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腺苷酸活化蛋白激酶对腹侧被盖区和黑质致密部神经元 ATP 敏感性钾电流的差异作用。

Differential actions of AMP kinase on ATP-sensitive K currents in ventral tegmental area and substantia nigra zona compacta neurons.

机构信息

Department of Neurology, Oregon Health & Science University, Portland, OR, USA.

Veterans Affairs Portland Health Care System, Portland, OR, 97239, USA.

出版信息

Eur J Neurosci. 2017 Dec;46(11):2746-2753. doi: 10.1111/ejn.13756. Epub 2017 Nov 6.

DOI:10.1111/ejn.13756
PMID:29057540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5716849/
Abstract

ATP-sensitive K (K-ATP) channels play significant roles in regulating the excitability of dopamine neurons in the substantia nigra zona compacta (SNC). We showed previously that K-ATP channel function is up-regulated by AMP-activated protein kinase (AMPK). This study extended these studies to the neurons adjacent to the SNC in the ventral tegmental area (VTA). Using patch pipettes to record whole-cell currents in slices of rat midbrain, we found that the AMPK activator A769662 increased the amplitude of currents evoked by the K-ATP channel opener diazoxide in presumed dopamine-containing VTA neurons. However, current evoked by diazoxide with A769662 was significantly smaller in VTA neurons compared to SNC neurons. Moreover, a significantly lower proportion of VTA neurons responded to diazoxide with outward current. However, A769662 was able to increase the incidence of diazoxide-responsive neurons in the VTA. In contrast, A769662 did not potentiate diazoxide-evoked currents in presumed non-dopamine VTA neurons. These results show that AMPK activation augments K-ATP currents in presumed dopamine neurons in the VTA and SNC, although diazoxide-evoked currents remain less robust in the VTA. We conclude that K-ATP channels may play important physiological roles in VTA and SNC dopamine neurons.

摘要

ATP 敏感性钾 (K-ATP) 通道在调节黑质致密部 (SNC) 多巴胺神经元的兴奋性方面发挥着重要作用。我们之前的研究表明,K-ATP 通道功能可被 AMP 激活的蛋白激酶 (AMPK) 上调。本研究将这些研究扩展到腹侧被盖区 (VTA) 中与 SNC 相邻的神经元。通过在大鼠中脑切片中使用膜片钳记录全细胞电流,我们发现 AMPK 激活剂 A769662 增加了 K-ATP 通道 opener 二氮嗪诱发的电流的幅度在假定含有多巴胺的 VTA 神经元中。然而,与 SNC 神经元相比,A769662 与二氮嗪一起诱发的电流在 VTA 神经元中明显较小。此外,VTA 神经元中对二氮嗪有外向电流反应的比例明显较低。然而,A769662 能够增加 VTA 中二氮嗪反应性神经元的发生率。相比之下,A769662 不能增强假定非多巴胺 VTA 神经元中二氮嗪诱发的电流。这些结果表明,AMPK 激活增强了 VTA 和 SNC 中假定的多巴胺神经元中的 K-ATP 电流,尽管二氮嗪诱发的电流在 VTA 中仍然较弱。我们得出结论,K-ATP 通道可能在 VTA 和 SNC 多巴胺神经元中发挥重要的生理作用。

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