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Hepatoprotective effect of Diospyros lotus leaf extract against acetaminophen-induced acute liver injury in mice
被引:14
作者:

Cho, Byoung Ok
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Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea
Jeonju Univ, Dept Hlth & Sci, Jeonju 55069, Jeonbuk, South Korea Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea

Yin, Hong Hua
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Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea

Fang, Chong Zhou
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h-index: 0
机构:
Jeonju Univ, Dept Hlth & Sci, Jeonju 55069, Jeonbuk, South Korea Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea

Kim, Sang Jun
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机构:
Jeonju Biomat Inst, Jeonju 54810, Jeonbuk, South Korea Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea

Jeong, Seung Il
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h-index: 0
机构:
Jeonju Biomat Inst, Jeonju 54810, Jeonbuk, South Korea Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea

Jang, Seon Il
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h-index: 0
机构:
Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea
Jeonju Univ, Dept Hlth & Sci, Jeonju 55069, Jeonbuk, South Korea Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea
机构:
[1] Ato Q&A Corp, Jeonju 55069, Jeonbuk, South Korea
[2] Jeonju Univ, Dept Hlth & Sci, Jeonju 55069, Jeonbuk, South Korea
[3] Jeonju Biomat Inst, Jeonju 54810, Jeonbuk, South Korea
关键词:
Diospyros lotus;
acetaminophen;
liver injury;
antioxidants;
anti-inflammation;
MEDIATED DNA-DAMAGE;
CARBON-TETRACHLORIDE;
INDUCED HEPATOTOXICITY;
CAFFEIC ACID;
ANTIOXIDANT;
PROTECTS;
RATS;
TOXICITY;
ANIMALS;
D O I:
10.1007/s10068-015-0294-6
中图分类号:
TS2 [食品工业];
学科分类号:
0832 ;
摘要:
The aim of this study was to investigate the protective effect of Diospyros lotus leaf extract (DLE) against acetaminophen (APAP)-induced acute liver injury in mice. Administration of DLE significantly attenuated the levels of serum aspartate aminotransferase, alanine aminotransferase, and liver lipid peroxidation in APAP-treated mice. Histopathological examination showed that DLE treatment decreased the incidence of liver lesions in APAP-treated mice. DLE treatment markedly increased superoxide dismutase, catalase, glutathione peroxidase activity, and glutathione levels in APAP-treated mice. Furthermore, DLE treatment significantly suppressed the production of proinflammatory factors such as the nitric oxide, IL-6, TNF-alpha, and iNOS in APAP-treated mice. These results suggest that DLE protects the liver from APAP-induced hepatic injury via antioxidant and antiinflammatory effects.
引用
收藏
页码:2205 / 2212
页数:8
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