Comparison of the role of local anesthetic properties with dopamine uptake blockade in the inhibition of striatal and nucleus accumbens [3H]acetylcholine release by cocaine

A. N. Gifford, K. M. Johnson

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Abstract

The effects of cocaine on the electrically evoked release of tritium from brain slices previously loaded with [3H]choline were examined and used as an index of acetylcholine (ACh) release. In the striatum, cocaine dose- dependently inhibited ACh release, with an IC50 of 2.9 μM. At 10 μM cocaine, D2 receptor blockade by sulpride resulted in only about a 45% reversal of the inhibition of ACh release, whereas inhibition due to either nomifensine or quinpirole was reversed by about 80%. 5-Hydroxytryptamine antagonists had no effect on the cocaine-induced inhibition of striatal ACh release, thus suggesting no involvement of this amine in cocaine's action. Antagonists against γ-aminobutyric acid(A), muscarinic, opioid and adenosine receptors were similarly ineffective at reversing cocaine's effect on ACh release. Comparison with the effect of procaine on striatal ACh release suggested that the inhibition of ACh release in the presence of sulpiride was due to the local anesthetic properties of cocaine. In the nucleus accumbens cocaine was about 5-fold less potent at inhibiting ACh release than in the striatum and sulpiride was much less effective at reversing the inhibitory effect of cocaine, suggesting that the local anesthetic effects of cocaine play a greater role in regulating ACh release in this area relative to dopamine uptake blockade. These data suggest that the local anesthetic effect of cocaine is prominent at concentrations found in the central nervous system after pharmacologically relevant systemic doses and depending on the degree of monoaminergic control of a particular brain area, may be even more important than the effects of cocaine arising from inhibition of reuptake.

Original languageEnglish (US)
Pages (from-to)757-761
Number of pages5
JournalJournal of Pharmacology and Experimental Therapeutics
Volume263
Issue number2
StatePublished - 1992

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Corpus Striatum
Nucleus Accumbens
Local Anesthetics
Cocaine
Acetylcholine
Dopamine
Sulpiride
Anesthetics
Nomifensine
Quinpirole
Aminobutyrates
Serotonin Antagonists
Procaine
Purinergic P1 Receptors
Tritium
Brain
Opioid Receptors
Muscarinic Receptors
Choline
Inhibitory Concentration 50

ASJC Scopus subject areas

  • Pharmacology

Cite this

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title = "Comparison of the role of local anesthetic properties with dopamine uptake blockade in the inhibition of striatal and nucleus accumbens [3H]acetylcholine release by cocaine",
abstract = "The effects of cocaine on the electrically evoked release of tritium from brain slices previously loaded with [3H]choline were examined and used as an index of acetylcholine (ACh) release. In the striatum, cocaine dose- dependently inhibited ACh release, with an IC50 of 2.9 μM. At 10 μM cocaine, D2 receptor blockade by sulpride resulted in only about a 45{\%} reversal of the inhibition of ACh release, whereas inhibition due to either nomifensine or quinpirole was reversed by about 80{\%}. 5-Hydroxytryptamine antagonists had no effect on the cocaine-induced inhibition of striatal ACh release, thus suggesting no involvement of this amine in cocaine's action. Antagonists against γ-aminobutyric acid(A), muscarinic, opioid and adenosine receptors were similarly ineffective at reversing cocaine's effect on ACh release. Comparison with the effect of procaine on striatal ACh release suggested that the inhibition of ACh release in the presence of sulpiride was due to the local anesthetic properties of cocaine. In the nucleus accumbens cocaine was about 5-fold less potent at inhibiting ACh release than in the striatum and sulpiride was much less effective at reversing the inhibitory effect of cocaine, suggesting that the local anesthetic effects of cocaine play a greater role in regulating ACh release in this area relative to dopamine uptake blockade. These data suggest that the local anesthetic effect of cocaine is prominent at concentrations found in the central nervous system after pharmacologically relevant systemic doses and depending on the degree of monoaminergic control of a particular brain area, may be even more important than the effects of cocaine arising from inhibition of reuptake.",
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