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绿咖啡提取物可改善高脂饮食喂养的 ApoE 小鼠的心脏代谢参数并调节肠道微生物群。

Green Coffee Extract Improves Cardiometabolic Parameters and Modulates Gut Microbiota in High-Fat-Diet-Fed ApoE Mice.

机构信息

Grupo Inmunomodulación-GIM, Universidad de Antioquia. Calle 70 No. 52-21, 050010 Medellín, Colombia.

Vidarium⁻Nutrition, Health and Wellness Research Center, Grupo Empresarial Nutresa. Calle 8 Sur No. 50-67, 050023 Medellín, Colombia.

出版信息

Nutrients. 2019 Feb 27;11(3):497. doi: 10.3390/nu11030497.

Abstract

Chlorogenic acids (CGA) are the most abundant phenolic compounds in green coffee beans and in the human diet and have been suggested to mitigate several cardiometabolic risk factors. Here, we aimed to evaluate the effect of a water-based standardized green coffee extract (GCE) on cardiometabolic parameters in ApoE mice and to explore the potential underlying mechanisms. Mice were fed an atherogenic diet without (vehicle) or with GCE by gavage (equivalent to 220 mg/kg of CGA) for 14 weeks. We assessed several metabolic, pathological, and inflammatory parameters and inferred gut microbiota composition, diversity, and functional potential. Although GCE did not reduce atherosclerotic lesion progression or plasma lipid levels, it induced important favorable changes. Specifically, improved metabolic parameters, including fasting glucose, insulin resistance, serum leptin, urinary catecholamines, and liver triglycerides, were observed. These changes were accompanied by reduced weight gain, decreased adiposity, lower inflammatory infiltrate in adipose tissue, and protection against liver damage. Interestingly, GCE also modulated hepatic IL-6 and total serum IgM and induced shifts in gut microbiota. Altogether, our results reveal the cooccurrence of these beneficial cardiometabolic effects in response to GCE in the same experimental model and suggest potential mediators and pathways involved.

摘要

绿原酸(CGA)是咖啡豆和人类饮食中含量最丰富的酚类化合物,有研究表明它可以减轻几种心血管代谢风险因素。在这里,我们旨在评估水基标准化绿原酸提取物(GCE)对 ApoE 小鼠心血管代谢参数的影响,并探讨其潜在的机制。小鼠在 14 周内喂食致动脉粥样硬化饮食(不添加或添加 GCE,相当于 220mg/kg 的 CGA)。我们评估了几种代谢、病理和炎症参数,并推断了肠道微生物群落的组成、多样性和功能潜力。尽管 GCE 并未减少动脉粥样硬化病变的进展或降低血浆脂质水平,但它诱导了重要的有益变化。具体而言,观察到空腹血糖、胰岛素抵抗、血清瘦素、尿儿茶酚胺和肝甘油三酯等代谢参数的改善。这些变化伴随着体重增加减少、脂肪减少、脂肪组织中炎症浸润减少以及对肝损伤的保护。有趣的是,GCE 还调节了肝脏中的 IL-6 和总血清 IgM,并诱导了肠道微生物群落的变化。总的来说,我们的结果揭示了在相同的实验模型中,GCE 对这些有益的心血管代谢作用的同时发生,并提出了可能涉及的潜在介质和途径。

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