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Protective effects of Amauroderma rugosum on dextran sulfate sodium-induced ulcerative colitis through the regulation of macrophage polarization and suppression of oxidative stress
Li, Jingjing1,6; Luo, Xi2; Shiu, Polly Ho Ting3; Cheng, Yanfen2; Nie, Xin4; Rangsinth, Panthakarn3; Lau, Benson Wui Man1; Zheng, Chengwen3; Li, Xuebo2; Li, Renkai3; Lee, Simon Ming Yuen5; Fu, Chaomei2; Seto, Sai Wang5,6; Zhang, Jinming2; Leung, George Pak Heng3
2024-07-01
Source PublicationBiomedicine and Pharmacotherapy
ISSN0753-3322
Volume176Pages:116901
Abstract

Background: Amauroderma rugosum (AR) is a medicinal mushroom commonly used to treat inflammation, gastric disorders, epilepsy, and cancers due to its remarkable anti-inflammatory and anti-oxidative properties. This study was designed to evaluate the pharmacological effects of AR and its underlying mechanism of action against ulcerative colitis (UC) in vitro and in vivo. Methods: A UC mouse model was established by administration of dextran sulfate sodium (DSS). AR extract was administered intragastrically to mice for 7 days. At the end of the experiment, histopathology, macrophage phenotype, oxidative stress, and inflammatory status were examined in vivo. Furthermore, RAW 264.7, THP-1, and Caco-2 cells were used to elucidate the mechanism of action of AR in vitro. Results: AR extract (0.5–2 mg/mL) significantly suppressed lipopolysaccharide (LPS) and interferon-gamma (IFN-γ)-induced M1 macrophage (pro-inflammatory) polarization in both RAW 264.7 and THP-1 cells. LPS-induced pro-inflammatory mediators (nitric oxide, TNF-α, IL-1β, MCP-1, and IL-6) were reduced by AR extract in a concentration-dependent manner. Similarly, AR extract downregulated MAPK signaling activity in LPS-stimulated RAW 264.7 cells. AR extract elicited a concentration-dependent increase in the mRNA expression of M2 (anti-inflammatory) phenotype markers (CD206, Arg-1, Fizz-1, and Ym-1) in RAW 264.7 cells. Moreover, AR extract suppressed DSS-induced ROS generation and mitochondrial dysfunction in Caco-2 cells. The in vivo experiment revealed that AR extract (200 mg/kg) increased colon length compared to the DSS-treated group. In addition, disease activity index, spleen ratio, body weight, oxidative stress, and colonic inflammation were markedly improved by AR treatment in DSS-induced UC mice. Finally, AR suppressed M1 and promoted M2 macrophage polarization in UC mice. Conclusion: The AR extract protected against DSS-induced UC by regulating macrophage polarization and suppressing oxidative stress. These valuable findings suggest that adequate intake of AR can prevent and/or treat UC.

KeywordAmauroderma Rugosum Macrophage Polarization Oxidative Stress Ulcerative Colitis
DOI10.1016/j.biopha.2024.116901
URLView the original
Indexed BySCIE
Language英語English
WOS Research AreaResearch & Experimental Medicine ; Pharmacology & Pharmacy
WOS SubjectMedicine, Research & Experimental ; Pharmacology & Pharmacy
WOS IDWOS:001258513200001
PublisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER, 65 RUE CAMILLE DESMOULINS, CS50083, 92442 ISSY-LES-MOULINEAUX, FRANCE
Scopus ID2-s2.0-85196038010
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Document TypeJournal article
CollectionInstitute of Chinese Medical Sciences
THE STATE KEY LABORATORY OF QUALITY RESEARCH IN CHINESE MEDICINE (UNIVERSITY OF MACAU)
Corresponding AuthorSeto, Sai Wang; Zhang, Jinming; Leung, George Pak Heng
Affiliation1.Department of Rehabilitation Sciences, Faculty of Health and Social Sciences, Hong Kong Polytechnic University, Kowloon, Hung Hom, Hong Kong
2.State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China
3.Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong
4.State Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, China
5.Department of Food Science and Nutrition, Faculty of Science, Hong Kong Polytechnic University, Kowloon, Hung Hom, Hong Kong
6.The Research Centre for Chinese Medicine Innovation, Hong Kong Polytechnic University, Kowloon, Hung Hom, Hong Kong
Recommended Citation
GB/T 7714
Li, Jingjing,Luo, Xi,Shiu, Polly Ho Ting,et al. Protective effects of Amauroderma rugosum on dextran sulfate sodium-induced ulcerative colitis through the regulation of macrophage polarization and suppression of oxidative stress[J]. Biomedicine and Pharmacotherapy, 2024, 176, 116901.
APA Li, Jingjing., Luo, Xi., Shiu, Polly Ho Ting., Cheng, Yanfen., Nie, Xin., Rangsinth, Panthakarn., Lau, Benson Wui Man., Zheng, Chengwen., Li, Xuebo., Li, Renkai., Lee, Simon Ming Yuen., Fu, Chaomei., Seto, Sai Wang., Zhang, Jinming., & Leung, George Pak Heng (2024). Protective effects of Amauroderma rugosum on dextran sulfate sodium-induced ulcerative colitis through the regulation of macrophage polarization and suppression of oxidative stress. Biomedicine and Pharmacotherapy, 176, 116901.
MLA Li, Jingjing,et al."Protective effects of Amauroderma rugosum on dextran sulfate sodium-induced ulcerative colitis through the regulation of macrophage polarization and suppression of oxidative stress".Biomedicine and Pharmacotherapy 176(2024):116901.
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