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. Author manuscript; available in PMC: 2009 Apr 3.
Published in final edited form as: Toxicology. 2008 Jan 6;246(1):63–72. doi: 10.1016/j.tox.2007.12.025

Table 3.

Esterification of E2 by liver microsomes from control and clofibrate-fed ACI rats

Treatment E2 mg in pellet E2-oleoyl-ester formed (pmol/mg protein/min) E2-oleoyl-ester formed (nmol/liver/min)
6 weeks
A. AIN-76A 0 12 ± 2 1.10 ± 0.17
B. AIN-76A 1 9 ± 2 1.08 ± 0.05
C. 0.4% Clofibrate 1 85 ± 3# 14.32 ± 1.67#
D. AIN-76A 3 8 ± 2 0.66 ± 0.15
E. 0.4% Clofibrate 3 74 ± 8# 13.21 ± 1.91#
F. 0.4% Clofibrate 0 72 ± 7* 12.50 ± 0.69*
12 weeks
A. AIN-76A 0 15 ± 2 1.30 ± 0.08
B. AIN-76A 1 14 ± 2 1.23 ± 0.12
C. 0.4% Clofibrate 1 55 ± 9# 10.53 ± 1.30#
D. AIN-76A 3 7 ± 2* 0.61 ± 0.12*
E. 0.4% Clofibrate 3 20 ± 3# 5.22 ± 1.26#
F. 0.4% Clofibrate 0 28 ± 5* 4.65 ± 0.91*

Liver microsomes (1 mg protein/ml) were incubated at 37 °C for 30 min with 50 μM [3H]-E2 (3 μCi), 100 μM oleoyl-CoA. Data are presented as the mean ± S.E. of five animals per group.

*

Statistically different from the control group receiving only a 20 mg cholesterol pellet,

#

Statistically different from the group receiving same amount of E2, P <0.05). (ANOVA followed by Bonferroni hoc post test)