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与钙通道拮抗剂的药代动力学相互作用(第二部分)。

Pharmacokinetic interactions with calcium channel antagonists (Part II).

作者信息

Schlanz K D, Myre S A, Bottorff M B

机构信息

Division of Clinical and Hospital Pharmacy, College of Pharmacy, University of Cincinnati Medical Center, Ohio.

出版信息

Clin Pharmacokinet. 1991 Dec;21(6):448-60. doi: 10.2165/00003088-199121060-00005.

Abstract

Since calcium channel antagonists are a diverse class of drugs frequently administered in combination with other agents, the potential for clinically significant pharmacokinetic drug interactions exists. These interactions occur most frequently via altered hepatic blood flow and impaired hepatic enzyme activity. Part I of the article, which appeared in the previous issue of the Journal, dealt with interactions between calcium antagonists and marker compounds, theophylline, midazolam, lithium, doxorubicin, oral hypoglycaemics and cardiac drugs. Part II examines interactions with cyclosporin, anaesthetics, carbamazepine and cardiovascular agents.

摘要

由于钙通道拮抗剂是一类多样的药物,常与其他药物联合使用,因此存在具有临床意义的药代动力学药物相互作用的可能性。这些相互作用最常通过肝血流量改变和肝酶活性受损而发生。该文章的第一部分发表在上一期《杂志》上,讨论了钙拮抗剂与标记化合物、茶碱、咪达唑仑、锂、阿霉素、口服降糖药和心脏药物之间的相互作用。第二部分研究了与环孢素、麻醉剂、卡马西平和心血管药物的相互作用。

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