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卡托普利和依那普利对自发性高血压大鼠局部血管α-肾上腺素能受体反应性的影响。

Influence of captopril and enalapril on regional vascular alpha-adrenergic receptor reactivity in SHR.

作者信息

Richer C, Doussau M P, Giudicelli J F

出版信息

Hypertension. 1984 Sep-Oct;6(5):666-74. doi: 10.1161/01.hyp.6.5.666.

Abstract

The effects of short-term oral treatment with captopril and enalapril (two angiotensin-I-converting-enzyme inhibitors [ACEIs] that were administered in equipotent antihypertensive doses) on the systemic vasopressor response and on the renal, mesenteric, and hindlimb vascular responses to cirazoline and UK-14,304 (alpha 1- and alpha 2-adrenergic receptor-specific agonists, respectively) were investigated in adult pithed spontaneously hypertensive rats (SHR) of the Okamoto-Aoki strain. In the nonbinephrectomized animal, captopril and enalapril reduced to the same extent the systemic blood pressure and renal and hindlimb vascular resistances. They also decreased to the same extent systemic pressor and regional vasoconstrictor responses to cirazoline and UK-14,304, especially in the renal and mesenteric vascular beds. Simultaneously, the effects of angiotensin I and angiotensin II on the pressor response were abolished and almost not modified. In the binephrectomized animals, captopril and enalapril no longer reduced the systemic blood pressure and regional vascular resistances, but whereas the sympathoinhibitory effect of captopril vs the systemic pressor and regional vasoconstrictor responses to cirazoline and UK-14,304 persisted, those of enalapril disappeared.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在冈本-青木品系的成年去脑自发性高血压大鼠(SHR)中,研究了短期口服卡托普利和依那普利(两种以等效降压剂量给药的血管紧张素转换酶抑制剂[ACEIs])对全身血管升压反应以及对可乐定和UK-14,304(分别为α1和α2肾上腺素能受体特异性激动剂)的肾、肠系膜和后肢血管反应的影响。在未双侧肾切除的动物中,卡托普利和依那普利同等程度地降低了全身血压以及肾和后肢血管阻力。它们还同等程度地降低了对可乐定和UK-14,304的全身升压和局部血管收缩反应,尤其是在肾和肠系膜血管床。同时,血管紧张素I和血管紧张素II对升压反应的作用被消除且几乎未改变。在双侧肾切除的动物中,卡托普利和依那普利不再降低全身血压和局部血管阻力,但是,卡托普利对可乐定和UK-14,304的全身升压和局部血管收缩反应的交感抑制作用仍然存在,而依那普利的这种作用消失了。(摘要截断于250字)

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