补充 Akkermansia Muciniphila 可改善高脂肪喂养的载脂蛋白 E 缺乏小鼠的高脂血症、心脏功能和肠道微生物群

IF 2.5 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

摘要

高脂血症、肥胖和肠道菌群失调是动脉粥样硬化性心血管疾病(ACVD)的关键风险因素。事实证明,补充 Akkermansia muciniphila(AKK)能有效预防和治疗肥胖及其他代谢紊乱。在这里,我们通过对粪便样本进行元基因组测序发现,AKK 在健康对照组中的含量高于 ACVD 患者。随后,我们研究了 AKK 在肥胖相关动脉粥样硬化中的作用和潜在机制。通过改善血脂异常,AKK干预部分逆转了载脂蛋白E-/-小鼠动脉粥样硬化病变形成的恶化。有趣的是,补充 AKK 能显著增强心脏功能并减轻体重。它还减少了血液循环中的促炎细胞因子IL-6,增加了抗炎细胞因子IL-10。此外,AKK定植还能极大地调节肠道微生物群,增加乳酸菌的丰度。我们的研究结果为 AKK 作为一种有益微生物治疗动脉粥样硬化相关心血管疾病的潜力提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Akkermansia Muciniphila supplementation improves hyperlipidemia, cardiac function, and gut microbiota in high fat fed apolipoprotein E–deficient mice

Hyperlipidemia, obesity and gut dysbiosis are pivotal risk factors for atherosclerotic cardiovascular disease (ACVD). Supplementation of Akkermansia muciniphila (AKK) has also been proven to be effective in the prevention and treatment of obesity and other metabolic disorders. Here we found that AKK was more abundant in healthy control than ACVD patients via metagenomic sequencing on fecal samples. Subsequently, we investigated the role and underlying mechanism of AKK on obesity-associated atherosclerosis. AKK intervention partially reversed the exacerbation of atherosclerotic lesion formation in ApoE-/- mice by improving dyslipidemia. Interestingly, replenishment with AKK significantly enhanced cardiac function and reduced the body weight. It also reduced pro-inflammatory cytokine IL-6 and increased anti-inflammatory IL-10 in the circulation. Additionally, AKK colonization dramatically regulated gut microbiota and increased the abundance of Lactobacillaceae. Our findings have provided novel insights into the therapeutic potential of AKK as a beneficial microbe for treating atherosclerotic-associated cardiovascular diseases.

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来源期刊
Prostaglandins & other lipid mediators
Prostaglandins & other lipid mediators 生物-生化与分子生物学
CiteScore
5.80
自引率
3.40%
发文量
49
审稿时长
2 months
期刊介绍: Prostaglandins & Other Lipid Mediators is the original and foremost journal dealing with prostaglandins and related lipid mediator substances. It includes basic and clinical studies related to the pharmacology, physiology, pathology and biochemistry of lipid mediators. Prostaglandins & Other Lipid Mediators invites reports of original research, mini-reviews, reviews, and methods articles in the basic and clinical aspects of all areas of lipid mediator research: cell biology, developmental biology, genetics, molecular biology, chemistry, biochemistry, physiology, pharmacology, endocrinology, biology, the medical sciences, and epidemiology. Prostaglandins & Other Lipid Mediators also accepts proposals for special issue topics. The Editors will make every effort to advise authors of the decision on the submitted manuscript within 3-4 weeks of receipt.
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