Tan Xiang, Pei Wenjing, Xie Chune, Wang Zhibin, Liu Jiali, Cheng Yuan, Mao Tangyou, Shi Lei, Zhao Xingjie, Lu Qiongqiong, Sun Zhongmei, Kou Fushun, Jiang Hui, Li Junxiang
Graduate School of Beijing University of Chinese Medicine, Beijing 100029, China.
Department of Gastroenterology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing 100078, China.
Evid Based Complement Alternat Med. 2021 Jun 18;2021:6679348. doi: 10.1155/2021/6679348. eCollection 2021.
Irritable bowel syndrome (IBS) is a functional gastrointestinal disease characterized by visceral hypersensitivity-related abdominal pain, in which diarrhea-predominant IBS (IBS-D) is the main subtype and has a high clinical incidence. Tongxie Anchang Decoction (TXACD) has been proved to significantly improve abdominal pain in patients with IBS-D, but its underlying therapeutic mechanism still remains unclear. In the present study, IBS-D model rats were induced by neonatal maternal separation (NMS) combined with restraint stress (RS). The therapeutic effect of TXACD was evaluated by fecal characteristics and abdominal withdrawal reflex (AWR) scores. After 14 days of intragastric administration, the colonic tissues of rats were collected to detect the protein and gene level of the NGF, TrkA, and TRPV1 using Western blotting and real-time polymerase chain reaction, respectively, and detect mast cells infiltration using toluidine blue staining. The abdominal aorta blood centrifuged was collected for detecting serum levels of SP, 5-HT, and CGRP with ELISA. The results revealed that TXACD could significantly improve visceral hypersensitivity in IBS-D rats, reflected in the decrease of AWR score and the serum levels of SP, 5-HT, and CGRP. In addition, TXACD treatment could alleviate mast cells infiltration. Moreover, the expression levels of the NGF, TrkA, and TRPV1 were repressed by TXACD. The findings of the present study indicated that the therapeutic effect of TXACD on visceral hypersensitivity might be closely related to the downregulation of the NGF/TrkA signaling pathway, the reversal of TRPV1 expression and mast cells infiltration, and the decreased release of neuroendocrine factors SP, 5-HT, and CGRP.
肠易激综合征(IBS)是一种功能性胃肠疾病,其特征为与内脏高敏感性相关的腹痛,其中腹泻型肠易激综合征(IBS-D)是主要亚型,临床发病率较高。痛泻要方(TXACD)已被证明可显著改善IBS-D患者的腹痛,但其潜在治疗机制仍不清楚。在本研究中,通过新生母鼠分离(NMS)联合束缚应激(RS)诱导建立IBS-D模型大鼠。通过粪便特征和腹部退缩反射(AWR)评分评估TXACD的治疗效果。灌胃给药14天后,收集大鼠结肠组织,分别采用蛋白质免疫印迹法和实时聚合酶链反应检测神经生长因子(NGF)、酪氨酸激酶受体A(TrkA)和瞬时受体电位香草酸亚型1(TRPV1)的蛋白和基因水平,并用甲苯胺蓝染色检测肥大细胞浸润情况。采集离心后的腹主动脉血,用酶联免疫吸附测定法检测血清中P物质(SP)、5-羟色胺(5-HT)和降钙素基因相关肽(CGRP)水平。结果显示,TXACD可显著改善IBS-D大鼠的内脏高敏感性,表现为AWR评分降低以及血清中SP、5-HT和CGRP水平降低。此外,TXACD治疗可减轻肥大细胞浸润。而且,TXACD可抑制NGF、TrkA和TRPV1的表达水平。本研究结果表明,TXACD对内脏高敏感性的治疗作用可能与下调NGF/TrkA信号通路、逆转TRPV1表达和肥大细胞浸润以及减少神经内分泌因子SP、5-HT和CGRP的释放密切相关。