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J Physiol Volume 558, Number 1, 193-211, July 1, 2004 DOI: 10.1113/jphysiol.2004.061416
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Burst generation in rat pyramidal neurones by regenerative potentials elicited in a restricted part of the basilar dendritic tree

Bogdan A. Milojkovic, Mihailo S. Radojicic, The Late Patricia S. Goldman-Rakic and Srdjan D. Antic

Department of Neurobiology, Yale University, 333 Cedar Street, New Haven, CT 06520-8001, USA

The common preconception about central nervous system neurones is that thousands of small postsynaptic potentials sum across the entire dendritic tree to generate substantial firing rates, previously observed in in vivo experiments. We present evidence that local inputs confined to a single basal dendrite can profoundly influence the neuronal output of layer V pyramidal neurones in the rat prefrontal cortical slices. In our experiments, brief glutamatergic stimulation delivered in a restricted part of the basilar dendritic tree invariably produced sustained plateau depolarizations of the cell body, accompanied by bursts of action potentials. Because of their small diameters, basolateral dendrites are not routinely accessible for glass electrode measurements, and very little is known about their electrical properties and their role in information processing. Voltage-sensitive dye recordings were used to follow membrane potential transients in distal segments of basal branches during sub- and suprathreshold glutamate and synaptic stimulations. Recordings were obtained simultaneously from multiple dendrites and multiple points along individual dendrites, thus showing in a direct way how regenerative potentials initiate at the postsynaptic site and propagate decrementally toward the cell body. The glutamate-evoked dendritic plateau depolarizations described here are likely to occur in conjunction with strong excitatory drive during so-called ‘UP states’, previously observed in in vivo recordings from mammalian cortices.

(Received 16 January 2004; accepted after revision 18 May 2004; first published online 21 May 2004)
Corresponding author S. D. Antic: Department of Neurobiology, Yale University, 333 Cedar Street, New Haven, CT 06520-8001, USA. Email: srdjan.antic{at}yale.edu


This paper is dedicated to the memory of Patricia Goldman-Rakic, our dear friend and colleague.




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