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The Journal of Neurophysiology Vol. 86 No. 1 July 2001, pp. 463-474
Copyright ©2001 by the American Physiological Society
1The Center for Neurobiology and Behavior and 2Department of Anatomy and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York 10032
Barazangi, Nobl and
Lorna W. Role.
Nicotine-Induced Enhancement of Glutamatergic and GABAergic
Synaptic Transmission in the Mouse Amygdala. J. Neurophysiol. 86: 463-474, 2001. Presynaptic nicotinic
acetylcholine receptors (nAChRs) are thought to mediate some of the
cognitive and behavioral effects of nicotine. The olfactory projection
to the amygdala, and intra-amygdaloid projections, are limbic relays
involved in behavioral reinforcement, a property influenced by
nicotine. Co-cultures consisting of murine olfactory bulb (OB) explants
and dispersed amygdala neurons were developed to reconstruct this
pathway in vitro. Whole cell patch-clamp recordings were obtained from
amygdala neurons contacted by OB explant neurites, and spontaneous and
evoked synaptic currents were characterized. The majority of the 108 innervated amygdala neurons exhibited glutamatergic spontaneous
postsynaptic currents (PSCs), 20% exhibited GABAergic spontaneous
PSCs, and 17% exhibited both. Direct extracellular stimulation of OB
explants elicited glutamatergic synaptic currents in amygdala neurons.
Antibodies to nAChR subunits co-localized with an antibody to synapsin
I, a presynaptic marker, along OB explant processes, consistent with the targeting of nAChR protein to presynaptic sites of the mitral cell
projections. Hence, we examined the role of presynaptic nAChRs in
modulating synaptic transmission in the OB-amygdala co-cultures. Focal
application of 500 nM to 1 µM nicotine for 5-60 s markedly increased
the frequency of spontaneous PSCs, without a change in the amplitude,
in 39% of neurons that exhibited glutamatergic spontaneous PSCs
(average peak fold increase = 125.2 ± 33.3). Nicotine also
enhanced evoked glutamatergic currents elicited by direct stimulation
of OB explant fibers. Nicotine increased the frequency of spontaneous
PSCs, without a change in the amplitude, in 35% of neurons that
exhibited GABAergic spontaneous PSCs (average peak fold increase = 63.9 ± 34.3). Thus activation of presynaptic nAChRs can modulate
glutamatergic as well as GABAergic synaptic transmission in the
amygdala. These results suggest that behaviors mediated by olfactory
projections may be modulated by presynaptic nAChRs in the amygdala,
where integration of olfactory and pheromonal input is thought to occur.
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