Crossland Randy F, Balasa Alfred, Ramakrishnan Rajesh, Mahadevan Sangeetha K, Fiorotto Marta L, Van den Veyver Ignatia B
Department of Obstetrics & Gynecology, Baylor College of Medicine, Houston, TX, United States of America.
Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, United States of America.
PLoS One. 2017 Jan 18;12(1):e0170127. doi: 10.1371/journal.pone.0170127. eCollection 2017.
Offspring of murine dams chronically fed a protein-restricted diet have an increased risk for metabolic and neurobehavioral disorders. Previously we showed that adult offspring, developmentally exposed to a chronic maternal low-protein (MLP) diet, had lower body and hind-leg muscle weights and decreased liver enzyme serum levels. We conducted energy expenditure, neurobehavioral and circadian rhythm assays in male offspring to examine mechanisms for the body-weight phenotype and assess neurodevelopmental implications of MLP exposure. C57BL/6J dams were fed a protein restricted (8%protein, MLP) or a control protein (20% protein, C) diet from four weeks before mating until weaning of offspring. Male offspring were weaned to standard rodent diet (20% protein) and single-housed until 8-12 weeks of age. We examined body composition, food intake, energy expenditure, spontaneous rearing activity and sleep patterns and performed behavioral assays for anxiety (open field activity, elevated plus maze [EPM], light/dark exploration), depression (tail suspension and forced swim test), sociability (three-chamber), repetitive (marble burying), learning and memory (fear conditioning), and circadian behavior (wheel-running activity during light-dark and constant dark cycles). We also measured circadian gene expression in hypothalamus and liver at different Zeitgeber times (ZT). Male offspring from separate MLP exposed dams had significantly greater body fat (P = 0.03), less energy expenditure (P = 0.004), less rearing activity (P = 0.04) and a greater number of night-time rest/sleep bouts (P = 0.03) compared to control. MLP offspring displayed greater anxiety-like behavior in the EPM (P<0.01) but had no learning and memory deficit in fear-conditioning assay (P = 0.02). There was an effect of time on Per1, Per 2 and Clock circadian gene expression in the hypothalamus but not on circadian behavior. Thus, transplacental and early developmental exposure of dams to chronic MLP reduces food intake and energy expenditure, increases anxiety like behavior and disturbs sleep patterns but not circadian rhythm in adult male offspring.
长期喂食蛋白质限制饮食的母鼠所产后代患代谢和神经行为障碍的风险增加。此前我们发现,成年后代在发育过程中暴露于慢性母体低蛋白(MLP)饮食,其体重和后腿肌肉重量较低,肝酶血清水平降低。我们对雄性后代进行了能量消耗、神经行为和昼夜节律测定,以研究体重表型的机制,并评估MLP暴露对神经发育的影响。C57BL/6J母鼠在交配前四周至后代断奶期间喂食蛋白质限制(8%蛋白质,MLP)或对照蛋白质(20%蛋白质,C)饮食。雄性后代断奶后喂食标准啮齿动物饮食(20%蛋白质),单笼饲养至8 - 12周龄。我们检查了身体组成、食物摄入量、能量消耗、自发竖毛活动和睡眠模式,并进行了焦虑行为测定(旷场活动、高架十字迷宫[EPM]、明暗探索)、抑郁行为测定(悬尾和强迫游泳试验)、社交行为测定(三室试验)、重复行为测定(埋大理石试验)、学习和记忆行为测定(恐惧条件反射)以及昼夜行为测定(明暗周期和持续黑暗周期中的转轮活动)。我们还在不同的授时因子时间(ZT)测量了下丘脑和肝脏中的昼夜节律基因表达。与对照组相比,来自不同MLP暴露母鼠的雄性后代体脂显著更高(P = 0.03),能量消耗更低(P = 0.004),竖毛活动更少(P = 0.04),夜间休息/睡眠次数更多(P = 0.03)。MLP后代在EPM中表现出更强的焦虑样行为(P<0.01),但在恐惧条件反射试验中没有学习和记忆缺陷(P = 0.02)。时间对下丘脑Per1、Per2和Clock昼夜节律基因表达有影响,但对昼夜行为没有影响。因此,母鼠经胎盘和早期发育暴露于慢性MLP会降低成年雄性后代的食物摄入量和能量消耗,增加焦虑样行为,扰乱睡眠模式,但不影响昼夜节律。