TABLE 1

Bisphenol A glucuronidation by hepatic microsomes

Michaelis-Menten apparent kinetic constants (Vmax and Km) for BPA glucuronidation by hepatic microsomal fractions of early-stage (54- to 57-day-old) and near-term (120- to 135-day-old) ovine fetuses and of adult sheep and humans after incubation with BPA for 20 minutes. Hepatic glucuronidation unbound intrinsic clearance (CLint,u) and extrapolated hepatic clearance (CLH) (mean ± S.D.).

SubjectsVmaxKmCLint,uCLH
pmol/mg microsomal protein per minµMml/min per g of liverml/kg per min
Ovine fetuses
 Early stagea
  Female (n = 3)b15.3 (S.E. 2.26)4.71 (S.E. 2.95)0.075NA
  Male (n = 3)b8.50 (S.E. 1.70)3.41 (S.E. 2.93)0.044NA
 Near-term
  Female (n = 3)519 ± 25810.8 ± 5.941.53 ± 1.164.76 ± 3.68
  Male (n = 3)446 ± 3168.38 ± 7.051.93 ± 1.216.40 ± 4.28
Adult
 Ewes (n = 3)6086 ± 86282.0 ± 18.13.93 ± 0.853.14 ± 0.43
 Humans (n = 3)2770 ± 25059.6 ± 15.69.00 ± 2.477.67 ± 1.35
  • NA, not applicable.

  • a At 54–57 days of pregnancy, several concentrations of BPA-G were below the LOQ (25 nM), so the data were computed together for each sex group to estimate Michaelis-Menten parameters and the associated standard errors (S.E.).

  • b Three pools of two fetuses.