Lewin Amanda E, Vicini Stefano, Richardson Janell, Dretchen Kenneth L, Gillis Richard A, Sahibzada Niaz
Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC, USA.
J Physiol. 2016 May 15;594(10):2661-79. doi: 10.1113/JP272069.
The dorsal motor nucleus of the vagus (DMV) in the brainstem consists primarily of vagal preganglionic neurons that innervate postganglionic neurons of the upper gastrointestinal tract. The activity of the vagal preganglionic neurons is predominantly regulated by GABAergic transmission in the DMV. The present findings indicate that the overwhelming GABAergic drive present at the DMV is primarily from somatostatin positive GABA (Sst-GABA) DMV neurons. Activation of both melanocortin and μ-opioid receptors at the DMV inhibits Sst-GABA DMV neurons. Sst-GABA DMV neurons may serve as integrative targets for modulating vagal output activity to the stomach.
We have previously shown that local GABA signalling in the brainstem is an important determinant of vagally-mediated gastric activity. However, the neural identity of this GABA source is currently unknown. To determine this, we focused on the somatostatin positive GABA (Sst-GABA) interneuron in the dorsal motor nucleus of the vagus (DMV), a nucleus that is intimately involved in regulating gastric activity. Also of particular interest was the effect of melanocortin and μ-opioid agonists on neural activity of Sst-GABA DMV neurons because their in vivo administration in the DMV mimics GABA blockade in the nucleus. Experiments were conducted in brain slice preparation of transgenic adult Sst-IRES-Cre mice expressing tdTomato fluorescence, channelrhodopsin-2, archaerhodopsin or GCaMP3. Electrophysiological recordings were obtained from Sst-GABA DMV neurons or DiI labelled gastric-antrum projecting DMV neurons. Our results show that optogenetic stimulation of Sst-GABA neurons results in a robust inhibition of action potentials of labelled premotor DMV neurons to the gastric-antrum through an increase in inhibitory post-synaptic currents. The activity of the Sst-GABA neurons in the DMV is inhibited by both melanocortin and μ-opioid agonists. These agonists counteract the pronounced inhibitory effect of Sst-GABA neurons on vagal pre-motor neurons in the DMV that control gastric motility. These observations demonstrate that Sst-GABA neurons in the brainstem are crucial for regulating the activity of gastric output neurons in the DMV. Additionally, they suggest that these neurons serve as targets for converging CNS signals to regulate parasympathetic gastric function.
脑干中的迷走神经背核(DMV)主要由支配上消化道节后神经元的迷走神经节前神经元组成。迷走神经节前神经元的活动主要受DMV中GABA能传递的调节。目前的研究结果表明,DMV中占主导地位的GABA能驱动主要来自生长抑素阳性GABA(Sst-GABA)DMV神经元。激活DMV中的黑皮质素受体和μ-阿片受体可抑制Sst-GABA DMV神经元。Sst-GABA DMV神经元可能是调节迷走神经向胃输出活动的整合靶点。
我们之前已经表明,脑干中的局部GABA信号是迷走神经介导的胃活动的重要决定因素。然而,目前尚不清楚这种GABA来源的神经身份。为了确定这一点,我们聚焦于迷走神经背核(DMV)中的生长抑素阳性GABA(Sst-GABA)中间神经元,该核密切参与调节胃活动。黑皮质素和μ-阿片激动剂对Sst-GABA DMV神经元神经活动的影响也特别令人感兴趣,因为它们在DMV中的体内给药模拟了该核中的GABA阻断作用。实验在表达tdTomato荧光、通道视紫红质-2、古紫质或GCaMP3的转基因成年Sst-IRES-Cre小鼠的脑片制备中进行。从Sst-GABA DMV神经元或DiI标记的投射到胃窦的DMV神经元获得电生理记录。我们的结果表明,对Sst-GABA神经元进行光遗传学刺激会通过增加抑制性突触后电流,强烈抑制标记的DMV运动前神经元向胃窦的动作电位。DMV中Sst-GABA神经元的活动受到黑皮质素和μ-阿片激动剂的抑制。这些激动剂抵消了Sst-GABA神经元对DMV中控制胃动力的迷走神经运动前神经元的显著抑制作用。这些观察结果表明,脑干中的Sst-GABA神经元对于调节DMV中胃输出神经元的活动至关重要。此外,它们表明这些神经元是汇聚中枢神经系统信号以调节副交感神经胃功能的靶点。