Effects of osthol on blood pressure and lipid metabolism in stroke-prone spontaneously hypertensive rats

被引:56
作者
Ogawa, Hiroshi
Sasai, Noriko
Kamisako, Toshinori
Baba, Kimiye
机构
[1] Kinki Univ, Sch Med, Dept Hyg, Sayama, Osaka 5898511, Japan
[2] Osaka Univ Pharmaceut Sci, Dept Pharmacognosy, Takatsuki, Osaka 5691094, Japan
基金
日本学术振兴会;
关键词
Cnidium monnieri; coumarin; osthol; hypertension; lipid metabolism; reverse transcription-polymerase chain reaction; stroke-prone spontaneously hypertensive rats;
D O I
10.1016/j.jep.2007.01.028
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Osthol, a coumarin compound, was isolated from the dried fruits of Cnidium monnieri (Umbelliferae) and the effect of dietary osthol on hypertension and lipid metabolism was examined in stroke-prone spontaneously hypertensive rats (SHRSP). Six-week-old male SHRSP were fed the experimental diet containing 0.05% osthol by weight for 4 weeks with free access to the diet and water. Elevation of systolic blood pressure was significantly suppressed on and after 3 weeks. In addition, significant decreases in cholesterol and triglyceride contents in the liver were recognized without any significant changes in serum lipids profiles. A comparative study on hepatic mRNA expression indicated that osthol induced a significant increase in 3-hydroxy-3-methylglutaryl coenzymeA (HMG-CoA) reductase mRNA expression, which may lead to decrease in hepatic cholesterol pool through inhibition of the enzyme activity. Moreover, osthol induced a significant increase in acyl-CoA oxidase mRNA expression associated with an increase in carnitine palmitoyl transferase I a mRNA expression, which suggests the acceleration of P-oxidation of hepatic fatty acids. This may be responsible, at least in part, for the reduction of hepatic triglyceride content in SHRSP. These beneficial effects of osthol could be useful for both prevention of atherosclerosis and suppression of hepatic lipid accumulation. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:26 / 31
页数:6
相关论文
共 35 条
[1]   Quantitative trait loci for cellular defects in glucose and fatty acid metabolism in hypertensive rats [J].
Aitman, TJ ;
Gotoda, T ;
Evans, AL ;
Imrie, H ;
Heath, KE ;
Trembling, PM ;
Truman, H ;
Wallace, CA ;
Rahman, A ;
Dore, C ;
Flint, J ;
Kren, V ;
Zidek, V ;
Kurtz, TW ;
Pravenec, M ;
Scott, J .
NATURE GENETICS, 1997, 16 (02) :197-201
[2]  
Beck K F, 1992, DNA Seq, V2, P359, DOI 10.3109/10425179209020817
[3]   Hepatic responses to inhibition of 3-hydroxy-3-methylglutaryl-CoA-reductase: a comparison of atorvastatin and simvastatin [J].
Bergstrom, JD ;
Bostedor, RG ;
Rew, DJ ;
Geissler, WM ;
Wright, SD ;
Chao, YS .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1998, 1389 (03) :213-221
[4]   REGULATION OF ACTIVITY OF LOW-DENSITY LIPOPROTEIN RECEPTOR IN HUMAN FIBROBLASTS [J].
BROWN, MS ;
GOLDSTEIN, JL .
CELL, 1975, 6 (03) :307-316
[5]   Vasorelaxing effect of coumarins from Cnidium monnieri on rabbit corpus cavernosum [J].
Chiou, WF ;
Huang, YL ;
Chen, CF ;
Chen, CC .
PLANTA MEDICA, 2001, 67 (03) :282-284
[6]   Peroxisome proliferator-activated receptors: Nuclear control of metabolism [J].
Desvergne, B ;
Wahli, W .
ENDOCRINE REVIEWS, 1999, 20 (05) :649-688
[7]  
ESSER V, 1993, J BIOL CHEM, V268, P5817
[8]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[9]  
HONDA G, 1984, Shoyakugaku Zasshi, V38, P221
[10]   METHOD FOR DETERMINATION OF ANGIOTENSIN-CONVERTING ENZYME-ACTIVITY IN BLOOD AND TISSUE BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
HORIUCHI, M ;
FUJIMURA, K ;
TERASHIMA, T ;
ISO, T .
JOURNAL OF CHROMATOGRAPHY, 1982, 233 (DEC) :123-130