Departments of Pharmacology and Physiology.
Pathology, Georgetown University Medical Center, Washington, DC 20007.
J Neurosci. 2022 Jun 29;42(26):5212-5228. doi: 10.1523/JNEUROSCI.0419-22.2022. Epub 2022 May 24.
Activity in the dorsal vagal complex (DVC) is essential to gastric motility regulation. We and others have previously shown that this activity is greatly influenced by local GABAergic signaling, primarily because of somatostatin (SST)-expressing GABAergic neurons. To further understand the network dynamics associated with gastric motility control in the DVC, we focused on another neuron prominently distributed in this complex, neuropeptide-Y (NPY) neurons. However, the effect of these neurons on gastric motility remains unknown. Here, we investigate the anatomic and functional characteristics of the NPY neurons in the nucleus tractus solitarius (NTS) and their interactions with SST neurons using transgenic mice of both sexes. We sought to determine whether NPY neurons influence the activity of gastric-projecting neurons, synaptically interact with SST neurons, and affect end-organ function. Our results using combined neuroanatomy and optogenetic and show that NPY neurons are part of the gastric vagal circuit as they are trans-synaptically labeled by a viral tracer from the gastric antrum, are primarily excitatory as optogenetic activation of these neurons evoke EPSCs in gastric-antrum-projecting neurons, are functionally coupled to each other and reciprocally connected to SST neurons, whose stimulation has a potent inhibitory effect on the action potential firing of the NPY neurons, and affect gastric tone and motility as reflected by their robust optogenetic response These findings indicate that interacting NPY and SST neurons are integral to the network that controls vagal transmission to the stomach. The brainstem neurons in the dorsal nuclear complex are essential for regulating vagus nerve activity that affects the stomach via tone and motility. Two distinct nonoverlapping populations of predominantly excitatory NPY neurons and predominantly inhibitory SST neurons form reciprocal connections with each other in the NTS and with premotor neurons in the dorsal motor nucleus of the vagus to control gastric mechanics. Light activation and inhibition of NTS NPY neurons increased and decreased gastric motility, respectively, whereas both activation and inhibition of NTS SST neurons enhanced gastric motility.
迷走神经背核(DVC)中的活动对胃动力调节至关重要。我们和其他人之前已经表明,这种活动受到局部 GABA 能信号的极大影响,主要是因为生长抑素(SST)表达的 GABA 能神经元。为了进一步了解与 DVC 中胃动力控制相关的网络动态,我们专注于该复合体中另一种分布明显的神经元,即神经肽 Y(NPY)神经元。然而,这些神经元对胃动力的影响尚不清楚。在这里,我们使用雌雄两性转基因小鼠研究了孤束核(NTS)中 NPY 神经元的解剖和功能特征及其与 SST 神经元的相互作用。我们试图确定 NPY 神经元是否影响胃投射神经元的活动,与 SST 神经元突触相互作用,并影响终末器官功能。我们使用联合神经解剖学和光遗传学的结果表明,NPY 神经元是胃迷走神经回路的一部分,因为它们被来自胃窦的病毒示踪剂顺行标记,作为光遗传学激活这些神经元会在胃窦投射神经元中诱发 EPSC,它们彼此功能连接并与 SST 神经元相互连接,刺激 SST 神经元对 NPY 神经元的动作电位放电具有强大的抑制作用,并反映在它们对光遗传学的强烈反应中,影响胃张力和动力。这些发现表明,相互作用的 NPY 和 SST 神经元是控制迷走神经向胃传递的网络的组成部分。背核复合体中的脑干神经元对于调节通过张力和动力影响胃的迷走神经活动至关重要。两个截然不同的非重叠的主要兴奋性 NPY 神经元和主要抑制性 SST 神经元群体在 NTS 中相互形成相互连接,并与迷走神经背侧运动核中的前运动神经元形成相互连接,以控制胃力学。NTS NPY 神经元的光激活和抑制分别增加和减少胃动力,而 NTS SST 神经元的激活和抑制都增强胃动力。