FoxO1 signaling as a therapeutic target for type 2 diabetes and obesity

被引:48
作者
Benchoula, Khaled [1 ]
Arya, Aditya [2 ,3 ,4 ]
Parhar, Ishwar S. [5 ]
Hwa, Wong Eng [1 ]
机构
[1] Taylors Univ, Sch Med, Fac Hlth & Med Sci, Subang Jaya, Malaysia
[2] Taylors Univ, Fac Hlth & Med Sci, Sch Med, Dept Pharmacol & Therapeut, Subang Jaya, Malaysia
[3] Univ Melbourne, Fac Med Dent & Hlth Sci, Dept Pharmacol & Therapeut, Parkville, Vic 3010, Australia
[4] Malaysian Inst Pharmaceut & Nutraceuticals IPharm, Gelugor, Pulau Pinang, Malaysia
[5] Monash Univ Malaysia BRIMS, Jeffrey Cheah Sch Med & Hlth Sci, Subang Jaya, Malaysia
关键词
FoxO1; Type; 2; diabetes; Obesity; Glucose homeostasis; Oxidative stress; Therapeutics; TRANSCRIPTION FACTOR FOXO1; INHIBITS HEPATIC GLUCONEOGENESIS; AMELIORATES INSULIN-RESISTANCE; BONE MORPHOGENETIC PROTEIN-7; BETA-CELL DEDIFFERENTIATION; FORKHEAD BOX O1; PI3K/AKT PATHWAY; SKELETAL-MUSCLE; GLUCOSE-METABOLISM; 3T3-L1; ADIPOCYTES;
D O I
10.1016/j.ejphar.2020.173758
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glucose production and the consumption of high levels of carbohydrate increase the chance of insulin resistance, especially in cases of obesity. Therefore, maintaining a balanced glucose homeostasis might form a strategy to prevent or cure diabetes and obesity. The activation and inhibition of glucose production is complicated due to the presence of many interfering pathways. These pathways can be viewed at the downstream level because they activate certain transcription factors, which include the Forkhead-O1 (FoxO1). This has been identified as a significant agent in the pancreas, liver, and adipose tissue, which is significant in the regulation of lipids and glucose. The objective of this review is to discuss the intersecting portrayal of FoxO1 and its parallel cross-talk which highlights obesity-induced insulin susceptibility in the discovery of a targeted remedy. The review also analyses current progress and provides a blueprint on therapeutics, small molecules, and extracts/phytochemicals which are explored at the pre-clinical level.
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收藏
页数:12
相关论文
共 146 条
[1]   FOXO1 functions as a master switch that regulates gene expression necessary for tumor necrosis factor-induced fibroblast apoptosis [J].
Alikhani, M ;
Alikhani, ZB ;
Graves, DT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (13) :12096-12102
[2]  
Alikhani M, 2010, MOL VIS, V16, P408
[3]  
[Anonymous], 2012, CURR GERONTOL GERIAT
[4]  
Asano RY, 2017, BRAZ J MED BIOL RES, V50, DOI [10.1590/1414-431X20176400, 10.1590/1414-431x20176400]
[5]  
Aslian S., 2018, ASLIAN YAZDANPARAST, V3, P1
[6]   Raspberry ketone and Garcinia Cambogia rebalanced disrupted insulin resistance and leptin signaling in rats fed high fat fructose diet [J].
Attia, Reem T. ;
Abdel-Mottaleb, Yousra ;
Abdallah, Dalaal M. ;
El-Abhar, Hanan S. ;
El-Maraghy, Nabila N. .
BIOMEDICINE & PHARMACOTHERAPY, 2019, 110 :500-509
[7]   Inhibition of JAK-STAT and NF-κB signalling systems could be a novel therapeutic target against insulin resistance and type 2 diabetes [J].
Bako, Hauwa'u Yakubu ;
Ibrahim, Mohammed Auwal ;
Isah, Muhammad Sani ;
Ibrahim, Sani .
LIFE SCIENCES, 2019, 239
[8]   Moringa concanensis Nimmo ameliorates hyperglycemia in 3T3-L1 adipocytes by upregulating PPAR-γ, C/EBP-α via Akt signaling pathway and STZ-induced diabetic rats [J].
Balakrishnan, Brindha Banu ;
Krishnasamy, Kalaivani ;
Choi, Ki Choon .
BIOMEDICINE & PHARMACOTHERAPY, 2018, 103 :719-728
[9]   Epigenetics and developmental origins of diabetes: correlation or causation? [J].
Bansal, Amita ;
Simmons, Rebecca A. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2018, 315 (01) :E15-E28
[10]   Effect of oral magnesium sulfate administration on blood glucose hemostasis via inhibition of gluconeogenesis and FOXO1 gene expression in liver and muscle in diabetic rats [J].
Barooti, Ayeshe ;
Kamran, Mitra ;
Kharazmi, Fatemeh ;
Eftakhar, Ebrahim ;
Malekzadeh, Kianoosh ;
Talebi, Ardeshir ;
Soltani, Nepton .
BIOMEDICINE & PHARMACOTHERAPY, 2019, 109 :1819-1825