Pellinen Jacob, Wang Hong, Eckel Robert H
1 University of Colorado School of Medicine, University of Colorado Anschutz Medical Campus , Aurora, Colorado.
Metab Syndr Relat Disord. 2014 Aug;12(6):339-46. doi: 10.1089/met.2013.0141. Epub 2014 Apr 14.
Three-month-old neuron-specific lipoprotein lipase (LPL)-depleted mice (NEXLP(-/-)) mice are preobese and have normal body weight before developing obesity by 4.5 months. This series of experiments investigated responses to novel environment stimuli and acute sleep deprivation in preobese NEXLPL(-/-)) mice to test the hypothesis that neuron-specific LPL deletion alters normal adaptive metabolic responses to environmental challenges.
Three-month-old, age- and weight-matched, male NEXLPL(-/-)) (n=10) and wild-type (WT) (n=10) mice were housed in individual metabolic chambers with a 12-hr dark cycle. Food and water intake, locomotor activity, and calorimetry data were recorded in 12-min intervals. Novel environmental responses were elicited by first-time introduction to chambers at dark onset, followed by acclimation, baseline recording, and 6-hr of sleep deprivation on subsequent experimental days.
NEXLPL(-/-)) mice displayed a 1.5-fold greater increase in activity in response to a novel environment than seen in WT controls (P=0.0308), and a two-fold greater increase in food intake following acute sleep deprivation (P=0.0117). NEXLPL(-/-)) mice averaged a 27% higher metabolic rate than WT mice throughout the experiments (P<0.0001). Body weight, composition, and temperature did not differ between murine groups throughout the experiments. Levels of free fatty acid, insulin, glucose, and triglycerides were similar between groups at the terminus.
A deficiency in neuronal LPL signaling disrupts normal responses to novel environmental exposure and acute sleep deprivation, a maladaptive response that may contribute to weight gain in genetically predisposed mice, and perhaps humans.
三个月大的神经元特异性脂蛋白脂肪酶(LPL)缺失小鼠(NEXLP(-/-))处于肥胖前期,在4.5个月出现肥胖之前体重正常。这一系列实验研究了肥胖前期NEXLPL(-/-)小鼠对新环境刺激和急性睡眠剥夺的反应,以检验神经元特异性LPL缺失会改变对环境挑战的正常适应性代谢反应这一假设。
将三个月大、年龄和体重匹配的雄性NEXLPL(-/-)小鼠(n = 10)和野生型(WT)小鼠(n = 10)饲养在具有12小时黑暗周期的个体代谢室中。每隔12分钟记录一次食物和水的摄入量、运动活动和热量测定数据。通过在黑暗开始时首次引入代谢室引发新环境反应,随后进行适应、基线记录,并在随后的实验天数进行6小时的睡眠剥夺。
与WT对照组相比,NEXLPL(-/-)小鼠对新环境的反应活动增加了1.5倍(P = 0.0308),急性睡眠剥夺后食物摄入量增加了两倍(P = 0.0117)。在整个实验过程中,NEXLPL(-/-)小鼠的平均代谢率比WT小鼠高27%(P < 0.0001)。在整个实验过程中,两组小鼠的体重、组成和体温没有差异。实验结束时,两组之间的游离脂肪酸、胰岛素、葡萄糖和甘油三酯水平相似。
神经元LPL信号的缺陷会破坏对新环境暴露和急性睡眠剥夺的正常反应,这种适应不良反应可能导致遗传易患小鼠,也许还有人类体重增加。