DocumentCode :
2569501
Title :
The protective effects of flavonoids from Astragalus complanatus on carbon tetrachloride induced hepatic fibrosis in mice
Author :
Sun, Li-Bing ; Gu, Zhen-Lun ; Kwok, Ci-Yi ; Wang, Wei-Ping
fYear :
2010
fDate :
16-18 April 2010
Firstpage :
374
Lastpage :
377
Abstract :
Aims: The aim of this study was to investigate the protective effects of FAC in hepatic fibrosis (HF) and the underlined mechanism. Methods: Using KM mice subjected to CCl4-induced HF. At the end of the experiment, the tissues of liver were removed for histopathological examination and SOD, MDA, HYP assays. The expressions of PPARγ were detected by immunohistochemistry. Result: we found that administration of FAC significantly reduced the tissue malondialdehyde (MDA), hydroxypmline (HYP) contents, and also significantly increased superoxide dismutase (SOD) activities compared with model group. As shown in transmission electron microscope and pathological section. FAC treatment could protect hepatocyte in HF mice. Furthermore, it enhanced the expression of peroxisome proliferator -activated receptors γ ( PPARγ).
Keywords :
biological tissues; carbon compounds; cellular biophysics; diseases; drugs; enzymes; injuries; liver; molecular biophysics; organic compounds; proteins; transmission electron microscopy; Astragalus Complanatus; FAC; HYP assay; KM mice; MDA assay; PPARγ; SOD assay; carbon tetrachloride; flavonoid; hepatic fibrosis; hepatocyte; hydroxypmline; immunohistochemistry; liver tissue; malondialdehyde; mice; peroxisome proliferator-activated receptors γ; superoxide dismutase; transmission electron microscope; Animals; Electrochemical machining; Immune system; Injuries; Liver; Mice; Organic materials; Petroleum; Protection; FAC; HF; MDA; PPARγ; SOD;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Bioinformatics and Biomedical Technology (ICBBT), 2010 International Conference on
Conference_Location :
Chengdu
Print_ISBN :
978-1-4244-6775-4
Type :
conf
DOI :
10.1109/ICBBT.2010.5478936
Filename :
5478936
Link To Document :
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