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1 型糖尿病小鼠肠道微生物群和宿主代谢组的性别依赖性影响。

Sex-dependent effects on the gut microbiota and host metabolome in type 1 diabetic mice.

机构信息

Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China; Institute of Metabonomics & Medical NMR, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.

Institute of Metabonomics & Medical NMR, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2021 Dec 1;1867(12):166266. doi: 10.1016/j.bbadis.2021.166266. Epub 2021 Sep 2.

DOI:10.1016/j.bbadis.2021.166266
PMID:34481869
Abstract

Sexual dimorphism exists in the onset and development of type 1 diabetes (T1D), but its potential pathological mechanism is poorly understood. In the present study, we examined sex-specific changes in the gut microbiome and host metabolome of T1D mice via 16S rRNA gene sequencing and nuclear magnetic resonance (NMR)-based metabolomics approach, and aimed to investigate potential mechanism of the gut microbiota-host metabolic interaction in the sexual dimorphism of T1D. Our results demonstrate that female mice had a greater shift in the gut microbiota than male mice during the development of T1D; however, host metabolome was more susceptible to T1D in male mice. The correlation network analysis indicates that T1D-induced host metabolic changes may be regulated by the gut microbiota in a sex-specific manner, mainly involving short-chain fatty acids (SCFAs) metabolism, energy metabolism, amino acid metabolism, and choline metabolism. Therefore, our study suggests that sex-dependent "gut microbiota-host metabolism axis" may be implicated in the sexual dimorphism of T1D, and the link between microbes and metabolites might contribute to the prevention and treatment of T1D.

摘要

性别二态性存在于 1 型糖尿病(T1D)的发病和发展中,但其潜在的病理机制尚不清楚。在本研究中,我们通过 16S rRNA 基因测序和基于核磁共振(NMR)的代谢组学方法,检测了 T1D 小鼠的肠道微生物组和宿主代谢组的性别特异性变化,并旨在研究肠道微生物群-宿主代谢相互作用在 T1D 性别二态性中的潜在机制。我们的研究结果表明,在 T1D 的发展过程中,雌性小鼠的肠道微生物组比雄性小鼠有更大的变化;然而,雄性小鼠的宿主代谢组对 T1D 更敏感。相关性网络分析表明,T1D 诱导的宿主代谢变化可能以性别特异性的方式受到肠道微生物组的调节,主要涉及短链脂肪酸(SCFA)代谢、能量代谢、氨基酸代谢和胆碱代谢。因此,我们的研究表明,依赖于性别的“肠道微生物群-宿主代谢轴”可能与 T1D 的性别二态性有关,微生物和代谢物之间的联系可能有助于 T1D 的预防和治疗。

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