Changji'an formula alleviates visceral hypersensitivity of a post-inflammatory IBS-D mouse model via NGF/TrkA signaling pathway.

Abstract

Background: Changji'an Formula (CJAF) is an effective Chinese herbal prescription to treat irritable bowel syndrome with predominant diarrhea (IBS-D), which is derived from two famous classical prescription: Sijunzi decoction and Tong-Xie-Yao-Fang. However, the molecular mechanism has not been well defined. This study aims to illustrate the molecular mechanism of CJAF in the treatment of IBS-D.

Methods: Chemical components of CJAF were determined by ultrahigh performance liquid chromatography-quadrupole/orbitrap high resolution mass spectrometry (UPLC-Q-Orbitrap HRMS) and further verified by reference standards. IBS-D model was induced in C57BL/6J mice by a single edema with colonic infusion of 0.1 mL trinitrobenzene sulfonic acid (TNBS, 50 mg/mL) combined with 7 days of restraint stress, 2 h/d. The treatment group was given rifaximin (100 mg/kg) and high, moderate and low doses of CJAF by gavage for 7 days, respectively (n = 7). After administration, the main symptoms of IBS-D were tested, and behavioral tests were conducted using sucrose preference test and open field test. The colonic tissues of mice were obtained. Gene and protein expression of mast cell tryptase, nerve growth factor (NGF), tyrosine kinase receptor A (TrkA), phosphorylated TrkA, growth associated protein 43(GAP43) and neuro-specific enolase (NSE) were determined by RT-PCR, western blot and immunohistochemistry.

Results: 36 compounds were identified by UPLC-Q-Orbitrap HRMS, and the determined components can be categorized into 7 chemical types, including 16 flavonoids, 7 triterpenoids, 4 alkaloids, 3 sesquiterpenoids, 2 monoterpene glycosides, 2 organic acids, 1 phenylpropanoids and 1 tannin. Animal experiment showed that the abdominal pain and diarrhea symptoms of IBS-D mice were alleviated by CJAF. The sucrose preference, total translocation distance and average velocity of movement in the open field test was upregulated. The mRNA and protein expression of mast cell marker tryptase, as well as NGF, phosphorylated TrkA, GAP43 and NSE in IBS-D mice colonic tissues were down-regulated by CJAF.

Conclusions: CJAF could effectively alleviate abdominal pain and diarrhea symptoms of IBS-D by inhibiting the activation of colonic mast cells and the resultant activation of NGF/TrkA signal pathway. Therefore, CJAF affords a potential candidate for the treatment of IBS-D.