nutritious beverage.
もちろん、本発明の肝中脂質蓄積抑制剤を含有する食品においては、糖液や糖アルコールまたは調味料等を加えて甘味を強くすることもできる。 Of course, in the food containing the hepatic lipid accumulation inhibitor of the present invention, sugar solution, sugar alcohol, seasoning or the like can be added to enhance the sweetness.
また、本発明の肝中脂質蓄積抑制剤を含有する食品の剤形については、必要に応じてハードカプセル、ソフトカプセルなどのカプセル剤、錠剤、もしくは丸剤などに、あるいは粉末状、顆粒状、茶状、ティーバッグ状、もしくは飴状などの形態に成形したり、そのまま飲料として用いたりすることができる。これらの形状または好みに応じて、そのまま食してもよく、あるいは水、湯、牛乳などに溶いて飲んでも良い。また、粉末化してティーバッグ状などの場合、成分を浸出させてから飲んでも良い。 The dosage form of the food containing the hepatic lipid accumulation inhibitor of the present invention may be a capsule such as a hard capsule or a soft capsule, a tablet or a pill as necessary, or a powder, granule or tea. It can be formed into a tea bag shape or a bowl shape or used as a beverage as it is. Depending on their shape or preference, they may be eaten as they are, or they may be dissolved in water, hot water, milk or the like. In the case of powdered tea bags, etc., the ingredients may be leached before drinking.
以下、実施例に基づいて本発明を説明する。なお、実施例の記載により、本発明を限定して解釈すべきではなく、特許請求の範囲における記載の範囲内において、本発明は種々の変更が可能である。 Hereinafter, the present invention will be described based on examples. Note that the present invention should not be construed as being limited by the description of the embodiments, and various modifications can be made within the scope of the claims.
(実施例1:肝中脂質改善効果の検討)
5週齢の雄性のSDラット(日本チャ−ルス・リバー株式会社)を用いて、以下のようにして、葛花処理物が有する肝臓中における脂質の蓄積に対する効果を検証した。まず、18匹のSDラットを標準飼料(MF飼料、オリエンタル酵母工業株式会社)で1週間馴化した。次いで、1群あたりの平均体重が均一となるように1群6匹の3群にわけた。
(Example 1: Examination of liver lipid improvement effect)
Using a 5-week-old male SD rat (Nippon Charles River Co., Ltd.), the effect of the processed Kuzuka product on lipid accumulation in the liver was examined as follows. First, 18 SD rats were acclimated with a standard feed (MF feed, Oriental Yeast Co., Ltd.) for 1 week. Subsequently, it was divided into 3 groups of 6 animals per group so that the average body weight per group was uniform.
1群は、標準飼料に2質量%の葛花抽出物(イソフラボン類を10質量%、サポニンを1質量%含有、株式会社太田胃散)、1質量%のコレステロール、0.25質量%のコール酸を含有するように、各成分を添加したもの(試験飼料1とする)を自由摂取させた。 One group consists of 2% by weight of Kuzuka extract (10% by weight of isoflavones, 1% by weight of saponin, Ota Sakusan Co., Ltd.), 1% by weight of cholesterol and 0.25% by weight of cholic acid in the standard feed. So that each component was added so as to contain (referred to as test feed 1).
もう1群には、標準飼料に1質量%のコレステロール、0.25質量%のコール酸を含有するように、各成分を添加したもの(高コレステロール負荷食。比較飼料1とする)を自由摂取させた。 In the other group, a standard diet containing 1% by mass cholesterol and 0.25% by mass cholic acid so that each component was added (high cholesterol-loaded diet, referred to as comparative diet 1) was freely ingested. I let you.
残りの1群には、標準飼料のみ(対照飼料1とする)を自由摂取させた。 The remaining group received only the standard diet (control diet 1).
自由摂取開始から28日目に各マウスの肝臓を摘出し、肝臓中の総脂質をFolch法により抽出した。次いで、中性脂肪量を測定キット(トリグリセライドG−テストワコー、和光純薬工業株式会社)および、総コレステロール量を測定キット(コレステロールE−テストワコー、和光純薬株式会社)を用いて各々測定した。結果を表1に示す。 On the 28th day from the start of free intake, the liver of each mouse was removed, and the total lipid in the liver was extracted by the Folch method. Subsequently, the amount of neutral fat was measured using a measurement kit (Triglyceride G-Test Wako, Wako Pure Chemical Industries, Ltd.) and the total cholesterol amount using a measurement kit (Cholesterol E-Test Wako, Wako Pure Chemical Industries, Ltd.). . The results are shown in Table 1.
表1の結果、高コレステロール負荷食に葛花抽出物を含んだ飼料(試験飼料1)を摂取した群は、高コレステロール負荷食である飼料(比較飼料1)を摂取した群に比べ、中性脂肪量の増加が抑制されていることがわかる。さらに、標準飼料のみ(対照飼料1)を摂取させた群と比べても、中性脂肪量の増加が抑制されていた。 As a result of Table 1, the group that ingested the feed containing kuzuka extract (test feed 1) in the high-cholesterol-loaded diet was more neutral than the group that ingested the feed that was a high-cholesterol-loaded diet (comparative feed 1). It can be seen that the increase in fat mass is suppressed. Furthermore, the increase in the amount of neutral fat was suppressed even compared with the group fed with only the standard feed (control feed 1).
また、試験飼料1を摂取した群は、比較飼料1と比べて総コレステロール量の増加も抑制されていることがわかる。 In addition, it can be seen that the group that ingested the test feed 1 also suppressed the increase in the total cholesterol level compared to the comparative feed 1.
従って、本発明の肝中脂質蓄積抑制剤は、優れた肝中中性脂肪蓄積抑制作用ならびに肝中総コレステロール蓄積抑制作用を有し、脂肪肝の予防または治療に有効であることがわかる。 Therefore, it can be seen that the liver lipid accumulation inhibitor of the present invention has an excellent liver neutral fat accumulation inhibitory effect and liver total cholesterol accumulation inhibitory effect, and is effective in the prevention or treatment of fatty liver.
さらに、本発明の肝中脂質蓄積抑制剤は、優れた肝中中性脂肪蓄積抑制作用ならびに肝中総コレステロール蓄積抑制作用を有することより、脂肪肝によりリスクが高まることが指摘されている、糖尿病、高脂血症、高血圧、動脈硬化等の症状の予防効果も期待できる。 Furthermore, it has been pointed out that the liver lipid accumulation inhibitor of the present invention has an excellent liver neutral fat accumulation inhibitory effect and liver total cholesterol accumulation inhibitory effect, which increases the risk of fatty liver. It can also be expected to prevent symptoms such as hyperlipidemia, hypertension, and arteriosclerosis.
本発明の葛花処理物を有効成分とする肝中脂質蓄積抑制剤は、優れた肝中脂質蓄積抑制効果を有するため有用である。
The hepatic lipid accumulation inhibitor comprising the processed kuzuhana product of the present invention as an active ingredient is useful because it has an excellent effect of inhibiting hepatic lipid accumulation.
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JP2013155154A (en) * | 2012-01-31 | 2013-08-15 | Toyo Shinyaku Co Ltd | Phosphodiesterase-3 inhibitor |
JP2014065683A (en) * | 2012-09-26 | 2014-04-17 | Toyo Shinyaku Co Ltd | Anti-glycation composition |
JP2015145431A (en) * | 2015-05-18 | 2015-08-13 | 株式会社東洋新薬 | Phosphodiesterase 3 inhibitor |
JP2022529085A (en) * | 2020-03-09 | 2022-06-16 | 江西中医薬大学 | Kakkonto polysaccharide and its manufacturing method and usage |
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KR101357119B1 (en) * | 2011-09-23 | 2014-02-05 | 경희대학교 산학협력단 | A pharmaceutical composition comprising extract of Puerariae Flos for prevention and treatment of endometriosis |
WO2013117007A1 (en) * | 2012-02-10 | 2013-08-15 | Nestec S.A. | Composition comprising phytosterols and kudzu for cardiovascular diseases |
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JP2013155154A (en) * | 2012-01-31 | 2013-08-15 | Toyo Shinyaku Co Ltd | Phosphodiesterase-3 inhibitor |
JP2014065683A (en) * | 2012-09-26 | 2014-04-17 | Toyo Shinyaku Co Ltd | Anti-glycation composition |
JP2015145431A (en) * | 2015-05-18 | 2015-08-13 | 株式会社東洋新薬 | Phosphodiesterase 3 inhibitor |
JP2022529085A (en) * | 2020-03-09 | 2022-06-16 | 江西中医薬大学 | Kakkonto polysaccharide and its manufacturing method and usage |
JP7285596B2 (en) | 2020-03-09 | 2023-06-02 | 江西中医薬大学 | Kudzu root polysaccharide and its production method and use |
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