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易卒中自发性高血压大鼠中的抗高血压药物。

Antihypertensive drugs in the stroke-prone spontaneously hypertensive rat.

作者信息

Richer C, Vacher E, Fornes P, Giudicelli J F

机构信息

Département de Pharmacologie, Faculté de Médecine Paris-Sud, Le Kremlin-Bicêtre, France.

出版信息

Clin Exp Hypertens. 1997 Jul-Aug;19(5-6):925-36. doi: 10.3109/10641969709083196.

Abstract

The stroke-prone spontaneously hypertensive rat (SHR-SP) is an experimental model that has been widely used to investigate the potential preventive effects vs stroke and mortality of numerous antihypertensive agents. Among the latter, angiotensin I-converting enzyme inhibitors, angiotensin II AT1-receptor blockers and calcium antagonists have proven to be very effective. The mechanisms involved in their beneficial effects include limitation of the age-related alterations of large cerebral arteries' functional parameters, prevention of fibrinoid necrosis formation in cerebral arterioles and, to a lesser extent, limitation of the blood pressure rise.

摘要

易卒中自发性高血压大鼠(SHR-SP)是一种实验模型,已被广泛用于研究多种抗高血压药物对卒中和死亡率的潜在预防作用。在这些药物中,血管紧张素I转换酶抑制剂、血管紧张素II AT1受体阻滞剂和钙拮抗剂已被证明非常有效。其有益作用的机制包括限制大脑大动脉功能参数的年龄相关性改变、预防脑小动脉纤维蛋白样坏死的形成,以及在较小程度上限制血压升高。

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