ROLE OF TISSUE RENIN-ANGIOTENSIN SYSTEM IN 2-KIDNEY, ONE-CLIP HYPERTENSIVE RATS

被引:26
作者
MORISHITA, R
HIGAKI, J
OKUNISHI, H
NAKAMURA, F
NAGANO, M
MIKAMI, H
ISHII, K
MIYAZAKI, M
OGIHARA, T
机构
[1] OSAKA UNIV, SCH MED,DEPT GERIATR MED,1-1-50 FUKUSHIMA, FUKUSHIMA KU, OSAKA 553, JAPAN
[2] OSAKA MED COLL, DEPT PHARMACOL, TAKATSUKI, OSAKA 569, JAPAN
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 264卷 / 03期
关键词
ADRENAL; VASCULAR; BRAIN; ANGIOTENSIN-II; GENE EXPRESSION;
D O I
10.1152/ajprenal.1993.264.3.F510
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
To investigate the molecular pathology of two-kidney, one-clip (2K-1C) rats, we examined the gene expressions of the renin-angiotensin system (RAS) and angiotensin II (ANG II) concentration in various tissues in the early (4 wk) and chronic (16 wk) phases of hypertension. Four weeks after clipping, the brain renin mRNA level was lower in 2K-1C rats than in control rats (P < 0.05). On the other hand, the levels of brain and renal angiotensinogen mRNA were not significantly different in the two groups. The brain and adrenal ANG II concentrations were significantly higher in 2K-1C rats than in control rats. Sixteen weeks after clipping, there was no significant difference in the brain renin mRNA levels in the two groups, and renal and brain angiotensinogen mRNA levels were normal. Moreover, the ANG II concentrations in the adrenals and brain (except the cortex) of 2K-1C rats were not significantly higher than those in control rats. These results show a differential pattern of tissue RAS gene expression in rats during the development of 2K-1C hypertension, which is regulated in a tissue-specific manner. Furthermore, the data suggest that brain ANG II may be affected by circulating ANG II, but not by the brain renin angiotensin system, and may regulate brain renin, probably by negative feedback through its own receptor.
引用
收藏
页码:F510 / F514
页数:5
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