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四周的尼古丁给药以饮食依赖的方式适度影响血液代谢特征和肠道微生物群。

Four-week administration of nicotinemoderately impacts blood metabolic profile and gut microbiota in a diet-dependent manner.

机构信息

Zhengzhou Tobacco Research Institute of CNTC, Zhengzhou, 450001, China.

Innovation Service Platform of Plant Gene and Genomic Research of Qinghai Province, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, 810008, China.

出版信息

Biomed Pharmacother. 2019 Jul;115:108945. doi: 10.1016/j.biopha.2019.108945. Epub 2019 May 14.

Abstract

As the primary active component in tobacco, nicotine affects many aspects of human metabolism. Diet and gut microbiota are key factors that profoundly influence human lipid and glucose metabolism. However, the diet-based differential impacts of nicotine on blood lipid and glucose levels as well as on the gut microbiota are still largely unknown. Here we show that 4-week oral administration of nicotine (2 mg/kg) resulted in bodyweight and fat decrease in both normal-chow (NCD)- and high-fat diet (HFD)-fed mice. But nicotine showed little influence on the plasma levels of lipids, glucose and inflammatory cytokines in NCD-fed mice but moderately deteriorated these parameters in HFD-fed ones. 16S sequencing showed that nicotine perturbed bacterial diversity and community composition of gut microbiota more pronouncedly in HFD mice. At genus level, nicotine dramatically increased Ruminococcaceae UCG-009 in HFD condition but not in NCD feeding. Interestingly, co-treatment with antibiotics (ampicillin + norfloxacin) substantially abolished the lipid-enhancing effect of nicotine in HFD-fed mice, suggesting an important role of gut microbes in the lipid-modulatory effect of nicotine. Together, our results indicate that the harmful effects of nicotine on metabolism and systemic inflammation are diet-dependent. Chronic exposure to nicotine may alter the gut microbiota especially in HFD-fed animals.

摘要

作为烟草中的主要活性成分,尼古丁影响着人类新陈代谢的许多方面。饮食和肠道微生物群是深刻影响人类脂质和葡萄糖代谢的关键因素。然而,尼古丁对血脂和血糖水平以及肠道微生物群的饮食相关差异影响仍在很大程度上不为人知。在这里,我们发现,4 周的尼古丁(2mg/kg)口服给药导致正常饮食(NCD)和高脂肪饮食(HFD)喂养的小鼠体重和脂肪减少。但是,尼古丁对 NCD 喂养小鼠的血浆脂质、葡萄糖和炎症细胞因子水平几乎没有影响,但在 HFD 喂养的小鼠中则适度恶化了这些参数。16S 测序表明,尼古丁在 HFD 小鼠中更明显地扰乱了肠道微生物群的细菌多样性和群落组成。在属水平上,尼古丁在 HFD 条件下显著增加了 Ruminococcaceae UCG-009,但在 NCD 喂养中则没有。有趣的是,抗生素(氨苄青霉素+诺氟沙星)联合治疗基本上消除了尼古丁在 HFD 喂养小鼠中的脂质增强作用,这表明肠道微生物在尼古丁的脂质调节作用中具有重要作用。总的来说,我们的结果表明,尼古丁对代谢和全身炎症的有害影响是饮食依赖性的。慢性暴露于尼古丁可能会改变肠道微生物群,特别是在 HFD 喂养的动物中。

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