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Cocaine actions on rat prefrontal cortical and hippocampal dentate granule neurons in vitro
Author(s) -
Jahromi Shokrollah S.,
Schertzer Stephen,
Carlen Peter L.
Publication year - 1993
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.890140204
Subject(s) - excitatory postsynaptic potential , afterhyperpolarization , inhibitory postsynaptic potential , neuroscience , postsynaptic potential , electrophysiology , chemistry , hippocampal formation , depolarization , membrane potential , hyperpolarization (physics) , biology , biophysics , receptor , biochemistry , organic chemistry , nuclear magnetic resonance spectroscopy
The electrophysiological actions of cocaine hydrochloride (COC) on medial prefrontal cortical (mpfc) and hippocampal dentate granule (DG) neurons were investigated in rat brain slices with intracellular recording techniques. The following parameters were measured: resting membrane potential (RMP), spike threshold, spike firing adaptation, postspike train afterhyperpolarization (AHP), excitatory postsynaptic potentials (EPSPs), and inhibitory postsynaptic potentials (IPSPs). In the mpfc, COC appeared to have both inhibitory and excitatory effects. In the majority of cells examined, the EPSP amplitude was attenuated by COC (200 nM–20 μM), whereas the amplitude of the postspike train afterhyperpolarization (AHP) was reduced (an excitatory effect). In DG neurons, 1 μM COC caused a small depolarization. COC potentiated the EPSPs at 1 μM but attenuated EPSPs and IPSPs at 10–100 μM. The amplitude of antidromically evoked EPSPs was also increased by 20 μM COC. At concentrations of 10 μM and greater, COC increased spike threshold. It is concluded that COC actions on mpfc and DG neurons are both excitatory and inhibitory and that these effects may be mediated by multiple neurotransmitters/modulators. © 1993 Wiley‐Liss, Inc.