...
首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Adrenergic Receptor Agonists' Modulation of Dopaminergic and Non-dopaminergic Neurons in the Ventral Tegmental Area
【24h】

Adrenergic Receptor Agonists' Modulation of Dopaminergic and Non-dopaminergic Neurons in the Ventral Tegmental Area

机译:肾上腺素能受体激动剂对腹侧区域中的多巴胺能和非多巴胺能神经元的调节

获取原文
获取原文并翻译 | 示例
           

摘要

The ventral tegmental area (VTA) neuronal population consists of dopaminergic (DAergic) and non-DAergic neurons (mainly GABAergic), the activity of which is intertwined with VTA behavioral functions. Both DAergic and GABAergic neurons in the VTA have been shown to express adrenergic receptors (ARs) and respond to AR stimulation. The aim of the present study was to demonstrate the effects of selective AR agonists on DAergic and non-DAergic neuronal activity in the central and lateral parts of the VTA using in vivo electrophysiological recording combined with microiontophoretic drug application in anaesthetized rats. Administration of phenylephrine, a selective alpha(1)-AR agonist, while having an inhibitory effect on putative DAergic neurons (11% decrease in firing rate), induced a clear excitatory effect (59% increase in firing rate) on putative non-DAergic neurons. In contrast, application of clonidine, a selective alpha(2)-AR agonist, or isoprenaline, a selective beta-adrenergic receptor agonist, did not change the firing rate of either DAergic or non-DAergic neurons but influenced the firing pattern of non-DAergic cells only. Our results suggest that noradrenaline modulates activity of VTA neurons in vivo primarily via alpha(1), but also via beta- and alpha(2)-AR to a lesser extent. Furthermore, we show that alpha(1)-AR activation has contrasting effects on putative DAergic and non-DAergic neurons. We hypothesize that the phenylephrine-induced inhibition of putative DAergic neurons results from activation of GABAergic terminals present at the site of drug application. Such a mechanism is further supported by the observed alpha(1)-AR-induced excitation of putative GABAergic VTA neurons. (C) 2017 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:腹侧腹部面积(VTA)神经元群由多巴胺能(DARICIC)和非晚期神经元(主要是胃肠杆菌剂)组成,其活性与VTA行为功能交织在一起。 VTA中的两个晚期和胃肠杆菌神经元都已显示出表达肾上腺素能受体(ARS)并响应AR刺激。本研究的目的是展示选择性Ar激动剂在VTA中的中央和横向部位中使用体内电生理记录的侧侧部和非晚期神经元活性的影响,所述在麻醉大鼠中的微观细胞药物应用结合。施用苯妥(1)-AR激动剂,同时对推定的晚期神经元具有抑制作用(烧制率降低11%),推定的非晚期诱导澄清的兴奋性效果(烧制率增加59%)神经元。相反,Clonidine的应用,选择性α(2) - A激动剂或异戊酮,一种选择性β-肾上腺素能受体激动剂没有改变DAIGIC或非天使神经元的烧制率,但影响了非的烧制模式只有晚期细胞。我们的研究结果表明,去甲肾上腺素通过α(1)来调节体内VTA神经元的活性,而且通过β-和α(2)-AR至较小程度。此外,我们表明,α(1)-AR激活对推定的恶性腺和非晚期神经元具有对比作用。我们假设苯妥膦诱导的推定的晚期神经元的抑制因药物施用部位存在的胃肠杆菌末端的激活而导致的抑制。通过观察到的α(1)-AR诱导推定的胃肠杆菌vTA神经元激发的这种机制进一步支持。 (c)2017年IBRO。 elsevier有限公司出版。保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号