Harris Ruth B S
Department of Physiology, Medical College of Georgia, Augusta University, Augusta, Georgia
Am J Physiol Endocrinol Metab. 2017 Aug 1;313(2):E134-E147. doi: 10.1152/ajpendo.00052.2017. Epub 2017 Apr 25.
We previously reported that low-dose leptin infusions into the third or fourth ventricle that do not affect energy balance when given independently cause rapid weight loss when given simultaneously. Therefore, we tested whether hindbrain leptin enhances the response to forebrain leptin or whether forebrain leptin enhances the response to hindbrain leptin. Rats received fourth-ventricle infusions of saline or 0.01, 0.1, 0.3, or 0.6 μg leptin/day for 13 days. On and , 0.1 μg leptin was injected into the third ventricle. The injection inhibited food intake for 36 h in saline-infused rats but for 60 h in those infused with 0.6 μg leptin/day. Leptin injection increased intrascapular brown fat temperature in leptin-infused, but not saline-infused, rats. In a separate experiment, rats received third-ventricle infusions of saline or 0.005, 0.01, 0.05, or 0.1 μg leptin/day and fourth-ventricle injections of 1.0 μg leptin on and Leptin injection inhibited food intake, respiratory exchange ratio, and 14-h food intake in rats infused with saline or the two lowest doses of leptin. There was no effect with higher-dose leptin infusions because food intake, body fat, and lean mass were already inhibited. These data suggest that activation of leptin receptors in the hindbrain enhances the response to third-ventricle leptin, whereas activation of forebrain leptin receptors does not enhance the response to fourth-ventricle leptin, consistent with our previous finding that weight loss in rats treated with fourth-ventricle leptin is associated with indirect activation of hypothalamic STAT3.
我们之前报道过,单独向第三或第四脑室输注低剂量瘦素时不会影响能量平衡,但同时输注时会导致体重快速下降。因此,我们测试了后脑瘦素是否会增强对前脑瘦素的反应,或者前脑瘦素是否会增强对后脑瘦素的反应。大鼠接受第四脑室输注生理盐水或每天0.01、0.1、0.3或0.6μg瘦素,持续13天。在第11天和第12天,向第三脑室注射0.1μg瘦素。该注射在输注生理盐水的大鼠中抑制食物摄入36小时,但在每天输注0.6μg瘦素的大鼠中抑制60小时。瘦素注射使输注瘦素而非输注生理盐水的大鼠肩胛间棕色脂肪温度升高。在另一项实验中,大鼠接受第三脑室输注生理盐水或每天0.005、0.01、0.05或0.1μg瘦素,并在第11天和第12天接受第四脑室注射1.0μg瘦素。瘦素注射抑制了输注生理盐水或两种最低剂量瘦素的大鼠的食物摄入、呼吸交换率和14小时食物摄入量。高剂量瘦素输注没有效果,因为食物摄入、体脂和瘦体重已经受到抑制。这些数据表明,后脑瘦素受体的激活增强了对第三脑室瘦素的反应,而前脑瘦素受体的激活并未增强对第四脑室瘦素的反应,这与我们之前的发现一致,即接受第四脑室瘦素治疗的大鼠体重减轻与下丘脑STAT3的间接激活有关。