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阴沟肠杆菌给药可诱导高脂饮食喂养的小鼠肝损伤和皮下脂肪堆积。

Enterobacter cloacae administration induces hepatic damage and subcutaneous fat accumulation in high-fat diet fed mice.

机构信息

Institute of Biomedicine, University of Turku, Turku, Finland.

Department of Clinical Microbiology, Turku University Hospital, Turku, Finland.

出版信息

PLoS One. 2018 May 30;13(5):e0198262. doi: 10.1371/journal.pone.0198262. eCollection 2018.

Abstract

Accumulating evidence indicates that gut microbiota plays a significant role in obesity, insulin resistance and associated liver disorders. Family Enterobacteriaceae and especially Enterobacter cloacae strain B29 have been previously linked to obesity and hepatic damage. The underlying mechanisms, however, remain unclear. Therefore, we comprehensively examined the effects of E. cloacae subsp. cloacae (ATCC® 13047™) administration on host metabolism of mice fed with high-fat diet (HFD). C57BL/6N mice were randomly divided into HFD control, chow control, and E. cloacae treatment groups. The E. cloacae treatment group received live bacterial cells in PBS intragastrically twice a week, every other week for 13 weeks. Both control groups received PBS intragastrically. After the 13-week treatment period, the mice were sacrificed for gene and protein expression and functional analyses. Our results show that E. cloacae administration increased subcutaneous fat mass and the relative proportion of hypertrophic adipocytes. Both subcutaneous and visceral fat had signs of decreased insulin signaling and elevated lipolysis that was reflected in higher serum glycerol levels. In addition, E. cloacae -treated mice had significantly higher hepatic AST and AST/ALT ratio, and their liver histology indicated fibrosis, demonstrating that E. cloacae subsp. cloacae administration promotes hepatic damage in HFD fed mice.

摘要

越来越多的证据表明,肠道微生物群在肥胖、胰岛素抵抗和相关的肝脏疾病中起着重要作用。家族肠杆菌科,特别是阴沟肠杆菌 B29 株,以前与肥胖和肝损伤有关。然而,其潜在机制尚不清楚。因此,我们全面研究了阴沟肠杆菌亚种(ATCC®13047™)给药对高脂肪饮食(HFD)喂养的宿主代谢的影响。C57BL/6N 小鼠被随机分为 HFD 对照组、标准饮食对照组和阴沟肠杆菌治疗组。阴沟肠杆菌治疗组每周两次经胃内给予活细菌细胞 PBS,每隔一周一次,共 13 周。两组对照组均给予 PBS 胃内给予。13 周治疗期结束后,处死小鼠进行基因和蛋白表达及功能分析。我们的结果表明,阴沟肠杆菌给药增加了皮下脂肪量和肥大脂肪细胞的相对比例。皮下脂肪和内脏脂肪均有胰岛素信号降低和脂肪分解升高的迹象,表现为血清甘油水平升高。此外,阴沟肠杆菌治疗组小鼠的肝 AST 和 AST/ALT 比值显著升高,其肝组织学显示纤维化,表明阴沟肠杆菌亚种。阴沟肠杆菌给药可促进 HFD 喂养小鼠的肝损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2038/5976205/597e0f4050c3/pone.0198262.g001.jpg

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