Okuno A, Ikeda K, Shiota M, Fujiwara T, Yoshioka S, Sugano T, Horikoshi H
Pharmacology and Molecular Biology Research Laboratories, Sankyo, Tokyo, Japan.
Metabolism. 1997 Jun;46(6):716-21. doi: 10.1016/s0026-0495(97)90019-6.
Troglitazone (CS-045) is a new type of antidiabetic agent that decreases plasma glucose by enhancing insulin action in insulin-resistant diabetic animals and non-insulin-dependent diabetes mellitus (NIDDM) patients. To examine the direct effect of troglitazone on glucose metabolism and insulin action in skeletal muscle, we infused troglitazone solution into perfused rat hindlimbs in the presence of 6 mmol/L glucose and in the absence or presence of insulin. In the absence of insulin, even 50 mumol/L troglitazone did not elicit glucose uptake. Troglitazone did increase lactate and pyruvate release at concentrations of 20 mumol/L and higher; however, it decreased the ratio of lactate to pyruvate (L/P ratio) and increased oxygen consumption at concentrations higher than 5 and 20 mumol/L, respectively. In hindlimb muscle, 20 mumol/L troglitazone decreased glycogen content without changing fructose 2,6-bisphosphate (F2,6P2) content in the absence of insulin. Insulin infusion with 250 microU/mL obtained half-maximal effects, causing a 2.8-fold increase in glucose uptake and a 1.5-fold increase in lactate and pyruvate release. When 20 mumol/L troglitazone was infused for 30 minutes together with 250 microU/mL insulin, insulin-induced glucose uptake significantly increased 30 minutes after troglitazone infusion, and this increase was further augmented after withdrawal of troglitazone. In insulin plus troglitazone infusion at 30 minutes after troglitazone removal, glycogen content in hindlimb muscle was significantly decreased compared with that obtained with insulin infusion alone. In summary, in the absence of insulin, troglitazone does not elicit glucose uptake, but causes an increase in glycolysis accompanied by a decrease in muscle glycogen content and L/P ratio and an increase in oxygen consumption. In the presence of insulin, troglitazone increases insulin-induced glucose uptake, and this increase is further augmented after troglitazone removal. Addition of troglitazone to insulin infusion decreased the glycogen content in hindlimb muscle. This decrease in muscle glycogen content may trigger an enhancement of insulin-induced glucose uptake similar to that observed during muscle contraction or epinephrine treatment.
曲格列酮(CS - 045)是一种新型抗糖尿病药物,它通过增强胰岛素抵抗型糖尿病动物和非胰岛素依赖型糖尿病(NIDDM)患者的胰岛素作用来降低血糖。为了研究曲格列酮对骨骼肌葡萄糖代谢和胰岛素作用的直接影响,我们在灌注大鼠后肢中,于存在6 mmol/L葡萄糖且有无胰岛素的情况下输注曲格列酮溶液。在无胰岛素时,即使50 μmol/L曲格列酮也不能引起葡萄糖摄取。曲格列酮在浓度为20 μmol/L及更高时确实会增加乳酸和丙酮酸释放;然而,它会降低乳酸与丙酮酸的比值(L/P比值),并分别在高于5 μmol/L和20 μmol/L的浓度时增加耗氧量。在无胰岛素的情况下,后肢肌肉中20 μmol/L曲格列酮会降低糖原含量,而不改变果糖2,6 - 二磷酸(F2,6P2)含量。输注250 μU/mL胰岛素可产生半数最大效应,使葡萄糖摄取增加2.8倍,乳酸和丙酮酸释放增加1.5倍。当20 μmol/L曲格列酮与250 μU/mL胰岛素一起输注30分钟时,曲格列酮输注30分钟后胰岛素诱导的葡萄糖摄取显著增加,且在停用曲格列酮后这种增加进一步增强。在停用曲格列酮30分钟后进行胰岛素加曲格列酮输注时,后肢肌肉中的糖原含量与单独输注胰岛素相比显著降低。总之,在无胰岛素时,曲格列酮不会引起葡萄糖摄取,但会导致糖酵解增加,同时伴有肌肉糖原含量和L/P比值降低以及耗氧量增加。在有胰岛素时,曲格列酮会增加胰岛素诱导的葡萄糖摄取,且在停用曲格列酮后这种增加会进一步增强。向胰岛素输注中添加曲格列酮会降低后肢肌肉中的糖原含量。肌肉糖原含量的这种降低可能会引发胰岛素诱导的葡萄糖摄取增强,类似于在肌肉收缩或肾上腺素治疗期间观察到的情况。