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-Aminobutyric AcidA Receptor Manipulation on Migrating Gonadotropin-Releasing Hormone Neurons through the Entire Migratory Route in Vivo and in Vitro1
Eunice Kennedy Shriver Center, Division of Biomedical Sciences, Waltham, Massachusetts 02452
Address all correspondence and requests for reprints to: Dr. Elizabeth Bless, Eunice Kennedy Shriver Center, 200 Trapelo Road, Waltham, Massachusetts 02452. E-mail: ebless{at}shriver.org
GnRH neurons originate in the nasal compartment and migrate along
vomeronasal fibers over the cribiform plate to the forebrain.
Previously, we found
-aminobutyric acid (GABA) present in GnRH
neurons during development. To clarify the influence of GABA across the
entire GnRH migration route, we examined the effects of muscimol and
bicuculline (GABAA agonist and antagonist) in
vivo and in vitro, maintaining the integrity of
the nasal-forebrain connection. For in vivo experiments,
mice were administered muscimol, bicuculline, or vehicle on days 1015
of pregnancy and were killed on embryonic day 15 (E15). For in
vitro experiments, 250-µm parasagittal slices of whole heads
of E13 mice were incubated with muscimol, bicuculline, or vehicle for 2
days. Muscimol inhibited GnRH cell migration and decreased extension of
GnRH fibers. Bicuculline treatment led to a disorganized distribution
of GnRH cells in the forebrain and a concomitant dissociation of GnRH
cells from fibers of guidance. These results suggest that GABAs
influence on GnRH development changes as the cells move out of the
nasal compartment and extend processes toward the median eminence.
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