AU764747B2 - Lipid metabolism improving agent - Google Patents

Description

S&FRef: 377111D1

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT

ORIGINAL

Name and Address of Applicant: Kyowa Hakko Kogyo Co., Ltd.

6-1, Ohtemachi 1-chome Chiyoda-ku Tokyo 100 Japan Actual Inventor(s): Address for Service: Goro Hori, Kazuhiro Matsuoka, Iwao Sato, Satoshi Nagaoka Spruson Ferguson St Martins Tower 31 Market Street Sydney NSW 2000 Invention Title: Lipid Metabolism Improving Agent 0 00 :0 0.000 0 0 The following statement is a full description of this invention, including the best method of performing it known to me/us:- 5845c

SPECIFICATION

LIPID METABOLISM IMPROVING AGENT Technical Field The present invention relates to a lipid metabolism improving agent and a functional food.

Background Art The term lipid metabolism refers to the in vivo process of catabolism (decomposition) and anabolism (accumulation) of lipids, which are mainly triglycerides derived from food, and is intended to include, in the broad sense, reactions for transforming lipids into energy, biosynthesis of fatty acids, biosynthesis of acylglycerol, phospholipid metabolism, and cholesterol metabolism [Akira Misaki, Biochemistry for Nutrition, Asakura Shoten (1993), p. 123-134].

In recent years, mortality from adult diseases, particularly cardiovascular disorders, is rapidly rising, and a correlation between occurrence of such disorders and cholesterol concentration in blood has been pointed out.

Some attempts have so far been made to lower the cholesterol concentration in blood by the use of specific food components. For example, the following proteins are S 25 known as proteins which lower the cholesterol concentration in blood: whey protein [Agric. Biol. Chem., 55, 813 (1991)]; soybean protein [Atherosclerosis, 722, 115 (1988)]; milk serum protein (Japanese Published Unexamined Patent Application No. 176713/93); and soybean protein hydrolyzate Nutr., 120, 977 (1990)].

It is also known that egg yolk phospholipid lowers the cholesterol concentration in blood [Agric. Biol. Chem., 53, 2469 (1989)].

An attempt has been made to lower the cholesterol concentration in blood by the use of a combination of lactalbumin, collagen, soybean protein, or wheat gluten, 2 and soybean lecithin 2.5 and [Nutr. Rep. Int., 28, 621 (1983)].

Also known is a method for lowering the cholesterol concentration in blood by the use of a textured soybean protein containing 6% of soybean lecithin [Ann. Nutr.Metab., 29, 348(1985)].

Summary of the Invention According to a first aspect of this invention, there is provided a lipid metabolism improving agent comprising a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein derived from wheat, soybean, corn or milk and is not hydrolyzed.

According to a second aspect of this invention, there is provided a cholesterol metabolism improving agent comprising a protein/phospholipid complex containing or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed.

According to a third aspect of this invention, there is provided a functional food comprising a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein derived from wheat, soybean, corn or milk and is not hydrolyzed.

According to a fourth aspect of this invention, there is provided a method for improving the lipid metabolism of an animal, which method comprises administering to S 20 the animal a protein/phospholipid complex containing 10w% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed.

According to a fifth aspect of this invention, there is provided a method for improving the cholesterol metabolism of an animal, which method comprises administering to the animal a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed.

According to a sixth aspect of this invention, there is provided a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein S 30 the protein is derived from wheat, soybean, cor or milk and not hydrolyzed, when used for improving the lipid metabolism, the cholesterol metabolism, or both, of an animal.

According to a seventh aspect of this invention, there is provided use of a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed, in the I:\DayLib\LIBUU\03290.doc 2a manufacture of a medicament for improving the lipid metabolism, the cholesterol metabolism, or both, of an animal.

Disclosure of the Invention The present invention relates to a protein/phospholipid or protein hydrolyzate/phospholipid complex containing 10 wt% or more of bound phospholipid, a lipid metabolism improving agent comprising the complex, and a functional food comprising the complex.

The proteins for use in the present invention may be derived from animals, plants or microorganisms. Suitable examples are wheat protein, soybean protein, corn protein and milk protein, among which wheat protein and soybean protein are preferred. As the wheat protein, wheat gluten is usually used. Wheat gluten, soybean protein, etc. of commercial origin are readily available.

Particularly disclosed in this application is a protein/phospholipid complex s1 containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn, or milk; a lipid metabolism improving agent comprising a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn, or milk; a cholesterol metabolism improving agent comprising a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn, or milk; a functional food comprising a protein/phospholipid complex containing 10wt% or more of :bound phospholipid wherein the protein is derived from wheat, soybean, corn, or milk.

Examples of the phospholipids are phosphatidyl choline, phosphatidyl ethanolamine, phosphatidyl inositol, phosphatidyl serine, sphingomyelin, phosphatidic acid, and lecithin, which is a mixture of the above members.

Lecithin derived from animals, plants or microorganisms may be used. Suitable examples are brain lecithin, liver lecithin, egg yolk lecithin, soybean lecithin and yeast lecithin, among which soybean lecithin and egg yolk lecithin are preferred.

Lecithin may be used as such, but enzyme-modified lecithin obtained by treating 30 lecithin with an enzyme such as phospholipase is preferably used. Lecithin and enzymemodified lecithin of commercial origin are readily available.

The term bound phospholipid as used herein refers to a phospholipid which remains bound to a protein after being I:\DayLib\LIBUU\03290.doc treated with a nonpolar organic solvent such as petroleum ether.

The amount of bound phospholipid is calculated as follows. The amount of total phospholipid contained in a protein hydrolyzate/phospholipid complex is determined.

Then, the complex is treated with a nonpolar organic solvent such as petroleum ether, and the amount of phospholipid extracted into the solvent (hereinafter referred to as free phospholipid) is determined. The amount of bound phospholipid is calculated as the difference between the amount of total phospholipid and that of free phospholipid.

The bound phospholipid content of a complex is calculated as the percentage of bound phospholipid in the complex The complex of the present invention contains 10% or more, preferably 10-50% of bound phospholipid.

Particularly preferred is the complex containing 20-50% of bound phospholipid.

As the protein/phospholipid complex, commercially available ones can be used. The protein/phospholipid complex can also be prepared by mixing 100 parts by weight of a protein and 10-100 parts by weight of a phospholipid using a stirring mixer, preferably in the presence of 25 water. By mixing a protein and a phospholipid at a ratio of 100:20-50 by weight, preferably 100:30-40, a desirable complex can be obtained wherein the bound phospholipid content is high and the ratio of bound phospholipid to total phospholipid is high. In an exemplary preparation process, a solution prepared by dispersing a phospholipid in water is added to a protein, followed by mixing at room temperature by using a high power mixer (50-200 or a homogenizer (5,000-15,000 The protein hydrolyzate/phospholipid complex can be prepared by mixing a protein hydrolyzate and a phospholipid, or by hydrolyzing in an aqueous medium the protein moiety of a complex prepared by mixing a protein and a phospholipid.

As the protein hydrolysate, hydrolysed products of proteins in an aqueous medium using a proteolytic enzyme or an acid can be used. Preferred are hydrolysates slightly soluble in water having a molecular weight of 5,000-30,000, particularly, those having a molecular weight of 10,000-20,000.

A typical example of the method for preparing such slightly water-soluble substances is given below. A protein is dispersed in water, and hydrochloric acid or sodium hydroxide is added to the solution to bring it to the optimum pH range for the proteolytic enzyme to be employed. The proteolytic enzyme is added to the solution in an amount of 0.5-2% based on the substrate protein, followed by reaction at the optimum pH and the optimum temperature for the enzyme for 20-30 hours.

o1 The enzyme reaction is terminated by heating at 85-950C for about one hour. After being neutralised with sodium hydroxide or hydrochloric acid, the reaction mixture is centrifuged to obtain the slightly water-soluble substance.

As the aqueous medium, water, buffers, alcohols, esters, ketones, amides, etc. can be used.

Water is preferably used.

As the proteolytic enzyme, pepsin, trypsin, pancreatin, papain, etc. can be used.

S. The protein hydrolysate/phospholipid complex can be prepared by mixing 100 parts by weight of a protein hydrolysate and 10-100 parts by weight of a phospholipid using a stirring mixer, preferably in the presence of water. By mixing a protein hydrolysate and a phospholipid at a ratio of 100:20-50 by weight, preferably 100:30-40, a desirable complex can be obtained wherein the bound phospholipid content is high and the ratio of bound phospholipid to total phospholipid is high. In an exemplary preparation process, a solution prepared by dispersing a phospholipid in water is added to a protein hydrolysate, followed by mixing at room temperature by using a high power mixer (50-200 or a homogeniser (5,000-15,000 The protein hydrolysate/phospholipid complex can also be prepared by the same method as in the preparation of a protein hydrolysate except that a protein/phospholipid complex is used instead of a protein. By this method, the protein moiety of the complex is hydrolysed to give the desired complex as a slightly water-soluble substance having a molecular weight of 5,000-30,000, preferably, 10,000- 20,000. The hydrolysis of the protein moiety of the complex is preferably carried out by the treatment with a proteolytic enzyme in an aqueous medium.

As the method for the preparation of the protein hydrolysate/phospholipid complex, the hydrolysis of the protein moiety of a protein/phospholipid complex in an aqueous medium is preferable to the mixing of a protein hydrolysate and a phospholipid, because the former gives a higher protein recovery.

The complex of the present invention may be utilised without being isolated from the reaction mixture, or after isolation and purification from the reaction mixture. The product obtained by drying [R:\LBAA]07644.doc:TAB the reaction mixture or the complex by freeze-drying or spray-drying and pulverising the dried product can also be utilised.

The protein hydrolysate/phospholipid complex is superior to the protein/phospholipid complex in lipid metabolism improving effect.

The lipid metabolism improving agent of the present invention may be in any of the dose forms such as tablets, powders, fine granules, granules, capsules, syrups, enteric coated tablets, troches, and liquid preparations for oral administration.

The administration route for the lipid metabolism improving agent of the present invention is not specifically limited, but oral administration is preferred.

[R:\LIBAA]07644.doc:TAB 6 In the case of oral administration, the complex of the present invention may be administered as it is, or in the form of compositions prepared by conventional methods using excipients which are acceptable as ingredients of food or drugs.

As the excipients, saccharides such as sorbitol, lactose and glucose, inorganic substances such as dextrin, starch, calcium carbonate and calcium sulfate, crystalline cellulose, distilled water, sesame oil, corn oil, olive oil, cottonseed oil, and other generally employed excipients can be used.

In preparing the compositions, additives such as binders, lubricants, dispersing agents, suspending agents, emulsifiers, diluents, buffers, antioxidants, and antibacterial agents may be used.

The dose of the composition will vary depending on various factors such as the patient's age, sex and physical condition, administration route, administration schedule, 20 and form of composition. For instance, when the 20 composition is orally administered to an adult, it is suitable to administer the composition in an amount of 2- 100 g/day in 1 to 4 parts. Administration may be made at a dose outside the above limit as may be required.

The lipid metabolism improving agent of the present S 25 invention can be used not only as a cholesterol metabolism improving agent but also as an agent for the treatment or prevention of diseases such as fatty liver, hypertension, hyperlipidemia, arteriosclerosis, obesity, diabetes, and myocardial infarction.

The functional food of the present invention can be produced by adding the protein hydrolyzate/phospholipid complex containing 10% or more of bound phospholipid to food materials in a conventional process for producing food. The functional food contains 0.1% or more, preferably 0.1-50%, more preferably 0.5-30% of the complex.

The functional food may additionally be formulated to contain a protein, a sugar, a fat, a trace element, a vitamin, an emulsifier, a flavor, and the like.

The term functional food as used herein refers to food designed and processed so that food ingredients may fully perform their functions for the biophylaxis, regulation of -biorhythm, and regulation of physical condition relating to the prevention of and recovery from diseases.

Examples of the food are juice, soft drinks, tea, lactic acid beverages, ices, milk, dairy products (e.g.

butter, cheese, yogurt, processed milk, and skim milk), meat, meat products ham, sausage, and hamburger), fish, fish products steamed, baked or fried fish paste), egg, egg products fried or steamed foods made of beaten eggs), confectionery cookies, jelly, and snacks), bread, noodles, pickles, smoked fish and meat, dried fish, preserved foods boiled down with soy, salted foods, soup, and seasonings.

.":The functional food of the present invention may be in the form of ordinary food, or in the form of liquid food, 20 pre-digested nutrient food, elemental diet, liquid nutrient food, or the like.

The functional food of the present invention can be used not only for improving lipid metabolism, particularly cholesterol metabolism, but also for treating, preventing 25 or alleviating diseases such as fatty liver, hypertension, hyperlipidemia, arteriosclerosis, obesity, diabetes, and myocardial infarction. It is suitable to give the functional food to an adult in an amount of 2-100 g/day.

The effect of the complexes of the present invention is shown below by Test Examples.

Test Example 1 Test Method Five-weeks-old male Wistar rats were used as test animals. The rats were fed with a commercially available solid feed (MF, Oriental Yeast Co., Ltd.) for three days, and then divided into groups each consisting of 6 animals in such a way that there is no significant difference in body weight of the animals between the groups. The test feed compositions were formulated, as shown in Table 1, to respectively contain a protein at a protein level of and to contain sucrose in amounts adjusted so as to make the total weights of all the compositions equal. After groups of test animals were fed with equal amounts of the respective feed compositions for 10 days, the total cholesterol concentration in serum, the high density lipoprotein (HDL) cholesterol concentration in serum, and the total cholesterol concentration in liver were measured for each rat.

__Table 1 Test Group Ingredient 1 2 3 4 Protein* 1 23.05 28.65 28.45 30.05 (Protein level) (20) (20) (20) Methionine* 2 0.1 0.1 0.1 0.1 Lard 5 5 5 Corn oil 1 1 1 1 Mineral mixture* 3 3.5 3.5 3.5 (AIN-76) Vitamin mixture 1 1 1 1 (AIN-76) Choline chloride 0.2 0.2 0.2 0.2 Cellulose 5 5 5 Sucrose 60.4 54.8 55.0 53.4 Cholesterol 0.5 0.5 0.5 Sodium cholate 0.25 0.25 0.25 0.25 9 Notes) *1 (Protein) Group 1: Promic P (isolated soybean protein) (bound phospholipid content: 1%) Group 2: Mixture of Promic P and SLP-White (soybean lecithin) obtained in Comparative Example 1 (bound phospholipid content: free phospholipid content: Group 3: Protein/phospholipid complex obtained in Example 3 (Promic P/SLP-White complex) (bound phospholipid content: 20%, free phospholipid content: Group 4: Protein/enzyme-modified phospholipid complex obtained in Example 2 (Promic P/Elmizer AC complex) (bound phospholipid content: free phospholipid content: Methionine, an essential amino acid, was added in order to make the nutritive values of all the compositions equal.

20 American Institute of Nutrition of Nutrition, 107, 1340 (1977)] The results are shown in Table 2.

S 25 *e 25 Table 2 4 4** .4.

Total HDL Arterio- Total Test Cholesterol Cholesterol sclerosis Cholesterol Group Cone. in Serum Conc. in Serum Index* Cone. in Liver (mg/dl) (mg/dl) .(mg/g of liver) 1 111.0±10.0 14.3±1.0 0.14±0.01 25.1±1.3 2 80.8± 6.4 20.0±0.9 0.25±0.02 22.3±1.0 3 79.3± 7.1 25.5±1.7 0.33±0.02 19.2±1.2 4 77.2± 4.5 26.2±1.0 0.35±0.02 16.3±1.3 (Numerical value: mean standard error) Note)* The arteriosclerosis index shows the value of (HDL cholesterol cone. in serum)/(total cholesterol conc. in serum).

As shown in the above table, Test Groups 3 and 4 were almost equal to Test Group 2 in total cholesterol concentration in serum, but showed higher HDL cholesterol concentration in serum as compared with Test Groups 1 and 2. The relationship between the total cholesterol concentration in serum and the HDL cholesterol concentration in serum was expressed as the arteriosclerosis index. Test Groups 3 and 4 showed higher arteriosclerosis index as compared with Test Groups 1 and 2, which indicates that the cholesterol metabolism in serum was improved in Test Groups 3 and 4. Test groups 3 and 4 also showed lower total cholesterol concentration in liver as compared with Test Groups 1 and 2. No significant difference was observed in feed intake or increase in body weight between the test groups.

Test Example 2 The test was carried out in the same manner as in Test Example 1, except that the feed compositions shown in Table 20 3 were used. The results are shown in Table 4.

fee *000 0 o f oooo Table 3 Test Group Ingredient 5 6 Protein* 1 34.35 32.65 (Protein) (20) Lard 5 Corn oil 1 1 Mineral mixture 3.5 (AIN-76) Vitamin mixture 1 1 (AIN-76) Choline chloride 0.2 0.2 Cellulose 5 Sucrose 49.2 50.9 Cholesterol 0.5 Sodium cholate 0.25 0.25 Note) *1 (Protein) Group 5: Mixture of Promic P hydrolyzate and SLP-White obtained in Comparative Example 3 (bound phospholipid content: free phospholipid content: Group 6: Protein hydrolyzate/phospholipid complex obtained in Example 9 (Promic P hydrolyzate/ SLP-White complex) (bound phospholipid content: 20%, free phospholipid content: Table 4 Total HDL Arterio- Total Test Cholesterol Cholesterol sclerosis Cholesterol Group Conc. in Serum Cone. in Serum Index Cone. in Liver (mg/dl) (mg/dl) (mg/g of liver) 72.7±3.1 35.2±1.3 0.49±0.03 7.4±0.7 6 68.3±3.6 32.0±2.3 0.49±0.03 4.7±0.4 (Numerical value: mean standard error) As shown in the above table, Test Group 6 was equal to Test Group 5 in arteriosclerosis index, but showed lower total cholesterol concentration in liver. No significant difference was observed in feed intake or increase in body weight between the test groups.

Test Example 3 The test was carried out in the same manner as in Test Example 1, except that the feed compositions shown in Table 5 were used. The results are shown in Table 6.

Table Test Group Ingredient 7 8 9 Protein* 1 23.05 32.3 34.8 (Protein level) (20) (20) Methionine 0.1 0.04 0.04 Tryptophan 0 0.01 0.01 Lard 5 5 Corn oil 1 1 1 Mineral mixture 3.5 3.5 (AIN-76) Vitamin mixture 1 1 1 (AIN-76) Choline chloride 0.2 0.2 0.2 Cellulose 5 5 Sucrose 60.4 51.2 48.7 Cholesterol 0.5 0.5 Sodium cholate 0.25 0.25 0.25 Note) *1 (Protein) Group 7: Promic P (bound phospholipid content: 1%) Group 8: Hydrolyzate of soybean protein/enzyme-modified lecithin complex (Promic P/Elmizer AC complex) Group 9: obtained in Example 5 (bound phospholipid content: 20%, free phospholipid content: Soybean protein hydrolyzate/enzyme-modified lecithin complex obtained in Example 8 (Promic P hydrolyzate/Elmizer AC complex) (bound phospholipid content: 20%, free phospholipid content: Table 6 Total HDL Arterio- Total Test Cholesterol Cholesterol sclerosis Cholesterol Group Cone. in Serum Conc. in Serum Index Cone. in Liver (mg/dl) (mg/dl) (mg/g of liver) 7 103.8±9.7 34.7±2.5 0.35±0.04 28.7±1.5 8 75.4±5.3 53.4±3.1 0.71±0.02 4.3±0.3 9 81.4±4.7 53.5±2.7 0.73±0.02 5.3±0.3 (Numerical value: mean standard error) As shown in the above table, the arteriosclerosis indices of Test Groups 8 and 9 were higher than that of Test Group 7, which indicates that the cholesterol metabolism in serum was improved in Test Groups 8 and 9.

In addition, Test Groups 8 and 9 showed total cholesterol concentration in liver much lower than that of Test Group 7; the total cholesterol concentration in liver of Test Group 8 was lower than that of Test Group 9. No significant difference was observed in feed intake or increase in body weight between the test groups.

Test Example 4 The test was carried out in the same manner as in Test Example 1, except that the feed compositions shown in Table 7 were used. The results are shown in Table 8.

14 Table 7 Test Group Ingredient 10 11 12 13 14 Protein*l 27.59 28.69 28.69 37.15 40.65 (Protein level) (20) (20) (20) (20) Tryptophan 0.04 0.04 0.04 0.02 0.02 Lysine 0.82 0.82 0.82 0.72 0.72 Threonine 0.2 0.2 0.2 0.16 0.16 Lard 5 5 5 5 Corn oil 1 1 1 1 1 Mineral mixture* 3 3.5 3.5 3.5 3.5 (AIN-76) Vitamin mixture 1 1 1 1 1 (AIN-76) Choline chloride 0.2 0.2 0.2 0.2 0.2 Cellulose 5 5 5 5 Sucrose 54.9 53.8 53.8 45.5 42.0 Cholesterol 0.5 0.5 0.5 0.5 Sodium cholate 0.25 0.25 0.25 0.25 0.25 Note) *1 (Protein) Group 10: Wheat gluten (bound phospholipid content: 0.3%) Group 11: Mixture of wheat gluten and enzyme-modified lecithin obtained in Comparative Example 2 (bound phospholipid content: free phospholipid content: Group 12: Wheat gluten/enzyme-modified lecithin complex obtained in Example 1 (bound phospholipid content: 10%, free phospholipid content: Group 13: Hydrolyzate of wheat gluten/enzyme-modified lecithin complex obtained in Example 4 (bound

I*

I

phospholipid content: 10%, free phospholipid content: 0.3%) Group 14: Wheat gluten hydrolyzate/enzyme-modified lecithin complex obtained in Example 7 (bound phospholipid content: 10%, free phospholipid Table 8 Total HDL Arterio- Total Test Cholesterol Cholesterol sclerosis Cholesterol Group Conc. in Serum Cone. in Serum Index Conc. in Liver (mg/dl) (mg/dl) (mg/g of liver) 132.5± 7.4 16.7±1.4 0.13±0.02 22.8±1.0 11 113.7±10.3 15.8±1.2 0.14±0.01 26.5±2.5 12 83.5± 6.9 21.5±1.8 0.27±0.03 19.9±1.3 13 62.2± 5.6 34.8±1.8 0.58±0.04 7.3±0.4 14 79.6± 6.7 28.7±2.4 0.37±0.03 18.9±1.5 (Numerical value: mean standard error) As shown in the above table, the arteriosclerosis indices of Test Groups 12-14 were higher than those of Test Groups 10 and 11, which indicates that the cholesterol metabolism in serum was improved in Test Groups 12-14. In addition, Test Groups 12-14 showed lower total cholesterol concentration in liver as compared with Test Groups 10 and 11; in particular, the total cholesterol concentration in liver of Test Group 13 was much the lowest. No significant difference was observed in feed intake or increase in body weight between the test groups.

Certain embodiments of the invention are illustrated in the following Examples and Comparative Examples.

Best Mode for Carrying Out the Invention Example. 1 To 1 kg of Regular Gluten A (wheat gluten, Bunge, bound phospholipid content: was added 2.4 1 of a 16 solution prepared by dispersing Elmizer AC (enzyme-modified lecithin, Kyowa Hakko Kogyo Co., Ltd.) in water. The mixture was kneaded by using a baker's mixer (100 at room temperature for 10 minutes. The resulting reaction mixture was freeze-dried and then pulverized to obtain about-1.1 kg of a protein/phospholipid complex (bound phospholipid content: 10%, free phospholipid content: Example 2 To 1 kg of Promic P (isolated soybean protein, Kyowa Hakko Kogyo Co., Ltd., bound phospholipid content: was added 10 L of a 2.5% solution prepared by dispersing Elmizer AC in water. The mixture was stirred rapidly 15 (10,000 at room temperature for 10 minutes. The resulting reaction mixture was freeze-dried and then pulverized to obtain 1.1 kg of a protein/phospholipid complex (bound phospholipid content: 20%, free phospholipid content: Example 3 The same procedure as in Example 2 was repeated, except that SLP-White (purified soybean lecithin, True Lecithin mfg. Co., Ltd.) was used in place of Elmizer AC, whereby about 1.1 kg of a protein/phospholipid complex S(bound phospholipid content: 20%, free phospholipid content: was obtained.

Example 4 The protein/phospholipid complex obtained in Example 1 (1 kg) was dispersed in 9 L of water, followed by addition of 2 N hydrochloric acid to adjust the solution to pH 2.

To the resulting solution was added pepsin [activity; 1:10,000 (this means that 1 g of the pepsin is capable of hydrolyzing 10,000 g of egg white protein at 50 0 C in 2 hours under acidic conditions with hydrochloric acid), 4 Li 17 Nacalai Tesque, Inc.] in an amount of 1% based on the protein/phospholipid complex. The mixture was allowed to stand at 37 0 C for 24 hours, followed by heating at 90 0 C for one hour to stop the reaction. The reaction mixture was neutralized with 2 N sodium hydroxide, and then -centrifuged. To the obtained precipitate was added water, and the mixture was centrifuged again. This procedure was repeated twice, whereby the precipitate was washed. The precipitate was freeze-dried and then pulverized to obtain 200 g of a hydrolyzate of the protein/phospholipid complex which is slightly soluble in water (molecular weight: ca.

15,000, bound phospholipid content: 10%, free phospholipid content: The molecular weight was determined by sodium dodecyl sulfate (SDS)-polyacrylamide gel 15 electrophoresis (the same method was employed for the determination of molecular weight in the following Examples) Example The same procedure as in Example 4 was repeated, except that the protein/phospholipid complex obtained in Example 2 was used in place of the protein/phospholipid complex obtained in Example 1, whereby 200 g of a hydrolyzate of the protein/phospholipid complex which is slightly soluble in water (molecular weight: ca. 15,000, bound phospholipid content: 20%, free phospholipid content: was obtained.

The nitrogen contents of the protein used as the starting material and the protein contained in the obtained hydrolyzate of the protein/phospholipid complex were respectively determined by the Kjeldahl method.

Multiplication of the obtained values by a conversion factor of 6.25 gave the weights of the proteins, and the protein recovery calculated as the ratio of the amount of the protein contained in the hydrolyzate to that of the protein used as the starting material was 19.1%.

18 Example 6 The same procedure as in Example 4 was repeated, except that the protein/phospholipid complex obtained in Example 3 was used in place of the protein/phospholipid complex obtained in Example 1, whereby 200 g of a hydrolyzate of the protein7phospholipid complex which is slightly soluble in water (molecular weight: ca. 15,000, bound phospholipid content: 20%, free phospholipid content: was obtained.

Example 7 Regular Gluten A (bound phospholipid content: (1 kg) was dispersed in 9 f of water, followed by addition of 2 N hydrochloric acid to adjust the solution to pH 2. To the 15 resulting solution was added pepsin (activity; 1:10,000, Nacalai Tesque, Inc.) in an amount of 1% based on Regular Gluten A. The mixture was allowed to stand at 37 0 C for 24 hours, followed by heating at 90°C for one hour to stop the reaction. The reaction mixture was neutralized with 2 N sodium hydroxide, and then centrifuged. To the obtained precipitate was added water, and the mixture was centrifuged again. This procedure was repeated twice, whereby the precipitate was washed. The precipitate was freeze-dried and then pulverized to obtain 200 g of a protein hydrolyzate (molecular weight: ca. 15,000). To 200 g of the obtained protein hydrolyzate was added 1.0 e of a solution prepared by dispersing Elmizer AC in water, and the mixture was stirred rapidly (10,000 The resulting reaction mixture was freeze-dried and then pulverized to obtain 220 g of a protein hydrolyzate/ phospholipid complex (bound phospholipid content: 10%, free phospholipid content: Example 8 Promic P (bound phospholipid content: (1 kg) was dispersed in 9 e of water, followed by addition of 2 N hydrochloric acid to adjust the solution to pH 2. To the resulting solution was added pepsin (activity; 1:10,000, Nacalai Tesque, Inc.) in an amount of 1% based on Promic P.

The mixture was allowed to stand at 37 0 C for 24 hours, followed by heating at 90 0 C for one hour to stop the reaction. The reaction mixture was neutralized with 2 N sodium hydroxide, and then centrifuged. To the obtained precipitate was added water, and the mixture was centrifuged again. This procedure was repeated twice, whereby the precipitate was washed. The precipitate was freeze-dried and then pulverized to obtain 200 g of a protein hydrolyzate (molecular weight: ca. 15,000). To 200 g of the obtained protein hydrolyzate was added 2.0 e of a 2.5% solution prepared by dispersing Elmizer AC in water, 15 and the mixture was stirred rapidly (10,000 The S resulting reaction mixture was freeze-dried and then pulverized to obtain 250 g of a protein hydrolyzate/ phospholipid complex (bound phospholipid content: 20%, free phospholipid content: 20 The protein recovery calculated as the ratio of the amount of the protein contained in the obtained protein hydrolyzate/phospholipid complex to that of the protein used as the starting material in the same manner as in Example 5 was 12.4%.

*4 Example 9 The same procedure as in Example 8 was repeated, except that SLP-White was used in place of Elmizer AC, whereby 250 g of a protein hydrolyzate/phospholipid complex (bound phospholipid content: 20%, free phospholipid content: was obtained.

Comparative Example 1 Promic P (bound phospholipid content: (1 kg) was mixed with 250 g of SLP-White to obtain 1250 g of a protein/phospholipid mixture (bound phospholipid content: free phospholipid content: Comparative Example 2 Regular Gluten A (bound phospholipid content: (1 kg) was mixed with 110 g of Elmizer AC to obtain 1110 g of a protein/enzyme-modified lecithin mixture (bound phospholipid content: free phospholipid content: Comparative Example 3 Promic P (bound phospholipid content: (1 kg) was dispersed in 9 e of water, followed by addition of 2 N hydrochloric acid to adjust the solution to pH 2. To the 15 resulting solution was added pepsin (activity; 1:10,000, Nacalai Tesque, Inc.) in an amount of 1% based on Promic P.

mixture was allowed to stand at 37 0 C for 24 hours, followed by heating at 90 0 C for one hour to stop the reaction. The reaction mixture was neutralized with 2 N sodium hydroxide, and then centrifuged. To the obtained precipitate was added water, and the mixture was centrifuged again. This procedure was repeated twice, whereby the precipitate was washed. The precipitate was freeze-dried and then pulverized to obtain 200 g of a 25 protein hydrolyzate (molecular weight: ca. 15,000). The obtained protein hydrolyzate (1 kg) was mixed with 250 g of SLP-White to obtain 1250 g of a protein hydrolyzate/ phospholipid mixture (bound phospholipid content: 0.8%, free phospholipid content: Example Hamburgers (two servings) are prepared from the following ingredients.

Onion Half Minced meat 100 g Water Lard 29.2 g 11.8 g Slightly water-soluble product obtained in Example Egg Crumbs Seasonings 9 g One Small quantity Small quantity from the following Example 11 Cookies (30 pieces) are prepared ingredients.

Soft flour Starch Water Slightly water-soluble product obtained in Example Baking powder Salt Egg Butter Milk Honey 100 g 74 g 14 g 9 g 2 Tsp.

1/2 Tsp.

One 80 g 2 Tbsp.

Small quantity r Example 12 A powdery protein to be used in a liquid preparation is prepared from the following ingredients.

Slightly water-soluble product obtained in Example Casein sodium L-Valine Ferric pyrophosphate (iron source) Phoscal EFC (calcium source, Nikko Fine Products) 80 g 17.5 g 0.5 g 0.1 g 1 g Vitamin Mix (Merck Co., Inc.) 1 g A liquid preparation is prepared by dispersing 20 g of the powdery protein in 180 ml of water.

Example 13 Tablets are prepared from the following ingredients.

Slightly water-soluble product 2 g obtained in Example Powdery sugar 2.6 g Ascorbic acid 150 mg Citric acid 0.1 g Sucrose stearate 150 mg Flavor 15 mg Industrial Applicability The present invention provides a lipid metabolism 20 improving agent and a functional food.

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Claims (28)

1. A lipid metabolism improving agent comprising a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed.

2. The lipid metabolism improving agent according to claim 1 in an effective amount which is in pharmaceutically acceptable dosage form comprising a pharmaceutically acceptable carrier.

3. A cholesterol metabolism improving agent comprising a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed.

4. The cholesterol metabolism improving agent according to claim 3 in an effective amount which is in pharmaceutically acceptable dosage form comprising a pharmaceutically acceptable carrier. A functional food comprising a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed.

6. The functional food according to claim 5 which contains 0.lwt% or more of the complex.

7. The functional food according to claim 4 or 5 having lipid metabolism improving activity.

8. The functional food according to claim 4 or 5 having cholesterol metabolism improving activity.

9. A method for improving the lipid metabolism of an animal, which method comprises administering to the animal a protein/phospholipid complex containing or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed. A method for improving the cholesterol metabolism of an animal, which method comprises administering to the animal a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, 30 soybean, corn or milk and not hydrolyzed.

11. A protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed, when used for improving the lipid metabolism, the cholesterol metabolism, or both, of an animal. I:\DayLib\LIBUU\03290.doc 24

12. Use of a protein/phospholipid complex containing 10wt% or more of bound phospholipid wherein the protein is derived from wheat, soybean, corn or milk and not hydrolyzed, in the manufacture of a medicament for improving the lipid metabolism, the cholesterol metabolism, or both, of an animal.

13. The agent according to any one of claims 1 to 4 wherein the complex contains 10-50wt% of bound phospholipid.

14. The agent according to any one of claims 1 to 4 wherein the complex contains

20-50wt% of bound phospholipid. The agent according to any one of claims 1 to 4 wherein the phospholipid is lecithin. 16. The agent according to any one of claims 1 to 4 wherein the phospholipid is enzyme modified lecithin. 17. The functional food according to any one of claims 5 to 8 wherein the complex contains 10-50wt% of bound phospholipid. 18. The functional food according to any one of claims 5 to 8 wherein the complex contains 20-50wt% of bound phospholipid. 19. The functional food according to any one of claims 5 to 8 wherein the phospholipid is lecithin. The functional food according to any one of claims 5 to 8 wherein the phospholipid is enzyme modified lecithin.

21. The method according to claim 9 or 10 wherein the complex contains 10-50wt% of bound phospholipid.

22. The method according to claim 9 or 10 wherein the complex contains 20-50wt% of bound phospholipid.

23. The method according to claim 9 or 10 wherein the phospholipid is lecithin.

24. The method according to claim 9 or 10 wherein the phospholipid is enzyme- modified lecithin. The complex according to claim 11 wherein the complex contains 10-50wt% of bound phospholipid. 30 26. The complex according to claim 11 wherein the complex contains 20-50wt% of bound phospholipid.

27. The complex according to claim 11 wherein phospholipid is lecithin.

28. The complex according to claim 11 phospholipid is enzyme-modified lecithin.

29. The use according to claim 12 wherein the complex contains 10-50wt% of bound phospholipid. I:\DayLib\LIBUU\03290.doc The use according to claim 12 wherein the complex contains 20-50wt% of bound phospholipid.

31. The use according to claim 12 wherein phospholipid is lecithin.

32. The use according to claim 12 wherein the phospholipid is enzyme-modified lecithin.

33. A lipid metabolism improving agent substantially as hereinbefore described with reference to any one of the examples but excluding the comparative examples.

34. A cholesterol metabolism improving agent as hereinbefore described with reference to any one of the examples but excluding the comparative examples.

35. A functional food substantially as hereinbefore described with reference to any one of the examples but excluding the comparative examples.

36. A method for improving the lipid metabolism of an animal, said method substantially as hereinbefore described with reference to any one of the examples but excluding the comparative examples.

37. A method for improving the cholesterol metabolism of an animal, said method substantially as hereinbefore described with reference to any one of the examples but excluding the comparative examples.

38. A protein/phospholipid complex substantially as hereinbefore described with reference to any one of the examples but excluding the comparative examples. Dated 7 July 2003 Kyowa Hakko Kogyo Co., Ltd. Patent Attorneys for the Applicant/Nominated Person SPRUSON FERGUSON S S *ot I;\DayLib\LIBUU\03290.doc