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成年大鼠辣椒素和迷走神经切断诱导的神经损伤后结状神经节神经元的可塑性。

Plasticity of nodose ganglion neurons after capsaicin- and vagotomy-induced nerve damage in adult rats.

机构信息

Department of Veterinary and Comparative Anatomy, Pharmacology, and Physiology, College of Veterinary Medicine, Washington State University, Pullman, WA 99163-6520, USA.

出版信息

Neuroscience. 2010 Jun 2;167(4):1227-38. doi: 10.1016/j.neuroscience.2010.02.049. Epub 2010 Mar 1.

Abstract

Previous reports show that vagal afferent innervation of the stomach eventually regenerates from surviving nodose ganglion (NG) neurons after subdiaphragmatic vagotomy. Systemic capsaicin treatment destroys gastric vagal afferent neurons expressing vanilloid receptor 1 (VR1). However, it is not known whether gastric innervation lost after neuronal destruction can be restored. Here, we report that capsaicin-induced damage of NG neurons innervating the stomach in adult rats is followed by restoration of vagal afferent projections. Specifically, we compared measures of neuronal plasticity in NG and vagi after subdiaphragmatic vagotomy or capsaicin treatment. The numbers of VR1-immunoreactive neurons projecting to the stomach were significantly reduced 10 days after either capsaicin treatment or vagotomy. However, the VR1-immunoreactive afferent innervation of the stomach was restored to levels exceeding those of vagotomized rats by 37 days after capsaicin, whereas neither total afferent innervation nor VR1-immunoreactive innervation reached control levels, even by 67 days after vagotomy. Capsaicin treatment significantly increased NG neuronal nitric oxide synthase (nNOS) immunoreactivity at 10 days after capsaicin, and this increase was sustained for the duration of the study, indicating higher nNOS demand in restoration of vagal projections. Vagotomy was associated with a much smaller increase in the number of nNOS-immunoreactive NG neurons, detectable only at 10 days after surgery. The number of nNOS-immunopositive gastric-projecting neurons was dramatically reduced 10 days after either capsaicin treatment or vagotomy but returned to the control level in both groups at 67 days. We found a significantly higher number of growth cones in capsaicin-treated animals compared with controls. Capsaicin significantly increased the number of nNOS-immunopositive and nNOS-immunonegative growth cones in NG at all time points. Vagotomy did not increase the number of nNOS(-) growth cones in NG. We conclude that capsaicin treatment may result in more significant restorative capacities than vagotomy, mainly because of sprouting of capsaicin-insensitive nerve fibers.

摘要

先前的报告表明,在膈下迷走神经切断术后,胃的迷走传入神经支配最终会从存活的结状神经节(NG)神经元再生。全身辣椒素处理会破坏表达香草素受体 1(VR1)的胃迷走传入神经元。然而,尚不清楚神经元破坏后丧失的胃传入神经能否得到恢复。在这里,我们报告在成年大鼠中,辣椒素诱导的胃 NG 神经元损伤后,迷走传入投射得到恢复。具体而言,我们比较了膈下迷走神经切断术或辣椒素处理后 NG 和迷走神经中的神经元可塑性测量值。在接受辣椒素处理或迷走神经切断术后 10 天,投射到胃的 VR1-免疫反应性神经元数量明显减少。然而,在接受辣椒素处理后 37 天,VR1-免疫反应性传入胃的支配恢复到超过迷走神经切断大鼠的水平,而即使在迷走神经切断后 67 天,传入神经支配总数或 VR1-免疫反应性传入神经支配也未达到对照水平。辣椒素处理在接受辣椒素处理后 10 天显着增加了 NG 神经元一氧化氮合酶(nNOS)免疫反应性,并且这种增加持续到研究结束,表明在恢复迷走神经投射时需要更高的 nNOS 需求。迷走神经切断术与 NG 中 nNOS-免疫反应性神经元数量的增加相关,这种增加仅在手术后 10 天可检测到。在接受辣椒素处理或迷走神经切断术后 10 天,nNOS-免疫阳性胃投射神经元的数量显着减少,但两组均在 67 天恢复到对照水平。我们发现接受辣椒素处理的动物的神经生长锥数量明显高于对照组。在所有时间点,辣椒素均显着增加了 NG 中 nNOS-免疫阳性和 nNOS-免疫阴性神经生长锥的数量。迷走神经切断术并未增加 NG 中 nNOS(-)神经生长锥的数量。我们的结论是,与迷走神经切断术相比,辣椒素处理可能导致更显着的修复能力,这主要是由于辣椒素不敏感神经纤维的发芽。

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