دورية أكاديمية

Vanillic acid alleviates liver fibrosis through inhibiting autophagy in hepatic stellate cells via the MIF/CD74 signaling pathway

التفاصيل البيبلوغرافية
العنوان: Vanillic acid alleviates liver fibrosis through inhibiting autophagy in hepatic stellate cells via the MIF/CD74 signaling pathway
المؤلفون: Lifeng Qin, Jiawu Tan, Xiaoping Lv, Jiqiao Zhang
المصدر: Biomedicine & Pharmacotherapy, Vol 168, Iss , Pp 115673- (2023)
بيانات النشر: Elsevier, 2023.
سنة النشر: 2023
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: Vanillic acid, Liver fibrosis, Autophagy, Hepatic stellate cells, MIF/CD74, Therapeutics. Pharmacology, RM1-950
الوصف: MIF/CD74 signaling pathway and autophagy may be closely related to liver fibrosis. Vanillic acid (VA) is likely to have an anti-liver fibrosis effect, although related studies have not been reported. The aim of this study was to verify the role of hepatic stellate cells (HSCs) autophagy and the MIF/CD74 signaling pathway in the pathogenesis of liver fibrosis, and to investigate the effect of VA on liver fibrosis through in vivo and in vitro experiments. Our results showed that VA significantly attenuated CCl4-induced liver fibrosis. The alleviation of liver fibrosis with VA treatment was associated with a reduction of MIF, CD74, α-SMA, LC3B and Collagen 1. In addition, VA, MIF inhibitor (ISO-1) and autophagy inhibitor (3-MA) markedly inhibited the proliferation and migration of HSCs. This study indicates that VA could protect against HSCs activation, proliferation and migration by inhibiting the autophagy in HSCs via the MIF/CD74 signaling pathway so that alleviates liver fibrosis.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0753-3322
Relation: http://www.sciencedirect.com/science/article/pii/S0753332223014713; https://doaj.org/toc/0753-3322
DOI: 10.1016/j.biopha.2023.115673
URL الوصول: https://doaj.org/article/641765da197147c4a7d74cedd218301d
رقم الأكسشن: edsdoj.641765da197147c4a7d74cedd218301d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:07533322
DOI:10.1016/j.biopha.2023.115673