Riegel Arthur C, Williams John T
Vollum Institute, Oregon Health and Science University, Portland, OR 97239, USA.
Neuron. 2008 Feb 28;57(4):559-70. doi: 10.1016/j.neuron.2007.12.029.
Changes in cytosolic calcium are crucial for numerous processes including neuronal plasticity. This study investigates the regulation of cytosolic calcium by corticotropin-releasing factor (CRF) in midbrain dopamine neurons. The results demonstrate that CRF stimulates the release of intracellular calcium from stores through activation of adenylyl cyclase and PKA. Imaging and photolysis experiments showed that the calcium originated from dendrites and required both functional IP3 and ryanodine receptor channels. The elevation in cytosolic calcium potentiated calcium-sensitive potassium channels (sK) activated by action potentials and metabotropic Gq-coupled receptors for glutamate and acetylcholine. This increase in cytosolic calcium activated by postsynaptic Gs-coupled CRF receptors may represent a fundamental mechanism by which stress peptides and hormones can shape Gq-coupled receptor-mediated regulation of neuronal excitability and synaptic plasticity in dopamine neurons.
胞质钙的变化对包括神经元可塑性在内的众多过程至关重要。本研究调查了促肾上腺皮质激素释放因子(CRF)对中脑多巴胺神经元胞质钙的调节作用。结果表明,CRF通过激活腺苷酸环化酶和蛋白激酶A刺激细胞内钙从储存库中释放。成像和光解实验表明,钙源自树突,并且需要功能性的肌醇三磷酸(IP3)和兰尼碱受体通道。胞质钙的升高增强了由动作电位以及代谢型Gq偶联的谷氨酸和乙酰胆碱受体激活的钙敏感钾通道(sK)。由突触后Gs偶联的CRF受体激活的胞质钙增加可能代表了一种基本机制,通过该机制应激肽和激素可以塑造Gq偶联受体介导的多巴胺神经元的神经元兴奋性和突触可塑性调节。
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