Endothelin-1 modulates angiotensin II in the development of hypertension in fructose-fed rats

被引:42
作者
Tran, L. T. [1 ]
MacLeod, K. M. [1 ]
McNeill, J. H. [1 ]
机构
[1] Univ British Columbia, Fac Pharmaceut Sci, Div Pharmacol & Toxicol, Vancouver, BC V6T 1Z3, Canada
关键词
Insulin resistance; Hypertension; Endothelin-1; Angiotensin II; Bosentan; L-158,809; CONVERTING ENZYME-INHIBITOR; DOCA-SALT HYPERTENSION; ETA-RECEPTOR BLOCKADE; INSULIN-RESISTANCE; BLOOD-PRESSURE; OXIDATIVE STRESS; AT1-RECEPTOR ANTAGONIST; GLUCOSE-TOLERANCE; MODEL; TROGLITAZONE;
D O I
10.1007/s11010-008-0023-z
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Two of the most potent vasoconstrictors, endothelin-1 (ET-1) and angiotensin II (Ang II), are upregulated in fructose hypertensive rats. It is unknown whether an interrelationship exists between these peptides that may contribute to the development of fructose-induced hypertension. The objective of this study was to investigate the existence of an interaction between the endothelin and renin angiotensin systems that may play a role in the development of fructose-induced hypertension. High fructose feeding and treatment with either bosentan, a dual endothelin receptor antagonist, or with L-158,809, an angiotensin type 1 receptor antagonist, were initiated simultaneously in male Wistar rats. Systolic blood pressure, fasted plasma parameters, insulin sensitivity, plasma Ang II, and vascular ET-1-immunoreactivity were determined following 6 weeks of high fructose feeding. Rats fed with a high fructose diet exhibited insulin resistance, hyperinsulinemia, hypertriglyceridemia, hypertension, and elevated plasma Ang II. Treatment with either bosentan or L-158,809 significantly attenuated the rise in blood pressure with no effect on insulin levels or insulin sensitivity in fructose-fed rats. Bosentan treatment significantly reduced plasma Ang II levels, while L-158,809 treatment significantly increased vascular ET-1-immunoreactivity in fructose-fed rats. Thus, treatment with the endothelin receptor antagonist prevented the development of fructose-induced hypertension and decreased plasma Ang II levels. These data suggest that ET-1 contributes to the development of fructose-induced hypertension through modulation of Ang II levels.
引用
收藏
页码:89 / 97
页数:9
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