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α2 and β-adrenoceptor agonists modulate [3H]dopamine release from rat nucleus accumbens slices: Implications for research into depression

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Abstract

The modulatory effects of noradrenergic agonists on the 25 mM K+-induced release of [3H]dopamine (3H-DA) from rat brain nucleus accumbens slices was investigated, using a superfusion technique. The K+-induced release of3H-DA was Ca2+ dependent, significantly enhanced (25–32%;p<0.02) by the β-adrenoceptor agonist isoproterenol (10 μM), and significantly decreased (13–25%;p<0.05) by the α2-adrenoceptor agonist clonidine (10 μM). At these concentrations neither drug affected basal release of3H-DA. Clonidine (100 μM) increased the basal release of3H-DA, while decreasing the K+-induced release by 19% (p<0.01). The inclusion of desipramine in the incubation medium, to prevent accumulation of3H-DA into noradrenergic neurons, did not alter the inhibitory effect of clonidine (10 μM) on3H-DA release. This study provides direct evidence that noradrenergic neurons can modulate dopaminergic neurotransmission in the mesolimbic system.

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References

  1. Kostowski, W. 1981. Brain noradrenaline, depression and antidepressant drugs: Facts and hypothesis. TIPS 2:314–317.

    Google Scholar 

  2. Jenner, P., Sheehy, M., andMarsden, C. D. 1983. Noradrenaline and 5-hydroxytryptamine modulation of brain dopamine function: Implications for the treatment of Parkinson's disease. Br. J. Clin. Pharmacol. 15:277S-289S.

    Google Scholar 

  3. Fibiger, H. C., andPhillips, A. G. 1981. Increased intracranial self-stimulation in rats after long-term administration of desipramine. Science 214:683–685.

    Google Scholar 

  4. Garrigues, A., andCazala, P. 1983. Central catecholamine metabolism and hypothalamic self-stimulation behaviour in two inbred strains of mice. Brain Res. 265:265–271.

    Google Scholar 

  5. Antelman, S. M., andCaggiula, A. R. 1977. Norepinephrine-dopamine interactions and behaviour. Science 195:646–653.

    Google Scholar 

  6. Kostowski, W. 1980. Noradrenergic interactions among central neurotransmitters. Pages 47–65,in Essman, W. B. (ed.), Neurotransmitters, Receptors and Drug Action, Spectrum Publ. Inc., New York.

    Google Scholar 

  7. Starke, K. 1981. Presynaptic receptors. Ann. Rev. Pharmacol. Toxicol. 21:7–30.

    Google Scholar 

  8. De Belleroche, J. S., andBradford, H. F. 1980. Presynaptic control of the synthesis and release of dopamine from striatal synaptosomes: A comparison between the effects of 5-hydroxytryptamine, acetylcholine, and glutamate. J. Neurochem. 35:1227–1234.

    Google Scholar 

  9. Ennis, C., Kemp, J. D., andCox, B. 1981. Characterisation of inhibitory 5-hydroxytryptamine receptors that modulate dopamine release in the striatum. J. Neurochem. 36:1515–1520.

    Google Scholar 

  10. Westfall, T. C., andTittermary, V. 1982. Inhibition of the electrically induced release of [3H]dopamine by serotonin from superfused rat striatal slices. Neurosci. Lett. 28:205–209.

    Google Scholar 

  11. De Belleroche, J., andGardiner, I. M. 1982. Contrasting effects of 5-hydroxytryptamine on the release of dopamine and acetylcholine in the nucleus accumbens of rat. J. Neural. Trans. 55:227–242.

    Google Scholar 

  12. McCarthy, B. W., Reyneke, L., Rousseau, J., Taljaard, J. J. F., andNeethling, A. C. 1982. Neurotransmitter release studies: A versatile approach to data handling. S. Afr. J. Sci. 78:333–334.

    Google Scholar 

  13. De Langen, C. D. J., Hogenboom, F., andMulder, A. H. 1979. Presynaptic noradrenergic α-receptors and modulation of3H-noradrenaline release from rat brain synaptosomes. Eur. J. Pharmacol. 60:79–89.

    Google Scholar 

  14. Rubin, R. P. 1970. The role of calcium in the release of neurotransmitter substances and hormones. Pharmacol. Rev. 22:389–428.

    Google Scholar 

  15. Cerrito, F., Casazza, G., Levi, G., andRaiteri, M. 1980. Evidence for a similar compartmentation of recaptured and endogenously synthesized dopamine in striatal synaptosomes. Neurochem. Res. 5:115–121.

    Google Scholar 

  16. Mulder, A. H. Van Den Berg, W. B., andStoof, J. C. 1975. Calcium-dependent release of radiolabeled catecholamines and serotonin from rat brain synaptosomes in a superfusion system. Brain Res. 99:419–424.

    Google Scholar 

  17. Hoffmann, I. S., Naylor, R. J., andCubeddu, L. X. 1980. Presynaptic effects of 2-aminotetralins on striatal dopaminergic neurons. J. Pharmacol. Exp. Therap. 215:486–493.

    Google Scholar 

  18. Fischer, J. F., andCho, A. K. 1979. Chemical release of dopamine from striatal homogenates: Evidence for an exchange diffusion model. J. Pharmacol. Exp. Therap. 208:203–209.

    Google Scholar 

  19. George, S. R. andVan Loon, G. R. 1982. Characterization of high affinity dopamine uptake into the dopamine neurons of the hypothalamus. Brain Res 234:339–355.

    Google Scholar 

  20. Ueda, H., Goshima, Y., andMisu, Y. 1983. Presynaptic mediation by α1-,β12-adrenoceptors of endogenous noradrenaline and dopamine release from slices of rat hypothalamus. Life Sci. 33:371–376.

    Google Scholar 

  21. Liang, N. Y., andRutledge, C. O. 1982. Evidence for carrier-mediated efflux of dopamine from corpus striatum. Biochem. Pharmacol. 31:2479–2484.

    Google Scholar 

  22. Lindvall, O., andBjörklund, A. 1974. The organization of the ascending catecholamine neuron systems in the rat brain as revealed by the glyoxylic acid fluorescence method. Acta Physiol. Scand. 412 (suppl.):1–48.

    Google Scholar 

  23. O'Donohue, T. L., Crowley, W. R., andJacobwitz, D. M. 1979. Biochemical mapping of the noradrenergic ventral bundle projection sites: Evidence for a noradrenergic-dopaminergic interaction. Brain Res. 172:87–100.

    Google Scholar 

  24. Kelly, P. H., Seviour, P. W., andIversen, S. D. 1975 Amphetamine and apomorphine responses in the rat following 6-OHDA lesions of the nucleus accumbens septi and corpus striatum. Brain Res. 94:507–522.

    Google Scholar 

  25. Spyraki, C., andFibiger, H. C. 1981. Behavioural evidence for supersensitivity of postsynaptic dopamine receptors in the mesolimbic system after chronic administration of desipramine. Eur. J. Pharmacol. 74:195–206.

    Google Scholar 

  26. Maj, J., Rogóz, Z., Skuza, G., andSowínska, H. 1983. Reserpine-induced locomotor stimulation in mice chronically treated with typical and atypical antidepressants. Eur. J. Pharmacol. 87:469–474.

    Google Scholar 

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Nurse, B., Russell, V.A. & Taljaard, J.J.F. α2 and β-adrenoceptor agonists modulate [3H]dopamine release from rat nucleus accumbens slices: Implications for research into depression. Neurochem Res 9, 1231–1238 (1984). https://doi.org/10.1007/BF00973036

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