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PMID: 6289964 Published · ppublish English Journal Article

Responses of intracellularly recorded cortical neurons to the iontophoretic application of dopamine.

Brain research ·Vol. 245 ·No. 2 ·1982-08-12 ·Pages 267-74

Bernardi G, Cherubini E, Marciani MG, Mercuri N, Stanzione P

Abstract

Considering that a well-defined dopaminergic projection from the mesencephalic structures to the rat frontal cortex has been demonstrated, the purpose of this research was to study the action of iontophoretically applied dopamine (DA) on intracellularly recorded rat frontal neurons. The stimulation of the substantia nigra (SN) and the ventral tegmental area (VTA) evoked EPSP-IPSP sequences in these cells. About 50% of the tested neurons, widely distributed in all the frontal cortex, responded to DA application and no difference in the response to DA was observed between neurons with monosynaptic inputs and neurons with polysynaptic inputs. The catecholamine depolarized the cell membrane and decreased the firing rate, generally without significant changes in membrane resistance, as already observed in rat and cat striatal cells. In some neurons the decrease of the spikes preceded the membrane depolarization. Considering the complex effect of DA on the electrical properties of these neurons, these results seem to be indicative of a mechanism of action dependent on metabolic changes.

MeSH Terms
Animals Dopamine/pharmacology Evoked Potentials/drug effects Frontal Lobe/drug effects Glutamates/pharmacology Intracellular Fluid/drug effects Male Neural Pathways/drug effects Neurons/drug effects Rats Rats, Inbred Strains Substantia Nigra/drug effects Synaptic Transmission/drug effects Tegmentum Mesencephali/drug effects
Chemicals
Glutamates Dopamine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Bernardi G
Cherubini E
Marciani M G
Mercuri N
Stanzione P
Article Info
Journal
Brain research
Abbr.
Brain Res
ISSN
0006-8993
Published
1982-08-12
Pages
267-74
Language
English
Region
Netherlands
NLM ID
0045503
Subset
IM
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