The Research Center for Integrative Medicine, School of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, P. R. China.
Hunan University of Chinese Medicine, Changsha 410000, Hunan Province, P. R. China.
Am J Chin Med. 2022;50(7):1905-1925. doi: 10.1142/S0192415X22500811. Epub 2022 Oct 3.
Patchouli alcohol (PA) has been widely used for the treatment of diarrhea-predominant irritable bowel syndrome (IBS-D) in traditional Chinese medicine, and the related mechanism remains to be fully understood. Our previous study has indicated that PA significantly reduced visceral sensitivity and defecation area in IBS-D rats. In this study, we prepared an IBS-D rat model and observed the dynamic intestinal motility and colonic longitudinal muscle and myenteric plexus (LMMP) neurons, as well as their subtypes at D14, D21, and D28. After PA administration, we observed the effects on the changes in intestinal motility, colonic LMMP neurons, and LMMP Myosin Va in IBS-D rats and their co-localization with inhibitory neurotransmitter-related proteins. The results indicated that PA treatment could alleviate IBS-D symptoms, regulate the abnormal expression of LMMP neurons, increase Myosin Va expression, up-regulate co-localization levels of Myosin Va with neuronal nitric oxide synthase (nNOS), and promote co-localization levels of Myosin Va with vasoactive intestinal polypeptide (VIP). In conclusion, this study demonstrated the neuropathic alterations in the colon of chronic restraint stress-induced IBS-D rat model. PA reversed the neuropathological alteration by affecting the transport process of nNOS and VIP vesicles via Myosin Va and the function of LMMP inhibitory neurons, and these effects were related to the mechanism of enteric nervous system (ENS) remodeling.
香豆素醇(PA)已广泛用于中医治疗腹泻型肠易激综合征(IBS-D),但其相关机制仍未完全阐明。我们之前的研究表明,PA 可显著降低 IBS-D 大鼠的内脏敏感性和排便面积。在本研究中,我们制备了 IBS-D 大鼠模型,并观察了 D14、D21 和 D28 时的肠道动力和结肠纵行肌及肌间神经丛(LMMP)神经元的动态变化,以及它们的亚型。在给予 PA 后,观察其对 IBS-D 大鼠肠道动力变化、LMMP 神经元和 LMMP 肌球蛋白 Va 的影响,以及它们与抑制性神经递质相关蛋白的共定位。结果表明,PA 治疗可缓解 IBS-D 症状,调节 LMMP 神经元的异常表达,增加肌球蛋白 Va 的表达,上调肌球蛋白 Va 与神经元型一氧化氮合酶(nNOS)的共定位水平,并促进肌球蛋白 Va 与血管活性肠肽(VIP)的共定位水平。总之,本研究证明了慢性束缚应激诱导的 IBS-D 大鼠模型结肠的神经病变改变。PA 通过影响肌球蛋白 Va 介导的 nNOS 和 VIP 囊泡的转运过程以及 LMMP 抑制性神经元的功能,逆转了神经病理改变,这些作用与肠神经系统(ENS)重塑的机制有关。