Effects of vitamin K-2 (menatetrenone) on atherosclerosis and blood coagulation in hypercholesterolemic rabbits

被引:36
作者
Kawashima, H
Nakajima, Y
Matubara, Y
Nakanowatari, J
Fukuta, T
Mizuno, S
Takahashi, S
Tajima, T
Nakamura, T
机构
[1] Pharmacological Evaluation Section, Tokyo Research Laboratories, Eisai Co., Ltd., Bunkyo-ku, Tokyo 112-88
关键词
vitamin K-2 (menatetrenone); hypercholesterolemia; atherosclerosis; blood coagulation; factor X;
D O I
10.1254/jjp.75.135
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
gamma-Carboxyglutamic acid (Gla)-containing protein, synthesized in the presence of vitamin K, has been found in atherogenic plaques, but the pharmacological effect of vitamin K on atherosclerosis is unclear. We examined whether vitamin K-2 (menatetrenone) could affect the progression of both atherosclerosis and hypercoagulability in hypercholesterolemic rabbits. Vitamin K-2 in daily doses of 1, 10 and 100 mg/kg was given with a 0.5% cholesterol diet for 10 weeks to 8 rabbits each. The plasma levels of total-cholesterol in the vitamin Ka-treated groups were clearly lower than that of the hypercholesterolemic control group. The excessive dose of vitamin K-2, even at the high dose of 100 mg/kg/day for 10 weeks, did not accelerate the progression of atherosclerosis and did not promote the coagulative tendency in the rabbits. In contrast, the vitamin K-2 treatment (1 to 10 mg/kg/day) suppressed the progression of atherosclerotic plaques, intima-thickening and pulmonary atherosclerosis, the increase of ester-cholesterol deposition in the aorta, and both the elevation in plasma factor X level and increase in Hepaplastin(R)test value in the rabbits. These results indicate that the pharmacological dose of vitamin K-2 prevents both the progression of atherosclerosis and the coagulative tendency by reducing the total-cholesterol, lipid peroxidation and factor X activity in plasma, and the ester-cholesterol deposition in the aorta in hypercholesterolemic rabbits.
引用
收藏
页码:135 / 143
页数:9
相关论文
共 37 条
[1]   EFFECTS OF MENATETRENONE ON BONE LOSS INDUCED BY OVARIECTOMY IN RATS [J].
AKIYAMA, Y ;
HARA, K ;
OHKAWA, I ;
TAJIMA, T .
JAPANESE JOURNAL OF PHARMACOLOGY, 1993, 62 (02) :145-153
[2]   PLATELET ACTIVATION BY OXIDATIVELY MODIFIED LOW-DENSITY LIPOPROTEINS [J].
ARDLIE, NG ;
SELLEY, ML ;
SIMONS, LA .
ATHEROSCLEROSIS, 1989, 76 (2-3) :117-124
[3]   OXIDIZED LDL, CEROID, AND PROSTAGLANDIN METABOLISM IN HUMAN ATHEROSCLEROSIS [J].
ARMSTRONG, DA .
MEDICAL HYPOTHESES, 1992, 38 (03) :244-248
[4]  
CORSINI A, 1995, AM J CARDIOL, V76, pA21
[5]   GLUNICATE (LG 13979) PROTECTS THE ARTERIAL-WALL FROM CHOLESTEROL-INDUCED ATHEROSCLEROTIC CHANGES IN THE RABBIT WITHOUT AFFECTING PLASMA-LIPIDS [J].
CRISCUOLI, M ;
RENZETTI, AR ;
SUBISSI, A .
ATHEROSCLEROSIS, 1984, 53 (01) :59-68
[6]  
DATI F, 1987, THROMB HAEMOSTASIS, V58, P856
[7]   CORONARY ARTERIAL CALCIFICATION AS AN ACTIVE PROCESS - A NEW PERSPECTIVE ON AN OLD PROBLEM [J].
DOHERTY, TM ;
DETRANO, RC .
CALCIFIED TISSUE INTERNATIONAL, 1994, 54 (03) :224-230
[8]  
ESMON CT, 1989, J BIOL CHEM, V264, P4743
[9]   ROLE OF VITAMIN-E IN PREVENTING THE OXIDATION OF LOW-DENSITY-LIPOPROTEIN [J].
ESTERBAUER, H ;
DIEBERROTHENEDER, M ;
STRIEGL, G ;
WAEG, G .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 53 (01) :S314-S321
[10]   THE MOLECULAR-BASIS OF BLOOD-COAGULATION [J].
FURIE, B ;
FURIE, BC .
CELL, 1988, 53 (04) :505-518