κ-阿片受体对腹外侧导水管周围灰色多巴胺神经元gaba能输入的调节

Chia Li, T. Kash
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引用次数: 10

摘要

κ-阿片受体(KOR)系统参与了包括疼痛在内的许多行为的调节。虽然有许多研究表明,KOR对疼痛的调节是通过脊柱介导的,但也有报道称,中枢KOR信号调节了疼痛样行为。特别是,催产素诱导的镇痛似乎是由腹外侧导水管周围灰质(vlPAG)内的KOR受体介导的。我们最近发现,vlPAG内多巴胺(DA)神经元的激活具有抗感受性。在本研究中,我们试图确定KOR信号对gabaergy输入到vlPAG DA神经元的影响,以及KOR影响这些输入的机制。我们发现,激活KOR可减少gaba能在vlPAG DA神经元上的传递。此外,我们的数据表明这种作用是通过G蛋白βγ-亚基在突触前介导的。他们提出了KOR激活解除vlPAG DA神经元抑制的可能性,这可能导致疼痛相关行为的调节改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
κ-Opioid Receptor Modulation of GABAergic Inputs onto Ventrolateral Periaqueductal Gray Dopamine Neurons
The κ-opioid receptor (KOR) system has been implicated in the regulation of many behaviors including pain. While there are numerous studies suggesting KOR regulation of pain being mediated spinally, there have been reports of pain-like behaviors regulated by central KOR signaling. In particular, oxytocin-induced analgesia appears to be mediated by KOR receptors within the ventrolateral periaqueductal gray (vlPAG). We recently found that activation of dopamine (DA) neurons within the vlPAG is antinociceptive. In this study, we sought to determine the impact of KOR signaling on GABAergic inputs onto vlPAG DA neurons, and the mechanism through which KOR impacts these inputs. We found that activation of KOR reduced GABAergic transmission onto vlPAG DA neurons. In addition, our data suggest this effect is mediated presynaptically via the G protein βγ-subunit. They raise the possibility that KOR activation disinhibits vlPAG DA neurons, which could lead to altered regulation of pain-related behaviors.
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