Nandivada Prathima, Fell Gillian L, Pan Amy H, Nose Vania, Ling Pei-Ra, Bistrian Bruce R, Puder Mark
Vascular Biology Program and Department of Surgery, Boston Children's Hospital, Harvard Medical School, 300 Longwood Ave, Boston, MA, 02115, USA.
Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Lipids. 2016 Jun;51(6):703-14. doi: 10.1007/s11745-016-4156-7. Epub 2016 Apr 27.
Dietary strategies to alter the immune response to acute inflammation have the potential to improve outcomes in critically ill patients. A eucaloric ketogenic diet (EKD), composed predominantly of fat with very small amounts of carbohydrate, can provide adequate caloric support while minimizing spikes in blood glucose and reducing oxidative stress. The purpose of this study was to evaluate the effects of an EKD on glycemic control and the inflammatory response after acute endotoxemia in mice. Mice received either an EKD or a carbohydrate-based control diet (CD) for 4 weeks. Animals subsequently underwent either a 2-h fast (postprandial) or an overnight fast (postabsorptive), and half of the animals in each diet group were randomized to receive either intraperitoneal lipopolysaccharide (1 mg/kg) or an equivalent volume of saline. Glycemic response, insulin resistance, inflammatory cytokine levels, and the expression of key inflammatory and metabolic genes were measured. After endotoxin challenge, hypoglycemia was more frequent in mice fed a CD than an EKD in the postprandial period. This was due in part to the preservation of hepatic glycogen stores despite endotoxin exposure and prolonged fasting in mice fed an EKD. Furthermore, mice fed the CD had higher levels of IL-6 and TNF-α in the postabsorptive period, with a fivefold higher expression of hepatic NFκB compared to mice fed the EKD in both fasting periods. These results suggest that the unique metabolic state induced by an EKD can alter the response to acute inflammation in mice.
改变对急性炎症免疫反应的饮食策略有可能改善重症患者的预后。一种以脂肪为主、碳水化合物含量极少的正常热量生酮饮食(EKD),可以在提供足够热量支持的同时,使血糖峰值最小化并减轻氧化应激。本研究的目的是评估EKD对小鼠急性内毒素血症后血糖控制和炎症反应的影响。小鼠接受EKD或基于碳水化合物的对照饮食(CD)4周。随后,动物们经历了2小时禁食(餐后)或过夜禁食(吸收后),每个饮食组中的一半动物被随机分配接受腹腔注射脂多糖(1mg/kg)或等量的生理盐水。测量了血糖反应、胰岛素抵抗、炎症细胞因子水平以及关键炎症和代谢基因的表达。在内毒素攻击后,餐后喂食CD的小鼠比喂食EKD的小鼠更频繁地出现低血糖。这部分归因于尽管暴露于内毒素且喂食EKD的小鼠禁食时间延长,但肝脏糖原储备得以保留。此外,在吸收后阶段,喂食CD的小鼠IL-6和TNF-α水平更高,与两个禁食期喂食EKD的小鼠相比,肝脏NFκB的表达高五倍。这些结果表明,EKD诱导的独特代谢状态可以改变小鼠对急性炎症的反应。