首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Regulation of somatodendritic dopamine release by corticotropin-releasing factor via the inhibition of voltage-operated Ca2+ channels.
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Regulation of somatodendritic dopamine release by corticotropin-releasing factor via the inhibition of voltage-operated Ca2+ channels.

机译:促肾上腺皮质激素释放因子通过抑制电压操纵的Ca2 +通道来调节树突状多巴胺的释放。

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摘要

Dopamine (DA) neurons in the substantia nigra pars compacta release DA from their somata and dendrites, which regulate motor activity and muscle tone. Previously, we reported that Ca(2+) influx through voltage-operated Ca(2+) channels (VOCCs) contributes to spontaneous somatodendritic DA release. Since corticotropin-releasing factor (CRF) regulates VOCC, we sought to determine whether urocortin affects somatodendritic DA release in the isolated DA neurons using amperometry method. The application of urocortin reversibly inhibited both VOCC and the frequency of DA release events via the activation of type-1 CRF receptor. The blockers for L- and T-type Ca(2+) channels effectively abolished the effects of urocortin both on the frequency of DA release events and on Ca(2+) current. These results indicate that CRF inhibits somatodendritic DA release by inhibiting L- and T-type Ca(2+) channels. Thus, the inhibition of somatodendritic DA release by stress hormone may be one of the molecular mechanisms underlying the effect of stress on motor function.
机译:黑质致密部中的多巴胺(DA)神经元从其躯体和树突中释放DA,从而调节运动活动和肌肉张力。以前,我们报告通过电压操作的Ca(2+)通道(VOCCs)流入Ca(2+)有助于自发性体细胞树突状细胞释放。由于促肾上腺皮质激素释放因子(CRF)调节VOCC,我们试图使用安培法确定尿皮质素是否影响分离的DA神经元中的树突状细胞DA释放。 urocortin的应用通过1型CRF受体的激活可逆地抑制VOCC和DA释放事件的频率。 L型和T型Ca(2+)通道的阻滞剂有效地消除了尿皮质素对DA释放事件的频率和Ca(2+)电流的影响。这些结果表明,CRF通过抑制L型和T型Ca(2+)通道来抑制树突状细胞DA的释放。因此,应激激素对树突状细胞DA释放的抑制可能是应激对运动功能影响的分子机制之一。

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