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J Neurophysiol 78: 1735-1739, 1997;
0022-3077/97 $5.00
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The Journal of Neurophysiology Vol. 78 No. 3 September 1997, pp. 1735-1739
Copyright ©1997 The American Physiological Society

RAPID COMMUNICATION


Differential Impact of Miniature Synaptic Potentials on the Soma and Dendrites of Pyramidal Neurons In Vivo

Denis Paré1, Elen Lebel1, and Eric J. Lang2

1 Département de Physiologie, Faculté de Médecine, Université Laval, Quebec G1K 7P4, Canada; and 2 Department of Physiology and Neuroscience, New York University Medical Center, New York, New York 10016

Paré, Denis, Elen LeBel, and Eric J. Lang. Differential impact of miniature synaptic potentials on the somata and dendrites of pyramidal neurons in vivo. J. Neurophysiol. 78: 1735-1739, 1997. We studied the impact of transmitter release resistant to tetrodotoxin (TTX) in morphologically identified neocortical pyramidal neurons recorded intracellularly in barbiturate-anesthetized cats. It was observed that TTX-resistant release occurs in pyramidal neurons in vivo and at much higher frequencies than was previously reported in vitro. Further, in agreement with previous findings indicating that GABAergic and glutamatergic synapses are differentially distributed in the somata and dendrites of pyramidal cells, we found that most miniature synaptic potentials were sensitive to gamma -aminobutyric acid-A (GABAA) or alpha -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) antagonists in presumed somatic and dendritic impalements, respectively. Pharmacological blockage of spontaneous synaptic events produced large increases in input resistance that were more important in dendritic (approx 50%) than somatic (approx 10%) impalements. These findings imply that in the intact brain, pyramidal neurons are submitted to an intense spike-independent synaptic bombardment that decreases the space constant of the cells. These results should be taken into account when extrapolating in vitro findings to intact brains.




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