Taleux N, De Potter I, Deransart C, Lacraz G, Favier R, Leverve X M, Hue L, Guigas B
Université catholique de Louvain and Institute of Cellular Pathology, Hormone and Metabolic Research Unit, Brussels, Belgium.
Int J Obes (Lond). 2008 Apr;32(4):639-47. doi: 10.1038/sj.ijo.0803759. Epub 2007 Dec 4.
The AMP-activated protein kinase (AMPK) is involved in the control of food intake by the hypothalamus. The aim of this work was to investigate if modification of hypothalamic AMPK regulation could be related to the spontaneous food restriction of Lou/C rats, a strain resistant to obesity exhibiting a 40% reduction in caloric intake compared with their lean Wistar counterparts.
Three-month-old male Lou/C rats were compared with age-matched male Wistar rats in both fed ad libitum and 24-h food deprivation state.
We first confirmed that starvation activated both isoforms of AMPK catalytic alpha subunits and enhanced the phosphorylation state of its downstream targets acetyl-CoA carboxylase and elongation factor 2 in the hypothalamus of Wistar rats. These changes were not observed in the hypothalamus of Lou/C rats. Interestingly, the starvation-induced changes in hypothalamic mRNA levels of the main orexigenic and anorexigenic neuropeptides were also blunted in the Lou/C rats. Analysis of the concentrations of circulating substrates and hormones known to regulate hypothalamic AMPK indicated that the starvation-induced changes in ghrelin, adiponectin and leptin were not observed in Lou/C rats. Furthermore, an increased phosphorylation state of signal transducer and activator of transcription 3 (STAT3), which admittedly mediates leptin signaling, was evidenced in the hypothalamus of the starved Lou/C rats, as well as modifications of expression of the leptin-sensitive genes suppressor of cytokine signaling-3 and stearoyl-coenzyme A desaturase 1. In addition, despite reduced leptin level in fed Lou/C rats, the phosphorylation state of hypothalamic STAT3 remained similar to that found in fed Wistar rats, an adaptation that could be explained by the concomitant increase in ObRb leptin receptor mRNA expression.
Activation of hypothalamic AMPK by starvation, which stimulates food intake through changes in (an)orexigenic neuropeptides in the normal rats, was not observed in the spontaneously hypophagic Lou/C rats.
AMP激活的蛋白激酶(AMPK)参与下丘脑对食物摄入的调控。本研究旨在探讨下丘脑AMPK调节的改变是否与Lou/C大鼠的自发性食物限制有关,Lou/C大鼠是一种抗肥胖品系,与瘦型Wistar大鼠相比,其热量摄入减少40%。
将3月龄雄性Lou/C大鼠与年龄匹配的雄性Wistar大鼠在自由进食和24小时食物剥夺状态下进行比较。
我们首先证实,饥饿激活了Wistar大鼠下丘脑AMPK催化α亚基的两种同工型,并增强了其下游靶点乙酰辅酶A羧化酶和延伸因子2的磷酸化状态。在Lou/C大鼠的下丘脑中未观察到这些变化。有趣的是,Lou/C大鼠下丘脑中主要促食欲和抑食欲神经肽的饥饿诱导mRNA水平变化也不明显。对已知调节下丘脑AMPK的循环底物和激素浓度的分析表明,Lou/C大鼠未出现饥饿诱导的胃饥饿素、脂联素和瘦素变化。此外,在饥饿的Lou/C大鼠下丘脑中,信号转导子和转录激活子3(STAT3)的磷酸化状态增加,STAT3公认介导瘦素信号传导,同时瘦素敏感基因细胞因子信号传导抑制因子3和硬脂酰辅酶A去饱和酶1的表达也发生了改变。此外,尽管喂食的Lou/C大鼠瘦素水平降低,但其下丘脑STAT3的磷酸化状态仍与喂食的Wistar大鼠相似,这种适应性变化可能是由于ObRb瘦素受体mRNA表达的同时增加所致。
在正常大鼠中,饥饿通过改变(促)食欲神经肽来刺激食物摄入,从而激活下丘脑AMPK,但在自发性少食的Lou/C大鼠中未观察到这种情况。