Kruszynska Y T, McCormack J G, McIntyre N
Department of Medicine, Royal Free Hospital School of Medicine, London, UK.
Diabetologia. 1991 Apr;34(4):205-11. doi: 10.1007/BF00405077.
The effects of increased tissue glycogen stores on insulin sensitivity, and on the response of insulin-stimulated glucose utilisation to an acute elevation in plasma fatty acid levels (approximately 1.5 mmol/l), were investigated in conscious rats using the hyperinsulinaemic euglycaemic clamp. Studies were performed in two groups of rats; (a) fasted 24 h; (b) fasted 4.5 h, but infused with glucose for 4 h (0.5 g/h) of this period before the clamp (fed, glucose infused rats). Clamp glucose requirement and 3-3H-glucose turnover were 20-25% lower in the fed, glucose-infused rats. In these rats, elevation of plasma fatty acid levels resulted in impaired suppression of hepatic glucose output (residual hepatic glucose output: 41 +/- 4 vs 8 +/- 6 mumol.min-1.kg-1, p less than 0.001) but did not further decrease 3-3H-glucose turnover. Elevated non-esterified fatty acid levels had no significant effect on glucose kinetics in 24 h fasted rats. In the fed glucose-infused rats, at low plasma fatty acid levels, there was no deposition of glycogen in muscle during the clamp and liver glycogen levels fell. With elevation of non-esterified fatty acid levels muscle glycogen deposition was stimulated in both groups, and there was no fall in liver glycogen during the clamps in the fed glucose-infused rats. Increased non-esterified fatty acid availability during the clamps decreased pyruvate dehydrogenase activity in liver, heart, adipose tissue and quadriceps muscle, in both groups of rats. The findings are consistent with an inhibition of glycolysis in liver, skeletal muscle and heart by increased fatty acid availability.(ABSTRACT TRUNCATED AT 250 WORDS)
使用高胰岛素正常血糖钳夹技术,在清醒大鼠中研究了组织糖原储备增加对胰岛素敏感性以及胰岛素刺激的葡萄糖利用对血浆脂肪酸水平急性升高(约1.5 mmol/l)的反应的影响。研究在两组大鼠中进行:(a) 禁食24小时;(b) 禁食4.5小时,但在钳夹前的这段时间内输注葡萄糖4小时(0.5 g/h)(喂食、输注葡萄糖的大鼠)。喂食、输注葡萄糖的大鼠钳夹时的葡萄糖需求量和3-3H-葡萄糖周转率降低了20-25%。在这些大鼠中,血浆脂肪酸水平升高导致肝葡萄糖输出抑制受损(残余肝葡萄糖输出:41±4 vs 8±6 μmol·min-1·kg-1,p<0.001),但未进一步降低3-3H-葡萄糖周转率。非酯化脂肪酸水平升高对禁食24小时大鼠的葡萄糖动力学无显著影响。在喂食、输注葡萄糖的大鼠中,在低血浆脂肪酸水平时,钳夹期间肌肉中没有糖原沉积,肝糖原水平下降。随着非酯化脂肪酸水平升高,两组肌肉糖原沉积均受到刺激,喂食、输注葡萄糖的大鼠在钳夹期间肝糖原没有下降。钳夹期间非酯化脂肪酸可用性增加降低了两组大鼠肝脏、心脏、脂肪组织和股四头肌中的丙酮酸脱氢酶活性。这些发现与脂肪酸可用性增加抑制肝脏、骨骼肌和心脏中的糖酵解一致。(摘要截断于250字)