2009•Journal of Hepatobiliary SurgeryRequires access

EFFECTS FO EICOSAPENTAENOIC ACID ON PROLIFERATION OF HEPG2 CELLS

Jingyu Cao

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Abstract

Objective To study the effets of eicosapentaenoic acid (EPA)on the proliferation of HepG2 cells.Methods In,the EPA was added in the culture for the HepG2 cells.The proliferation of HepG2 cells was detected by MTT method,and the cell configuration was evaluated by fluorescent staining and transmission electron microspe,and the apoptosis was detected by flow cytometry (FCM).Results Compared with control group,the inhibition ration of the HepG2 cells in concentrations of EPA 45 μg/ml and 60 μg/ml is 36.7% and 52.1%,68.1% and 94.8%,94.2% and 99.7% on the 24 h,48 h and 72.An increasing of apoptosis on the test group was found by fluorescent staining,TEM,and FCM.Conclusions The HepG2 cells were inhibited by EPA and its effect depended on time and concentration of EPA.The phenomenon may be related with the apoptosis.

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Objective To study the effets of eicosapentaenoic acid (EPA)on the proliferation of HepG2 cells.Methods In,the EPA was added in the culture for the HepG2 cells.The proliferation of HepG2 cells was detected by MTT method,and the cell configuration was evaluated by fluorescent staining and transmission electron microspe,and the apoptosis was detected by flow cytometry (FCM).Results Compared with control group,the inhibition ration of the HepG2 cells in concentrations of EPA 45 μg/ml and 60 μg/ml is 36.7% and 52.1%,68.1% and 94.8%,94.2% and 99.7% on the 24 h,48 h and 72.An increasing of apoptosis on the test group was found by fluorescent staining,TEM,and FCM.Conclusions The HepG2 cells were inhibited by EPA and its effect depended on time and concentration of EPA.The phenomenon may be related with the apoptosis.

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Available abstract

Objective To study the effets of eicosapentaenoic acid (EPA)on the proliferation of HepG2 cells.Methods In,the EPA was added in the culture for the HepG2 cells.The proliferation of HepG2 cells was detected by MTT method,and the cell configuration was evaluated by fluorescent staining and transmission electron microspe,and the apoptosis was detected by flow cytometry (FCM).Results Compared with control group,the inhibition ration of the HepG2 cells in concentrations of EPA 45 μg/ml and 60 μg/ml is 36.7% and 52.1%,68.1% and 94.8%,94.2% and 99.7% on the 24 h,48 h and 72.An increasing of apoptosis on the test group was found by fluorescent staining,TEM,and FCM.Conclusions The HepG2 cells were inhibited by EPA and its effect depended on time and concentration of EPA.The phenomenon may be related with the apoptosis.

Key concepts: Eicosapentaenoic acid, Apoptosis, Flow cytometry, Fluorescent staining, Staining, Cell growth, Medicine, Molecular biology

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