Changani K K, Bell J D, Iles R A
Cellular Mechanisms Research Group, Medical Unit, Royal London Hospital and Medical School, Whitechapel, London E1 2AD, UK.
Biochim Biophys Acta. 1998 Apr 10;1380(2):198-208. doi: 10.1016/s0304-4165(97)00140-2.
In vivo -NMR was employed to determine the hepatic fate of infused [1-]-d-glucose (200 mg/kg) following ad libitum or routine meal feeding (RMF) regimes imposed during pregnancy. Hepatic glycogen synthesis was measured immediately following the last meal in virgin, 10 and 20 day pregnant rats. No detectable incorporation of -glucose into glycogen was observed in 20 day pregnant and control fed virgin rats. In 20 day pregnant RMF rats, glycogen synthesis from -glucose occurred at a linear rate of 0.10/s (S.D. 0.018/s). By 50 min post-infusion, 13C-glycogen levels were 131% (p<0.01) higher than those seen for the 22 h starved and 2 h refed virgin group. Following 10 days of gestation, glucose incorporation into glycogen was maximal in both the ad libitum and RMF groups. Compared with the 20 day pregnant RMF group, the 10 day pregnant ad libitum and RMF rats produced 146% (p<0.001) and 315% (p<0.001) more incorporation of -glucose into the glycogen macromolecule, respectively. Hepatic glycogen values were similar for both 10 and 20 day pregnant ad libitum rats (65.7+/-4.7 and 58.8+/-4.5 mg/g weight) but lower in the RMF groups by 58% and 48%, respectively. In conclusion, meal feeding regimes in the pregnant rat alter carbohydrate control of the liver producing increased glycogen synthesis initially via direct incorporation of glucose into the macromolecule.
采用体内核磁共振技术,以确定在孕期自由采食或常规进餐(RMF)模式下,注入的[1-] -D-葡萄糖(200毫克/千克)在肝脏中的代谢情况。在末次进食后,立即测定未孕、妊娠10天和20天大鼠肝脏中的糖原合成情况。在妊娠20天的大鼠和对照喂养的未孕大鼠中,未观察到葡萄糖掺入糖原的情况。在妊娠20天的RMF大鼠中,葡萄糖合成糖原的速率呈线性,为0.10/秒(标准差0.018/秒)。输注后50分钟,13C-糖原水平比饥饿22小时后再喂食2小时的未孕组高131%(p<0.01)。妊娠10天后,自由采食组和RMF组中葡萄糖掺入糖原的量均达到最大值。与妊娠20天的RMF组相比,妊娠10天的自由采食组和RMF组大鼠中,葡萄糖掺入糖原大分子的量分别多146%(p<0.001)和315%(p<0.001)。妊娠10天和20天的自由采食大鼠肝脏糖原值相似(分别为65.7±4.7和58.8±4.5毫克/克体重),但RMF组分别低58%和48%。总之,妊娠大鼠的进餐模式改变了肝脏对碳水化合物的控制,最初通过葡萄糖直接掺入大分子导致糖原合成增加。