Department of Nutrition, Food Science, Physiology and Toxicology, University of Navarra, C/Irunlarrea 1, Pamplona, Spain.
J Physiol Biochem. 2011 Sep;67(3):479-86. doi: 10.1007/s13105-011-0087-1. Epub 2011 Apr 2.
Lipoic acid (LA) is an antioxidant with therapeutic properties on several diseases like diabetes and obesity. Apelin is a novel adipokine with potential beneficial actions on glucose metabolism and insulin resistance. The aim of this study was to examine in 3T3-L1 adipocytes the effects of LA on apelin gene expression and secretion, as well as elucidate the signaling pathways involved. We also tested the regulation of adipose apelin gene expression by LA supplementation in a model of high-fat diet-induced obesity. LA increased apelin secretion but not apelin gene expression in 3T3-L1 adipocytes. The AMPK inhibitor Compound C induced an increase in LA-stimulated apelin production, and, on the contrary, the AMPK activator AICAR completely reversed the LA stimulatory effects on apelin secretion, also inducing a significant reduction in apelin mRNA levels in this in vitro model. Apelin mRNA levels were increased in those animals fed with the high-fat diet, while the caloric restriction decreased apelin mRNA to control levels. However, apelin gene expression was not significantly modified in rats treated with LA compared with the obese group. The current data suggest the ability of LA to modulate apelin secretion by adipocytes. However the insulin-sensitizing effect of LA in vivo is not related to changes in apelin gene expression in our model of diet-induced obesity.
硫辛酸(LA)是一种具有治疗多种疾病(如糖尿病和肥胖症)特性的抗氧化剂。Apelin 是一种新型脂肪因子,对葡萄糖代谢和胰岛素抵抗具有潜在的有益作用。本研究旨在研究 3T3-L1 脂肪细胞中 LA 对 Apelin 基因表达和分泌的影响,并阐明涉及的信号通路。我们还测试了 LA 补充对高脂肪饮食诱导肥胖模型中脂肪组织 Apelin 基因表达的调节。LA 增加了 3T3-L1 脂肪细胞中 Apelin 的分泌,但不增加 Apelin 的基因表达。AMPK 抑制剂 Compound C 诱导 LA 刺激的 Apelin 产生增加,而相反,AMPK 激活剂 AICAR 完全逆转了 LA 对 Apelin 分泌的刺激作用,同时也使体外模型中的 Apelin mRNA 水平显著降低。在高脂肪饮食喂养的动物中,Apelin mRNA 水平增加,而热量限制则使 Apelin mRNA 降低至对照水平。然而,与肥胖组相比,LA 治疗的大鼠中 Apelin 基因表达没有明显改变。目前的数据表明,LA 能够调节脂肪细胞的 Apelin 分泌。然而,在我们的饮食诱导肥胖模型中,LA 在体内的胰岛素增敏作用与 Apelin 基因表达的变化无关。