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. 2017 Feb 14;11:19–30. doi: 10.2174/2213988501711010019

Table 1.

Cytotoxicity of well-characterized human nephrotoxicants in HK-2 and SA7K Cells.

Nephrotoxicants Cell viability (IC50, µM) Caspase 3/7 (EC50, µM) MMP (IC50, µM)
HK-2 SA7K HK-2 SA7K HK-2 SA7K
Cyclosporine A 19.92±4.17 Inactive Inactive 11.12±1.80 Inactive 10.34±1.86
Potassium dichromate 65.75±14.83 18.65±5.27 Inactive 23.39±1.90 Inactive 72.54±4.91
Cadmium (II) chloride 26.98±4.60 65.23±11.73 Inactive Inactive Inactive Inactive
Citrinin 78.2±0 87.75±0 Inactive 98.46± 0 78.56±9.03 73.96±6.01
Adefovir dipivoxil 64.65±4.38 91.71±11.69 63.23±14.46 84.57±5.51 Inactive 78.21±0
Puromycin 1.30±0.64 3.95±0.64 3.37±0.22 2.55±0.82 Inactive 5.28±2.68
Arsenic trioxide 13.15±1.07 17.19±4.29 Inactive 15.16±6.0 Inactive Inactive
Rifampin 84.57±5.51 69.70±0 Inactive 82.98±6.75 26.89±3.70 15.67±5.70
Tacrolimus Inactive Inactive Inactive Inactive 49.93±0 22.30±0
Tetracycline Inactive Inactive Inactive Inactive Inactive 9.85±0

Data are presented as mean ± SD from two to three experiments. Compounds showing no concentration response were defined as inactive.