Samuel Varman T, Choi Cheol Soo, Phillips Trevor G, Romanelli Anthony J, Geisler John G, Bhanot Sanjay, McKay Robert, Monia Brett, Shutter John R, Lindberg Richard A, Shulman Gerald I, Veniant Murielle M
TAC S269, P.O. Box 9012, 300 Cedar St., Yale University School of Medicine, New Haven, CT 06510, USA.
Diabetes. 2006 Jul;55(7):2042-50. doi: 10.2337/db05-0705.
Fasting hyperglycemia, a prominent finding in diabetes, is primarily due to increased gluconeogenesis. The transcription factor Foxo1 links insulin signaling to decreased transcription of PEPCK and glucose-6-phosphatase (G6Pase) and provides a possible therapeutic target in insulin-resistant states. Synthetic, optimized antisense oligonucleotides (ASOs) specifically inhibit Foxo1 expression. Here we show the effect of such therapy on insulin resistance in mice with diet-induced obesity (DIO). Reducing Foxo1 mRNA expression with ASO therapy in mouse hepatocytes decreased levels of Foxo1 protein and mRNA expression of PEPCK by 48 +/- 4% and G6Pase by 64 +/- 3%. In mice with DIO and insulin resistance, Foxo1 ASO therapy lowered plasma glucose concentration and the rate of basal endogenous glucose production. In addition, Foxo1 ASO therapy lowered both hepatic triglyceride and diacylglycerol content and improved hepatic insulin sensitivity. Foxo1 ASO also improved adipocyte insulin action. At a tissue-specific level, this manifested as improved insulin-mediated 2-deoxyglucose uptake and suppression of lipolysis. On a whole-body level, the result was improved glucose tolerance after an intraperitoneal glucose load and increased insulin-stimulated whole-body glucose disposal during a hyperinsulinemic-euglycemic clamp. In conclusion, Foxo1 ASO therapy improved both hepatic insulin and peripheral insulin action. Foxo1 is a potential therapeutic target for improving insulin resistance.
空腹血糖过高是糖尿病的一个显著特征,主要归因于糖异生增加。转录因子Foxo1将胰岛素信号与磷酸烯醇式丙酮酸羧激酶(PEPCK)和葡萄糖-6-磷酸酶(G6Pase)转录减少联系起来,并为胰岛素抵抗状态提供了一个可能的治疗靶点。合成的、经过优化的反义寡核苷酸(ASO)可特异性抑制Foxo1表达。在此,我们展示了这种治疗方法对饮食诱导肥胖(DIO)小鼠胰岛素抵抗的影响。在小鼠肝细胞中用ASO疗法降低Foxo1 mRNA表达,可使Foxo1蛋白水平以及PEPCK的mRNA表达降低48±4%,G6Pase的mRNA表达降低64±3%。在患有DIO和胰岛素抵抗的小鼠中,Foxo1 ASO疗法降低了血浆葡萄糖浓度和基础内源性葡萄糖生成速率。此外,Foxo1 ASO疗法降低了肝脏甘油三酯和二酰甘油含量,并改善了肝脏胰岛素敏感性。Foxo1 ASO还改善了脂肪细胞的胰岛素作用。在组织特异性水平上,这表现为胰岛素介导的2-脱氧葡萄糖摄取改善以及脂解抑制。在全身水平上,结果是腹腔注射葡萄糖负荷后葡萄糖耐量改善,以及在高胰岛素-正常血糖钳夹期间胰岛素刺激的全身葡萄糖处置增加。总之,Foxo1 ASO疗法改善了肝脏胰岛素作用和外周胰岛素作用。Foxo1是改善胰岛素抵抗的一个潜在治疗靶点。