...
首页> 外文期刊>The biochemical journal >Pathways of glycogen synthesis from glucose during the glycogenic response to insulin in cultured foetal hepatocytes
【24h】

Pathways of glycogen synthesis from glucose during the glycogenic response to insulin in cultured foetal hepatocytes

机译:胎儿肝细胞对胰岛素的糖原反应过程中,葡萄糖合成糖原的途径

获取原文
           

摘要

pThe pathways of glycogen synthesis from glucose were studied using double-isotope procedures in 18-day cultured foetal-rat hepatocytes in which glycogenesis is strongly stimulated by insulin. When the medium containing 4 mM-glucose was supplemented with [2-3H,U-14C]glucose or [3-3H,U-14C]glucose, the ratios of 3H/14C in glycogen relative to that in glucose were 0.23 +/- 0.04 (n = 6) and 0.63 +/- 0.09 (n = 8) respectively after 2 h. This indicates that more than 75% of glucose was first metabolized to fructose 6-phosphate, whereas 40% reached the step of the triose phosphates prior to incorporation into glycogen. The stimulatory effect of 10 nM-insulin on glycogenesis (4-fold) was accompanied by a significant increase in the (3H/14C in glycogen)/(3H/14C in glucose) ratio with 3H in the C-2 position (0.29 +/- 0.05, n = 6, P less than 0.001) or in the C-3 position (0.68 +/- 0.09, n = 8, P less than 0.01) of glucose, whereas the effect of a 12 mM-glucose load (3.5-fold) did not alter these ratios. Fructose (4 mM) displaced [U-14C]glucose during labelling of glycogen in the presence and absence of insulin by 50 and 20% respectively, and produced under both conditions a similar increase (45%) in the (3H/14C in glycogen)/(3H/14C in glucose) ratio when 3H was in the C-2 position. 3-Mercaptopicolinate (1 mM), an inhibitor of gluconeogenesis from lactate/pyruvate, further decreased the already poor labelling of glycogen from [U-14C]alanine, whereas it increased both glycogen content and incorporation of label from [U-14C]serine and [U-14C]glucose with no effect on the relative 3H/14C ratios in glycogen and glucose with 3H in the C-3 position of glucose. These results indicate that an alternative pathway in addition to direct glucose incorporation is involved in glycogen synthesis in cultured foetal hepatocytes, but that insulin preferentially favours the classical direct route. The alternative foetal pathway does not require gluconeogenesis from pyruvate-derived metabolites, contrary to the situation in the adult liver./p
机译:>在18天培养的大鼠-大鼠肝细胞中,使用双同位素方法研究了葡萄糖合成糖原的途径,在该细胞中,胰岛素强烈刺激了糖原生成。当在含有4 mM葡萄糖的培养基中添加[2-3H,U-14C]葡萄糖或[3-3H,U-14C]葡萄糖时,糖原中3H / 14C的比例相对于葡萄糖的比例为0.23 + / -2小时后分别为0.04(n = 6)和0.63 +/- 0.09(n = 8)。这表明超过75%的葡萄糖首先被代谢为果糖6-磷酸,而40%的葡萄糖在掺入糖原之前达到了磷酸三糖的步骤。 10 nM胰岛素对糖原的刺激作用(4倍)伴随着(糖原中的3H / 14C)/(葡萄糖中的3H / 14C)比率显着增加,而C-2位置为3H(0.29 + /-0.05,n = 6,P小于0.001)或处于C-3位置(0.68 +/- 0.09,n = 8,P小于0.01),而12 mM葡萄糖负荷( 3.5倍)没有改变这些比例。在存在和不存在胰岛素的情况下,在糖原标记过程中,果糖(4 mM)取代了[U-14C]葡萄糖,分别增加了50%和20%,并且在两种条件下产生的糖原中(3H / 14C)的增加都相似(45%) )/(3H / 14C,以葡萄糖计)比,当3H位于C-2位置时。 3-Mercaptopicolinate(1 mM),一种从乳酸/丙酮酸中糖异生的抑制剂,进一步降低了[U-14C]丙氨酸中糖原已经很差的标记,而它同时增加了糖原含量和[U-14C]丝氨酸中标记的掺入[U-14C]葡萄糖对糖原和葡萄糖的相对3H / 14C比没有影响,而葡萄糖的C-3位为3H。这些结果表明,在培养的胎儿肝细胞中,除了直接掺入葡萄糖外,还存在其他途径参与糖原的合成,但是胰岛素优先支持经典的直接途径。与成人肝脏中的情况相反,替代性胎儿途径不需要丙酮酸衍生代谢产物的糖异生。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号