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婴儿源屎肠球菌WEFA23益生菌降胆固醇菌株对大鼠饮食诱导的代谢综合征的有益作用。

Beneficial effects of probiotic cholesterol-lowering strain of Enterococcus faecium WEFA23 from infants on diet-induced metabolic syndrome in rats.

作者信息

Zhang Fen, Qiu Liang, Xu Xiongpeng, Liu Zhengqi, Zhan Hui, Tao Xueying, Shah Nagendra P, Wei Hua

机构信息

School of Life Sciences, Nanchang University, Nanchang 330031, China.

Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China.

出版信息

J Dairy Sci. 2017 Mar;100(3):1618-1628. doi: 10.3168/jds.2016-11870. Epub 2016 Dec 29.

Abstract

The aim of this study was to select probiotic Enterococcus strains that have the potential to improve metabolic syndrome (MS). Ten Enterococcus strains isolated from healthy infants were evaluated for their probiotic properties in vitro, and Enterococcus faecium WEFA23 was selected due to its cholesterol removal ability (1.89 ± 0.07 mg/10 cfu), highest glycodeoxycholic acid-hydrolase activity (1.86 ± 0.01 U/mg), and strong adhesion capacity to Caco-2 cells (17.90 ± 0.19%). The safety of E. faecium WEFA23 was verified by acute oral administration in mice, and it was found to have no adverse effects on general health status, bacterial translocation, and gut mucosal histology. Moreover, the beneficial effects of E. faecium WEFA23 on high-fat diet-induced MS in rats were investigated, and we found WEFA23 significantly decreased body weight, serum lipid levels (total cholesterol, triacylglycerols, and low-density lipoprotein cholesterol), blood glucose level, and insulin resistance in rats fed with a high-fat diet. This indicated that administration of E. faecium WEFA23 improved almost all key markers of MS, including obesity, hyperlipidemia, hyperglycemia, and insulin resistance. Our results supported E. faecium WEFA23 as a candidate for cholesterol-lowering dairy products and improvement of MS. Our research provided novel insights on Enterococcus as a strategy to combat MS.

摘要

本研究的目的是筛选出具有改善代谢综合征(MS)潜力的益生菌肠球菌菌株。对从健康婴儿中分离出的10株肠球菌菌株进行了体外益生菌特性评估,屎肠球菌WEFA23因其胆固醇去除能力(1.89±0.07毫克/10 cfu)、最高的甘氨脱氧胆酸水解酶活性(1.86±0.01 U/毫克)以及对Caco-2细胞的强黏附能力(17.90±0.19%)而被选中。通过对小鼠进行急性口服给药验证了屎肠球菌WEFA23的安全性,发现其对一般健康状况、细菌易位和肠道黏膜组织学均无不良影响。此外,还研究了屎肠球菌WEFA23对高脂饮食诱导的大鼠MS的有益作用,我们发现WEFA23显著降低了高脂饮食喂养大鼠的体重、血脂水平(总胆固醇、三酰甘油和低密度脂蛋白胆固醇)、血糖水平以及胰岛素抵抗。这表明给予屎肠球菌WEFA23改善了MS的几乎所有关键指标,包括肥胖、高脂血症、高血糖和胰岛素抵抗。我们的结果支持屎肠球菌WEFA23作为降低胆固醇乳制品和改善MS的候选菌株。我们的研究为肠球菌作为对抗MS的策略提供了新的见解。

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