Ranganathan Gouri, Unal Resat, Pokrovskaya Irina, Yao-Borengasser Aiwei, Phanavanh Bounleut, Lecka-Czernik Beata, Rasouli Neda, Kern Philip A
Central Arkansas Veterans HealthCare System, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
J Lipid Res. 2006 Nov;47(11):2444-50. doi: 10.1194/jlr.M600248-JLR200. Epub 2006 Aug 7.
Acyl-coenzyme A:diacylglycerol transferase (DGAT), fatty acid synthetase (FAS), and LPL are three enzymes important in adipose tissue triglyceride accumulation. To study the relationship of DGAT1, FAS, and LPL with insulin, we examined adipose mRNA expression of these genes in subjects with a wide range of insulin sensitivity (SI). DGAT1 and FAS (but not LPL) expression were strongly correlated with SI. In addition, the expression of DGAT1 and FAS (but not LPL) were higher in normal glucose-tolerant subjects compared with subjects with impaired glucose tolerance (IGT) (P < 0.005). To study the effects of insulin sensitizers, subjects with IGT were treated with pioglitazone or metformin for 10 weeks, and lipogenic enzymes were measured in adipose tissue. After pioglitazone treatment, DGAT1 expression was increased by 33 +/- 10% (P < 0.05) and FAS expression increased by 63 +/- 8% (P < 0.05); however, LPL expression was not altered. DGAT1, FAS, and LPL mRNA expression were not significantly changed after metformin treatment. The treatment of mice with rosiglitazone also resulted in an increase in adipose expression of DGAT1 by 2- to 3-fold, as did the treatment of 3T3 F442A adipocytes in vitro with thiazolidinediones. These data support a more global concept suggesting that adipose lipid storage functions to prevent peripheral lipotoxicity.
酰基辅酶A:二酰甘油转移酶(DGAT)、脂肪酸合成酶(FAS)和脂蛋白脂肪酶(LPL)是在脂肪组织甘油三酯积累过程中起重要作用的三种酶。为了研究DGAT1、FAS和LPL与胰岛素的关系,我们检测了胰岛素敏感性(SI)范围广泛的受试者中这些基因的脂肪mRNA表达。DGAT1和FAS(而非LPL)的表达与SI密切相关。此外,糖耐量正常的受试者中DGAT1和FAS(而非LPL)的表达高于糖耐量受损(IGT)的受试者(P < 0.005)。为了研究胰岛素增敏剂的作用,对IGT受试者用吡格列酮或二甲双胍治疗10周,并测定脂肪组织中的生脂酶。吡格列酮治疗后,DGAT1表达增加33±10%(P < 0.05),FAS表达增加63±8%(P < 0.05);然而,LPL表达未改变。二甲双胍治疗后,DGAT1、FAS和LPL的mRNA表达无显著变化。用罗格列酮治疗小鼠也导致DGAT1的脂肪表达增加2至3倍,体外对3T3 F442A脂肪细胞用噻唑烷二酮处理也有同样效果。这些数据支持了一个更全面的概念,即脂肪脂质储存的功能是预防外周脂毒性。