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Vane 发现了阿司匹林的作用机制,改变了我们对其临床药理学的理解。

Vane's discovery of the mechanism of action of aspirin changed our understanding of its clinical pharmacology.

机构信息

The William Harvey Research Institute, St. Bartholomew's Hospital Medical College, Charterhouse Square, London EC1M 6BQ, UK.

出版信息

Pharmacol Rep. 2010 May-Jun;62(3):518-25. doi: 10.1016/s1734-1140(10)70308-x.

Abstract

Aspirin exerts its analgesic, antipyretic and anti-inflammatory actions by inhibiting the enzyme cyclooxygenase and thus preventing the formation and release of prostaglandins. The elucidation by John Vane of the mechanism of action of aspirin in 1971 was followed twenty years later by the discovery of a second cyclooxygenase enzyme, COX-2 and the rapid development of selective inhibitors of this enzyme. The COX-2 inhibitors are potent anti-inflammatory drugs without the damaging side effects on the stomach mucosa of the non-selective aspirin-like inhibitors. More recently, two enzymes have been identified inhibition of which may explain the mechanism of action of paracetamol. These are a putative cyclooxygenase-3 which is a variant of cyclooxygenase-1 and derives from the same gene, and a COX-2 variant, induced with diclofenac, which may be involved in the resolution of inflammation.

摘要

阿司匹林通过抑制环氧化酶来发挥其镇痛、解热和抗炎作用,从而阻止前列腺素的形成和释放。1971 年,约翰·万恩(John Vane)阐明了阿司匹林的作用机制,二十年后发现了第二种环氧化酶酶,即 COX-2,以及对这种酶的快速选择性抑制剂的发现。COX-2 抑制剂是一种强效抗炎药物,没有非选择性阿司匹林样抑制剂对胃黏膜的破坏性副作用。最近,又发现了两种可能解释对乙酰氨基酚作用机制的酶。一种是假定的环氧化酶-3,它是环氧化酶-1 的变体,来源于同一个基因,另一种是 COX-2 变体,它与双氯芬酸诱导有关,可能参与炎症的消退。

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