Département de biologie-médicale, Université de Montréal, Montréal, QC, Canada.
Horm Metab Res. 2013 Sep;45(10):716-21. doi: 10.1055/s-0033-1349853. Epub 2013 Aug 5.
The purpose of the study was to investigate the effects of acute exercise and fasting on glucagon receptor (GluR) binding characteristics, GluR-mRNA, and protein content in rat liver. Liver homogenates were prepared and plasma membranes were purified by aqueous 2-phase affinity partitioning in rats fed at rest (control) and after 180 min of swimming exercise and 24 h of fasting (7 rats/group). Saturation curve of plasma membranes incubated with [125I]-glucagon showed significant higher GluR density following exercise and fasting than in the control group (8.19±0.29 and 8.01±0.65 vs. 3.09±0.12 pmol/mg of proteins, respectively). When compared to control rats, GluR Kd was also higher following exercise and fasting (0.46±0.05 and 0.56±0.13 vs. 0.33±0.05 nM, respectively; significantly different for fasting only). Expression of GluR-mRNA and protein content were both significantly higher (~100% and ~90%, respectively) following the 24-h fast than in the control rats, but not following exercise. These results, in line with the literature showing an increased sensitivity of the liver to glucagon following exercise and fasting, indicate that an increased density of GluR on plasma membranes can be obtained by 2 complementary mechanisms: externalization of pre-existing GluR from intracellular pools operative in response to the prolonged exercise, and de novo synthesis of GluR operative only in response to fasting. The reduction in plasma insulin concentration and/or depletion of liver glycogen stores, which results from both prolonged exercise and fasting, could be involved in the control of these mechanisms.
本研究旨在探讨急性运动和禁食对大鼠肝脏中胰高血糖素受体(GluR)结合特性、GluR-mRNA 和蛋白含量的影响。在静息(对照)和游泳运动 180 分钟及禁食 24 小时(每组 7 只大鼠)后,通过水相 2 相亲和分配法从大鼠肝脏中制备肝匀浆并纯化质膜。用 [125I]-胰高血糖素孵育质膜的饱和曲线显示,运动和禁食后 GluR 密度显著高于对照组(8.19±0.29 和 8.01±0.65 对 3.09±0.12 pmol/mg 蛋白质,分别)。与对照大鼠相比,运动和禁食后 GluR Kd 也更高(0.46±0.05 和 0.56±0.13 对 0.33±0.05 nM,禁食差异显著)。禁食 24 小时后,GluR-mRNA 和蛋白含量均显著高于对照组(分别为100%和90%),但运动后无明显差异。这些结果与文献中显示的运动和禁食后肝脏对胰高血糖素敏感性增加一致,表明质膜上 GluR 密度的增加可以通过 2 种互补机制获得:长期运动引起细胞内池中原有的 GluR 向外翻转,以及仅在禁食时发生的 GluR 新合成。血浆胰岛素浓度降低和/或肝糖原储存耗尽,这是由长期运动和禁食引起的,可能参与了这些机制的控制。