甲氨蝶呤
医学
类风湿性关节炎
药理学
药物遗传学
作用机理
嘌呤
腺苷
毒性
内科学
生物化学
酶
化学
基因型
体外
基因
作者
Henghe Tian,Bruce N. Cronstein
出处
期刊:PubMed
日期:2007-01-01
卷期号:65 (3): 168-73
被引量:318
摘要
Methotrexate has been widely used for the treatment of rheumatoid arthritis (RA). The mechanisms of action of methotrexate are complex. Developed as a folic acid analogue, methotrexate inhibits purine and pyrimidine synthesis, which accounts for its efficacy in the therapy of cancer as well as for some of its toxicities. Recently, many studies have focused on the adenosine-mediated antiinflammatory effects of methotrexate. Certain aspects of methotrexate toxicities are also attributed to adenosine release. A better understanding of the mechanisms of action and toxicities of methotrexate will direct clinicians in their treatment approach and toxicity monitoring. Toward that objective, the latest developments in the pharmacokinetics, mechanism of action, pharmacogenetics, and toxicity of methotrexate are herein discussed.
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