دورية أكاديمية

The research progress of crosstalk mechanism of autophagy and apoptosis in diabetic vascular endothelial injury

التفاصيل البيبلوغرافية
العنوان: The research progress of crosstalk mechanism of autophagy and apoptosis in diabetic vascular endothelial injury
المؤلفون: Hanyu Liu, Qiyuan Yao, Xueru Wang, Hongyan Xie, Chan Yang, Hong Gao, Chunguang Xie
المصدر: Biomedicine & Pharmacotherapy, Vol 170, Iss , Pp 116072- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: Diabetic vascular endothelial injury, Apoptosis, Autophagy, Beclin1-Bcl2/Bcl-xL complex, PINK1/Parkin signal pathway, Therapeutics. Pharmacology, RM1-950
الوصف: In recent years, the widespread prevalence of diabetes has become a major killer that threatens the health of people worldwide. Of particular concern is hyperglycemia-induced vascular endothelial injury, which is one of the factors that aggravate diabetic vascular disease. During the process of diabetic vascular endothelial injury, apoptosis is an important pathological manifestation and autophagy is a key regulatory mechanism. Autophagy and apoptosis interact with each other. Hence, the crosstalk mechanism between the two processes is an important means of regulating diabetic vascular endothelial injury. This article reviews the research progress in apoptosis in the context of diabetic vascular endothelial injury and discusses the crosstalk mechanism of autophagy and apoptosis and its role in this injury. The purpose is to guide the prevention and treatment of diabetic vascular endothelial injury in the future.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0753-3322
Relation: http://www.sciencedirect.com/science/article/pii/S075333222301870X; https://doaj.org/toc/0753-3322
DOI: 10.1016/j.biopha.2023.116072
URL الوصول: https://doaj.org/article/377ee06882764df3a48c49f548f03389
رقم الأكسشن: edsdoj.377ee06882764df3a48c49f548f03389
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:07533322
DOI:10.1016/j.biopha.2023.116072