首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Regulation by the neuropeptide cholecystokinin (CCK-8S) of protein phosphorylation in the neostriatum.
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Regulation by the neuropeptide cholecystokinin (CCK-8S) of protein phosphorylation in the neostriatum.

机译:由神经肽胆囊收缩素(CCK-8S)调节新纹状体中蛋白质的磷酸化。

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摘要

Despite physiological evidence that cholecystokinin (CCK) is an excitatory neurotransmitter in the brain, little is known about its mechanism of action. CCK immunoreactivity in the brain, including projections to the striatum, is primarily attributable to the sulfated octapeptide CCK-8S. We report here that CCK-8S abolishes cAMP-dependent phosphorylation of a dopamine- and cAMP-regulated 32-kDa phosphoprotein (DARPP-32) in striatal neurons. The effect of CCK-8S is prevented by antagonists of CCKB and N-methyl-D-aspartate receptors. Our results support a model in which CCK-8S, originating from CCK or CCK/glutamate corticostriatal neurons, promotes the release of an excitatory neurotransmitter that causes the dephosphorylation and inactivation of DARPP-32, a potent protein phosphatase inhibitor, thereby modulating neuronal excitability.
机译:尽管有生理证据表明胆囊收缩素(CCK)是大脑中的一种兴奋性神经递质,但对其作用机理知之甚少。脑中的CCK免疫反应性(包括纹状体的投影)主要归因于硫酸化的八肽CCK-8S。我们在这里报告,CCK-8S消除了纹状体神经元中多巴胺和cAMP调节的32 kDa磷酸化蛋白(DARPP-32)的cAMP依赖性磷酸化。 CCKB和N-甲基-D-天冬氨酸受体的拮抗剂可预防CCK-8S的作用。我们的结果支持这样一种模型,其中源自CCK或CCK /谷氨酸皮质皮质神经元的CCK-8S促进兴奋性神经递质的释放,引起兴奋性神经递质DARPP-32(一种有效的蛋白磷酸酶抑制剂)的去磷酸化和失活,从而调节神经元兴奋性。

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