Department of Neural and Behavioral Sciences, Penn State University College of Medicine , Hershey, Pennsylvania.
J Neurotrauma. 2018 May 1;35(9):1079-1090. doi: 10.1089/neu.2017.5369. Epub 2018 Feb 9.
A profound reduction in colorectal transit time accompanies spinal cord injury (SCI), yet the colonic alterations after SCI have yet to be understood fully. The loss of descending supraspinal input to lumbosacral neural circuits innervating the colon is recognized as one causal mechanism. Remodeling of the colonic enteric nervous system/smooth muscle junction in response to inflammation, however, is recognized as one factor leading to colonic dysmotility in other pathophysiological models. We investigated the alterations to the neuromuscular junction in rats with experimental high-thoracic (T3) SCI. One day to three weeks post-injury, both injured and age-matched controls underwent in vivo experimentation followed by tissue harvest for histological evaluation. Spontaneous colonic contractions were reduced significantly in the proximal and distal colon of T3-SCI rats. Histological evaluation of proximal and distal colon demonstrated significant reductions of colonic mucosal crypt depth and width. Markers of intestinal inflammation were assayed by qRT-PCR. Specifically, Icam1, Ccl2 (MCP-1), and Ccl3 (MIP-1α) mRNA was acutely elevated after T3-SCI. Smooth muscle thickness and collagen content of the colon were increased significantly in T3-SCI rats. Colonic cross sections immunohistochemically processed for the pan-neuronal marker HuC/D displayed a significant decrease in colonic enteric neuron density that became more pronounced at three weeks after injury. Our data suggest that post-SCI inflammation and remodeling of the enteric neuromuscular compartment accompanies SCI. These morphological changes may provoke the diminished colonic motility that occurs during this same period, possibly through the disruption of intrinsic neuromuscular control of the colon.
结直肠通过时间的显著降低伴随着脊髓损伤(SCI),但 SCI 后结肠的改变尚未完全理解。对支配结肠的腰骶神经回路的下行至上的传入的丧失被认为是一个因果机制。然而,肠神经系统/平滑肌交界处对炎症的重塑被认为是导致其他病理生理模型中结肠动力障碍的一个因素。我们研究了实验性高胸(T3)SCI 大鼠的神经肌肉接头的改变。在损伤后 1 天至 3 周,受伤和年龄匹配的对照组接受体内实验,然后进行组织收获进行组织学评估。T3-SCI 大鼠的近端和远端结肠的自发性结肠收缩显著减少。近端和远端结肠的组织学评估显示结肠粘膜隐窝深度和宽度显著减少。通过 qRT-PCR 测定肠道炎症标志物。具体而言,Icam1、Ccl2(MCP-1)和 Ccl3(MIP-1α)mRNA 在 T3-SCI 后急性升高。T3-SCI 大鼠的结肠平滑肌厚度和胶原含量显著增加。对 pan-neuronal 标志物 HuC/D 进行的结肠横切片免疫组织化学处理显示结肠肠神经元密度显著降低,在损伤后 3 周时更为明显。我们的数据表明,SCI 后炎症和肠神经肌肉隔室的重塑伴随着 SCI。这些形态变化可能会引发同一时期发生的结肠蠕动减弱,可能是通过破坏结肠的固有神经肌肉控制。