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Laboratory of Neuroendocrinology, The Babraham Institute, Cambridge, United Kingdom CB2 4AT; and the Department of Neuroendocrinology, Division of Neuroscience, Imperial College Medical School (H.E.M., G.E.G.), London, United Kingdom W6 8RF
Address all correspondence and requests for reprints to: Dr. Allan E. Herbison, Laboratory of Neuroendocrinology, The Babraham Institute, Cambridge, United Kingdom CB2 4AT. E-mail: allan.herbison{at}bbsrc.ac.uk
The sexually dimorphic profile of GH secretion is thought to be
engendered by gonadal steroids acting in part on hypothalamic
periventricular somatostatin (SOM) neurons. The present study set out
to examine and characterize the development of sex differences in these
SOM neurons. In the first series of experiments, we used in
situ hybridization to examine SOM messenger RNA (mRNA)
expression within the periventricular nucleus (PeN) of male and female
rats on postnatal day 1 (P1), P5, and P10. Cellular SOM mRNA content
was found to increase from P1 to P10 in both sexes
(P < 0.01), but was 24% (P <
0.05) and 38% (P < 0.01) higher in males on P5
and P10, respectively. A second series of experiments examined the SOM
peptide content of the PeN in developing rats and found increasing
levels from P1 to P10, with a 44% higher SOM content in males compared
with females on P10 (P < 0.05). The third series
of experiments questioned the role of gonadal steroids in engendering
sex differences in SOM mRNA expression by determining the effects of
neonatal gonadectomy (GDX) and replacement of dihydrotestosterone or
estradiol benzoate. The SOM mRNA content of PeN neurons in P5 males
gonadectomized on the day of birth was the same as that in P5 females
and was significantly reduced compared with that in sham-operated P5
males (P < 0.05). Male rats GDX on P1 and treated
with estradiol benzoate from P1 to P5 had cellular SOM mRNA levels
similar to those in intact males on P5, whereas dihydrotestosterone
treatment had no effect. Treatment of intact males with an androgen
receptor antagonist, cyproterone acetate, on P1 had no effect on
cellular SOM mRNA on P5, whereas male rats given the aromatase
inhibitor 1,4,6-androstatriene-3,17-dione from P1 to P5 had lower
(P < 0.05) SOM mRNA levels than controls. In the
final set of experiments, dual labeling immunocytochemistry showed that
SOM neurons in the PeN of P5 rats did not contain estrogen
receptor-
, but expressed androgen receptors in a sexually dimorphic
manner. These results demonstrate that a sex difference in SOM
biosynthesis, which persists into adulthood, develops between P1 and P5
in PeN neurons. Despite the absence of estrogen receptor-
in these
neurons, the organizational influence of testosterone only occurs after
its aromatization to estrogen.
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