CNC-Center for Neuroscience and Cell Biology, University of Coimbra, 3004-517 Coimbra, Portugal; CFE-Center for Functional Ecology, University of Coimbra, Apartado 3046, 3001-401 Coimbra, Portugal; Department of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, 3001-401 Coimbra, Portugal.
Comp Biochem Physiol A Mol Integr Physiol. 2013 Nov;166(3):399-405. doi: 10.1016/j.cbpa.2013.07.013. Epub 2013 Jul 17.
Sources of blood glucose in European seabass (initial weight 218.0±43.0g; mean±S.D., n=18) were quantified by supplementing seawater with deuterated water (5%-(2)H2O) for 72h and analyzing blood glucose (2)H-enrichments by (2)H NMR. Three different nutritional states were studied: continuously fed, 21-day of fast and 21-day fast followed by 3days of refeeding. Plasma glucose levels (mM) were 10.7±6.3 (fed), 4.8±1.2 (fasted), and 9.3±1.4 (refed) (means±S.D., n=6), showing poor glycemic control. For all conditions, (2)H-enrichment of glucose position 5 was equivalent to that of position 2 indicating that blood glucose appearance from endogenous glucose 6-phosphate (G6P) was derived by gluconeogenesis. G6P-derived glucose accounted for 65±7% and 44±10% of blood glucose appearance in fed and refed fish, respectively, with the unlabeled fraction assumed to be derived from dietary carbohydrate (35±7% and 56±10%, respectively). For 21-day fasted fish, blood glucose appearance also had significant contributions from unlabeled glucose (52±16%) despite the unavailability of dietary carbohydrates. To assess the role of hepatic enzymes in glycemic control, activity and mRNA levels of hepatic glucokinase (GK) and glucose 6-phosphatase (G6Pase) were assessed. Both G6Pase activity and expression declined with fasting indicating the absence of a classical counter-regulatory stimulation of hepatic glucose production in response to declining glucose levels. GK activities were basal during fed and fasted conditions, but were strongly stimulated by refeeding. Overall, hepatic G6Pase and GK showed limited capacity in regulating glucose levels between feeding and fasting states.
通过在海水中添加重水(5%-(2)H2O)72 小时,并通过(2)H NMR 分析血糖(2)H 丰度,量化了欧洲鲈鱼(初始体重 218.0±43.0g;平均值±标准差,n=18)的血糖来源。研究了三种不同的营养状态:连续喂养、21 天禁食和 21 天禁食后 3 天再喂养。血浆葡萄糖水平(mM)分别为 10.7±6.3(喂养)、4.8±1.2(禁食)和 9.3±1.4(再喂养)(平均值±标准差,n=6),表明血糖控制不佳。对于所有条件,葡萄糖位置 5 的(2)H 丰度与位置 2 的(2)H 丰度相等,表明血液葡萄糖来自内源性葡萄糖 6-磷酸(G6P)是通过糖异生产生的。G6P 衍生的葡萄糖分别占喂养和再喂养鱼血液葡萄糖出现的 65±7%和 44±10%,未标记部分假定来自膳食碳水化合物(分别为 35±7%和 56±10%)。对于 21 天禁食的鱼,尽管没有可利用的膳食碳水化合物,血液葡萄糖的出现也有显著的未标记葡萄糖贡献(52±16%)。为了评估肝酶在血糖控制中的作用,评估了肝葡萄糖激酶(GK)和葡萄糖 6-磷酸酶(G6Pase)的活性和 mRNA 水平。随着禁食的进行,G6Pase 活性和表达均下降,表明在葡萄糖水平下降时,肝脏葡萄糖生成没有经典的反向调节刺激。GK 活性在喂养和禁食条件下均处于基础状态,但在再喂养时受到强烈刺激。总的来说,肝 G6Pase 和 GK 在进食和禁食状态之间调节血糖水平的能力有限。