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Neurobiology of Aging Laboratories and Fishberg Research Center for Neurobiology (M.M.A., R.A.F., A.C.G.), and Henry L. Schwartz Department of Geriatrics and Adult Development (A.C.G.), Mount Sinai School of Medicine, New York, New York 10029
Address all correspondence and requests for reprints to: Andrea C. Gore, Ph.D., Mount Sinai School of Medicine, Neurobiology of Aging Laboratories, One Gustave L. Levy Place, Box 1639, New York, New York 10029. E-mail: gore{at}msvax.mssm.edu
During the neonatal period, the brain is subject to profound
alterations in neuronal circuitry due to high levels of synaptogenesis
and gliogenesis. In neuroendocrine regions such as the preoptic
area-anterior hypothalamus (POA-AH), the site of GnRH perikarya, these
changes could affect the maturation of GnRH neurons. Because the GnRH
system is developmentally regulated by glutamatergic neurons, we
hypothesized that changes in the
N-methyl-D-aspartate (NMDA) receptor system
begin early in postnatal development, before the onset of puberty,
thereby playing a role in establishing the appropriate environment for
the subsequent maturation of GnRH neurons. To this end, we determined
developmental changes in NMDA receptors, alterations in GnRH gene
expression, and the regulation of GnRH neurons by the NMDA receptor
system in developing male and female rats. In Exp I, NMDA receptor
subunit (NR) 1 mRNA levels in the POA-AH were found to increase
significantly (
5-fold) from E18 through P10 in both males and
females. NR2b mRNA increased significantly between P0 and P5 in both
males and females. In contrast, NR2a subunit mRNA, which was in very
low abundance in both males and females, increased only in males
between P10 and P15. In Exp II we determined that GnRH gene expression
changes differentially in developing male and female rats, with
increases from P0 to P5 in males, and decreases from P5 to P10 in
females. This latter effect in females is attributed to a change in
GnRH gene transcription because GnRH primary transcript RNA levels
paralleled changes in GnRH mRNA levels. In Exp III, we tested effects
of treatment with an NMDA receptor analog on GnRH mRNA levels and found
that only P5 and P10 male rats responded to NMDA receptor activation
with an increase in GnRH mRNA levels, via a posttranscriptional
mechanism. This greater responsiveness of males to NMDA receptor
stimulation may be due to differences in the composition and levels of
NMDA receptor subunits. Exp IV examined the localization of NR1 in the
POA-AH during neonatal development. No GnRH neurons were immunopositive
for NR1, indicating that effects of glutamate on GnRH neurons are
mediated by interneurons or other glutamate receptor subunits or types.
Taken together, these data indicate that glutamatergic inputs to the
POA-AH change dramatically during the early postnatal period, before
puberty and before the GnRH system is fully responsive to glutamate,
consistent with the hypothesis that the maturation of inputs to GnRH
neurons, and the establishment of the proper neurotransmitter
"milieu" enabling the activation of GnRH neurons, occurs before the
onset of puberty.
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