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Xie Zhuo Tiao Zhi formula ameliorates chronic alcohol-induced liver injury in mice.
Chang, Kaixin; Guo, Rui; Hu, Wenbo; Wang, Xuezhu; Cao, Feiwei; Qiu, Jiannan; Li, Jiaomei; Han, Qiang; Du, Zhongyan; Dou, Xiaobing; Li, Songtao.
Affiliation
  • Chang K; School of Life Science, Zhejiang Chinese Medical University, Hangzhou, China.
  • Guo R; School of Public Health, Zhejiang Chinese Medical University, Hangzhou, China.
  • Hu W; The First School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou, China.
  • Wang X; School of Public Health, Zhejiang Chinese Medical University, Hangzhou, China.
  • Cao F; School of Public Health, Zhejiang Chinese Medical University, Hangzhou, China.
  • Qiu J; School of Life Science, Zhejiang Chinese Medical University, Hangzhou, China.
  • Li J; School of Public Health, Zhejiang Chinese Medical University, Hangzhou, China.
  • Han Q; School of Public Health, Zhejiang Chinese Medical University, Hangzhou, China.
  • Du Z; Key Laboratory of Blood-Stasis-Toxin Syndrome of Zhejiang Province, Zhejiang Engineering Research Center for 'Preventive Treatment' Smart Health of Traditional Chinese Medicine, School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
  • Dou X; School of Life Science, Zhejiang Chinese Medical University, Hangzhou, China.
  • Li S; School of Public Health, Zhejiang Chinese Medical University, Hangzhou, China.
Front Pharmacol ; 15: 1363131, 2024.
Article in En | MEDLINE | ID: mdl-38681193
ABSTRACT
This study aimed to evaluate the protective role and potential mechanisms of Xie Zhuo Tiao Zhi decoction (XZTZ) on alcohol-associated liver disease (ALD). XZTZ significantly alleviated alcohol-induced liver dysfunction, based on histological examinations and biochemical parameters after 4-week administration. Mechanically, alcohol-stimulated hepatic oxidative stress was ameliorated by XZTZ, accompanied by the improvement of Nrf2/Keap1 expression and alcohol-activated phosphorylation of pro-inflammatory transcription factors, including JNK, P38, P65, and IκBα, were rescued by XZTZ. In conclusion, XZTZ demonstrates potential in alleviating alcohol-induced liver injury, oxidative stress, and inflammation possibly through modulation of Nrf2/Keap1 and MAPKs/NF-κB signaling pathways, suggesting its potential as a therapeutic option for patients with alcoholic liver disease.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2024 Document type: Article Affiliation country: China