Skip to main content
Log in

Effect of ethanol on [3H]Dopamine release in rat nucleus accumbens and striatal slices

  • Original Articles
  • Published:
Neurochemical Research Aims and scope Submit manuscript

Abstract

Ethanol (10–200 mM) transiently increased tritium overflow from superfused rat nucleus accumbens slices previously incubated with [3H]dopamine (DA) and [14C]choline. The effect was greater in striatal tissue and did not appear to be a non-specific membrane effect since [14C]acetylcholine (ACh) release was not affected. Lack of antagonism by picrotoxin suggested that γ-aminobutyric acid (GABA) receptors were not involved. Calcium was not a requirement and the DA uptake blocker, nomifensine, was without effect. Ethanol appeared to be causing [3H]DA release into the cytoplasm. K+-stimulated release of [3H]DA and [14C]ACh from nucleus accumbens and striatal slices was not affected. Clonidine-mediated inhibition of the K+-evoked release of [3H]DA remained unaltered. Ethanol attenuated the isoproterenol-induced enhancement of [3H]DA release. Ethanol therefore appeared to interact with components of the DA terminal causing a transient increase in the release of neurotransmitter without impairing K+-evoked release but apparently interfering with the isoproterenol-induced effect.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Hunt, W. A. 1981. Neurotransmitter function in the basal ganglia after acute and chronic ethanol treatment. Fed. Proc. 40:2077–2081.

    Google Scholar 

  2. Majchrowicz, E. 1981. Reversal in central nervous system function during ethanol withdrawal in humans and experimental animals. Fred. Proc. 40:2065–2072.

    Google Scholar 

  3. Di Chiara, G., and Imperato, A. 1985. Ethanol preferentially stimulates dopamine release in the nucleus accumbens of freely moving rats. Eur. J. Pharmacol. 115:131–132.

    Google Scholar 

  4. Mereu, G., Fadda, F., and Gessa, G. L. 1984. Ethanol stimulates the firing rate of nigral dopaminergic neurons in unanesthetized rats. Brain Res. 292:63–69.

    Google Scholar 

  5. Mereu, G., and Gessa, G. L. 1985. Low doses of ethanol inhibit the firing of neurons in the substantia nigra, pars reticulata: a GABA-ergic Effect? Brain Res. 360:325–330.

    Google Scholar 

  6. Suzdak, P. D., Schwartz, R. D., Skolnick, P., and Paul, S. M. 1986. Ethanol stimulates γ-aminobutyric acid receptormediated chloride transport in rat brain synaptoneurosomes. Proc. Natl. Acad. Sci. U.S.A. 83:4071–4075.

    Google Scholar 

  7. Gessa, G. L., Muntoni, F., Collu, M., Vargiu, L., and Mereu, G. 1985. Low doses of ethanol activate dopaminergic neurons in the ventral tegmental area. Brain Res. 348:201–203.

    Google Scholar 

  8. Esposito, R. U., Parker, E. S., and Weingartner, H. 1984. Enkephalinergic-dopaminergic “reward” Pathways: a critical substrate for the stimulatory, euphoric and memory-enhancing actions of alcohol—a hypothesis. Subst. Alcohol Actions/misuse. 5:111–119.

    Google Scholar 

  9. Spyraki, C., Fibiger, H. C., and Phillips, A. G. 1983. Attenuation of heroin reward in rats by disruption of the mesolimbic dopamine system. Psychopharmacol. 79:278–283.

    Google Scholar 

  10. Pettit, H. O., Ettenberg, A., Bloom, F.E., and Koob, G. F. 1984. Destruction of dopamine in the nucleus accumbens selectively attenuates cocaine but not heroin self-administration in rats. Psychopharmacol. 84:167–173.

    Google Scholar 

  11. Willner, P. 1983. Dopamine and depression: A review of recent evidence. II. Theoretical Approaches. Brain Res. Revs. 6:225–236.

    Google Scholar 

  12. Holman, R. B., and Snape, B. M. 1985. Effects of ethanol in vitro and in vivo on the release of endogenous catecholamines from specific regions of rat brain. J Neurochem. 44:357–363.

    Google Scholar 

  13. Gysling, K., Bustos, G., Concha, I., and Martinez, G. 1976. Effect of ethanol on dopamine synthesis and release from rat corpus striatum. Biochem. Pharmacol. 25:157–162.

    Google Scholar 

  14. Murphy, J. M., Cunningham, S. D., and McBride, W. J. 1985. Effects of 250 mg% ethanol on monoamine and amino acid release from rat striatal slices. Brain Res. Bull. 14:439–442.

    Google Scholar 

  15. Samuel, D., Lynch, M. A., and Littleton, J. M. 1983. Picrotoxin inhibits the effect of ethanol on the spontaneous efflux of3H-dopamine from superfused slices of rat corpus striatum. Neuropharmacol. 22:1413–1415.

    Google Scholar 

  16. Seeman, P., and Lee, T. 1974. The dopamine-releasing actions of neuroleptics and ethanol. J. Pharmacol. Exp. Therap. 190:131–140.

    Google Scholar 

  17. Lynch, M. A., Samuel, D., and Littleton, J. M. 1985. Altered characteristics of3H-dopamine release from superfused slices of corpus striatum obtained from rats receiving ethanol in vivo. Neuropharmacol. 24:479–485.

    Google Scholar 

  18. Nurse, B., Russell, V. A., and Taljaard, J. J. F. 1984. 492-1 and β-adrenoceptor agonists modulate3H-dopamine release from rat nucleus accumbens slices: Implications for Research into Depression. Neurochem. Res. 9:1231–1238.

    Google Scholar 

  19. Nurse, B., Russell, V. A., and Taljaard, J. J. F. 1985. Effect of chronic desipramine treatment on adrenoceptor modulation of3H-dopamine release from rat nucleus accumbens slices. Brain Res. 334:235–242.

    Google Scholar 

  20. Russell, V. A., Lamm, M. C. L., de Viliers, A. S., Taljaard, J. J. F., and Chalton, D. O. 1985. Effects of combined administration of L-tryptophan and tricyclic antidepressants on α2- and β-adrenoceptors and monoamine levels in rat brain. Neurochem. Res. 10:1661–1671.

    Google Scholar 

  21. Zumstein, A., Karduck, W., and Starke, K. 1981. Pathways of dopamine metabolism in the rabbit caudate nucleus in vitro. Naunyn-Schmiedeberg's Arch. Pharmacol. 316:205–217.

    Google Scholar 

  22. Cubeddo, L. X., Hoffmann, I. S., and Ferrari, G. B. 1979. Metabolism and efflux of3H-dopamine in rat neostriatum: Presynaptic origin of 3,4-3H-dihydroxyphenylacetic acid. J. Pharmacol. Exp. Therap. 209:165–175.

    Google Scholar 

  23. Martz, A., Deitrich, R. A., and Harris, R. A. 1983. Behavioural evidence for the involvement of γ-aminobutyric acid in the actions of ethanol. Eur. J. Pharmacol. 89:53–62.

    Google Scholar 

  24. Mendelson, W. B., Martin, J. V., Wagner, R., Roseberry, C., Skolnick, P., Weissman, B. A., and Squires, R. 1985. Are the toxicities of pentobarbital and ethanol mediated by the GABA-benzodiazepine receptor-chloride ionophore complex? Eur. J. Pharmacol. 108:63–70.

    Google Scholar 

  25. Carlen, P. L., Gurevich, N., Davies, M. F., Blaxter, T. J., and O'Beirne, M. 1985. Enhanced neuronal K+ conductance: a possible common mechanism for sedative-hypnotic drug action. Can. J. Physiol. Pharmacol. 63:831–837.

    Google Scholar 

  26. Richelson, E., and Pfenning, M. 1984. Blockade by antidepressants and related compounds of biogenic amine uptake into rat brain synaptosomes: most antidepressants selectivety block norepinephrine uptake. Eur. J. Pharmacol. 104:277–286.

    Google Scholar 

  27. Russell, V. A., Nurse, B., Lamm, M. C. L., and Taljaard, J. J. F. 1987. Effect of chronic antidepressant treatment on noradrenergic modulation of3H dopamine release from rat nucleus accumbens and striatal slices. Brain Res. 410:78–82.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Russell, V.A., Lamm, M.C.L. & Taljaard, J.J.F. Effect of ethanol on [3H]Dopamine release in rat nucleus accumbens and striatal slices. Neurochem Res 13, 487–492 (1988). https://doi.org/10.1007/BF01268885

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01268885

Key Words

Navigation