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促肾上腺皮质激素释放因子信号传导:中枢神经系统中药物靶向的分子特异性

CRF signaling: molecular specificity for drug targeting in the CNS.

作者信息

Arzt Eduardo, Holsboer Florian

机构信息

Laboratorio de Fisiología y Biología Molecular, Departamento Fisiología y Biología Molecular y Celular, Facultad de Ciencias Exactas y Naturales (FCEN), Universidad de Buenos Aires, 1428 Buenos Aires, Argentina.

出版信息

Trends Pharmacol Sci. 2006 Oct;27(10):531-8. doi: 10.1016/j.tips.2006.08.007. Epub 2006 Aug 28.

Abstract

Corticotrophin-releasing factor (CRF) is the key mediator of the central nervous system response needed to adapt to stress. If adaptation fails, hypersecretion of CRF continues and produces, via CRF type 1 receptors, symptoms pertaining to cognition, appetite, sleep and anxiety, implicating CRF as a causal factor in affective disorders. Clinical studies with CRF receptor 1 antagonists support a novel pharmacological strategy for treating stress-related disorders. Here we summarize recent information obtained on CRF receptor 1 signaling and propose the concept of a more focused pharmacological intervention based on the signaling pathways involved. Recent findings suggest that CRF activates, via the same CRF receptor 1, different signaling pathways in specific areas of the brain. This intracellular and neuroanatomical signaling specificity will facilitate the search for less pleiotropic antagonists and new chemical compounds that modulate signal transduction in a site-specific manner.

摘要

促肾上腺皮质激素释放因子(CRF)是适应应激所需的中枢神经系统反应的关键介质。如果适应失败,CRF的分泌持续亢进,并通过1型CRF受体产生与认知、食欲、睡眠和焦虑相关的症状,这表明CRF是情感障碍的一个致病因素。使用CRF受体1拮抗剂的临床研究支持了一种治疗应激相关疾病的新的药理学策略。在这里,我们总结了最近获得的关于CRF受体1信号传导的信息,并基于所涉及的信号通路提出了一种更具针对性的药理学干预概念。最近的研究结果表明,CRF通过相同的CRF受体1在大脑的特定区域激活不同的信号通路。这种细胞内和神经解剖学上的信号特异性将有助于寻找作用较少的拮抗剂和以位点特异性方式调节信号转导的新化合物。

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