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Vol. 30, Issue 2, 141-147, February 2002
Laboratories of Biochemistry, University of Pennsylvania School of
Veterinary Medicine, Philadelphia, Pennsylvania
Rat liver, as well as other species, contains numerous
sex-dependent isoforms of cytochrome P450 (P450) that are
regulated by the sexually dimorphic profiles of circulating growth
hormone. During puberty, young adulthood, and senescence, changes in
the hormonal profiles appear to be responsible for alterations in age-associated expression levels of selective P450 isoforms. In contrast, little is known about the growth hormone secretory profiles and their P450-dependent expression levels during middle age. In the
present study, we observed subtle changes in the hormonal concentrations, and frequencies of peaks and interpulse periods in the
sexually dimorphic growth hormone profiles of 1-year-old male and
female rats correlated to suppression of male-specific isoforms CYP2C11
and CYP2C13 and female-predominant CYP2C7. To identify possible causes
for the age-associated changes in the circulating growth hormone
profiles, the responsiveness of the hypothalamic-pituitary axis to
growth hormone secretagogues clonidine and growth hormone-releasing
factor (GRF) were examined in middle-aged male and female rats. In
spite of the same sexually dimorphic response in young adult and
middle-aged rats to both secretogogues (males > females), the
pituitary somatotrophs in the older animals exhibited a dramatic
decrease in sensitivity to clonidine, characterized by subnormal growth
hormone release levels and an inordinate delay in pituitary response to
clonidine stimulation. Results from similar studies conducted on
middle-aged arcuate nucleus-lesioned rats suggest that a decline in GRF
secretion is a possible contributor to the age-associated alterations
in plasma growth hormone profiles during middle age. These changes in
GRF-induced, sexually dimorphic secretory growth hormone profiles and
the accompanying decline in P450 expression levels may anticipate
similar, but more profound, changes to occur during senescence.
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