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P物质拮抗剂:新药是否与旧药相同?来自转基因动物模型的见解。

Substance P antagonists: meet the new drugs, same as the old drugs? Insights from transgenic animal models.

作者信息

Santarelli Luca, Saxe Michael D

机构信息

Center for Neurobiology and Behavior, Columbia University, New York, New York 10032, USA.

出版信息

CNS Spectr. 2003 Aug;8(8):589-96. doi: 10.1017/s1092852900018861.

Abstract

Antidepressants that primarily target the reuptake of monoamines have been highly successful treatments. However, therapies with these drugs still have several drawbacks, namely severe side effects, delays in the onset of action, and a significant percentage of non-responders. Recently, non-peptidic antagonists of the neurokinin 1 receptor, or substance P antagonists, have emerged as a novel class of drugs with antidepressant efficacy that is comparable to current drugs, but a potentially reduced side effect profile. This review summarizes the pre-clinical evidence derived from pharmacological and transgenic animal studies that suggests an important role for the substance P/neurokinin 1 system in anxiety and depression. Also, potential mechanisms by which substance P antagonists may produce their therapeutic effects are discussed.

摘要

主要作用于单胺再摄取的抗抑郁药一直是非常成功的治疗方法。然而,使用这些药物进行治疗仍存在几个缺点,即严重的副作用、起效延迟以及相当比例的无反应者。最近,神经激肽1受体的非肽类拮抗剂,即P物质拮抗剂,已成为一类新型药物,其抗抑郁疗效与现有药物相当,但副作用可能更少。本综述总结了来自药理学和转基因动物研究的临床前证据,这些证据表明P物质/神经激肽1系统在焦虑和抑郁中起重要作用。此外,还讨论了P物质拮抗剂可能产生治疗作用的潜在机制。

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