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[内皮素的生理与病理生理意义]

[The physiological and pathophysiological significance of endothelins].

作者信息

Aardal S

机构信息

Anestesi-og intensivavdeling Haukeland Sykehus, Bergen.

出版信息

Tidsskr Nor Laegeforen. 1994 Aug 10;114(18):2120-4.

PMID:7992271
Abstract

Endothelin-1 (ET-1) is a vasoconstrictor peptide of endothelial origin belonging to a family of four isopeptides consisting of ET-1, ET-2, ET-3, and vasoactive intestinal constrictor also called ET-4. These peptides show considerable homology with the sarafotoxins which are cardiotoxic molecules present in the venom of the snake Israeli burrowing asp. ET-1 is the most potent vasoconstrictor known, ten times more potent than angiotensin II. It is synthesized in response to stress, hypoxia, and other vasoactive substances. The physiological role of the endothelins and site of synthesis for ET-2 and ET-3 are still unknown. Two endothelin receptors have been cloned. Elevated plasma levels of ET-1 have been measured in patients suffering from various diseases such as myocardial infarction, cardiogenic shock, septic shock, renal failure, subarachnoid haemorrhage and pre-eclampsia. ET-receptor antagonists and ET-1 synthesis inhibitors are now available. It has been shown that these inhibitors, and also ET-1 antibodies, ameliorate the consequences of severely impaired blood flow in the kidney and in the brain. In animals, infusion of endothelin antibody has been shown to limit the size of myocardial infarction. ET-1 inhibitors can be expected to play a therapeutic role in the future.

摘要

内皮素-1(ET-1)是一种内皮源性血管收缩肽,属于由ET-1、ET-2、ET-3和血管活性肠收缩肽(也称为ET-4)组成的四种异肽家族。这些肽与存在于以色列穴蝰蛇毒液中的心脏毒性分子沙巴毒素有相当大的同源性。ET-1是已知最强效的血管收缩剂,其效力比血管紧张素II强十倍。它是在应激、缺氧和其他血管活性物质的刺激下合成的。内皮素的生理作用以及ET-2和ET-3的合成部位仍不清楚。已经克隆出两种内皮素受体。在患有各种疾病(如心肌梗死、心源性休克、感染性休克、肾衰竭、蛛网膜下腔出血和先兆子痫)的患者中,已检测到血浆ET-1水平升高。现在有内皮素受体拮抗剂和ET-1合成抑制剂。已经表明,这些抑制剂以及ET-1抗体可改善肾脏和大脑中严重受损的血流后果。在动物中,输注内皮素抗体已被证明可限制心肌梗死的面积。预计ET-1抑制剂在未来将发挥治疗作用。

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