Shen Ling, Lo Chunmin C, Woollett Laura A, Liu Min
Department of Pathology and Laboratory Medicine, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Department of Biomedical Sciences and Diabetes Institute, Ohio University, Athens, OH, USA.
Biochem Biophys Res Commun. 2017 Dec 9;494(1-2):152-157. doi: 10.1016/j.bbrc.2017.10.063. Epub 2017 Oct 14.
Apolipoprotein A-IV (apoA-IV) is a satiation factor that acts in the hypothalamus, however, the intracellular mechanisms responsible for this action are still largely unknown. Here we report that apoA-IV treatment elicited a rapid activation of the phosphatidylinositol-3-kinase (PI3K) signaling pathway in cultured primary hypothalamic neurons, and this effect was significantly attenuated by pretreatment with LY294002, an inhibitor of the PI3K pathway. To determine if the activation of PI3K is required for apoA-IV's inhibitory effect on food intake, apoA-IV was administered intracerebroventricularly. We found that apoA-IV significantly reduced food intake and activated PI3K signaling in the hypothalamus, and these effects were abolished by icv pre-treatment with LY294002. To identify the distinct brain sites where apoA-IV exerts its anorectic action, apoA-IV was administered into the ventromedial hypothalamus (VMH) through implanted bilateral cannula. At a low dose (0.5 μg), apoA-IV significantly inhibited food intake and activated PI3K signaling pathway in the VMH of lean rats, but not in high-fat diet-induced obese (DIO) rats. These results collectively demonstrate a critical role of the PI3K/Akt pathway in apoA-IV's anorectic action in lean rats and suggest a defective PI3K pathway in the VMH is responsible for the impaired apoA-IV's anorectic action in the DIO animals.
载脂蛋白A-IV(apoA-IV)是一种在下丘脑中发挥作用的饱腹感因子,然而,负责这一作用的细胞内机制仍 largely未知。在此我们报告,apoA-IV处理可在原代培养的下丘脑神经元中迅速激活磷脂酰肌醇-3-激酶(PI3K)信号通路,而PI3K通路抑制剂LY294002预处理可显著减弱这一效应。为确定PI3K的激活是否是apoA-IV抑制食物摄入所必需的,将apoA-IV脑室内给药。我们发现,apoA-IV可显著减少食物摄入并激活下丘脑的PI3K信号,而这些效应可被LY294002脑室内预处理消除。为确定apoA-IV发挥其厌食作用的不同脑区,通过植入双侧套管将apoA-IV注入腹内侧下丘脑(VMH)。低剂量(0.5μg)时,apoA-IV可显著抑制瘦大鼠VMH中的食物摄入并激活PI3K信号通路,但对高脂饮食诱导的肥胖(DIO)大鼠则无此作用。这些结果共同表明PI3K/Akt通路在apoA-IV对瘦大鼠的厌食作用中起关键作用,并提示VMH中PI3K通路缺陷是DIO动物中apoA-IV厌食作用受损的原因。