Guo J, Zhu Y, Yang Y, Wang X, Chen B, Zhang W, Xie B, Zhu Z, Yue Y, Cheng J
Second School of Clinical Medical, Nanjing University of Chinese Medicine, Nanjing, China.
Centre of Physical Medicine and Rehabilitation, Hainan Provincial Nongken General Hospital, Hainan, China.
Spinal Cord. 2016 Dec;54(12):1139-1144. doi: 10.1038/sc.2016.76. Epub 2016 Jul 5.
Study designExperimental study.ObjectiveTo determine the effects of electroacupuncture (EA) at Zusanli (ST36) on colonic motility and neuronal nitric oxide synthase (nNOS) expression in rats with neurogenic bowel dysfunction (NBD) after spinal cord injury (SCI).SettingSecond School of Clinical Medical, Nanjing University of Chinese Medicine, Jiangsu, China.MethodsWe divided 30 adult Sprague-Dawley rats into a sham group (10 rats), a model group (SCI alone, 10 rats) and a EA group (SCI+EA at ST36, 10 rats). Defecation time was recorded as the time from activated carbon administration (on day 15) to evacuation of the first black stool. Immunohistochemical, real-time PCR and western blot analyses were performed to assess changes in nNOS-immunoreactive cells, and nNOS messenger RNA (mRNA) and protein, respectively, after 14 experimental days.ResultsDefecation time was lower in the EA group than in the model group (P<0.01). On immunohistochemical analysis, nNOS was localized in the myenteric plexus of the colon. The number of nNOS-immunoreactive cells and the intensity of nNOS staining were greater in the model group than in the sham group and lesser in the EA group than in the model group. Consistent with the immunohistochemical findings, nNOS mRNA and protein expression was higher in the model group than in the sham group and lower in the EA group than in the model group (P<0.05 for both).ConclusionIncreased colonic nNOS expression can induce/aggravate NBD in SCI rats. EA at ST36 ameliorated NBD, possibly by downregulating colonic nNOS expression.
实验性研究。
确定电针足三里(ST36)对脊髓损伤(SCI)后神经源性肠功能障碍(NBD)大鼠结肠动力及神经元型一氧化氮合酶(nNOS)表达的影响。
中国江苏省南京中医药大学第二临床医学院。
将30只成年Sprague-Dawley大鼠分为假手术组(10只大鼠)、模型组(单纯SCI,10只大鼠)和电针组(SCI + 电针ST36,10只大鼠)。排便时间记录为从给予活性炭(第15天)到排出第一粒黑色粪便的时间。在实验14天后,分别进行免疫组织化学、实时聚合酶链反应(PCR)和蛋白质印迹分析,以评估nNOS免疫反应性细胞、nNOS信使核糖核酸(mRNA)和蛋白质的变化。
电针组的排便时间低于模型组(P < 0.01)。免疫组织化学分析显示,nNOS定位于结肠肌间神经丛。模型组中nNOS免疫反应性细胞数量和nNOS染色强度高于假手术组,电针组低于模型组。与免疫组织化学结果一致,模型组中nNOS mRNA和蛋白质表达高于假手术组,电针组低于模型组(两者均P < 0.05)。
结肠nNOS表达增加可诱导/加重SCI大鼠的NBD。电针ST36改善了NBD,可能是通过下调结肠nNOS表达实现的。