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

AI Article Synopsis

  • - Chlorogenic acids (CGA), found in green coffee beans, may help reduce cardiometabolic risk factors, and a study investigated the effects of a water-based green coffee extract (GCE) on mice with a specific diet for 14 weeks.
  • - While GCE didn't lower blood fat levels or prevent artery damage, it led to positive changes like improved fasting glucose, reduced insulin resistance, and lower liver fat, alongside reduced weight gain and inflammation.
  • - The study also showed that GCE influenced liver-related immune factors and altered gut microbiota, indicating potential pathways for its health benefits in cardiometabolic conditions.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470615PMC
http://dx.doi.org/10.3390/nu11030497DOI Listing

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