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载脂蛋白A-IV基因敲除小鼠中高脂饮食诱导肥胖时肠道微生物群和代谢物组成的终生变化

Lifetime Changes in Gut Microbiota and Metabolite Composition in High-Fat Diet-Induced Obesity in Apolipoprotein A-IV Gene Knockout Mice.

作者信息

Zeber-Lubecka Natalia, Kulecka Maria, Balabas Aneta, Czarnowski Pawel, Pyśniak Kazimiera, Dąbrowska Michalina, Ostrowski Jerzy, Hennig Ewa E

机构信息

Department of Gastroenterology, Hepatology and Clinical Oncology, Centre of Postgraduate Medical Education, 02-781 Warsaw, Poland.

Department of Genetics, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, Poland.

出版信息

Biology (Basel). 2025 Sep 17;14(9):1278. doi: 10.3390/biology14091278.

Abstract

Apolipoprotein A-IV (ApoA-IV) has been implicated in modulating the gut microbiota. However, chronic high-fat diet (HFD) consumption impairs ApoA-IV signaling and disrupts gut microbial balance, contributing to obesity and insulin resistance. This study aimed to investigate the role of ApoA-IV in shaping the gut microbiota and associated metabolic profiles throughout the lifespan of mice exposed to an HFD. Fecal samples were collected from ApoA-IV knockout (KO) and wild-type mice at five time points for microbiota and metabolite profiling using 16S rRNA gene sequencing and gas chromatography-mass spectrometry, respectively. Lifespan was longest in ApoA-IV-KO mice on a normal diet, while the HFD reduced survival across genotypes. Microbiota analysis revealed diet- and age-dependent shifts, including an elevated Firmicutes/Bacteroidota ratio, altered abundance of and reduced in ApoA-IV-KO mice on the HFD. Metabolic profiling showed a stronger impact of diet than genotype, with early and persistent increases in branched-chain amino acids and reductions in short-chain fatty acids (SCFAs). ApoA-IV deficiency modulated lifespan microbial and metabolic changes and shaped distinct responses to dietary stress. Despite age-related convergence in microbiota structure, genotype-specific differences in metabolite profiles and SCFA-producing bacteria correlations persisted into old age, demonstrating the lasting impact of ApoA-IV on host metabolic adaptation.

摘要

载脂蛋白A-IV(ApoA-IV)与调节肠道微生物群有关。然而,长期食用高脂饮食(HFD)会损害ApoA-IV信号传导并破坏肠道微生物平衡,导致肥胖和胰岛素抵抗。本研究旨在调查ApoA-IV在暴露于HFD的小鼠整个生命周期中对塑造肠道微生物群和相关代谢谱的作用。分别在五个时间点从ApoA-IV基因敲除(KO)小鼠和野生型小鼠收集粪便样本,使用16S rRNA基因测序和气相色谱-质谱法进行微生物群和代谢物分析。正常饮食的ApoA-IV-KO小鼠寿命最长,而HFD降低了各基因型小鼠的存活率。微生物群分析揭示了饮食和年龄依赖性变化,包括HFD喂养的ApoA-IV-KO小鼠中厚壁菌门/拟杆菌门比例升高、特定菌属丰度改变以及某菌属减少。代谢物分析表明,饮食对代谢物的影响比基因型更强,支链氨基酸早期持续增加,短链脂肪酸(SCFA)减少。ApoA-IV缺乏调节了寿命、微生物和代谢变化,并塑造了对饮食应激的不同反应。尽管微生物群结构在年龄增长过程中趋同,但代谢物谱和SCFA产生菌相关性的基因型特异性差异持续到老年,表明ApoA-IV对宿主代谢适应具有持久影响。

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