Protective Effects of Zhi Ciweipi Water Extracts on Dextran Sulfate Sodium Salt⁃Induced Ulcerative Colitis in Mice
10.13865/j.cnki.cjbmb.2023.09.1237
- Author:
Zhi-Kai XIAHOU
1
;
Jun HAN
2
Author Information
1. Teaching and Research Office, Scientific Research Center, China Sport and Health Research Institute, Beijing Sport University
2. National and Local United Engineering Research Center of Key Technology of Traditional Chinese Medicinal Granules, Research Institute of Traditional Chinese Medicine, Beijing Tcmages Pharmaceutical Co., Ltd
- Publication Type:Journal Article
- Keywords:
colonic inflammatory factor(CIF);
colonic M1 macrophages;
Hedgehog skin fried with talcum powder (ZCWP);
single-cell sequencing;
transcriptome sequencing
- From:
Chinese Journal of Biochemistry and Molecular Biology
2023;39(11):1638-1649
- CountryChina
- Language:Chinese
-
Abstract:
Ulcerative colitis (UC) is a disease characterized by chronic inflammation of the intestinal mucosa. However, its exact pathogenesis is not fully understood. Zhi Ciweipi (ZCWP), as a traditional Chinese medicine (TCM), has demonstrated suitable anti-inflammatory effects in the treatment of patients with bloody stool and hemorrhoids. However, its therapeutic effects on ulcerative colitis have yet to be investigated in depth. The aim of this study was to investigate the protective effect of the aqueous extract of ZCWP against dextran sulfate sodium salt (DSS)-induced ulcerative colitis in mice and its possible mechanism of action. Successful simulation of ulcerative colitis was achieved by providing mice with drinking water containing 3% DSS. The HE staining results revealed that the aqueous extract of ZCWP could significantly reduce DSS-induced colonic injuries. Transcriptome sequencing analysis identified 10 key inflammation-related genes (IL⁃6, IL⁃1β, CSF2, TNF, IL10, IFN⁃γ, CXCL1, CXCL2, CXCL9, CXCL10), all of which were significantly downregulated (P<0. 05) in response to treatment with the aqueous extract of ZCWP according to qRT-PCR and Western blotting analyses. The immunofluorescence results further indicated that the aqueous extract of ZCWP was able to reduce the DSS-induced increase in the proportion of M1-type macrophages in the colon. Using single-cell sequencing, we thoroughly investigated the signaling relationships between different cell types, which revealed particularly strong communication between M1-type macrophages and fibroblasts. Subsequent qRT-PCR and Western blot analyses verified that the aqueous extract of ZCWP significantly downregulated the expression of DSS-induced fibrosis-related genes in colonic tissues (P<0. 05). In conclusion, the results of this study suggest that the aqueous extract of prepared ZCWP exerts a protective effect against DSS-induced ulcerative colitis by inhibiting M1-type macrophage polarization, downregulating the expression of inflammatory factors, and preventing strong communication between M1-type macrophages and fibroblasts. These findings not only reveal the therapeutic mechanism by which ZCWP aqueous extract treats colitis, but also provide a new theoretical basis for its application in clinical practice.
