CA2268437C

CA2268437C - Naringin and naringenin as 3-hydroxy-3-methylglutaryl coa(hmg-coa) reductase inhibitor

Info

Publication number: CA2268437C
Application number: CA002268437A
Authority: CA
Inventors: Song Hae Bok; Kwang Hee Son; Tae Sook Jeong; Byoung Mog Kwon; Young Kook Kim; Doil Choi; Sung Uk Kim; Ki Hwan Bae; Yong Bok Park; Myung Sook Choi; Ingyu Hwang; Surk Sik Moon; Yong Kook Kwon; Jung Ah Ahn; Eun Sook Lee
Original assignee: Korea Advanced Institute of Science and Technology KAIST
Current assignee: Korea Advanced Institute of Science and Technology KAIST
Priority date: 1996-10-14
Filing date: 1997-10-13
Publication date: 2003-07-29
Anticipated expiration: 2017-10-13
Also published as: CA2268439A1; DE69728064D1; CN1233174A; WO1998016239A1; KR100213898B1; DE69718030T2; EP1014968B1; DE69718030D1; CN1106840C; HK1022105A1; CA2268439C; DE69728064T2; US5763414A; KR100213895B1; CA2268438C; CN1233175A; KR19980027074A; CA2268437A1; CN1104897C; DE69727707T2

Abstract

A pharmaceutical composition for inhibiting the activity of 3-hydroxy-3-methylglutaryl CoA(HMG-CoA) reductase in mammals comprises an effective amount of naringin or naringenin as an active ingredient together with a pharmaceutically acceptable carrier, and a food or beverage composition for inhibiting the 3-hydroxy-3-methylglutaryl CoA(HMG-CoA) reductase activity in mammals comprises an effective amount of naringin or naringenin.

Description

WO 98116221 PCT/Iat97/00191 - 1~ -METHYLGLUTARYL COA(HMG-COA) REDUCTASE INHIBITOR
FIELD OF THE INVENTION
' The present invention relates to a pharmaceutical composition for inhibiting the activity of 3-hydroxy-3-methylglutaryl CoA(HMG-CoA) reductase in a mammal, which comprises an effective amount of naringin or naringenin as an active ingredient together with a pharmaceutically acceptable carrier, and a food or beverage composition for inhibiting the HMG-CoA reductase activity, which comprises an effective amount of naringin or naringenin.
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 reported that an elevated plasma cholesterol level causes the deposition of fat, macrophages and foam .cells on the wall of blood vessels, 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 lower the rate of cholesterol biosynthesis which takes place in the liver. It has been reported that hypercholesterolemia can be treated effective-ly by reducing the rate of cholesterol biosynthesis through the inhibition of HMG-CoA reductase which mediates the synthesis of mevalonic acid, an intermediate in the biosynthesis of sterols or isoprenoids(Cardiovascular Pharmacology, William W. Parmley and Ranu Chatterjee Ed., Wolfe Publishing, pages 8.6-8.7, 1994).
Therefore, numerous efforts have been made to develop WO 98/I622I PCT/IQt97100191 medicines to inhibit HMG-CoA reductase; and, as a result, several compounds derived from Penicillium sp. and Asner9~illus sp. have been commercialized. Specifically, Lovastatin~ and Simvastatin~ developed by Merck Co., U.S.A., and Pravastatin~ developed by Sankyo Co., Japan, have been commercialized(C.D.R. Dunn, Stroke: Trends. Treatment and Markets, SCRIPT Report, PJB Publications Ltd., 1995).
However, these medicines are very expensive and a long-term administration thereof is known to induce an adverse side effect of increasing creatine kinase in the liver.
Accordingly, there has continued to exist a need to develop an inexpensive and non-toxic inhibitor of HMG-CoA reductase.
Naringin and the aglycon of naringin, naringenin, are flavonoids found in lemons, grapefruits, tangerines and oranges(Citrus sinensis) and they have the following structures(Horowitz, Gentili, Tetrahedron, 19, 773(1963)):
Oit L1i=OH
H H
OH H
!10 H
H
H
O O
2 5 ~ CH j H H
H H
OH OH
Naringin RO
-Naringenin WO 98/16221 PCT/IQt97/00191 Naringin has been used as a bitter tasting agent, sweater or chewing gum base. However, there has been no report on the HMG-CoA reductase inhibitory activity of naringin or naringenin.
SUN~IARY OF THE INVENTION
Accordingly, it is an object of the present invention to provide a pharmaceutical composition for inhibiting the HMG-CoA reductase activity in mammals.
It is another object of the present invention to provide a food or beverage composition for inhibiting the HMG-CoA reductase activity in mammals.
In accordance with one aspect of the present invention, there is provided a pharmaceutical composition for inhibiting the activity of 3-hydroxy-3-methylglutaryl CoA(HMG-CoA) reductase in mammal, which comprises an effective amount of naringin or naringenin as an active ingredient together with a pharmaceutically acceptable carrier.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides a pharmaceutical composition for inhibiting the HMG-CoA reductase activity, which comprises naringin or naringenin as an active ingredient, in combination with pharmaceutically acceptable excipients, carriers or diluents.
Naringin and naringenin may be extracted from the peel of citrus or synthesized according to the process described by Rosenmund, Rosenmund, Ber., 61, 2608(1958) and Zemplen, Bognar, Ber., 75, 648(1942). Further, naringenin can be prepared by the hydrolysis of naringin.
Naringin or naringenin exerts an inhibitory effect on the HMG-CoA reductase at a dose of 0.05 mg/kg/day or more, the inhibitory effect increasing with the dose thereof.

WO 98/16221 PCT/I~t97/00191 Moreover, in spite of their potent efficacies, naringin and naringenin show little toxicity or mitogenicity in tests using mice. More specifically, naringin exhibits no toxicity when it is orally administered to a mouse at a dosage of 1,000 mg/kg, which corresponds to oral administration dose of 50 to 100 g/kg body weight of aaringin for a person weighing 50 kg. Further, naringin and naringenin exert no adverse effects on the liver function.
A pharmaceutical formulation may be prepared by using the composition in accordance with any of the conventional procedures. In preparing the formulation, naringin or naringenin is preferably admixed or diluted with a carrier, or enclosed 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, emulsion, 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 fillers, 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 formulation of the present invention WO 98116221 PCT/K1t97/00191 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 0.05 to 300 mg/kg body weight, preferably 0.5 to 30 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 and naringenin can be incorporated in foods or beverages for the purpose of inhibiting the HMG-CoA reductase activity. Accordingly, the present invention also provide a food or beverage composition for inhibiting the HMG-CoA reductase activity, which comprises an effective amount of naringin or naringenin.

As described above, naringin or naringenin can be used as an effective, non-toxic pharmaceutical agent for inhibiting HMG-CoA reductase activity.

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 reactions were carried out at room temperature, unless specifically indicated otherwise.

Example 1: Administration of Naringin and Naringenin to an Animal 30 four-week-old Sprague-Dawley rats(Taihan laboratory animal center, Rorea) 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), 1%
cholesterol plus 0.1% naringin(Naringin group), and 1%
cholesterol plus 0.1% naringenin(Naringenin group), respectively. The compositions of diets fed to the three groups are shown in Table I.
Table I
Dietary group Control Naringin Naringenin Component group group group 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's 5 5 5 Mineral mixture's 3.5 3.5 3.5 Vitamin mixture's 1 1 1 Choline citrate 0.2 0.2 0.2 Corn oil 5 5 5 Cholesterol 1 1 l Naringin*Z 0 . 1 Naringenin*Z 0.1 Total 100 100 100 *~: . Purchased from TERLAD Premier Co. (Madison, WI, U.S.A. ) .
*2: Purchased from Sigma Chemical Company(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 recorded 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 observed no significant difference _ 7 -among the three groups in terms of the feed ingestion amount and the~weight gain.
EXSmDle 2: Determination of Total Cholesterol, HDL-cholesterol and Neutral Lipid Content in plasma .
The effect of administering naringin and naringenin to rats on the plasma cholesterol and neutral lipid content was determined as follows.
Hlood 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 Rit Cat. No. 352-100(Sigma Chemical Co., U.S.A.)(Allain et al., Clin. Chem., 20, 470-475(1974)).
Neutral lipids level was determined by using -Sigma Diagnostic Kit Cat. No. 339-50(Bucolo, G. and David, H., Clin. Chem., ~9, 476-482{1973)). The result is shown in Table II, wherein the total plasma cholesterol level decreased by 32% in the naringin fed rat group and by 18% in the naringenin fed rat group, as compared with that of the control group.
Table II
Group Control Naringin 'Naringenin Lipids Conc. grou p group group Total-C (mg/dl) 147.834.8 100.816.1 I20.9t25.9 HDL-C (mg/dl) 22.2 24.0 23.4 HDL-C

(%) 15.715.3 23.917.6 20.89.1 Total-C

TG (mg/dl) 99.2118.9 86.714.6 103.418.2 * Total-C: Total-cholesterol * HDL-C: HDL-cholesterol * TG: Triglyceride WO 98/16221 fCTlHIt97/00191 g _ Example 3: Activity of Naringin and Naringenin in HMG-CoA
Reductase Inhibition (Step 1) Preparation of microsomes To determine the effect of naringin and naringenin feeding to rats on the activity of HMG-CoA.reductase, a . regulatory enzyme of the cholesterol synthesis in the liver, microsomes were separated from the liver tissue to be used as an enzyme source.
First, the rats of the three groups were sacrificed by decapitation and the livers were excised and immediately placed in an ice-cold homogenization medium(50 mM KHzP04(pH

7.0}, 0.2M sucrose, 2 mM dithiothreitol(DTT)}. The livers were homogenized in the homogenization medium(2 ml medium/g of the liver} with a WaringTM blendor-for l5 sec. (three strokes with a motor-driven TeflonTM nestle in a Potter-Elvehjem type glass homogenizer). The homogenate was centrifuged at 15, 000xg for 10 min. and the supernatant thus obtained was centrifuged at 100,000xg for '75 min. to obtain microsomal pellets, which.were then resuspended in the homogenization medium containing 50 mM EDTA and centrifuged at 100,OOOxg for 60 min. The supernatant containing the microsome was used as an enzyme source.
(Step 2) HMG-CoA reductase assay The activity of HMG-CaA reductase was determined by employing [~~C~HMG-CoA, in accordance with the method of Shapiro et al.(Biochemica et Biophysica Acta, 370, 369-377(1974}) as follows.
The enzyme in the supernatant containing the microsome obtained in (Step 1) was activated at 37°C for 30 min.
Added to a reaction tube were 20 ~C1 of HMG-CoA reductase 3~~ assay buffer(0.25M KHZP04(pH 7.0), 8.75 mM EDTA, 25 mM DTT, 0 , 45 M KC1 and 0. 2~ mg/m1 BSAa , 5 ~r1 0~ 50 mM NADPH, 5 u1 of WO 98/16221 PCT/IQt97/00191 - g ~14C)~G-CoA(0.05 NCi/tube, final conc. 120 pM), and 10 p1 of activated microsomal enzyme(0.03-0.04 mg), and the mixture was incubated at 37°C for 30 min. The reaction was terminated by adding 10 u1 of 6 M HC1 to the mixture, and the mixture was incubated at 37°C for 15 min. to allow r complete lactonization of the product(mevalonate). The precipitate was removed by centrifugation at 10,000xg for 1 min. and the supernatant was applied to a Silica gel 60G TLC
plate(Altech, Inc., Newark, U.S.A.) and then developed with benzene:acetone(1:1, v/v). A region having a Rf value ranging from 0.65 to 0.75 was removed by scraping with a disposable cover slips and assayed for radioactivity with 1450 Microbeta liquid scintillation counter(Wallacoy, Finland). Enzyme activities were calculated as picomoles mevalonic acid synthesized per min. per mg protein(pmoles/min/mg protein). The result is shown in Table III.
Table III
Group Control Naringin Naringenin group group group HMG-CoA reductase 147 111.1 101.4 activity 112.5 f14 7.3 (pmole/min/mg protein As can be seen from Table III, the control group rats showed a relatively high HMG-CoA reductase activity, while the HMG-CoA activities observed with the naringin-fed tat group and the naringenin-fed rat group are lower than that of the control group by 25% and 31%, respectively.
Example 4: Toxicity of Orally Administered Naringin 7 to 8 week-old, specific pathogen-free ICR female mice ( 8 heads ) each weighing about 25 to 29 g and male mice ( 8 heads) each weighing about 34 to 38 g were bred under a condition of temperature 22f1°C, moisture 5515% and WO 98/16221 PGT/IQt97/00191 photoperiod 12L/12D. Fodder(Cheiljedang Co., mouse and rat fodder) and water were sterilized and fed to the mice.
Naringin was dissolved in 0.5% 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 observed 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. Further, on the 10th day, the mice were sacrificed and the internal organs were visually examined.
All the mice were alive at day 10 and naringin 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 observed during the 10 day test period. Accordingly, it was concluded that naringin is not toxic when orally administered to an animal.
The following Formulation Example is for illustration only and not intended to limit the scope of the invention in any way.
Formulation Example Hard gelatin capsules were prepared using the following ingredients:
Quantity (mQ/capsule) Active ingredient(naringin) 20 Starch, dried 160 Magnesium stearate 20 Total 200 mg 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 appended claims.
:;r. ~,.,..~~.'xJ'%1.~1~~

Claims

What is claimed is:

1. A use of naringin or naringenin for inhibiting the activity of 3-hydroxy-3-methylglutaryl CoA reductase in a mammal.

2. The use of claim 1, wherein the mammal is human.

3. The use of claim 1, wherein naringin or naringenin for administration to the mammal is in the form a composition containing same and pharmaceutically or sitologically acceptable excipients, carriers or diluents, said composition being selected from the group consisting of:
a pharmaceutical composition, a food composition and a beverage composition.

4. The use of claim 3, wherein an effective amount of naringin or naringenin contained in the composition ranges from 0.5 to 300 mg/kg body weight/day when administered to the mammal.