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口面运动的调节:多巴胺受体机制和突变模型。

Regulation of orofacial movement: dopamine receptor mechanisms and mutant models.

机构信息

Molecular and Cellular Therapeutics, Royal College of Surgeons in Ireland, Dublin 2, Ireland.

出版信息

Int Rev Neurobiol. 2011;97:39-60. doi: 10.1016/B978-0-12-385198-7.00002-3.

Abstract

Orofacial movements involve complex processes that include generators for down-stream patterns, with up-stream regulatory mechanisms. While the neurotransmitter dopamine plays a fundamental role, the role of individual dopamine receptor subtypes and their associated transduction mechanisms is unclear. Here we review systematic, comparative studies of orofacial function in mutant mice with "knockout" of D1, D2, D3, D4 or D5 receptors, or of their critical transduction component DARPP-32 at four levels: general orofacial behaviors within the mouse repertoire, as assessed naturalistically; individual components of orofacial movement, as assessed under non-naturalistic conditions; each of the above, as assessed also under challenge with a D1-like vs a D2-like agonist. Studies in these "knockouts" provide novel insights into the motoric "building blocks" that regulate orofacial function.

摘要

口面部运动涉及复杂的过程,包括下游模式的发生器,以及上游调节机制。虽然神经递质多巴胺起着至关重要的作用,但个别多巴胺受体亚型及其相关转导机制的作用尚不清楚。在这里,我们综述了对具有“敲除” D1、D2、D3、D4 或 D5 受体或其关键转导成分 DARPP-32 的突变小鼠的口面部功能的系统、比较研究,在四个层面上评估:在小鼠范围内的一般口面部行为,自然评估;非自然条件下的口面部运动的各个组成部分;在使用 D1 样激动剂与 D2 样激动剂进行挑战的情况下,对上述每一种情况进行评估。这些“敲除”研究为调节口面部功能的运动“构建块”提供了新的见解。

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