JIANG Zhi-tao, WANG Xue, WANG Jian-chun, et al. Effect of Sedi Herba Total Flavanones and Isorhamnetin on APAP-induced Injured L02 Cells[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(6): 121-125.
JIANG Zhi-tao, WANG Xue, WANG Jian-chun, et al. Effect of Sedi Herba Total Flavanones and Isorhamnetin on APAP-induced Injured L02 Cells[J]. Chinese journal of experimental traditional medical formulae, 2018, 24(6): 121-125. DOI: 10.13422/j.cnki.syfjx.20180631.
Objective: To study the protective effect of Sedi Herba total flavanones and isorhamnetin on the acetaminophen (APAP)-induced injury of human normal hepatocytes (L02).Method: L02 cells were stimulated with different concentrations of APAP to prepare the injury model
and the effective stimulating concentration of APAP was screened. APAP-induced L02 cell injury models were thencopied
and the effect of Sedi Herba total flavanones and isorhamnetin on the activity of L02 cells induced by APAP was analyzed by cell counting kit-8 (CCK-8) method.The contents of malondialdehyde (MDA) and glutathione (GSH)
activity of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px)
and levels of alanine aminotransferase (ALT)
andaspartate aminotransferase (AST) in supernatant were measured.Result: As compared with the normal group
the activity of L02 cells treated with different concentrations of APAP was significantly decreased
and the selected modeling condition was 10 mmol · L-1 for 24 h. The MDA content in the supernatant of the model group was increased and the GSH content was decreased
SOD and GSH-Px activity decreased
AST and ALT levels increased(P<0.05
P<0.01). As compared with the model group
the Sedi Herba total flavanones and isorhamnetin could significantly increase the survival rate of APAP-injured cells
decrease the content of MDA
increase the content of GSH
increase the activity of SOD and GSH-Px activity
and lower the release of ALT and AST(P<0.05
P<0.01).Conclusion: The Sedi Herba total flavanones and isorhamnetin have a good protective effect on APAP-injured L02 cells.