在突触之外思考:超突触NMDA受体中的甘氨酸
1Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94143, USA. john.gray@ucsf.edu
Cell
|August 7, 2012
概括
甘氨酸作为超突触NMDA受体 (NMDARs) 的主要协兴剂,与突触协兴剂d-serine不同. 这一发现揭示了这些受体在生理学和疾病中的作用.
科学领域:
- 神经科学是一个神经科学.
- 分子生物学分子生物学
- 接受器药理学 接受器药理学
背景情况:
- 外突触NMDA受体 (NMDARs) 在神经元功能和功能障碍中起着至关重要的作用.
- 外突触NMDARs的内源性协激剂在很大程度上仍未确定,阻碍了对其特定功能的研究.
- 已知突触性NMDARs与d-serine进行协同激活.
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