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자료유형
학술저널
저자정보
Jang, Sun Hee (Department of Acupuncture & Moxibution Medicine, College of Korean Medicine, Dong-Eui University) Yoon, Hyun Min (Department of Acupuncture & Moxibution Medicine, College of Korean Medicine, Dong-Eui University) Kim, Bum Hoi (Department of Anatomy, College of Korean Medicine, Dong-Eui University) Jang, Kyung Jeon (Department of Acupuncture & Moxibution Medicine, College of Korean Medicine, Dong-Eui University) Kim, Cheol Hong (Department of Acupuncture & Moxibution Medicine, College of Korean Medicine, Dong-Eui University)
저널정보
대한침구의학회 대한침구의학회지 Journal of acupuncture research 제32권 제1호
발행연도
2015.1
수록면
13 - 22 (10page)

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Objectives : Alcohol-related liver disease is a major cause of morbidity and mortality worldwide. The present study was undertaken to determine whether Ganoderma lucidum pharmacopuncture(GLP) could protect against chronic liver injury induced by ethanol intoxication in rats. Methods : Sprague-Dawley rats were divided into 4 groups: normal, control, normal saline pharmacopuncture(NP), and GLP, with 8 animals in each. Each group, except normal, received ethanol orally. The NP and GLP groups were treated daily with NP and GLP respectively. The control group was not treated. All rats except the normal group were intoxicated for 4 weeks by oral administration of EtOH(6 g/kg BW). Two acupuncture points were used: Qimen($LR_{14}$) and Taechung($LR_3$). Body weight, histopathological analysis, liver function, activities of antioxidant enzymes, and immunohistochemistry were assessed. Results : GLP reduced the histological changes due to chronic liver injury induced by EtOH and significantly reduced the increase in the alanine aminotransferase(ALT) and aspartate aminotransferase(AST) enzymes. It significantly reversed the superoxide dismutase(SOD) and the catalase activities(CAT). It also significantly decreased BAX and increased Bcl-2 immunoreactivity expression. Conclusions : This study showed the protective efficacy of GLP against EtOH-induced chronic liver injury in SD rats by modulating ethanol metabolizing enzymes activity, attenuating oxidative stress, and inhibiting mitochondrial damage-mediated apoptosis.

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