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Effect of quamoclit angulata extract supplementation on oxidative stress and inflammation on hyperglycemia-induced renal damage in type 2 diabetic mice

Authors
Park J.E.Lee H.Rho H.Hong S.M.Kim S.Y.Lim Y.
Issue Date
Jun-2020
Publisher
MDPI AG
Keywords
Apoptosis; Fibrosis; Inflammation; Kidney damage; Oxidative stress; Quamoclit angulata; Type 2 diabetes
Citation
Antioxidants, v.9, no.6
Journal Title
Antioxidants
Volume
9
Number
6
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/77459
DOI
10.3390/antiox9060459
ISSN
2076-3921
Abstract
Type 2 diabetes mellitus (T2DM) is caused by abnormalities of controlling blood glucose and insulin homeostasis. Especially, hyperglycemia causes hyper-inflammation through activation of NLRP3 inflammasome, which can lead to cell apoptosis, hypertrophy, and fibrosis. Quamoclit angulata (QA), one of the annual winders, has been shown ameliorative effects on diabetes. The current study investigated whether the QA extract (QAE) attenuated hyperglycemia-induced renal inflammation related to NLRP inflammasome and oxidative stress in high fat diet (HFD)-induced diabetic mice. After T2DM was induced, the mice were treated with QAE (5 or 10 mg/kg/day) by gavage for 12 weeks. The QAE supplementation reduced homeostasis model assessment insulin resistance (HOMA-IR), kidney malfunction, and glomerular hypertrophy in T2DM. Moreover, the QAE treatment significantly attenuated renal NLRP3 inflammasome dependent hyperinflammation and consequential renal damage caused by oxidative stress, apoptosis, andfibrosis in T2DM. Furthermore, QAE normalized aberrant energy metabolism (downregulation of p-AMPK, sirtuin (SIRT)-1, and PPARγ-coactivator α (PGC-1 α)) in T2DM mice. Taken together, the results suggested that QAE as a natural product has ameliorative effects on renal damage by regulationof oxidative stress and inflammation in T2DM. © 2020 by the authors.
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