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Diacerein attenuates vascular dysfunction by reducing inflammatory response and insulin resistance in type 2 diabetic rats.

Authors :
He, An
Shen, Jian
Xue, Yuzhou
Xiang li
Li, Yuanjing
Huang, Longxiang
Lv, Dingyi
Luo, Minghao
Source :
Biochemical & Biophysical Research Communications. Dec2021, Vol. 585, p68-74. 7p.
Publication Year :
2021

Abstract

To examine the effect of diacerein on vascular dysfunction in type 2 diabetic rats and elucidate the mechanism of diacerein. In a rat model, type 2 diabetes was induced by high-fat diet and streptozotocin. Vascular function was assessed in vascular reactivity experiment. The effect of diacerein (10 or 20 mg/kg/day) on blood glucose, inflammation and insulin signaling, and modulators in vascular tissue in diabetic rats were investigated by molecular and biochemical approaches. In this study, diacerein inhibited diabetes-induced vascular dysfunction. Diacerein treatment normalized blood glucose, insulin tolerance test, inflammatory cytokine levels and nitric oxide synthases expression in diabetic rats. Moreover, diacerein inhibited NF-κB and NLRP3 pathways and activated insulin signaling pathway related proteins IRS-1 and AKT in diabetic rats. Diacerein improved vascular function effectively in diabetic rats by suppressing inflammation and reducing insulin resistance. These results suggest that diacerein may represent a novel therapy for patients with diabetes. • In our study, we found diacerein inhibited diabetes-induced vascular dysfunction for the first time. • Diacerein treatment normalized blood glucose, insulin resistance, inflammatory cytokine levels and endothelial nitric oxide synthase and inducible nitric oxide synthase expression in diabetic rats. • Diacerein inhibited NF-κB and NLRP3 pathways and activated insulin signaling pathway related proteins IRS-1 and AKT in diabetic rats. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
585
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
153783591
Full Text :
https://doi.org/10.1016/j.bbrc.2021.11.017