Non-steroidal Anti-inflammatory Drugs (NSAIDS): Chemistry, Mechanism and their Adverse events.

R. Tonk, Sumit Tewatia, S. Majeed, Manish Dagar
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Abstract

More than 15 different non-steroidal anti-inflammatory drugs (NSAIDs) are available commercially, and these agents are used worldwide for their analgesic antipyretic and antiinflammatory effects in patients with multiple medical conditions. NSAIDs, including aspirin, do not generally change the course of the disease process in those conditions, where they are used for symptomatic relief. The main mechanism of action of NSAIDs is the inhibition of the enzyme cyclooxygenase (COX). Cyclooxygenase is required to convert arachidonic acid into thromboxane’s, prostaglandins, and prostacyclin’s. Assessment of toxicity and therapeutic response to a given NSAID must take into account the time needed to reach the steady state plasma concentration (roughly equal to three to five half-lives of the drug). NSAIDs have wellknown adverse effects affecting the gastric mucosa, renal system, cardiovascular system, hepatic system, and hematologic system.
非甾体抗炎药(NSAIDS):化学、机理及其不良反应。
目前市面上有超过 15 种不同的非甾体抗炎药(NSAIDs),这些药物因其镇痛、解热和消炎作用而在全球范围内被多种疾病患者所使用。包括阿司匹林在内的非甾体抗炎药一般不会改变这些疾病的病程,只是用于缓解症状。非甾体抗炎药的主要作用机制是抑制环氧化酶(COX)。环氧化酶需要将花生四烯酸转化为血栓素、前列腺素和前列环素。评估特定非甾体抗炎药的毒性和治疗反应时,必须考虑到达到血浆稳态浓度所需的时间(大致相当于药物的三到五个半衰期)。非甾体抗炎药对胃黏膜、肾脏系统、心血管系统、肝脏系统和血液系统有众所周知的不良影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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