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在麻醉猫身上进行的血管紧张素II与(去天冬氨酸)-血管紧张素II的对比研究。

A comparative study with angiotensin II and (des-aspartic acid) -angiotensin II in the anesthetized cats.

作者信息

Türker R K, Ercan Z S

出版信息

Res Commun Chem Pathol Pharmacol. 1978 Jul;21(1):15-26.

PMID:684273
Abstract

The effects of angiotensin II and angiotensin III were studied in chloralose anesthetized and bilaterally adrenalectomized cats. Both peptides caused a dose-dependent increase in blood pressure and reduced the intraluminal pressure of the terminal ileum which was chosen as a parameter for the adrenergic actions of the peptides. Compared to angiotensin II, angiotensin III had 40 times lower agonistic potency in blood pressure but 200 times lower potency in intraluminal pressure. The competitive angiotensin antagonist Sar1-Ile8-angiotensin II, equally inhibited the agonistic effects of both peptides in blood pressure and intestinal motility. From these results it was concluded that specific angiotensin receptors are responsible for pressure as well as adrenergic effects of angiotensin II and angiotensin III.

摘要

在水合氯醛麻醉且双侧肾上腺切除的猫身上研究了血管紧张素II和血管紧张素III的作用。两种肽均引起血压呈剂量依赖性升高,并降低了回肠末端的腔内压力,回肠末端被选作这些肽肾上腺素能作用的一个参数。与血管紧张素II相比,血管紧张素III在升高血压方面的激动活性低40倍,但在降低腔内压力方面的活性低200倍。竞争性血管紧张素拮抗剂Sar1-Ile8-血管紧张素II同样抑制了两种肽在血压和肠道运动方面的激动作用。从这些结果得出结论,特定的血管紧张素受体介导了血管紧张素II和血管紧张素III的升压及肾上腺素能效应。

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