Raymond R M, Harkema J M, Emerson T E
Circ Shock. 1981;8(4):425-33.
The ability of insulin to promote glucose diffusion into skeletal muscle before and during gram-negative endotoxin shock was studied in mongrel dogs anesthetized with sodium pentobarbital. The in vivo, isolated, innervated, constant-flow-perfused gracilis muscle preparation was used. Prior to shock induction, close intraarterial insulin infusion resulted in a 320% increase in muscle glucose uptake. However, at one, two, and three hours of endotoxin shock, gracilis muscle glucose uptake was unaltered by insulin infusion. This loss of responsiveness to insulin occurred with no alteration in gracilis muscle oxygen uptake, muscle venous PO2, or muscle blood flow. During control experiments, however, the muscle response to intraarterial infusion of insulin (increased glucose uptake) was unaltered during the three-hour control period. These data demonstrate that skeletal muscle insulin resistance develops early and is maintained during three hours of endotoxin shock in the dog.
在用戊巴比妥钠麻醉的杂种狗身上,研究了胰岛素在革兰氏阴性内毒素休克前及休克期间促进葡萄糖扩散进入骨骼肌的能力。采用了体内分离、有神经支配、恒流灌注的股薄肌制备方法。在诱导休克前,通过动脉内近距离输注胰岛素使肌肉葡萄糖摄取增加了320%。然而,在内毒素休克1小时、2小时和3小时时,输注胰岛素并未改变股薄肌的葡萄糖摄取。这种对胰岛素反应性的丧失发生时,股薄肌的氧摄取、肌肉静脉血氧分压或肌肉血流量均未改变。然而,在对照实验中,在3小时的对照期内,肌肉对动脉内输注胰岛素的反应(葡萄糖摄取增加)未发生改变。这些数据表明,在狗身上,骨骼肌胰岛素抵抗在早期就出现,并在内毒素休克的3小时内持续存在。