Nakano Ryosuke, Kurosaki Eiji, Shimaya Akiyoshi, Shibasaki Masayuki
Pharmacology Research Laboratories, Drug Discovery Research, Astellas Pharma Inc., 5-2-3, Toukoudai, Tsukuba-shi, Ibaraki 300-2698, Japan.
J Pharmacol Sci. 2006 Aug;101(4):311-7. doi: 10.1254/jphs.fp0060360. Epub 2006 Aug 5.
The novel hypoglycemic agent YM440 ((Z)-1,4-bis{4-[(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)methyl] phenoxy}but-2-ene) is a ligand of the peroxisome proliferator-activated receptor (PPAR) gamma. YM440 has unique pharmacological profiles both in vitro and in vivo, but, it is not clear whether the compound has a significant effect on hepatic or peripheral insulin response throughout the body. The aim of this study is to examine the effects of YM440 on hepatic and peripheral insulin resistance in Zucker fatty (ZF) rats using the euglycemic-hyperinsulinaemic clamp technique. Treatment of ZF rats with YM440 (300 mg/kg per day) for 2 weeks significantly decreased plasma concentrations of glucose and insulin without inducing obesity. YM440 caused a 2-fold increase in the glucose infusion rate during euglycemic clamping compared with the vehicle control. YM440 also decreased the percent change in hepatic glucose production rate caused by intravenous insulin infusion in ZF rats. YM440 had no significant effect on the glucose disposal rate. These results indicate that YM440 ameliorates hepatic, but not peripheral insulin resistance in ZF rats. These findings strongly suggest that the main target organ of YM440 is the liver, unlike other PPARgamma agonist.
新型降糖药物YM440((Z)-1,4-双{4-[(3,5-二氧代-1,2,4-恶二唑烷-2-基)甲基]苯氧基}丁-2-烯)是过氧化物酶体增殖物激活受体(PPAR)γ的配体。YM440在体外和体内均具有独特的药理特性,但尚不清楚该化合物对全身肝脏或外周胰岛素反应是否有显著影响。本研究的目的是使用正常血糖-高胰岛素钳夹技术,研究YM440对Zucker肥胖(ZF)大鼠肝脏和外周胰岛素抵抗的影响。用YM440(每天300 mg/kg)治疗ZF大鼠2周,可显著降低血浆葡萄糖和胰岛素浓度,且不会导致肥胖。与溶媒对照组相比,YM440在正常血糖钳夹期间使葡萄糖输注率提高了2倍。YM440还降低了ZF大鼠静脉注射胰岛素引起的肝脏葡萄糖生成率的变化百分比。YM440对葡萄糖处置率无显著影响。这些结果表明,YM440可改善ZF大鼠的肝脏胰岛素抵抗,但不能改善外周胰岛素抵抗。这些发现强烈表明,与其他PPARγ激动剂不同,YM440的主要靶器官是肝脏。