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卡托普利诱导大鼠低血压机制的研究。

Studies on the mechanism of captopril induced hypotension in rats.

作者信息

Clarke D E, Wagner L B, Wagner L A

出版信息

Res Commun Chem Pathol Pharmacol. 1981 Jan;31(1):13-30.

PMID:7020011
Abstract

The mechanism of the hypotensive response to captopril was investigated in pithed and urethane anesthetized rats. Cumulative intravenous doses of captopril produced dose-dependent hypotensive responses which were correlated with blockade of the pressor response to angiotensin I. Angiotensin II responses were unaffected. Infusions of saralasin, an angiotensin receptor antagonist, inhibited the hypotensive action of captopril, the degree of antagonism being correlated with inhibition of angiotensin II pressor responses. Bilateral nephrectomy lowered blood pressure to approximately the same level as captopril and completely abolished the hypotensive effect of captopril. No evidence was obtained for the involvement of endogenous bradykinin or prostaglandins in the hypotensive action of captopril. It is concluded that in pithed and urethane anesthetized rats, captopril mediates its hypotensive response by removing the renal renin-angiotensin system, most probably via inhibition of angiotensin I - converting enzyme. The results contrast with similar studies conducted in anesthetized dogs. In this species, the mechanism of action of captopril remains for further resolution.

摘要

在脊髓切断和氨基甲酸乙酯麻醉的大鼠中研究了卡托普利降压反应的机制。静脉注射累积剂量的卡托普利可产生剂量依赖性的降压反应,这与对血管紧张素I升压反应的阻断相关。血管紧张素II反应未受影响。输注血管紧张素受体拮抗剂沙拉新可抑制卡托普利的降压作用,拮抗程度与血管紧张素II升压反应的抑制相关。双侧肾切除使血压降至与卡托普利大致相同的水平,并完全消除了卡托普利的降压作用。未获得内源性缓激肽或前列腺素参与卡托普利降压作用的证据。结论是,在脊髓切断和氨基甲酸乙酯麻醉的大鼠中,卡托普利通过消除肾素-血管紧张素系统来介导其降压反应,很可能是通过抑制血管紧张素I转换酶。这些结果与在麻醉犬中进行的类似研究形成对比。在该物种中,卡托普利的作用机制仍有待进一步阐明。

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