Effect of Oral Administration of Weissella confusa on Fecal and Plasma Ethanol Concentrations, Lipids and Glucose Metabolism in Wistar Rats Fed High Fructose and Fat Diet.

IF 2.6 Q2 GASTROENTEROLOGY & HEPATOLOGY
Hepatic Medicine : Evidence and Research Pub Date : 2020-06-26 eCollection Date: 2020-01-01 DOI:10.2147/HMER.S254195
Fouad M F Elshaghabee, Darab Ghadimi, Diana Habermann, Michael de Vrese, Wilhelm Bockelmann, Hans-Jürgen Kaatsch, Knut J Heller, Jürgen Schrezenmeir
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引用次数: 11

Abstract

Background and purpose: In previous investigations, Weissella confusa was shown to lack the metabolic pathway from fructose to mannitol and to produce ethanol when cultivated in the presence of fructose. Hence, we assessed the effect of oral administration of W. confusa (strain NRRL-B-14171) on blood and fecal ethanol concentrations, glucose and lipid metabolism and traits of the metabolic syndrome in Wistar rats (n=27) fed diets with two different fat and fructose levels and with or without the addition of W. confusa during a total intervention time of 15 weeks (105 days).

Materials and methods: From week 1 to 6, rats were given a medium fructose and fat (MFru-MF) diet containing 28% fructose and 10% fat without the addition of W. confusa (control group, n=13) or mixed with 30 g per kg diet of lyophilized W. confusa (10.56 ± 0.20 log CFU/g; W. confusa group, n=14). From week 7 to 15, the percentage of dietary fructose and fat in the control and W. confusa group was increased to 56% and 16%, respectively (high fructose-high fat (HFru-HF) diet).

Results: In HFru-HF-fed rats, W. confusa was detected in feces, regardless of whether W. confusa was added to the diet or not, but not in rats receiving the MFru-MF diet without added W. confusa or in an additional control group (n=10) fed standard rat food without fructose, increased fat content and W. confusa. This indicates that fecal W. confusa may be derived from orally administered W. confusa as well as - in the case of high fructose and fat intake and obesity of rats - from the intestinal microbiota. As shown by multifactorial ANOVA, blood ethanol, the relative liver weight, serum triglycerides, and serum cholesterol as well as fecal ethanol, ADH, acetate, propionate and butyrate, but not lactate, were significantly higher in the W. confusa - compared to the control group.

Discussion: This is the first in vivo trial demonstrating that heterofermentative lactic acid bacteria lacking the mannitol pathway (like W. confusa) can increase fecal and blood ethanol concentrations in mammals on a high fructose-high fat diet. This may explain why W. confusa resulted in hyperlipidemia and may promote development of NAFLD in the host.

口服鸢尾草对高果糖高脂饲料Wistar大鼠粪便和血浆乙醇浓度、脂质和葡萄糖代谢的影响。
背景和目的:在之前的研究中,研究人员发现,在有果糖存在的环境下培养的Weissella confusa缺乏从果糖到甘露醇的代谢途径,也无法产生乙醇。因此,我们在总干预时间为15周(105天)的情况下,评估了在饲喂两种不同脂肪和果糖水平的饲料以及添加或不添加鸢尾草的情况下,口服鸢尾草(菌株NRRL-B-14171)对Wistar大鼠(n=27)血液和粪便乙醇浓度、葡萄糖和脂质代谢以及代谢综合征特征的影响。材料与方法:第1 ~ 6周,给大鼠饲喂含28%果糖和10%脂肪的中果糖-脂肪(mfruf - mf)饲粮(对照组,n=13)或每kg饲粮中加入30 g冻干黄芪(10.56±0.20 log CFU/g;W. confusa组,n=14)。第7 ~ 15周,对照组和紫花苜蓿组饲粮中果糖和脂肪的比例分别提高到56%和16%(高果糖-高脂肪饲粮)。结果:在hfru - hf喂养的大鼠中,无论是否添加黄芪,粪便中均检测到黄芪,而在未添加黄芪的MFru-MF喂养的大鼠中,以及在另一个对照组(n=10)中,喂食不含果糖、脂肪含量增加和黄芪的标准大鼠食物中,均未检测到黄芪。这表明,粪粪可能来源于口服的粪菌,也可能来源于肠道微生物群——在高果糖和高脂肪摄入和肥胖大鼠的情况下。多因素方差分析显示,与对照组相比,血乙醇、相对肝脏重量、血清甘油三酯、血清胆固醇以及粪便乙醇、ADH、醋酸盐、丙酸盐和丁酸盐显著高于对照组,但乳酸盐不高于对照组。讨论:这是第一个体内试验,证明缺乏甘露醇途径的异发酵乳酸菌(如W. confusa)可以增加高果糖高脂肪饮食中哺乳动物粪便和血液中的乙醇浓度。这可能解释了为什么W. confusa导致高脂血症,并可能促进宿主NAFLD的发展。
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来源期刊
Hepatic Medicine : Evidence and Research
Hepatic Medicine : Evidence and Research GASTROENTEROLOGY & HEPATOLOGY-
自引率
0.00%
发文量
15
审稿时长
16 weeks
期刊介绍: Hepatic Medicine: Evidence and Research is an international, peer-reviewed, open access, online journal. Publishing original research, reports, editorials, reviews and commentaries on all aspects of adult and pediatric hepatology in the clinic and laboratory including the following topics: Pathology, pathophysiology of hepatic disease Investigation and treatment of hepatic disease Pharmacology of drugs used for the treatment of hepatic disease Although the main focus of the journal is to publish research and clinical results in humans; preclinical, animal and in vitro studies will be published where they will shed light on disease processes and potential new therapies. Issues of patient safety and quality of care will also be considered. As of 1st April 2019, Hepatic Medicine: Evidence and Research will no longer consider meta-analyses for publication.
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