ReferenceID 5669

Mangiferin protects against alcoholic liver injury via suppression of inflammation-induced adipose hyperlipolysis

Food Funct

Adipose dysfunction is closely associated with alcoholic liver disease. The impact of mangiferin on ethanol-induced liver injury and the probable underlying molecular mechanism has not been sufficiently addressed. In the

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Reference Id
5669
Evidence Id
22259
Core Evidence Id
22259
Source Reference Id
4586
Herb2 Reference Id
HBREF005383
Subject Paper Key
HBIN034394_32969440
Pubmed Id
32969440
Doi
10.1039/d0fo01436b
Paper Title
Mangiferin protects against alcoholic liver injury via suppression of inflammation-induced adipose hyperlipolysis
Paper Abstract
Adipose dysfunction is closely associated with alcoholic liver disease. The impact of mangiferin on ethanol-induced liver injury and the probable underlying molecular mechanism has not been sufficiently addressed. In the present study, mice were subjected to a chronic plus a single binge ethanol feeding to induce liver injury. In addition, the differentiated adipocytes from primary mouse adipocytes were isolated and used for the mechanism studies. Our study demonstrated that mangiferin protects against ethanol induced adipose hyperlipolysis by restoring PDE3B stability, which is associated with activating the AMPK/TBK1 signaling and suppressing the noncanonical NF-kappaB activation, leading to the reduction of free fatty acid release and the amelioration of ethanol-induced liver injury. Our findings identify that mangiferin ameliorates alcoholic liver injury via suppression of inflammation-induced adipose hyperlipolysis, suggesting that mangiferin might be a potential effective agent for the management of alcoholic liver injury.
Journal
Food Funct
Publish Year
2020
Experiment Subject
mouse
Experiment Type
Animal & Cell Experiment
Phenotype Related
Alcoholic Liver Disease; Alcoholic Liver Injury; Ethanol-induced Liver Injury; Adipose Dysfunction; Liver Injury
Paper Title Cn
Paper Title En
Mangiferin protects against alcoholic liver injury via suppression of inflammation-induced adipose hyperlipolysis
Bilingual Status
semi_complete