High uric acid directly inhibits insulin signalling and induces insulin resistance

•Hyperuricemic mice showed impaired glucose tolerance with insulin resistance.•Hyperuricemia inhibited insulin signaling in liver, muscle and fat tissues.•HUA levels induced oxidative stress in HepG2 cells.•NAC blocked the HUA-induced insulin signalling impairment in HepG2 cells. Accumulating clinic...

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Veröffentlicht in:Biochemical and biophysical research communications 2014-05, Vol.447 (4), p.707-714
Hauptverfasser: Zhu, Yuzhang, Hu, Yaqiu, Huang, Tianliang, Zhang, Yongneng, Li, Zhi, Luo, Chaohuan, Luo, Yinfeng, Yuan, Huier, Hisatome, Ichiro, Yamamoto, Tetsuya, Cheng, Jidong
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Sprache:eng
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Zusammenfassung:•Hyperuricemic mice showed impaired glucose tolerance with insulin resistance.•Hyperuricemia inhibited insulin signaling in liver, muscle and fat tissues.•HUA levels induced oxidative stress in HepG2 cells.•NAC blocked the HUA-induced insulin signalling impairment in HepG2 cells. Accumulating clinical evidence suggests that hyperuricemia is strongly associated with abnormal glucose metabolism and insulin resistance. However, how high uric acid (HUA) level causes insulin resistance remains unclear. We aimed to determine the direct role of HUA in insulin resistance in vitro and in vivo in mice. An acute hyperuricemia mouse model was created by potassium oxonate treatment, and the impact of HUA level on insulin resistance was investigated by glucose tolerance test, insulin tolerance test and insulin signalling, including phosphorylation of insulin receptor substrate 1 (IRS1) and Akt. HepG2 cells were exposed to HUA treatment and N-acetylcysteine (NAC), reactive oxygen species scavenger; IRS1 and Akt phosphorylation was detected by Western blot analysis after insulin treatment. Hyperuricemic mice showed impaired glucose tolerance with insulin resistance. Hyperuricemia inhibited phospho-Akt (Ser473) response to insulin and increased phosphor-IRS1 (Ser307) in liver, muscle and fat tissues. HUA induced oxidative stress, and the antioxidant NAC blocked HUA-induced IRS1 activation and Akt inhibition in HepG2 cells. This study supplies the first evidence of HUA directly inducing insulin resistance in vivo and in vitro. Increased uric acid level may inhibit IRS1 and Akt insulin signalling and induce insulin resistance. The reactive oxygen species pathway plays a key role in HUA-induced insulin resistance.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2014.04.080