Table 2

Formation of hydroxylated testosterone metabolites in freshly isolated and cryopreserved rat liver PC held in suspension at 37°C for up to 2 h

MetaboliteHydroxylated Testosterone Metabolite Formed in
Freshly isolated cellsCryopreserved cells
t = 0 mint = 30 mint = 60 mint = 120 mint = 0 mint = 30 mint = 60 mint = 120 min
pmol/min/mg protein
16α-OHT582  ± 150522  ± 108530  ± 89505  ± 103557  ± 158523  ± 133478  ± 104355  ± 97
2α-OHT523  ± 166498  ± 150459  ± 125430  ± 129421  ± 126352  ± 110350  ± 94238  ± 77
6β-OHT226  ± 34177  ± 25167  ± 50128  ± 27* 180  ± 38204  ± 36135  ± 2286  ± 18*
2β-OHT60  ± 1542  ± 1831  ± 7* 17  ± 3* 41  ± 1631  ± 722  ± 614  ± 4*
7α-OHT57  ± 1542  ± 1040  ± 1338  ± 1136  ± 1139  ± 1031  ± 724  ± 7
15β-OHT56  ± 1255  ± 949  ± 850  ± 1053  ± 755  ± 1149  ± 841  ± 7

Data are expressed as mean ± S.D. of four independent rat PC isolations and their corresponding cryopreserved counterparts.

  • ∗, significantly different from the corresponding t = 0 value (p < .05, Dunnett's test).