Abstract:
This work aims to investigate the role of simvastatin (SIM) in renal tubular epithelial cells (HK-2)
proliferation. The apoptosis model of HK-2 cells induced by high glucose was established; HK-2 cells were cultured in
vitro and randomly divided into control group, model group, SIM low-dose group, SIM medium-dose group and SIM
high-dose group. After 24 h culture, the inhibitory effect of SIM on high glucose- induced proliferation of HK-2 cells
was evaluated by MTT method. The expression of cysteinyl aspartate specific proteinase (Caspase-3) in apoptosisrelated protein was evaluated by Western blotting; miR-92a expression in HK-2 cells was measured by RT-qPCR. High
glucose group had significantly lower HK-2 cell survival rate than the control group (p<0.05); SIM middle-dose and
high-dose groups had higher HK-2 cell survival rate than the model group, (p<0.05); SIM low, medium and high-dose
groups had lower HK-2 cell apoptosis rate, Caspase-3 protein and miR-92a expression levels than the model group
(p<0.05), all showing dose-dependence.
