Key result
Wampee extract attenuated metabolic cardiomyopathy in mice by improving heart function, reducing intestine permeability, and suppressing inflammation via modulation of gastrointestinal microbiota.
Why the study?
Wampee has various biological functions, prompting an evaluation of its protective effects against metabolic cardiomyopathy by focusing on gastrointestinal microbiota.
Wampee extract attenuates metabolic cardiomyopathy in a mouse model by modulating gastrointestinal microbiota and promoting cardio-protective metabolites.
Answers are grounded in this paper and cite their sources.
No clinical adoption warranted from animal data; leaves open wampee alkaloids' role in metabolic cardiomyopathy.
Wampee has various biological functions, and the current study assesses its protective effects against metabolic cardiomyopathy (CMP) by focusing on gastrointestinal microbiota. The composition of wampee extract (WE) was determined, and mice were subjected to CMP model induction before handled with WE. WE improved heart function, reduced intestine permeability, and suppressed inflammation, and the function was attributed to alkaloids including girinimbine and stachydrine. The CMP model and WE had little influence on the alpha diversity, while CMP model changed the beta-diversity of mice microbiota. Duncaniella, Ruminococcus, Aspergillus, and Penicillium were positively correlated with the progression of metabolic CMP, while Muribaculum, Paramuribaculum, and Prevotella were negatively correlated, the abundance of which were restored by WE. The changes in microbes increased function enrichment in pathways related to immune responses and produced cardio-protective metabolites such as norleucine. WE induced a new homeostasis in the GI microbiota of CMP mice, thereby attenuating metabolic CMP.
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Shu et al. (2023) studied Metabolic cardiomyopathy. Wampee extract (WE) was evaluated on Heart function, intestine permeability, inflammation, and gastrointestinal microbiota composition. Wampee extract attenuated metabolic cardiomyopathy in mice by improving heart function, reducing intestine permeability, and suppressing inflammation via modulation of gastrointestinal microbiota.
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