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在内毒素血症葡萄糖输注期间糖异生对糖原补充的贡献。

The contribution of gluconeogenesis to glycogen repletion during glucose infusion in endotoxemia.

作者信息

Lang C H, Bagby G J, Buday A Z, Spitzer J J

出版信息

Metabolism. 1987 Feb;36(2):180-7. doi: 10.1016/0026-0495(87)90015-1.

Abstract

Glycogen repletion rates in liver and skeletal muscle were quantitated, and the contribution of gluconeogenesis to hepatic glycogen repletion and glucose output were determined during glucose infusion in hemodynamically stable endotoxemic animals. Four hours after the injection of endotoxin (or saline), rats were infused with 235 mumol/min/kg of glucose (or saline) containing [6-3H]-glucose for up to four additional hours. Glucose infusion increased the plasma glucose concentration, which plateaued between 14 to 17 mmol/L, in the control rats. The glucose concentration of the endotoxin group receiving glucose was consistently greater than in control rats and failed to reach a plateau. The rate of muscle glycogen synthesis was not altered after endotoxin, but hepatic glycogen repletion was decreased by 55%. The percentage of glycogen repletion derived directly from blood glucose in liver and muscle was similar in control and endotoxin-treated rats receiving glucose. Therefore, the direct incorporation of glucose into glycogen appeared to predominate over the contribution by gluconeogenesis. However, gluconeogenesis continued during the glucose infusion in both control and endotoxemic animals. The calculated rate of total gluconeogenesis was 160% higher in the endotoxin glucose-infused rats compared to the control animals receiving glucose. This increase was due primarily to the attenuated suppression of hepatic glucose output in the endotoxin group (52 +/- 4%) compared to controls (84 +/- 3%). Thus, gluconeogenically derived glucose-6-phosphate appears to be diverted from hepatic glycogen storage to glucose output in endotoxin-treated rats during glucose infusion.

摘要

在血流动力学稳定的内毒素血症动物葡萄糖输注过程中,对肝脏和骨骼肌中的糖原补充率进行了定量,并确定了糖异生对肝脏糖原补充和葡萄糖输出的贡献。注射内毒素(或生理盐水)4小时后,给大鼠输注含[6-³H]葡萄糖的235μmol/(min·kg)葡萄糖(或生理盐水),持续4小时。葡萄糖输注使对照大鼠的血浆葡萄糖浓度升高,在14至17mmol/L之间达到平稳状态。接受葡萄糖输注的内毒素组的葡萄糖浓度始终高于对照大鼠,且未达到平稳状态。内毒素处理后肌肉糖原合成速率未改变,但肝脏糖原补充减少了55%。在接受葡萄糖输注的对照大鼠和内毒素处理大鼠中,肝脏和肌肉中直接来源于血糖的糖原补充百分比相似。因此,葡萄糖直接掺入糖原似乎比糖异生的贡献更为突出。然而,在对照动物和内毒素血症动物的葡萄糖输注过程中,糖异生均持续存在。与接受葡萄糖输注的对照动物相比,内毒素葡萄糖输注大鼠的总糖异生计算速率高出160%。这种增加主要是由于与对照组(84±3%)相比,内毒素组肝脏葡萄糖输出的抑制减弱(52±4%)。因此,在葡萄糖输注期间,在内毒素处理的大鼠中,糖异生来源的6-磷酸葡萄糖似乎从肝脏糖原储存转向了葡萄糖输出。

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