Glycogen synthase kinase-3: A potential target for diabetes

被引:19
|
作者
Teli, Divya M. [1 ]
Gajjar, Anuradha K. [1 ]
机构
[1] LM Coll Pharm, Dept Pharmaceut Chem & Qual Assurance, Ahmadabad 380009, Gujarat, India
关键词
Glycogen synthase kinase-3; Glycogen metabolism; Diabetes; Inhibitors; ALZHEIMERS-DISEASE; GSK-3; INHIBITORS; PROTEIN-KINASE; SUBSTRATE-SPECIFICITY; MOLECULAR-MECHANISM; TAU PHOSPHORYLATION; PEPTIDE INHIBITORS; STRUCTURAL BASIS; PHASE-II; INSULIN;
D O I
10.1016/j.bmc.2023.117406
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Elevated circulating glucose level due to & beta;-cell dysfunction has been a key marker of Type-II diabetes. Glycogen synthase kinase-3 (GSK-3) has been recognized as an enzyme involved in the control of glycogen metabolism. Consequently, inhibitors of GSK-3 have been explored for anti-diabetic effects in vitro and in animal models. Further, the mechanisms governing the regulation of this enzyme have been elucidated by means of a combination of structural and cellular biological investigations. This review article examines the structural analysis of GSK-3 as well as molecular modeling reports from numerous researchers in the context of the design and development of GSK-3 inhibitors. This article centers on the signaling pathway of GSK-3 relevant to its potential as a target for diabetes and discusses advancements till date on different molecular modification approaches used by researchers in the development of novel GSK-3 inhibitors as potential therapeutics for the treatment of Type II diabetes.
引用
收藏
页数:19
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