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Publication Name World Journal of Gastroenterology
Manuscript ID 123033
DOI 10.3748/wjg.123033
Country China
Category Endocrinology & Metabolism
Manuscript Type Basic Study
Article Title Integrating proteomics, metabolomics, and molecular docking to elucidate the mechanism of Jiangtang Qingre formula against metabolic dysfunction-associated steatohepatitis
Manuscript Source Unsolicited Manuscript
All Author List Li-Juan Zhou, Jin-Lin Wu, Hang Wang, Rui Han, Cai Tang, Fang Fang and Dan-Ping Zhu
Funding Agency and Grant Number
Funding Agency Grant Number
Chongqing Clinical Research Center for Metabolic Diseases (Integrated Traditional Chinese and Western Medicine) SQMS2025DXB-006
Chongqing Clinical Research Center for Metabolic Diseases (Integrated Traditional Chinese and Western Medicine) SQMS2026DXB-001
Chongqing Clinical Research Center for Metabolic Diseases (Integrated Traditional Chinese and Western Medicine) SQMS2026DXB-003
Corresponding Author Dan-Ping Zhu, Department of Endocrinology and Metabolism, Chongqing Traditional Chinese Medicine Hospital, Department of Endocrinology and Metabolism, Chongqing Traditional Chinese Medicine Hospital, Chongqing, 400021, China. zdp790203@163.com., Chongqing 400021, China. zdp790203@163.com
Key Words Metabolic dysfunction-associated steatohepatitis; Jiangtang Qingre formula; Multi-omics; Oxidative stress; Leiomodin 3; Timosaponins
Core Tip This study demonstrated that Jiangtang Qingre formula (JQF) ameliorates metabolic dysfunction-associated steatohepatitis through multi-target mechanisms. Multi-omics revealed arachidonic acid metabolism, and glutathione metabolism, with multiple targets implicated including Lmod3. Molecular docking confirmed timosaponins exhibited the strongest binding affinity to these targets. Knockdown of Lmod3 partially alleviated free fatty acids-induced AML12 cell injury, an effect further augmented by JQF. Additionally, timosaponin A III and timosaponin B II were effectively absorbed into the bloodstream and enriched in the liver, while their secondary metabolite sarsasapogenin was detected at high abundance in feces, further supporting the role of timosaponins as key pharmacologically active substances.
Citation Zhou LJ, Wu JL, Wang H, Han R, Tang C, Fang F, Zhu DP. Integrating proteomics, metabolomics, and molecular docking to elucidate the mechanism of Jiangtang Qingre formula against metabolic dysfunction-associated steatohepatitis. World J Gastroenterol 2026; In press
PDF 123033-in-press.pdf
Received
2026-05-07 08:18
Peer-Review Started
2026-05-07 08:19
First Decision by Editorial Office Director
2026-06-03 11:26
Return for Revision
2026-06-03 11:26
Revised
2026-07-01 09:50
Publication Fee Transferred
2026-07-07 04:50
Second Decision by Editor
2026-09-02 02:54
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2026-09-04 09:13
Articles in Press
2026-09-04 09:13
Edit the Manuscript by Language Editor
Typeset the Manuscript
ISSN 1007-9327 (print) and 2219-2840 (online)
Open Access This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See Permissions. Published by Baishideng Publishing Group Inc.
Copyright ©Author(s) (or their employer(s)) 2026. No commercial re-use. See Permissions. Published by Baishideng Publishing Group Inc.
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