肥胖年龄组Zucker大鼠的动脉血压和主动脉反应。

D Sanchez, M Miguel, A Aleixandre
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引用次数: 2

摘要

内皮功能障碍是高血压的许多被提出的机制之一,它可能证明,至少部分地,高血压受试者血压升高。然而,肥胖Zucker大鼠高血压的确切机制尚不清楚。本研究采用尾袖法测量四组肥胖雌性Zucker大鼠的动脉血压,每组7只。1 ~ 4组大鼠分别为9 ~ 12、15 ~ 18、21 ~ 24、27 ~ 30周龄。我们还评估了这些动物的主动脉环对KCl、甲氧基胺和乙酰胆碱的反应。主动脉环依次暴露于80mm KCl和甲氧胺(10(-8)-10(-5)M)中,甲氧胺预收缩组织(预收缩接近甲氧胺最大作用的80%)也建立了对乙酰胆碱(10(-9)-10(-5)M)的内皮依赖性松弛。当这些动物的年龄增加时,观察到动脉血压明显升高。血压升高的大鼠主动脉环对KCl和甲氧沙明的收缩反应较低。15-18、21-24和27-30周龄大鼠的环对乙酰胆碱的反应低于年轻组。总之,肥胖的Zucker大鼠出现高血压和内皮功能障碍。然而,老龄肥胖Zucker大鼠去极化或α(1)-肾上腺素能受体刺激引起的动脉收缩减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Arterial blood pressure and aortic responses in obese, age-grouped Zucker rats.

Endothelial dysfunction is one of the many proposed mechanisms of hypertension and it may justify, at least in part, the increased blood pressure of hypertensive subjects. Nevertheless, the exact mechanisms involved in the hypertensive condition of obese Zucker rats are unclear. In this study, we measured the arterial blood pressure (tail cuff method) of four groups of seven, female, obese Zucker rats each. The rats of groups 1-4 were 9-12, 15-18, 21-24 and 27-30 weeks old respectively. We also evaluated the responses of aortic rings to KCl, methoxamine and acetylcholine, in these animals. Aortic rings were successively exposed to 80 mM KCl and to methoxamine (10(-8)-10(-5) M). The endothelium-dependent relaxation to acetylcholine (10(-9)-10(-5) M) was also established in the methoxamine-precontracted tissue (precontraction close to 80% of the maximum effect of methoxamine). A clear increase in the arterial blood pressure was observed when the age of these animals increased. The contractile responses to KCl and methoxamine were lower in the aortic rings of rats with increased arterial blood pressure. The response to acetylcholine was lower in the rings from 15-18, 21-24 and 27-30 weeks old rats, than in the younger groups. In conclusion, obese Zucker rats develop hypertension and endothelial dysfunction. Nevertheless, the arterial contractions elicited by depolarization or by α(1)-adrenoceptor stimulation decrease in aged, obese Zucker rats.

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