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The Journal of Neurophysiology Vol. 81 No. 5 May 1999, pp. 2398-2405
Copyright ©1999 by the American Physiological Society
Department of Neurobiology and Behaviour, State University of New York at Stony Brook, Stony Brook, New York 11794-5230
Seebach, Bradley S.,
Viktor Arvanov, and
Lorne M. Mendell.
Effects of BDNF and NT-3 on Development of Ia/Motoneuron
Functional Connectivity in Neonatal Rats. J. Neurophysiol. 81: 2398-2405, 1999.
Effects of BDNF and NT-3 on development of Ia/motoneuron functional
connectivity in neonatal rats. The effects of neurotrophin administration and neurotrophin removal via administration of tyrosine
kinase (trk) immunoadhesins (trk receptor extracellular domains
fused with IgG heavy chain) on the development of segmental reflexes
were studied in neonatal rats. Brain derived neurotrophic factor
(BDNF), neurotrophin-3 (NT-3), trkB-IgG, and trkC-IgG were delivered via subcutaneous injection on days 0, 2, 4, and 6 of postnatal life. Electrophysiological analysis of EPSPs recorded intracellularly in L5 motoneurons in response to
stimulation of dorsal root L5 was carried out on postnatal
day 8 in the in vitro hemisected spinal cord. Treatment with BDNF
resulted in smaller monosynaptic EPSPs with longer latency than those
in controls. EPSP amplitude became significantly larger when BDNF was
sequestered with trkB-IgG, suggesting that BDNF has a tonic action on
the development of this synapse in neonates. Treatment with NT-3
resulted in larger EPSPs, but the decrease noted after administration
of trkC-IgG was not significant. Neurotrophins had little effect on the
response to high-frequency dorsal root stimulation or on motoneuron
properties. Polysynaptic components were exaggerated in BDNF-treated
rats and reduced after NT-3 compared with controls. As in control
neonates the largest monosynaptic EPSPs in NT-3 and trkB-IgG-treated
preparations were observed in motoneurons with relatively large values
of rheobase, probably those that are growing the most rapidly. We
conclude that supplementary NT-3 and BDNF administered to neonates can
influence developing Ia/motoneuron synapses in the spinal cord but with
opposite net effects.
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