Reduced expressions of inducible nitric oxide synthase and cyclooxygenase-2 in vascular smooth muscle cells of stroke-prone spontaneously hypertensive rats

被引:25
作者
Hirafuji, M [1 ]
Tsunoda, M
Machida, T
Hamaue, N
Endo, T
Miyamoto, A
Minami, M
机构
[1] Hlth Sci Univ Hokkaido, Dept Pharmacol, Fac Pharmaceut Sci, Ishikari, Hokkaido 0610293, Japan
[2] Sapporo Med Univ, Sch Med, Dept Pharmacol, Sapporo, Hokkaido 0608556, Japan
关键词
nitric oxide; inducible nitric oxide synthase; prostaglandin I-2; cyclooxygenase; vascular smooth muscle cells; stroke-prone spontaneously hypertensive rats;
D O I
10.1016/S0024-3205(01)01464-3
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2 are expressed in vascular smooth muscle cells stimulated with interleukin-1beta (IL-1beta), resulting in the production of nitric oxide (NO) and prostaglandins (PGs) such as PGI(2). The iNOS and COX-2 proteins and their mRNA expressions in cultured vascular smooth muscle cells isolated from 6-7 week-old stroke-prone spontaneously hypertensive rats (SHRSP) were compared with those in the cells isolated from age-matched normotensive Wistar Kyoto rats (WKY). The IL-1beta-induced NO production and iNOS expression in vascular smooth muscle cells of SHRSP were significantly lower than those in cells of WKY. Similarly, PGI(2) production and COX-2 expression were significantly lower in vascular smooth muscle cells of SHRSP than WKY, whereas there was no difference in the COX-1 expression. There were no significant differences in iNOS and COX-2 mRNA expressions between the two strains, suggesting that these protein expression may be reduced at the post- transcriptional level in cells of SHRSP. These results further suggest that the reduction of iNOS and COX-2 expressions in vascular smooth muscle cells may have relevance to the pathophysiology in SHRSP. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:917 / 926
页数:10
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