Department of Physical Education and Recreation Studies, Mount Royal University, 4825 Mount Royal Gate SW, Calgary, AB, Canada.
Br J Nutr. 2012 Feb;107(4):601-13. doi: 10.1017/S0007114511003163. Epub 2011 Jul 18.
There is a growing interest in modulating gut microbiota with diet in the context of obesity. The purpose of the present study was to evaluate the dose-dependent effects of prebiotics (inulin and oligofructose) on gut satiety hormones, energy expenditure, gastric emptying and gut microbiota. Male lean and obese JCR:LA-cp rats were randomised to either of the following: lean 0 % fibre (LC), lean 10 % fibre (LF), lean 20 % fibre (LHF), obese 0 % fibre (OC), obese 10 % fibre (OF) or obese 20 % fibre (OHF). Body composition, gastric emptying, energy expenditure, plasma satiety hormone concentrations and gut microbiota (using quantitative PCR) were measured. Caecal proglucagon and peptide YY mRNA levels were up-regulated 2-fold in the LF, OF and OHF groups and 3-fold in the LHF group. Ghrelin O-acyltransferase mRNA levels were higher in obese v. lean rats and decreased in the OHF group. Plasma ghrelin response was attenuated in the LHF group. Microbial species measured in the Bacteroidetes division decreased, whereas those in the Firmicutes increased in obese v. lean rats and improved with prebiotic intake. Bifidobacterium and Lactobacillus increased in the OHF v. OC group. Bacteroides and total bacteria negatively correlated with percentage of body fat and body weight. Enterobacteriaceae increased in conjunction with glucose area under the curve (AUC) and glucagon-like peptide-1 AUC. Bacteroides and total bacteria correlated positively with ghrelin AUC yet negatively with insulin AUC and energy intake (P < 0·05). Several of the mechanisms through which prebiotics act (food intake, satiety hormones and alterations in gut microbiota) are regulated in a dose-dependent manner. The combined effects of prebiotics may have therapeutic potential for obesity.
人们越来越感兴趣的是在肥胖背景下通过饮食来调节肠道微生物群。本研究的目的是评估益生元(菊粉和低聚果糖)对肠道饱腹感激素、能量消耗、胃排空和肠道微生物群的剂量依赖性影响。雄性瘦型和肥胖型 JCR:LA-cp 大鼠随机分为以下几组:瘦型 0%纤维(LC)、瘦型 10%纤维(LF)、瘦型 20%纤维(LHF)、肥胖型 0%纤维(OC)、肥胖型 10%纤维(OF)或肥胖型 20%纤维(OHF)。测量身体成分、胃排空、能量消耗、血浆饱腹感激素浓度和肠道微生物群(使用定量 PCR)。LF、OF 和 OHF 组的胰高血糖素原和肽 YY mRNA 水平上调 2 倍,LHF 组上调 3 倍。Ghrelin O-酰基转移酶 mRNA 水平在肥胖型大鼠中高于瘦型大鼠,并在 OHF 组中降低。LHF 组的血浆 ghrelin 反应减弱。在厚壁菌门中测量的微生物种类减少,而在拟杆菌门和厚壁菌门中测量的微生物种类在肥胖型大鼠中增加,并随着益生元的摄入而改善。与 OC 组相比,双歧杆菌和乳杆菌在 OHF 组中增加。拟杆菌和总细菌与体脂百分比和体重呈负相关。肠杆菌科与血糖曲线下面积(AUC)和胰高血糖素样肽-1 AUC 一起增加。拟杆菌和总细菌与 ghrelin AUC 呈正相关,与胰岛素 AUC 和能量摄入呈负相关(P<0.05)。益生元作用的几种机制(食物摄入、饱腹感激素和肠道微生物群的改变)呈剂量依赖性调节。益生元的联合作用可能对肥胖具有治疗潜力。