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基于联合效应的抗惊厥药作用机制的等效线图分析

Isobolographic analysis of the mechanisms of action of anticonvulsants from a combination effect.

作者信息

Matsumura Nobuko, Nakaki Toshio

机构信息

Department of Pharmacology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.

Department of Pharmacology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.

出版信息

Eur J Pharmacol. 2014 Oct 15;741:237-46. doi: 10.1016/j.ejphar.2014.08.001. Epub 2014 Aug 19.

Abstract

The nature of the pharmacodynamic interactions of drugs is influenced by the drugs׳ mechanisms of action. It has been hypothesized that drugs with different mechanisms are likely to interact synergistically, whereas those with similar mechanisms seem to produce additive interactions. In this review, we describe an extensive investigation of the published literature on drug combinations of anticonvulsants, the nature of the interaction of which has been evaluated by type I and II isobolographic analyses and the subthreshold method. The molecular targets of antiepileptic drugs (AEDs) include Na(+) and Ca(2+) channels, GABA type-A receptor, and glutamate receptors such as NMDA and AMPA/kainate receptors. The results of this review indicate that the nature of interactions evaluated by type I isobolographic analyses but not by the two other methods seems to be consistent with the above hypothesis. Type I isobolographic analyses may be used not only for evaluating drug combinations but also for predicting the targets of new drugs.

摘要

药物的药效学相互作用的性质受药物作用机制的影响。据推测,具有不同作用机制的药物可能产生协同相互作用,而具有相似机制的药物似乎产生相加相互作用。在本综述中,我们描述了一项对已发表的关于抗惊厥药物联合使用文献的广泛研究,其相互作用的性质已通过I型和II型等效线图分析及阈下剂量法进行评估。抗癫痫药物(AEDs)的分子靶点包括Na(+)和Ca(2+)通道、GABA A型受体以及谷氨酸受体,如NMDA和AMPA/海人藻酸受体。本综述结果表明,通过I型等效线图分析而非其他两种方法评估的相互作用性质似乎与上述假设一致。I型等效线图分析不仅可用于评估药物联合使用,还可用于预测新药的靶点。

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