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Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury.

Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury. Research Abstract Details 

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  • Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury. Abstract Text:

    hua xuHua Xu,guang-fan haiGuang-Fan Hai,ji-zhou xiangJi-Zhou Xiang,cheng-can yaoCheng-Can Yao,qing zhengQing Zheng,qi-hao zhangQi-Hao Zhang,hai hongHai Hong,

    Aim: To study whether non-mitogenic human acidic fibroblast growth factor (nm-haFGF) has protective effects on H(2)O(2)-induced hepatocyte injury in vitro and CCl(4)-induced hepatocyte injury in vivo. Methods: (i) HL-7702 hepatocytes were incubated with different concentrations of nm-haFGF for 12 h, and then the activity of lactate dehydrogenase (LDH) in culture medium was detected, and genomic DNA electrophoresis analysis was observed after being exposed to H(2)O(2) (8 mmol/L) for 4 h. Proximately, apoptotic rates and protein expressions of Bcl-2 and Bax of HL-7702 cell were detected after being exposed to H(2)O(2) (0.2 mmol/L) for 20 h. (ii) Being injected intraperitoneally with nm-haFGF, mice were treated with CCl(4) intraperitoneally to induce hepatic injury. Twenty-four hours later, serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were measured and histopathologic changes were evaluated. Results: (i) In vitro tests: LDH activities and apoptotic rates decreased, the protein expression of Bcl-2 increased and Baxdecreased in nm-haFGF-treated groups at the concentrations of 100 150 and 200 ng/mL, compared with that in the model control group, which was treated with H(2)O(2) alone. The genomic DNA remained nearly intact at the concentrations of 150 and 200 ng/mL. (ii) In vivo tests: serum ALT and AST in nm-haFGF-treated groups (10 mug/kg and 20 mug/kg) were much lower as compared to the model control group, which was treated with CCl(4) alone. Histological examination showed that nm-haFGF markedly ameliorated hepatocytes vacuolation, cloudy swelling and inflammatory cells infiltration induced by CCl(4). Conclusion: nm-haFGF had protective effects against H(2)O(2)-induced hepatocyte injury in vitro and CCl(4)-induced acute liver injury in vivo.

    Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury. Publishing Authors By Initials

    h xuH Xu,gf haiGF Hai,jz xiangJZ Xiang,cc yaoCC Yao,q zhengQ Zheng,qh zhangQH Zhang,h hongH Hong,

    For similar abstracts research abstracts see: abstracts research

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    Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Hepatology research : the official journal of the

    VOLUME: 37

    Page Numbers: 836-44

    Journal Abbreviation: Hepatol. Res.

    ISSN: 1386-6346

    DAY: 15

    MONTH: 06

    YEAR: 2007

    Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury. Information

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    LANGUAGE: eng

    NlmUniqueID: 9711801

    Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury. Keywords Mesh Terms:

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    Grant and Affiliation Information for Protective effect of non-mitogenic human acidic fibroblast growth factor on hepatocyte injury.

    AFFILIATION: Tongji Medical College, Huazhong University of Science and Technology, Wuhan, and Pharmacy College, Ji-nan University, Guangzhou, China.

    Country: Netherlands

    Netherlands Research PublicationNetherlands Research Publication

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    MEDLINETA: Hepatol Res

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