A Review on SIRtuins in Diabetes

被引:61
作者
Aditya, R. [1 ]
Kiran, A. Ravi [2 ]
Varma, D. Sai [3 ]
Vemuri, Ravichandra [4 ]
Gundamaraju, Rohit [4 ]
机构
[1] Daewoong Pharmaceut Co Ltd, Hyderabad, Andhra Pradesh, India
[2] G Pulla Reddy Coll Pharm, Hyderabad, Andhra Pradesh, India
[3] Aurobindo Pharma Ltd, Hyderabad, Andhra Pradesh, India
[4] Univ Tasmania, Sch Hlth Sci, Launceston, Tas 7248, Australia
关键词
SIRT1; Type II diabetes mellitus; resveratrol; activator; clinical trials; insulin secretion; ACTIVATED PROTEIN-KINASE; PANCREATIC BETA-CELLS; TRANSCRIPTIONAL COACTIVATOR PGC-1; STIMULATED INSULIN-SECRETION; FATTY-ACID OXIDATION; GENE-EXPRESSION; CALORIE RESTRICTION; SKELETAL-MUSCLE; ERR-ALPHA; MITOCHONDRIAL BIOGENESIS;
D O I
10.2174/1381612823666170125153334
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Background: Type-2 Diabetes is a long lasting disease characterized by high glucose concentration in the blood due to insulin resistance. One of the recent treatment strategies is using activators against SIRT-1, which has been in clinical trials. Hence, it is necessary to know the effects of the SIRT-1 modulators against various metabolic pathways. Methods: Many cellular processes, including insulin secretion, cell cycle, and apoptosis are imperatively regulated by a family of mediators called SIRTuins. First known mammalian sirtuin, SIRT1 is a positive regulator of insulin secretion, which triggers glucose uptake and utilization. For the past decade, a major outstanding question is whether SIRT1 activation is a safe therapy for human diseases such as diabetes? Results: This review summarizes and discusses the advances of the past decade and the challenges that will brazen out perplexity of this field. We also cover the physiological regulation of sirtuin (SIRT1) activity and how these modes of regulation may be exploited to manipulate SIRT1 activity in cells. Designing of drugs using advanced computational methods that specifically target SIRT1, and also, involvement of advanced biological methods for further understanding of sirtuin1 biology to afford new optimized treatments for diabetes and several age related human diseases. Conclusion: Hence, this review is a serial perspective of all the above topics.
引用
收藏
页码:2299 / 2307
页数:9
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