دورية أكاديمية

Resveratrol inhibits high glucose-induced activation of AP-1 and NF-κB via SphK1/S1P2 pathway to attenuate mesangial cells proliferation and inflammation

التفاصيل البيبلوغرافية
العنوان: Resveratrol inhibits high glucose-induced activation of AP-1 and NF-κB via SphK1/S1P2 pathway to attenuate mesangial cells proliferation and inflammation
المؤلفون: Yanhui Deng, Wenyan Gong, Qiang Li, Xian Wu, Liyao Wu, Xiaoxia Zheng, Wenying Chen, Heqing Huang
المصدر: Journal of Functional Foods, Vol 55, Iss , Pp 86-94 (2019)
بيانات النشر: Elsevier, 2019.
سنة النشر: 2019
المجموعة: LCC:Nutrition. Foods and food supply
مصطلحات موضوعية: Resveratrol, Diabetic nephropathy, Sphingosine kinase 1, Sphingosine 1-phosphate, AP-1, NF-κB, Nutrition. Foods and food supply, TX341-641
الوصف: Diabetes nephropathy (DN) is the most common microvascular complications of diabetes, as hyperglycemia induces mesangial cell (MC) proliferation and inflammation and subsequently contributes to the development of renal fibrosis. Sphingosine kinase 1 (SphK1)/sphingosine 1-phosphate receptor 2 (S1P2) signaling pathway could activate AP-1 and NF-κB, which played a key regulatory role in the pathological progression of DN. This study investigates whether resveratrol (RSV) plays a regulatory role by SphK1/S1P2 pathway in MCs proliferation and inflammation under high glucose condition. Herein, we found that RSV inhibited MCs proliferation and attenuated high glucose (HG)-induced FN, TGF-β1, ICAM-1, iNOS, SphK1 and S1P2 expression and inhibited SphK1 activity andS1P production, which was also in accordance with MCs transfected with wild-type SphK1WT plasmid. Furthermore, RSV remarkably reduced AP-1 and NF-κB activation. Overall, these results indicated that RSV could be a potential and valuable resource of natural compounds for DN treatment via SphK1/S1P2 pathway.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1756-4646
Relation: http://www.sciencedirect.com/science/article/pii/S1756464619300775; https://doaj.org/toc/1756-4646
DOI: 10.1016/j.jff.2019.02.014
URL الوصول: https://doaj.org/article/d2ccba15d8284f889875a98ad94555eb
رقم الأكسشن: edsdoj.2ccba15d8284f889875a98ad94555eb
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17564646
DOI:10.1016/j.jff.2019.02.014