Mapping Txnip: Key connexions in progression of diabetic nephropathy

被引:32
作者
Kumar, Anil [1 ]
Mittal, Ruchika [1 ]
机构
[1] Panjab Univ, UGC Ctr Adv Study, Univ Inst Pharmaceut Sci, Neuropharmacol Div, Chandigarh, India
关键词
Diabetic nephropathy; Txnip; Inflammation; mTOR pathway; THIOREDOXIN-INTERACTING-PROTEIN; CARBOHYDRATE RESPONSE ELEMENT; BETA-CELL APOPTOSIS; OXIDATIVE STRESS; ENDOTHELIAL-CELLS; GENE-EXPRESSION; NLRP3; INFLAMMASOME; BINDING PROTEIN-2; HIGH GLUCOSE; MITOCHONDRIAL-FUNCTION;
D O I
10.1016/j.pharep.2017.12.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Studies demonstrates the major involvement of inflammatory and apoptotic pathway in the pathophysiology of diabetic nephropathy. The cross talk between inflammatory and apoptotic pathway suggests Txnip as a molecular connexion in progression of disease state. Txnip modulates inflammatory pathway (via ROS production and NLRP3 inflammasome activity) and apoptotic pathway (via mTOR pathway). The key contribution of Txnip in both the pathways, reflects, its crucial role in diabetic nephropathy. In the present review, we have first provided an overview of diabetic nephropathy and Txnip system, followed by the mechanistic insight of Txnip in the progression of diabetic nephropathy. This new mechanistic approach suggests to explore Txnip modulators as a promising therapeutic drug target in diabetic nephropathy. (c) 2017 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Sp. z o.o. All rights reserved.
引用
收藏
页码:614 / 622
页数:9
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