L. Dicroce et al., INDEPENDENT BEHAVIOR OF RAT-LIVER LDL RECEPTOR AND HMGCOA REDUCTASE UNDER ESTROGEN-TREATMENT, Biochemical and biophysical research communications, 224(2), 1996, pp. 345-350
The main molecules of hepatic cholesterol homeostasis are HMGCoA reduc
tase, the key enzyme of the biosynthetic pathway, and LDL receptor, re
sponsible for the uptake of plasma lipoproteins. Estrogens are reporte
d to cause hypolipidemia in mammalians inducing hepatic LDL receptor.
The effect of such hormones on HMGCoA reductase is very ambiguous. The
mechanism and the time-dependence of the effects of these hormones on
HMGCoA reductase and LDL receptor in rat liver have been investigated
at mRNA and protein levels, at different times after estrogen adminis
tration. Estrogens cause an early increase of LDLr, at both mRNA and p
rotein level, and an increase of HMGCoA reductase, just at protein lev
el, detectable only after 5 days. The independent behavior of LDLr and
HMGCoA reductase under estrogen treatment suggests a not coordinate r
egulation by these hormones. (C) 1996 Academic Press, Inc.