| Literature DB >> 27264958 |
Cong Zhang1, Caiyun Sun1, Bin Wang1, Peipei Yan1, Amin Wu1, Guokun Yang1, Wensheng Li2.
Abstract
Orexins are hypothalamic neuropeptides involved in the central regulation of feeding behavior, sleep-wake cycle and other physiological functions. Orexin-A can regulate energy metabolism and increase glucose uptake, suggesting a role in glucose metabolism. In this study, we investigated the effects of orexin-A on GLUT4 mRNA and protein levels and the intracellular signaling mechanisms mediating orexin-A activity in the hepatocytes of grouper. Our results demonstrate that intraperitoneal injection of orexin-A increased the expression of GLUT4 in the liver, and this effect was significantly enhanced by co-injection of glucose. Treatment of primary cultured hepatocytes with either orexin-A or glucose alone had no effect on the expression of GLUT4, while co-treatment with orexin-A and glucose significantly increased the expression of GLUT4. This stimulatory effect was partially blocked by inhibitors to ERK1/2, JNK or p38 MAPK and was further blocked by an orexin receptor antagonist, which indicates that orexin-A could stimulate the expression of GLUT4 in a glucose dependent manner in primary hepatocytes via ERK1/2, JNK and p38 signaling. Our results suggest that orexin-A could play a pivotal role in stimulating glucose utilization in grouper, for a long-term goal, which might be useful in reducing costs in the aquaculture industry.Entities:
Keywords: GLUT4; Glucose; Hepatocytes; Orexin-A; Signaling pathway
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Year: 2016 PMID: 27264958 DOI: 10.1016/j.cbpa.2016.05.027
Source DB: PubMed Journal: Comp Biochem Physiol A Mol Integr Physiol ISSN: 1095-6433 Impact factor: 2.320