دورية أكاديمية

Icariin ameliorates viral myocarditis by inhibiting TLR4-mediated ferroptosis

التفاصيل البيبلوغرافية
العنوان: Icariin ameliorates viral myocarditis by inhibiting TLR4-mediated ferroptosis
المؤلفون: Wei Luo, Yi Lu, Jun-Hua Deng, Peng Liu, Yan Huang, Wan-Xi Liu, Chun-Li Huang
المصدر: Asian Pacific Journal of Tropical Biomedicine, Vol 14, Iss 3, Pp 106-114 (2024)
بيانات النشر: Wolters Kluwer Medknow Publications, 2024.
سنة النشر: 2024
المجموعة: LCC:Arctic medicine. Tropical medicine
LCC:Biology (General)
مصطلحات موضوعية: viral myocarditis, cvb3, tlr4, ferroptosis, icariin, Arctic medicine. Tropical medicine, RC955-962, Biology (General), QH301-705.5
الوصف: Objective: To explore the mechanism by which icariin alleviates viral myocarditis. Methods: CVB3-induced cardiomyocytes were used as an in vitro model of viral myocarditis to assess the effects of icariin treatment on cell viability, inflammation, and apoptosis. Moreover, the effects of icariin on ferroptosis and TLR4 signaling were assessed. After AC16 cells were transfected with TLR4 overexpression plasmids, the role of TLR4 in mediating the regulatory effect of icariin in viral myocarditis was investigated. Results: Icariin significantly elevated cell viability and reduced inflammatory factors TNF-α, IL-1β, IL-6, and IL-18. Flow cytometry revealed that icariin decreased apoptosis rate, and the protein expression of Bax and cleaved caspase 3 and 9 in CVB3-induced cardiomyocytes. Additionally, it suppressed ferroptosis including lipid peroxidation and ferrous ion, as well as the TLR4 signaling. However, TLR4 overexpression abrogated the modulatory effects of icariin. Conclusions: Icariin mitigates CVB3-induced myocardial injury by inhibiting TLR4-mediated ferroptosis. Further animal study is needed to verify its efficacy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2221-1691
2588-9222
Relation: http://www.apjtb.org/article.asp?issn=2221-1691;year=2024;volume=14;issue=3;spage=106;epage=114;aulast=Luo; https://doaj.org/toc/2221-1691; https://doaj.org/toc/2588-9222
DOI: 10.4103/apjtb.apjtb_588_23
URL الوصول: https://doaj.org/article/cbf3a8f4eed94d2389f332c2673c68c3
رقم الأكسشن: edsdoj.bf3a8f4eed94d2389f332c2673c68c3
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22211691
25889222
DOI:10.4103/apjtb.apjtb_588_23