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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Effects of exogenous nesfatin-1 on gastric distention-sensitive neurons in the central nucleus of the amygdala and gastric motility in rats
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Effects of exogenous nesfatin-1 on gastric distention-sensitive neurons in the central nucleus of the amygdala and gastric motility in rats

机译:外源性nesfatin-1对杏仁核中枢胃胀敏感神经元和胃动力的影响

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Nesfatin-1 is a novel brain-gut peptide identified in several brain regions associated with feeding and gastrointestinal function. Our study explored the effects of nesfatin-1 in the central nucleus of the amygdala (CNA) on the activity of gastric distention (GD)-sensitive neurons, gastric motility, and the potential regulation mechanisms by the dorsal motor nucleus of the vagus (DMV). Following retrograde injection of fluorogold (FG) into the DMV, we found that nesfatin-1/FG dual-labeled neurons were detected in the CNA, which indicates that some of the nesfatin-1-immunoreactive neurons arising from the DMV may project to the CNA. Single unit discharges in the CNA were recorded extracellularly, and gastric motility was monitored by implantation of a force transducer into the stomach of conscious rats. These results showed that nesfatin-1 administration to the CNA excited most of the GD-excitatory neurons, inhibited GD-inhibitory neurons, and dose-dependently reduced gastric motility. All of the above effects induced by nesfatin-1 could be partially blocked by pretreatment with the melanocortin 3/4 receptors antagonist, SHU9119. Electrical stimulation of the DMV excited the majority of the nesfatin-1-responsive GD neurons in the CNA. Additionally, pretreatment with an anti-NUCB2esfatin-1 antibody in the CNA increased the firing rate of nesfatin-1-responsive GD-inhibitory neurons but decreased the firing rate in nesfatin-1-responsive GD-excitatory neurons following electrical stimulation of the DMV. Finally, a subdiaphragmatic vagotomy eliminated the diminished gastric motility induced by nesfatin-1 injection. Taken together, these findings suggest that nesfatin-1 regulates the activity of GD-sensitive neurons and gastric motility via the melanocortin pathway in the CNA. Furthermore, the DMV may be involved in this regulatory pathway. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
机译:Nesfatin-1是一种新颖的脑肠肽,在与进食和胃肠功能有关的几个脑区域中鉴定出。我们的研究探索了杏仁核(CNA)中的nesfatin-1对胃扩张(GD)敏感神经元的活性,胃动力以及迷走神经背运动核(DMV)潜在调节机制的影响)。向DMV逆行注入氟金(FG)后,我们发现在CNA中检测到nesfatin-1 / FG双标记神经元,这表明DMV产生的某些nesfatin-1免疫反应神经元可能投射到CNA。在细胞外记录CNA中的单个单位放电,并通过将力传感器植入意识大鼠的胃中来监测胃动力。这些结果表明,向CNA施用nesfatin-1可使大多数GD兴奋性神经元兴奋,抑制GD抑制性神经元,并剂量依赖性地降低胃动力。 nesfatin-1诱导的所有上述作用都可以通过用黑皮质素3/4受体拮抗剂SHU9119进行预处理而部分阻止。 DMV的电刺激使CNA中的大多数nesfatin-1反应性GD神经元兴奋。另外,在CNA中用抗NUCB2 / nesfatin-1抗体进行预处理会增加电刺激神经节苷脂1反应性GD抑制神经元的放电率,但会降低nesfatin-1反应性GD兴奋性神经元的放电率。 DMV。最后,dia下迷走神经切断术消除了由nesfatin-1注射引起的胃动力减弱。综上,这些发现表明,nesfatin-1通过CNA中的黑皮质素途径调节GD敏感神经元的活性和胃动力。此外,DMV可能参与了该调节途径。 (C)2014 Elsevier Ireland Ltd.保留所有权利。

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