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Korean Red Ginseng Extract Suppresses the Progression of Alcoholic Fatty Liver in a Rat Model

Authors
Park, Yoo-SinKang, Ju-Seop
Issue Date
Dec-2011
Publisher
PHARMACEUTICAL SOC JAPAN
Keywords
Korean red ginseng; alcoholic fatty liver; fibrosis
Citation
JOURNAL OF HEALTH SCIENCE, v.57, no.6, pp.512 - 520
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF HEALTH SCIENCE
Volume
57
Number
6
Start Page
512
End Page
520
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/166963
DOI
10.1248/jhs.57.512
ISSN
1344-9702
Abstract
Alcoholic fatty liver (AFL) is the most common liver disease among Korean men, and Korean red ginseng has been used as a folk medicine to diverse diseases in Korea. Therefore, we examined if Korean red ginseng extract (KRG) could be a suppressive agent on AFL in a rat model or not. Experimental rats were fed the Lieber DeCarli diet with 36% of energy intake from ethanol, and divided into three groups which daily co-administered KRG 0, 700 and 1400 mg/kg for six weeks, respectively. Naive rats were fed iso-caloric control diet without ethanol and KRG. We investigated histopathological hepatic characteristics, hepatic and plasma lipid concentrations, hepatic hydroxyproline contents, heart/liver radioactivity ratio of (201)Thallium and liver/body weight of the rats at the end point. Ethanol intake brought about steatotic, inflammatory, necrotic and fibrotic changes of livers significantly, and it also lead the rats to increase hepatic triglyceride and hydroxyproline contents, plasma total cholesterol and low density lipoprotein cholesterol levels, and liver/body weight. However, co-administration of KRG 1400 mg/kg suppressed fat accumulation and fibrotic initiation in AFL rat model significantly. It was also inclined to attenuate inflammatory cell infiltration, hydroxyproline accumulation, and increasing liver/body weight, even though plasma lipid levels and heart/liver ratios were not successfully improved by six-week-long intakes of KRG. In conclusions, co-administration of KRG 1400 mg/kg could significantly suppress steatosis in AFL rat model, and it might need longer ingestion of KRG than six weeks to improve plasma lipid imbalance.
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