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新纹状体中生长抑素的突触前调制。

Presynaptic modulation by somatostatin in the neostriatum.

作者信息

Lopez-Huerta Violeta Gisselle, Tecuapetla Fatuel, Guzman Jaime N, Bargas Jose, Galarraga Elvira

机构信息

Departamento de Biofísica, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, PO Box 70-253, Mexico City, DF, 04510, Mexico.

出版信息

Neurochem Res. 2008 Aug;33(8):1452-8. doi: 10.1007/s11064-007-9579-3. Epub 2008 Feb 13.

Abstract

Medium spiny projection neurons (MSNs) are the main neuronal population in the neostriatum. MSNs are inhibitory and GABAergic. MSNs connect with other MSNs via local axon collaterals that produce lateral inhibition, which is thought to select cell assemblies for motor action. MSNs also receive inhibitory inputs from GABAergic local interneurons. This work shows, through the use of the paired pulse protocol, that somatostatin (SST) acts presynaptically to regulate GABA release from the terminals interconnecting MSNs. This SST action is reversible and not mediated through the release of dopamine. It is blocked by the SST receptor (SSTR) antagonist ciclosomatostatin (cicloSST). In contrast, SST does not regulate inhibition coming from interneurons. Because, SST is released by a class of local interneuron, it is concluded that this neuron helps to regulate the selection of motor acts.

摘要

中等棘状投射神经元(MSNs)是新纹状体中的主要神经元群体。MSNs具有抑制性且是γ-氨基丁酸能的。MSNs通过产生侧向抑制的局部轴突侧支与其他MSNs相连,这种侧向抑制被认为用于选择运动动作的细胞集合。MSNs还接受来自γ-氨基丁酸能局部中间神经元的抑制性输入。这项研究通过使用配对脉冲协议表明,生长抑素(SST)在突触前起作用,以调节连接MSNs的终末释放γ-氨基丁酸。这种SST作用是可逆的,且不是通过多巴胺的释放介导的。它被SST受体(SSTR)拮抗剂环孢生长抑素(cicloSST)阻断。相比之下,SST不调节来自中间神经元的抑制。由于SST由一类局部中间神经元释放,因此得出结论,这种神经元有助于调节运动动作的选择。

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