BACKGROUND OF THE INVENTION In recent years, coronary cardio-circulary diseases, e. g., atherosclerosis and hypercholesterolemia, have increasingly become a major cause of deaths. It has been reporte that an elevated plasma cholesterol level causes the deposition of fat, macrophages and foam cells on the wall of blood vesses, such deposit leading to plaque formation and then to atherosclerosis (Ross, R., Nature, 362, 801-809 (1993)). One of the methods for decreasing the plasma cholesterol level is alimentotherapy to reduce the ingestion of cholesterol and lipids. Another method is to inhibit the absorption of cholesterol by inhibiting enzymes involved therein.

Acyl CoA-cholesterol-o-acyltransferase (ACAT) promotes the esterification of cholesterol in blood. Foam cells are formed by the action of ACAT and contain a large amount of cholesterol ester carried by low density lipoproteins. The formation of foam cells on the wall of artery increases with the ACAT activity, and, accordingly, an inhibitor of ACAT may also be an agent for preventing atherosclerosis.

Further, it has been reporte that the blood level of LDL- cholesterol can be reduced by inhibiting the ACAT

activity (Witiak, D. T. and D. R. Feller (eds.), Anti- LiPidemic Druas: Medicinal, Chemical and Biochemical Aspects, Elsevier, pop159-195 (1991)).

On the other hand, deterioration of hepatic functions may occur due to an excessive intake of alcohol or foods having a high lipid content, or an infection of hepatitis B or C virus, and it may develop into hepatitis, hepatocirrhosis or hepatic cancer. In particular, the excessive intake of fat-containing foods and alcohol causes fatty liver wherein a large amount of lipids is deposited in the liver tissue and the levels of serum GOT (glutamate- oxaloacetate transaminase), GPT (glutamate-pyruvate transaminase) and y-GTP (y-glutamyl transpeptidase) are elevated (T. Banciu et al., Med. Interne., 20,69-71 (1982); and A. Par et al., Acta. Med. Acad. Sci. Hune., 33,309- 319(1976)).

Numerus efforts have been made to develop medicines which inhibit ACAT activity; and, as a result, several compound isolated from the cultures of various microorganisms have been reporte. Examples of such compound include pyripyropenes isolated from the culture of Asperqillus fumigatus (S. Omura et al., J. Antibiotics, A6, 1168-1169 (1993)) and Acaterin isolated from Pseudomonas sp. (S. Nagamura et al., J. Antibiotics, 45,1216- 1221(1992)).

Further, as a treating agent for hypercholesterolemia, a HMG-CoA reductase inhibitor named Lovastatine has been developed and marketed by Merck Co., U. S. A. However, this medicine is known to induce adverse side effect of increasing creatin kinase in the liver.

Accordingly, there has continued to exist a need to develop non-toxic inhibitors of ACAT and macrophage-lipid complex accumulation on the arterial epithelium, and a preventive or treating agent for the hepatic diseases.

The present inventors have endeavored to develop a novel and potent ACAT inhibitor, macrophage-lipid complex accumulation inhibitor and treating agent for the hepatic

diseases from natural materials, and, as a result, have discovered that naringin or naringenin has a potent ACAT inhibitory activity, macrophage-lipid complex accumulation inhibitory activity, and preventive or treating activity on the hepatic diseases.

Naringin (C27H32014, M. W.: 580. 53) and the aglycon of naringin, naringenin (C15H1205, M. W.: 272.25), are flavonoids found in lemons, grapefruits, tangerines, citrons and oranges (Citrus sinensis) (Horowitz, Gentil, Tetrahedron, L9, 773(1963)).

It has been reporte that naringin or naringenin has anti-cancer, anti-viral and cholesterol lowering activities (Monforte, M. T., et al., Farmaco., 50 (9), 595-599 (1995, Sep.) ; JP 95-86929; JP 95-86930; Felica, V., et al., J. Med. Virol., 15,71-79 (1985); EP 0352147 A2 (1990.1.24); and Martin, M. J., et al., Pharmacal., 49, 144-150 (1994)).

Further, naringin has been used as a bitter tasting agent, sweetener or chewing gum base.

However, hitherto, none of the ACAT inhibitory activity, macrophage-lipid complex accumulation inhibitory activity and preventive or treating activity on the hepatic diseases of naringin or naringenin has been reporte.

SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide a novel use of naringin or naringenin for inhibiting the ACAT activity in a mammal.

Another object of the present invention is to provide a novel use of naringin or naringenin for inhibiting the accumulation of macrophage-lipid complex on the endothelial wall of an artery in a mammal.

A further object of the present invention is to provide a novel use of naringin or naringenin for preventing or treating hepatic diseases in a mammal.

BRIEF DESCRIPTION OF THE DRAWINGS The above and other objects and features of the present invention will become apparent from the following description of the invention, when taken in conjunction with the accompanying drawings, in which: Figs. 1A, 1B and 1C show the arteries of the rabbits administered with 1% cholesterol; 1% cholesterol plus 1 mg/kg Lovastatine; and 1% cholesterol plus 0.1% naringint respectively; and Figs. 2A, 2B and 2C present the microscopic features of the livers of the rabbits administered with 1% cholesterol; 1% cholesterol plus 1 mg/kg Lovastatine; and 1% cholesterol plus 0.1% naringin, respectively.

DETAILED DESCRIPTION OF THE INVENTION In accordance with one aspect of the present invention, there is provided a use of naringin or naringenin for inhibiting the acyl-CoA cholesterol-o-acyltransferase (ACAT) activity in a mammal.

In accordance with another aspect of the present invention, there is provided a use of naringin or naringenin for inhibiting the accumulation of macrophage-lipid complex on the endothelial wall of an artery in a mammal.

In accordance with a further aspect of the present invention, there is provided a use of naringin or naringenin for preventing or treating hepatic diseases in a mammal.

Naringin and naringenin may be extracted from the peel of citrus or synthesized according to the process described by Zemplen, Bognar, Ber., 75,1043 (1943) and Seka, Proche, Monatsh., 69,284 (1936). Further, naringenin can be prepared by the hydrolysis of naringin.

Naringin or naringenin exerts an inhibitory effect on the ACAT activity and the accumulation of macrophage-lipid complex on the endothelial wall of an artery, and a preventive or treating effect on hepatic diseases at a dose

of 0.1 mg/kg/day or more, the inhibitory effect increasing with the dose thereof.

Moreover, in spite of its potent efficacies, naringin or naringenin shows little toxicity or mitogenicity in tests using mice. More specifically, naringin or naringenin exhibits no toxicity when it is orally administered to a mouse at a dose of 1,000 mg/kg, which corresponds to an oral administration dose of 50 to 100 g/kg body weight of naringin or naringenin for a person weighing 50 kg.

Further, naringin and naringenin exert no adverse effects on the liver function.

The present invention also provides a pharmaceutical composition for inhibiting the ACAT activity and accumulation cf macrophage-lipid complex on the endothelial wall of an artery, and for preventing or treating hepatic diseases, which comprise naringin or naringenin as an active ingredient and pharmaceutically acceptable excipients, carriers or diluent.

A pharmaceutical formulation may be prepared in accordance with any of the conventional procedures. In preparing the formulation, the active ingredient is preferably admixed or diluted with a carrier, or enclose within a carrier which may be in the form of a capsule, sachet or other container. When the carrier serves as a diluent, it may be a solid, semi-solid or liquid material acting as a vehicle, excipient or medium for the active ingredient. Thus, the formulations may be in the form of a tablet, pill, powder, sachet, elixir, suspension, mulsion, solution, syrup, aerosol, soft and hard gelatin capsule, sterile injectable solution, sterile packaged powder and the like.

Examples of suitable carriers, excipients, and diluents are lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, alginates, gelatin, calcium phosphate, calcium silicate, cellulose, methyl cellulose, microcrystalline cellulose, polyvinylpyrrolidone, water, methylhydroxybenzoates, propylhydroxybenzoates, talc,

magnesium stearate and mineral oil. The formulations may additionally include filles, anti-agglutinating agents, lubricating agents, wetting agents, flavoring agents, emulsifiers, preservatives and the like. The compositions of the invention may be formulated so as to provide quick, sustained or delayed release of the active ingredient after their administration to a mammal by employing any of the procedures well known in the art.

The pharmaceutical composition of the present invention can be administered via various routes including oral, transdermal, subcutaneous, intravenous and intramuscular introduction. In case of human, a typical daily dose of naringin or naringenin may range from about 0.1 to 100 mg/kg body weight, preferably 3 to 10 mg/kg body weight, and can be administered in a single dose or in divided doses.

However, it should be understood that the amount of the active ingredient actually administered ought to be determined in light of various relevant factors including the condition to be treated, the chosen route of administration, the age, sex and body weight of the individual patient, and the severity of the patient's symptom; and, therefore, the above dose should not be intended to limit the scope of the invention in any way.

Moreover, naringin or naringenin can be incorporated in foods or beverages, as an additive or a dietary supplement, for the purpose of inhibiting the ACAT activity, inhibiting the accumulation of macrophage-lipid complex on the arterial endothelium and/or preventing or treating hepatic diseases.

The foods or beverages may include meats; juices such as a vegetable juice (e. g., carrot juice and tomato juice) and a fruit juice (e. g., orange juice, grape juice, pineapple juice, apple juice and banana juice); chocolats; snacks; confectionery; pizza; foods made from cereal flour such as breads, cakes, crackers, cookies, biscuits, noodles and the likes; gums; dairy products such as milk, cheese, yogurt and ice creams; soups; broths; pastes, ketchups and sauces; teas; alcoholic beverages; carbonate beverages such as

Coca-Colas and Pepsi-Cola@; vitamin complexes; and various health foods.

In this case, the content of naringin or naringenin in a food or beverage may range from 0.01 to 5% by weight. In particular, the beverage according to the present invention may comprise 200 to 10,000 mg of naringin or naringenin per 1000 ml of the beverage.

As described above, naringin or naringenin can be used as an effective, non-toxic pharmaceutical agent for inhibiting ACAT activity, inhibiting the accumulation of macrophage-lipid complex on the arterial endothelium, and/or preventing or treating hepatic diseases.

The following Examples are intended to further illustrate the present invention without limiting its scope.

Further, percentages given below for solid in solid mixture, liquid in liquid, and solid in liquid are on a wt/wt, vol/vol and wt/vol basis, respectively, and all the rections were carried out at room temperature, unless specifically indicated otherwise.

Example 1: Extraction of Naringin from Citrus Peel The peels of tangerines (Cheju Island, Rorea), citrons (Jeollanamdo, Korea), and oranges, grapefruits and lemons (California, CA, U. S. A.) were dried at a room temperature and powdered to a particle size ranging from 100 to 200 Hm. 50 me of methanol was added to 500 mg each of the citrus peel powder and extracted in a water bath at 50°C for 6 hours. The extract thus obtained was cooled and filtered, and then methanol was added to the filtrate to a volume of 50 m. 2.

To confirm the content of naringin in the extract obtained above, 5.0 HQ of the resulting extract was subjected to high performance liquid chromatography (HPLC) using Lichrosorb RP-8 column (5 Hm, 4 x 250 mm) which was pre-equilibrated with 37 % methanol and maintained at a temperature of 30°C. The extract was eluted with 37 %

methanol at a flow rate of 1.0 mQ/min. Standard solutions were prepared by dissolving naringin (Sigma Chemical Co.

U. S. A.) in methanol to final concentrations of 0.1,0.2, 0.3,0.4 and 0.5 mg/m2, and subjected to HPLC under the same condition as above. The eluates were detected at 280 nm with UV-VIS spectrophotometer and the content of naringin was calculated by comparing the areas of HPLC profiles of the citrus peel extract and the standard solution. The content (%) of naringin in various citrus peel extracts is shown in Table I.

Table I Naringin (%) Orange trace amount Lemon trace amount Tangerine trace amount grapefruit 4.70 citron0.80 Example 2: Toxicity of Orally Administered Naringin or Naringenin 7 to 8 week-old, specific pathogen-free ICR female mice (6 heads) each weighing about 25 to 29 g and male mice (6 heads) each weighing about 34 to 38 g were bred under a condition of temperature 221°C, moisture 55+5 t and photoperiod 12L/12D. Fodder (Cheiljedang Co., mouse and rat fodder) and water were sterilized and fed to the mice.

Naringin or naringenin was dissolve in 0.5 8 Tween 80 to a concentration of 100 mg/ml, and the solution was orally administered to the mice in an amount of 0.2 ml per 20 g of mouse body weight. The solution was administered once and the mice were observe for 10 days for signs of adverse effects or death according to the following schedule: 1,4, 8, and 12 hours after the administration and, every 12 hours

thereafter. The weight changes of the mice were recorded every day to examine the effect of naringin or naringenin.

Further, on the 10th day, the mice were sacrifice and the internal organs were visually examine.

All the mice were alive at day 10 and naringin or naringenin showed no toxicity at a dose of 1,000 mg/kg. The autopsy revealed that the mice did not develop any pathological abnormality, and no weight loss was observe during the 10 day test period. Accordingly, it was concluded that naringin or naringenin is not toxic when orally administered to an animal.

Example 3: Administration of Naringin or Naringenin to an Animal 30 four-week-old Sprague-Dawley rats (Taihan laboratory animal center, Korea) each weighing about 90 to 110 g were evenly divided into three dietary groups by a randomized block design. The rats of the three groups were fed with three different high-cholesterol diets, i. e., AIN-76 laboratory animal diet (ICN Biochemicals, Cleveland, OH, U. S. A.) containing 1 % cholesterol (Control group), and 1 % cholesterol plus 0.1% naringin or naringenin, respectively.

The compositions of diets fed to the three groups are shown in Table II.

Table II

Dietary group Control Naringin Naringenin group group group Ingredients Casein 20 20 20 D, L-methionine 0.3 0.3 0. 3 Corn starch 15 15 15 Sucrose 49 48.9 48.9 Cellulose powder*l 5 5 5 Mineral mixture*1 3.5 3.5 3.5 Vitamin mixture*1 1 1 Choline bitartrate 0.2 0.2 0.2 Corn oil 5 5 5 Cholesterol 1 1 1 Naringin*2 0.1- Naringenin*2--0.1 Total 100 100 100 *1 Purchased from TEKLAD premier Co. (Madison, WI, U. S. A.) *2 Purchased from Sigma Chemical Co. (St. Louis, Mo, U. S. A.) The rats were allowed to feed freely on the specified diet together with water for six weeks, the ingestion amount was recorde daily and the rats were weighed every 7 days, and then the record was analyzed. All rats showed a normal growth rate and there was observe no significant difference among the three groups in terms of the feed ingestion amount and the weight gain.

Example 4: Determination of Total Cholesterol, HDL- Cholesterol and Neutral Lipid Content in Plasma The effect of administering naringin or naringenin to rats on the plasma cholesterol and neutral lipid content was determined as follows.

Blood samples were taken from the rats of the three dietary groups and plasma HDL fractions were separated therefrom by using HDL-cholesterol reagent (Sigma Chemical Co., Cat. No. 352-3) containing dextran-sulfate. Total cholesterol and HDL-cholesterol levels were determined by using Sigma Diagnostic Kit Cat. No. 352-100 (Sigma Chemical Co., U. S. A.) (Allain et al., Clin. Chem., 20,470-475 (1974)).

Neutral lipid level was determined by using Sigma Diagnostic Kit Cat. No. 339--50 (Bucolo, G. and David, H., Clin. Chem., 19, 476-482(1973)). The result is shown in Table III, wherein the total plasma cholesterol levels in naringin and naringenin-fed rat groups decreased by 32 % and 18%, respectively, as compare with that of the control group.

Table III Group Control Naringin Naringenin Lipid Conc. group group group Total-C (mg/dl) 147.834.8 100.816.1 120.925.9 HDL-C (mg/dl) 22.2 24.0 23.4 HDL-C (%) 15. 75.3 23.97.6 20.89.1 Total-C TG (mg/dl) 99.218. 9'86. 714.6 103. 418.2 * Total-C: Total-cholesterol * HDL-C: HDL-cholesterol * TG: Triglyceride Example 5: Activity of Naringin and Naringenin in ACAT Inhibition (Step 1) Preparation of microsomes To determine the effects of naringin and naringenin feeding to rats on the activity of ACAT, microsomes were separated from the liver tissue to be used as an enzyme source.

First, the rats of the three groups prepared in Example 3 were sacrifice by decapitation and the livers were excise. 1 g each of the livers was homogenized in 5 ml of homogenization medium (0. 1 M KH2PO4, pH 7.4,0.1 mM EDTA and 10 mM 13-mercaptoethanol). The homogenate was centrifuged at 3, 000xg for 10 min. at 4°C and the supernatant thus obtained was centrifuged av 15, 000xg for 15 min. at 4°C to obtain a supernatant. The supernatant was put into an ultracentrifuge tube (Beckman) and centrifuged at 100, 000xg for 1 hour at 4°C to obtain microsomal pellets, which were then suspende in 3 ml of the homogenization medium and centrifuged at 100, 000xg for 1 hour at 4°C. The pellets thus obtained were suspende in 1 ml of the homogenization medium. The concentration of proteins in the resulting suspension was determined by Lowry's method and then adjusted to 4 to 8 mg/ml. The resulting suspension was stored in a deep FormaScientificInc.).(Biofreezer, (Step 2) ACAT assay _ 6.67 pl of 1 mg/ml cholesterol solution in acetone was mixed with 6 pl of 10 % Triton WR-1339 (Sigma Co.) in acetone and, then, acetone was removed from the mixture by evaporation using nitrogen gas. Distille water was added to the resulting mixture in an amount to adjust the concentration of cholesterol to 30 mg/ml.

To 10 yl of the resulting aqueous cholesterol solution were added 10 pl of 1 M KH2PO4 (pH 7.4), 5 pl of 0.6 mM bovine serum albumin (BSA), 10 pl of microsome solution obtained in (Step 1) and 55 pl of distille water (total 90 pal). The mixture was pre-incubated in a waterbath at 37°C for 30 min.

10 pl of (1-14C) oleoyl-CoA solution (0. 05 pCi, final concentration: 10 µM) was added to the pre-incubated mixture and the resulting mixture was incubated in a waterbath at 37°C for 30 min. To the mixture were added 500 pl of isopropanol: heptane mixture (4: 1 (v/v)), 300 pl of heptane and 200 pal of 0.1 M KH2PO4 (pH 7.4), and the mixture was mixed

violently by using a vortex and then allowed to stand at a room temperature for 2 min.

200 pl of the resulting supernatant was put in a scintillation bottle and 4 ml of scintillation fluid (Lumac) was added thereto. The mixture was assayed for radioactivity with 1450 Microbeta liquid scintillation counter (Wallacoy, Finland). ACAT activity was calculated as picomoles of cholesteryl oleate synthesized per min. per mg protein (pmoles/min/mg protein). The result is shown in Table IV.

Table IV ACAT activity % Inhibition on Group (pmole/min/mg protein) ACAT activity Control group 806.2 105.2 0 0.1% naringin 643.5 # 80.7 20.2 group 0.1% naringenin 666.3 # 65.3 17.4 group As can be seen from Table IV, ACAT activities observe in naringin and naringenin-fed rat groups are lower than that of the control group by 20.2% and 17. 4%, respectively.

Example 6: Inhibition of Plaque Formation Caused by Macrophage-Lipid Complex in Naringin and Naringenin-Fed Animals (Step 1) Administration of naringin and naringenin to animals 24 three-month-old New Zealand White rabbits (Yeonam Horticulture and Animal Husbandry College, Rorea) each weighing about 2.5 to 2.6 kg were bred under a condition of temperature 202°C, relative humidity 555 %, and photoperiod 12L/12D. The rabbits were divided by a group of 6 rabbis, and the rats of four groups were fed with four

different diets, i. e., RC4 diet (Oriental Yeast Co., Japan) containing 1 % cholesterol (Control group); 1 % cholesterol plus 1 mg/kg Lovastatine (Merck, U. S. A.) (Comparative group); 1 % cholesterol plus 0.1 % ;naringin and 1 % cholesterol plus 0.1 % naringenin, respectively. RC4 diet comprises 7.6 <BR> <BR> <BR> % moisture, 22.8 % crude protein, 2.8 % crude fat, 8.8 % crude ash, 14.4 % crude cellulose and 43.6 % soluble nitrogen-free substances. The rabbits were bred for 6 weeks while being allowed free access to the diets and water.

(Step 2) Analysis for fatty streak in the main artery The rabbits bred in (Step 1) were sacrifice and their chest were incise. The main artery was cut out therefrom in a length of about 5 cm downward from the site 1 cm above the aortic valve and the fat surrounding the main artery was removed. The main artery was incised in the middle along the longitudinal axis and pinned to a dish. The moist artery was photographed and, then, staining of fatty streak was carried out in accordance with the method of Esper, E., et al. (J. Lab. Clin. Med., 121,103-110 (1993)) as follows.

A part of the incised main artery was washed three times by 2 min. with anhydrous propylene glycol and stained for 30 min. with a saturated solution of Oil Red O (ORO, Sigma Co.) dissolve in propylene glycol. Thereafter, the artery was washed twice by 3 min. with 85 % propylene glycol to remove remaining staining solution and, then washed with physical saline. The artery was photographed and the photograph was traced. The area of stained region (fatty streak region) was determined with an image analyzer (LEICA, Q-600, Germany) and its proportion (%) to the total arterial area was calculated.

On the other hand, the other part of the main artery was stained in accordance with hematoxylin-eosin (H&E) and Masson's trichrome staining methods and observe under a microscope to confirm whether the macrophage-lipid complexes were accumulated in the intima, internus, elastic lamina and

media.

Further, blood samples were taken from the rabbits and total cholesterol and triglyceride levels were determined in accordance with the same procedure in Example 4.

The result is shown in Table V.

Table V Total Triglyceride M-L* cholesterol (mg/dl) complex Dietary Group (mg/dl) area Control group 1143 56 35 lmg/kgLovastatine group 1210 66 5 0.1% naringin group 1367 72 12 0.1% naringenin group 1350 70 13 * M-L complex: Macrophage-lipid complex As can be seen from Table V, the area of macrophage- lipid complex accumulated on the arterial endothelium decreased significantly in the 1 mg/kg Lovastatin, 0.1 % naringin and 0.1 % naringenin groups, as compare to the control group. Accordingly, it has been confirme that naringin and naringenin inhibit the accumulation of macrophage-lipid complex on the arterial endothelium. In particular, it is remarkable that the inhibitory activity of naringin and naringenin on the accumulation of macrophage- lipid complex was exhibited under the blood cholesterol levels above 1,100 mg/dl, which are much higher than that of normal rabbit, i. e., about 50 mg/dl. This result suggests that there may be a novel mechanism for preventing the onset of atherosclerosis, which is different from the blocking of cholesterol synthesis by a HMG-CoA reductase inhibitor, blocking of cholesterol absorption by an ACAT inhibitor, or blocking of cholesterol transfer by a CETP inhibitor.

Figs. 1A, 1B and 1C show the arteries of the rabbits<BR> <BR> <BR> <BR> <BR> <BR> <BR> administered with 1 % cholesterol (control group); 1 % cholesterol plus 1 mg/kg Lovastatin@ (comparative group); and 1 % cholesterol plus 0.1 % naringin, respectively. As shown in Figs. 1A, 1B and 1C, a thick layer of macrophage-lipid complex was observe on the arterial endothelium of the rabbit administered with 1 % cholesterol, while no or very thin layers of macrophage-lipid complex were observe on the arterial endotheliums of the rabbits administered with 1 % <BR> <BR> <BR> <BR> cholesterol plus 1 mg/kg Lovastatin#, and 1 8 cholesterol plus 0.1 % naringin, respectively.

Accordingly, it has been concluded that naringin and naringenin strongly inhibit the accumulation of macrophage- lipid complex on the arterial endothelium.

Example 7: Prevention of Hepatic Diseases by Naringin (Step 1) Administration of naringin to rats 20 four-week-old Sprague-Dawley rats (Taihan laboratory animal center, Korea) each weighing about 90 to 110 g were evenly divided into two dietary groups by a randomized block design. The rats of the two groups were fed with two different high-cholesterol diets, i. e., AIN-76 laboratory animal diet (ICN Biochemicals, Cleveland, OH, U. S. A.) <BR> <BR> <BR> <BR> containing 1 % cholesterol (Control group), and 1 % % cholesterol plus 0. 02% naringin, respectively. The compositions of the diets fed to the two groups are shown in Table VI.

Table VI Dietary group Control Naringin group group Ingredients Casein 20 10 D, L-methionine 0.3 0.3 Corn starch 15 15 Sucrose 39 38.98 Cellulose powder*1 5 5 Mineral mixture*1 3.5 3.5 Vitamin mixture*1 1 1 Choline bitartrate 0.2 0.2 Fat 15 15 Cholesterol 1 1 Naringin*2-0.02 Total 100 100

*1 Purchased from TEKLAD premier Co. (Madison, WI, U. S. A.) *2 Purchased from Sigma Chemical Co. (St. Louis, Mo, U. S. A.) The rats were allowed to feed freely on the specified diet together with water for six. weeks, the ingestion amount was recorde daily and the rats were weighed every 7 days, and then the record was analyzed. All rats showed a normal growth rate and there was observe no significant difference among the two groups in terms of the feed ingestion amount and the weight gain.

(Step 2) Determination of serum GOT and GPT levels The effect of administering naringin to rats on the function of the liver was examine as follows.

Blood samples were taken from the rats of the two dietary groups and serum GOT (glutamate-oxaloacetate transaminase) and GPT (glutamate-pyruvate transaminase) levels were determined in accordance with the method of

Reitman and Frankel (Reitman, S. and J. S. Frankel, Am. J.

Clin. Pathol., 28,56 (1956)). GOT and GPT are synthesized in the liver and heart, and released into blood stream upon the damage of these organes. Accordingly, GOT and GPT are representative markers of the liver-function and high serum GOT and GPT levels mean severe damage of the liver.

The result showed that GOT and GPT levels of naringin group were lower than those of the control group by about 30 % and 10 %, respectively.

(Step 3) Expriment using rabbits The same procedure as in (Step 1) was repeated except that 30 three-month old New Zealand White rabbits (Yeonam Horticulture and Animal Husbandry College, Korea) each weighing about 2.5 to 2.6 kg were used in place of the rats, and the rabbits were fed for six weeks with three different diets, i. e., RC4 diet containing 1 % cholesterol (Control group); 1 % cholesterol plus 1 mg/kg Lovastatine (Comparative group); and 1 % cholesterol plus 0.1 % naringin, respectively.

Thereafter, the livers were separated from the rabbits and the histopathological observations were carried out as follows.

The rabbits were anesthetized with an intramuscular injection of ketamine (75 mg/kg) and subjected to an abdominal incision. The color and degree of sclerosis of the liver were observe with eyes, and the liver separated from the rabbit was fixed in 10 % neutral buffered formalin for more than 24 hours. The fixed liver was washed sufficiently with water, dehydrated stepwise with 70 %, 80 %, 90 % and 100 % ethanol and, then, embedded in paraffin.

The embedded liver was sectioned in 4 pm thickness with a microtome and stained with hematoxylin and eosin. The stained liver specimen was made transparent with xylene, mounted with permount, and then observe under a microscope to confirm the presence of lesions.

Figs. 2A, 2B and 2C present the microscopic features of the livers of the rabbits administered with 1 % cholesterol (control group), 1 % cholesterol plus 1 mg/kg Lovastatine (comparative group), and 1 % cholesterol plus 0.1 % naringin, respectively. As shown in Figs. 2A and 2B, the hepatic cells of the control group and the comparative group are irregularly arrange and enlarged and a large amount of fat is deposited therein. In contras, as shown in Fig. 2C, the hepatic cells of naringin group are normal and the deposition of fat is not observe. This result shows that naringin strongly inhibits the occurrence of fatty liver without toxic adverse effect to the hepatic cells.

(Step 4) Expriment using human Naringin was orally administered to a 55-year-old man at a daily dose of 10 mg/kg for 68 days and serum GOT, GPT and YGTP levels were determined just before the administration (day 0), and 45 and 68 days after the administration (day 45 and day 68), respectively.

Consequently, serum GOT levels at day 45 and day 68 decreased by 17 %, respectively, in comparison to that of day 0. Serum GPT levels at day 45 and day 68 decreased by 15 % and l9 %, respectively, in comparison to that of day 0.

Further, serum yGTP levels at day 45 and day 68 decreased by 25 % and 51 %, respectively, in comparison to that of day 0.

Surprisingly, reduction of serum YGTP level at day 68 was more than 50 %, and this result suggests that naringin or naringenin has a strong liver-protective activity and preventive activity on the hepatic diseases such as hepatitis, fatty liver and alcoholic fatty liver.

On the other hand, naringin was orally administered to a 56-year-old man, who had drunk alcoholic beverages habitually in an amount of 100 cc per day, at a daily dose of 6 mg/kg for 30 days and serum yGTP level was determined just before the administration (day 0) and 30 days after the administration (day 30). Consequently, initial serum yGTP

level at day 0 was 129 IU/1, while that of day 30 decreased to 69 IU/1 which is within the normal range. This result demonstrates that naringin or naringenin has a high activity of preventing alcoholic fatty liver and hepatocirrhosis.

Example 9: Foods containing Naringin or naringenin Foods containing naringin or naringenin were prepared as follows.

(1) Preparation of tomato ketchup and sauce Naringin or naringenin was added to a tomato ketchup or sauce in an amount ranging from 0.01 to 5 wtZ to obtain a health-improving tomato ketchup or sauce.

(2) Preparation of wheat flour foods Naringin or naringenin was added to a wheat fleur in an amount ranging from 0.01 to 5 wt% and breads, cakes, cookies, crackers and noodles were prepared by using the mixture to obtain health-improving foods.

(3) Preparation of soups and gravies Naringin or naringenin was added to soups and gravies in an amount ranging from 0.01 to 5 wt% to obtain health- improving soups and gravies.

(4) Preparation of ground beef Naringin or naringenin was added to ground beef in an amount ranging from 0.01 to 5 wt% to obtain a health- improving ground beef.

(5) Preparation of dairy product Naringin or naringenin was added to milk in an amount ranging from 0.01 to 5 wt% and various dairy products such as butter and ice cream were prepared by using the milk.

However, in case of cheese preparation, naringin or naringenin was added to the coagulated milk protein; and, in

case of yogurt preparation, naringin or naringenin was added to the coagulated milk protein obtained after the fermentation.

Example 10: Beverages containing Naringin or naringenin (1) Preparation of vegetable juice 200 to 10,000 mg of naringin or naringenin was added to 1000 niR of a tomato or carrot Juice to obtain a health- improving vegetable juice.

(2) Preparation of fruit juice 200 to 10,000 mg of naringin or naringenin was added to 1000 mu ouf an apple or grape Juice to obtain a health- improving fruit juice.

(3) Preparation of carbonate drink 200 to 10,000 mg of naringin or naringenin was added to 1000 mR of Coca-Colas or Pepsi-Cola to obtain a health- improving carbonate drink.

While the invention has been described with respect to the above specific embodiments, it should be recognized that various modifications and changes may be made to the invention by those skilled in the art which also fall within the scope of the invention as defined by the appende claims.