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December 19, 2016Food & Function

Upregulation of caveolin-1 by mulberry leaf extract and its major components, chlorogenic acid derivatives, attenuates alcoholic steatohepatitis via inhibition of oxidative stress

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Key result

Mulberry leaf extract and its chlorogenic derivatives upregulated caveolin-1 and diminished EGFR/STAT3/iNOS signalling, alleviating alcohol-induced hepatocellular disorders in mice.

Why the study?

Does mulberry leaf extract and its chlorogenic acid derivatives attenuate alcoholic steatohepatitis in a high alcohol-fed mouse model?

Population

High alcohol-fed mouse model

Comparison

Mulberry leaf extract and its major components… vs Control (high alcohol-fed mice without treatment)

Design

Preclinical

Authors

YLYi‐Ju LeeJHJeng‐Dong HsuWLWea‐Lung Lin

Discussion

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Member takes

Overview

MLE attenuates alcoholic steatohepatitis in mice; leaves open clinical translation to humans.

Structured PICO

Does mulberry leaf extract and its chlorogenic acid derivatives attenuate alcoholic steatohepatitis in a high alcohol-fed mouse model?

P
Population
High alcohol-fed mouse model used to study alcoholic steatohepatitis.
I
Intervention
Mulberry leaf extract (MLE) and its major components chlorogenic acid (CGA) and neochlorogenic acid (nCGA)
C
Comparator
Control (high alcohol-fed mice without treatment)
O
Outcome
Attenuation of alcoholic steatohepatitis (hepatic injury markers, lipid accumulation, lipid peroxidation, and pro-apoptotic signals)surrogate

Mulberry leaf extract and its chlorogenic acid derivatives attenuate alcoholic steatohepatitis in mice by upregulating caveolin-1 and inhibiting oxidative stress and pro-apoptotic signaling.

Cite This Study

Lee et al. (2016) studied Alcoholic steatohepatitis. Mulberry leaf extract (MLE), chlorogenic acid (CGA), and neochlorogenic acid (nCGA) was evaluated on Hepatic injury markers, lipid accumulation, and lipid peroxidation. Mulberry leaf extract and its chlorogenic derivatives upregulated caveolin-1 and diminished EGFR/STAT3/iNOS signalling, alleviating alcohol-induced hepatocellular disorders in mice.

synapsesocial.com/papers/6a9fd1ffdfc81ffeb871e0afhttps://doi.org/10.1039/c6fo01539e
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