Translational Medicine Research Program, The Hospital for Sick Children, Toronto, ON, Canada.
Morosky College of Health Professions and Sciences, Gannon University, Erie, PA, United States of America.
PLoS One. 2018 Jul 2;13(7):e0199916. doi: 10.1371/journal.pone.0199916. eCollection 2018.
Early postnatal-life malnutrition remains prevalent globally, and about 45% of all child deaths are linked to malnutrition. It is not clear whether survivors of childhood malnutrition suffer from long-term metabolic effects, especially when they are later in life exposed to a fat and carbohydrate rich obesogenic diet. The lack of knowledge around this dietary "double burden" warrants studies to understand the long-term consequences of children previously exposed to malnutrition. We hypothesized that an early-life nutritional insult of low protein consumption in mice would lead to long-term metabolic disturbances that would exacerbate the development of diet-induced insulin resistance and non-alcoholic fatty liver disease (NAFLD). We investigated the effects of feeding a low protein diet (4% wt/wt) immediately after weaning for four weeks and subsequent feeding of a high carbohydrate high fat feeding for 16 weeks on metabolic function and development of NAFLD. Mice exposed to early-life protein restriction demonstrated a transient glucose intolerance upon recovery by regular chow diet feeding. However, protein restriction after weaning in mice did not exacerbate an obesogenic diet-induced insulin resistance or progression to NAFLD. These data suggest that transient protein restriction in early-life does not exacerbate an obesogenic diet-induced NAFLD and insulin resistance.
早期生命期营养不良在全球仍然普遍存在,约 45%的儿童死亡与营养不良有关。目前尚不清楚儿童期营养不良的幸存者是否会遭受长期的代谢影响,尤其是当他们以后的生活中接触到富含脂肪和碳水化合物的致肥胖饮食时。由于对这种饮食“双重负担”缺乏了解,因此需要开展研究以了解先前遭受营养不良的儿童的长期后果。我们假设,在小鼠中,生命早期的低蛋白饮食摄入不足会导致长期的代谢紊乱,从而加剧饮食诱导的胰岛素抵抗和非酒精性脂肪性肝病(NAFLD)的发展。我们研究了在断奶后立即进行四周的低蛋白饮食(4%wt/wt)喂养,以及随后进行 16 周的高碳水化合物高脂肪喂养对代谢功能和 NAFLD 发展的影响。暴露于生命早期蛋白质限制的小鼠在恢复正常饮食时表现出短暂性的葡萄糖不耐受。然而,断奶后蛋白质限制并未加剧肥胖饮食诱导的胰岛素抵抗或进展为 NAFLD。这些数据表明,生命早期的短暂蛋白质限制不会加剧肥胖饮食诱导的 NAFLD 和胰岛素抵抗。