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Glucose-Induced β-Cell Dysfunction In Vivo: Evidence for a Causal Role of C-jun N-terminal Kinase Pathway

Overview
Journal Endocrinology
Specialty Endocrinology
Date 2018 Sep 15
PMID 30215691
Citations 10
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Abstract

Prolonged elevation of glucose can adversely affect β-cell function. Oxidative stress, which has been implicated in glucose-induced β-cell dysfunction, can activate c-jun N-terminal kinase (JNK). However, whether JNK is causal in glucose-induced β-cell dysfunction in vivo is unclear. Therefore, we aimed at investigating the causal role of JNK activation in in vivo models of glucose-induced β-cell dysfunction. Glucose-induced β-cell dysfunction was investigated in the presence or absence of JNK inhibition. JNK inhibition was achieved using either (i) the JNK-specific inhibitor SP600125 or (ii) JNK-1-null mice. (i) Rats or mice were infused intravenously with saline or glucose with or without SP600125. (ii) JNK-1 null mice and their littermate wild-type controls were infused intravenously with saline or glucose. Following the glucose infusion periods in rats and mice, β-cell function was assessed in isolated islets or in vivo using hyperglycemic clamps. Forty-eight-hour hyperglycemia at ~20 mM in rats or 96-hour hyperglycemia at ~13 mM in mice impaired β-cell function in isolated islets and in vivo. Inhibition of JNK using either SP600125 or JNK-1-null mice prevented glucose-induced β-cell dysfunction in isolated islets and in vivo. Islets of JNK-1-null mice exposed to hyperglycemia in vivo showed an increase in Pdx-1 and insulin 2 mRNA, whereas islets of wild-type mice did not. Together, these data show that JNK pathway is involved in glucose-induced β-cell dysfunction in vivo and is thus a potential therapeutic target for type 2 diabetes.

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References
1.
Cicenas J, Zalyte E, Rimkus A, Dapkus D, Noreika R, Urbonavicius S . JNK, p38, ERK, and SGK1 Inhibitors in Cancer. Cancers (Basel). 2017; 10(1). PMC: 5789351. DOI: 10.3390/cancers10010001. View

2.
Deng H, Yu F, Chen J, Zhao Y, Xiang J, Lin A . Phosphorylation of Bad at Thr-201 by JNK1 promotes glycolysis through activation of phosphofructokinase-1. J Biol Chem. 2008; 283(30):20754-60. PMC: 2475697. DOI: 10.1074/jbc.M800024200. View

3.
Andreozzi F, DAlessandris C, Federici M, Laratta E, Del Guerra S, Del Prato S . Activation of the hexosamine pathway leads to phosphorylation of insulin receptor substrate-1 on Ser307 and Ser612 and impairs the phosphatidylinositol 3-kinase/Akt/mammalian target of rapamycin insulin biosynthetic pathway in RIN pancreatic.... Endocrinology. 2004; 145(6):2845-57. DOI: 10.1210/en.2003-0939. View

4.
Aguirre V, Uchida T, Yenush L, Davis R, White M . The c-Jun NH(2)-terminal kinase promotes insulin resistance during association with insulin receptor substrate-1 and phosphorylation of Ser(307). J Biol Chem. 2000; 275(12):9047-54. DOI: 10.1074/jbc.275.12.9047. View

5.
Kaneto H, Nakatani Y, Miyatsuka T, Kawamori D, Matsuoka T, Matsuhisa M . Possible novel therapy for diabetes with cell-permeable JNK-inhibitory peptide. Nat Med. 2004; 10(10):1128-32. DOI: 10.1038/nm1111. View