4.7 Article

Preproinsulin expression, insulin release, and hepatic glucose metabolism after a glucose load in the omnivorous GIFT tilapia Oreochromis niloticus

期刊

AQUACULTURE
卷 482, 期 -, 页码 183-192

出版社

ELSEVIER
DOI: 10.1016/j.aquaculture.2017.10.001

关键词

Insulin; Glucose tolerance; Metabolism; Liver; Tilapia

资金

  1. Natural Science Foundation of China [31502181]
  2. China Postdoctoral Science Foundation [2015M582505]
  3. Education and Teaching Reform of Southwest University [2015JY012]
  4. Chongqing Research Program of Basic Research and Frontier Technology [cstc2017jcyjAX0217]

向作者/读者索取更多资源

This study was performed to investigate the time course of changes in the expression of preproinsulin (ins) and insulin-degrading enzyme (ide), plasma insulin level and hepatic glucose metabolism after a glucose tolerance test (GTT) in genetically improved farmed Nile tilapia (GIFT), Oreochromis niloticus. Male adult fish were intraperitoneally injected with 1 g glucose/kg of body weight after 24 h of food deprivation, and then subjected to sampling at 0, 1, 2, 4, 6 and 12 h after the GTT. Compared with the control (4.3 mM/L), plasma glucose level peaked at 1 h (14.8 mM/L), decreased during 2-4 h (5.7-8.3 mM/L), and was restored after 6 h of the GTT. Although the expression of ins1, ins2 and ide were not affected in the Brockman body, plasma insulin level concomitantly increased with the increase of plasma glucose level during 1-4 h after the glucose injection. The expression of glucose transporter 1 sharply increased at 1 h after the GTT, indicating that hepatic glucose uptake was stimulated. The mRNA level of glucokinase was up-regulated during 1-4 h, and the activity of phosphofructokinase increased during 2-4 h, suggesting that hepatic glycolysis was active during 1-4 h after the glucose administration. The mRNA level of glycogen synthase 1 increased at 1 h, and liver glycogen level accumulated at 4 h after the GTT. Although the expression of glucose-6-phosphatase catalytic subunit a2 was suppressed during 1-2 h, neither the mRNA level of phosphoenolpyruvate carboxykinase 2 nor its activity was impacted by the glucose injection, which might have prolonged the glucose clearance of tilapia. Hepatic lipogenesis was effectively stimulated to dispose excess glucose absorbed by the hepatocytes, as up-regulation of mRNA levels of ATP citrate lyase a (during 1-4 h), acetyl-CoA carboxylase alpha (during 4-12 h) and fatty acid synthase (during 2-12 h) were accompanied by the GTT. Taken together, it was concluded that glucose was an effective insulin secretagogue in tilapia, and liver played an important role to clear the glucose load through stimulation of glucose uptake, glycolysis, glycogenesis and lipogenesis.

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