Magnoflorine alleviates dextran sulfate sodium‐induced ulcerative colitis via inhibiting JAK2/STAT3 signaling pathway

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Main Authors: Jianxia Wen, Yi Yang, Lu Li, Jiachen Xie, Junjie Yang, Fangling Zhang, Liting Duan, Junjie Hao, Yuling Tong, Yuxin He
Format: Artículo Open Access
Published: Wiley 2024
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author Jianxia Wen
Yi Yang
Lu Li
Jiachen Xie
Junjie Yang
Fangling Zhang
Liting Duan
Junjie Hao
Yuling Tong
Yuxin He
author_facet Jianxia Wen
Yi Yang
Lu Li
Jiachen Xie
Junjie Yang
Fangling Zhang
Liting Duan
Junjie Hao
Yuling Tong
Yuxin He
Jianxia Wen
Yi Yang
Lu Li
Jiachen Xie
Junjie Yang
Fangling Zhang
Liting Duan
Junjie Hao
Yuling Tong
Yuxin He
collection Wiley Open Access
contents Magnoflorine alleviates dextran sulfate sodium‐induced ulcerative colitis via inhibiting JAK2/STAT3 signaling pathway Jianxia Wen Yi Yang Lu Li Jiachen Xie Junjie Yang Fangling Zhang Liting Duan Junjie Hao Yuling Tong Yuxin He Phytotherapy Research AbstractMagnoflorine (Mag), a natural alkaloid component originating from the Ranunculaceae Juss. Family, has a various of pharmacological activities. This study aimed to investigate the therapeutic effects and potential mechanism of Mag on dextran sulfate sodium (DSS)‐induced ulcerative colitis (UC) based on comprehensive approaches. Therapeutic effects of Mag on 3% DSS‐induced UC mice were analyzed. UHPLC‐Q‐TOF/MS was performed to investigate the potential metabolites and signaling pathway of Mag on DSS‐induced UC. Furthermore, the predicted mRNA and protein levels of JAK2/STAT3 signaling pathway in colon tissue were verified and assessed by qRT‐PCR and Western Blotting, respectively. Therapeutic effects of Mag on UC mice were presented in down‐regulation serum biochemical indices, alleviating histological damage of colon tissue. Serum untargeted metabolomics analysis showed that the potential mechanism of Mag on UC is mainly associated with the regulation of six biomarkers and 11 pathways, which may be responsible for the therapeutic efficacy of UC. The “component–metabolites–targets” interactive network indicated that Mag exerts its anti‐UC effect by regulating PTGS1 and PTGS2, thereby regulating arachidonic acid. Moreover, the results of qRT‐PCR showed that Mag could substantially decrease the relative mRNA expression level of Hub genes. In addition, it was found that Mag could inhibit the relative mRNA and protein expression of JAK2/STAT3 signaling pathway. The present results highlighted the role of Mag ameliorated colon injury in DSS‐induced UC mice by inhibiting the JAK2/STAT3 signaling pathway. These results suggest that Mag may be an effective agent for the treatment of UC. 10.1002/ptr.8271 http://onlinelibrary.wiley.com/termsAndConditions#vor
doi_str_mv 10.1002/ptr.8271
format Artículo Open Access
id wiley_oa_10_1002_ptr_8271
institution Wiley Open Access
license_str_mv http://onlinelibrary.wiley.com/termsAndConditions#vor
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle Magnoflorine alleviates dextran sulfate sodium‐induced ulcerative colitis via inhibiting JAK2/STAT3 signaling pathway
Jianxia Wen
Yi Yang
Lu Li
Jiachen Xie
Junjie Yang
Fangling Zhang
Liting Duan
Junjie Hao
Yuling Tong
Yuxin He
Phytotherapy Research
Magnoflorine alleviates dextran sulfate sodium‐induced ulcerative colitis via inhibiting JAK2/STAT3 signaling pathway Jianxia Wen Yi Yang Lu Li Jiachen Xie Junjie Yang Fangling Zhang Liting Duan Junjie Hao Yuling Tong Yuxin He Phytotherapy Research AbstractMagnoflorine (Mag), a natural alkaloid component originating from the Ranunculaceae Juss. Family, has a various of pharmacological activities. This study aimed to investigate the therapeutic effects and potential mechanism of Mag on dextran sulfate sodium (DSS)‐induced ulcerative colitis (UC) based on comprehensive approaches. Therapeutic effects of Mag on 3% DSS‐induced UC mice were analyzed. UHPLC‐Q‐TOF/MS was performed to investigate the potential metabolites and signaling pathway of Mag on DSS‐induced UC. Furthermore, the predicted mRNA and protein levels of JAK2/STAT3 signaling pathway in colon tissue were verified and assessed by qRT‐PCR and Western Blotting, respectively. Therapeutic effects of Mag on UC mice were presented in down‐regulation serum biochemical indices, alleviating histological damage of colon tissue. Serum untargeted metabolomics analysis showed that the potential mechanism of Mag on UC is mainly associated with the regulation of six biomarkers and 11 pathways, which may be responsible for the therapeutic efficacy of UC. The “component–metabolites–targets” interactive network indicated that Mag exerts its anti‐UC effect by regulating PTGS1 and PTGS2, thereby regulating arachidonic acid. Moreover, the results of qRT‐PCR showed that Mag could substantially decrease the relative mRNA expression level of Hub genes. In addition, it was found that Mag could inhibit the relative mRNA and protein expression of JAK2/STAT3 signaling pathway. The present results highlighted the role of Mag ameliorated colon injury in DSS‐induced UC mice by inhibiting the JAK2/STAT3 signaling pathway. These results suggest that Mag may be an effective agent for the treatment of UC. 10.1002/ptr.8271 http://onlinelibrary.wiley.com/termsAndConditions#vor
title Magnoflorine alleviates dextran sulfate sodium‐induced ulcerative colitis via inhibiting JAK2/STAT3 signaling pathway
topic Phytotherapy Research
url https://onlinelibrary.wiley.com/doi/10.1002/ptr.8271