环氧合酶
酶
花生四烯酸
基因亚型
前列腺素
炎症
药理学
前列腺素H2
医学
化学
生物化学
免疫学
基因
作者
Marco Turini,Raymond N. DuBois
出处
期刊:Annual Review of Medicine
[Annual Reviews]
日期:2002-02-01
卷期号:53 (1): 35-57
被引量:654
标识
DOI:10.1146/annurev.med.53.082901.103952
摘要
▪ Abstract Cyclooxygenase (COX), also known as prostaglandin endoperoxide synthase, is the key enzyme required for the conversion of arachidonic acid to prostaglandins. Two COX isoforms have been identified, COX-1 and COX-2. In many situations, the COX-1 enzyme is produced constitutively (e.g., in gastric mucosa), whereas COX-2 is highly inducible (e.g., at sites of inflammation and cancer). Traditional nonsteroidal anti-inflammatory drugs (NSAIDs) inhibit both enzymes, and a new class of COX-2 selective inhibitors (COXIBs) preferentially inhibit the COX-2 enzyme. This review summarizes our current understanding of the role of COX-1 and COX-2 in normal physiology and disease.
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