Skip to main content
Log in

Uptake and release ofmeta-tyramine,para-tyramine, and dopamine in rat striatal slices

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

Abstract

The uptakes of high-affinity concentrations (10−8 M) ofmeta-tyramine (m-TA),para-tyramine (p-TA), and dopamine (DA) into rat striatal slices have been shown to be inhibited by DNP and ouabain. We now demonstrate that cocaine (5×10−6 M) and low concentrations of sodium ion (26×10−3 M) also reduced these uptakes. The spontaneous efflux and the release [induced by an elevated concentration of potassium ion (5×10−2 M)] of each of the previously accumulated amines were studied in the presence and absence of added calcium ions. The spontaneous efflux of each amine (especially the tyramines) was enhanced by the absence of calcium ions. Part of this enhancement seemed to be due to an inhibition of a calcium-dependent reuptake. The elevated concentration of potassium ion proved to be an effective releaser of each amine; and for DA, such release was decreased by the removal of calcium. Form- andp-TA, however, the removal of calcium either did not reduce or completely abolished the releases depending upon the duration of the calcium removal. The significance of these findings is discussed.

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. Petrali, E. H., andDyck, L. E. 1976. Tyramine and dopamine uptake in the striatum and hypothalamus of the rat. Proc. Can. Fed. Biol. Soc. 19:182.

    Google Scholar 

  2. Burgen, A. S. V., andIversen, L. L. 1965. The inhibition of noradrenaline uptake by sympathomimetic amines in the isolated rat heart. Br. J. Pharmacol. Chemother. 25:34–49.

    Google Scholar 

  3. Nash, C. W., Wolff, S. A., andFerguson, B. A. 1968. Release of tritiated noradrenaline from perfused rat hearts by sympathomimetic amines. Can. J. Physiol. Pharmacol. 46:35–42.

    Google Scholar 

  4. Raiteri, M., Del Carmine, R., Bertollini, A., andLevi, G. 1977. Effect of sympathomimetic amines on the synaptosomal transport of noradrenaline, dopamine and 5-hydroxytryptamine. Eur. J. Pharmacol. 41:133–143.

    Google Scholar 

  5. Giachetti, A., andShore, P. A. 1966. Studies in vitro of amine uptake mechanisms in heart. Biochem. Pharmacol. 15:607–614.

    Google Scholar 

  6. Ross, S. B., andRenyi, A. L. 1966. Uptake of some tritiated sympathomimetic amines by mouse brain cortex slices in vitro. Acta Pharmacol. Toxicol. 24:297–309.

    Google Scholar 

  7. Ross, S. B., andRenyi, A. L. 1966. Uptake of tritiated tyramine and (+)-amphetamine by mouse heart slices. J. Pharm. Pharmacol. 18:756–757.

    Google Scholar 

  8. Ross, S. B., Renyi, A. L., andBrunefelter, B. 1968. Cocaine-sensitive uptake of sympathomimetic amines in nerve tissue. J. Pharm. Pharmacol. 20:283–288.

    Google Scholar 

  9. Ross, S. B., andRenyi, A. L. 1971. Uptake and metabolism of β-phenylethylamine and tyramine in mouse brain and heart slices. J. Pharm. Pharmacol. 23:276–279.

    Google Scholar 

  10. Commarato, M. A., Brody, T. M., andMcNeill, J. H. 1969. The effect of various drugs on the uptake and metabolism of tyramine-3H in the rat heart. J. Pharmacol. Exp. Ther. 167:151–158.

    Google Scholar 

  11. Commaroto, M. H., Brody, T. M., andMcNeill, J. H. 1969. Further studies on the effets of various drugs on the uptake of tyramine-3H and formation of octopamine-3H in the rat heart. Can. J. Physiol. Pharmacol. 47:511–514.

    Google Scholar 

  12. Steinberg, M. I., andSmith, C. B. 1970. Effects of desmethylimipramine and cocaine on the uptake, retention and metabolism of H3-tyramine in rat brain slices. J. Pharmacol. Exp. Ther. 173:176–192.

    Google Scholar 

  13. Baldessarini, R. J., andVogt, M. 1971. The uptake and subcellular distribution of aromatic amines in the brain of the rat. J. Neurochem. 18:2519–2533.

    Google Scholar 

  14. Baldessarini, R. J. 1971. Release of aromatic amines from brain tissues of the rat in vitro. J. Neurochem. 18:2509–2518.

    Google Scholar 

  15. Baldessarini, R. J., andVogt, M. 1972. Regional release of aromatic amines from tissues of the rat brain in vitro. J. Neurochem. 19:755–761.b

    Google Scholar 

  16. Stoof, J. C., Liem, A. L., andMulder, A. H. 1976. Release and receptor stimulating properties ofp-tyramine in rat brain. Arch. Int. Pharmacodyn. 220:62–71.

    Google Scholar 

  17. Saldate, M. C., andOrrego, F. 1977. Differences in the electrically-induced release of3H-labelled β-phenylethylamine, tyramine, octopamine and norepinephrine from rat neocortical slices. Pages 159–177,in Mosnaim, A. D., and Wolf, M. E. (eds.), Phenylethylamine: Biological Mechanisms and Clinical Aspects, Marcel Dekker, New York (in press).

    Google Scholar 

  18. Arnfred, L., Hertz, L., Lolle, L., andLund-Anderson, H. 1970. An improved holder for transfer of brain slices during in vitro incubation. Exp. Brain Res. 11:373–375.

    Google Scholar 

  19. McCaman, M. W., McCaman, R. E., andLees, G. J. 1972. Liquid cation exchange—a basis for sensitive radiometric assays for aromatic amino acid decarboxylases. Anal. Biochem. 45:242–252.

    Google Scholar 

  20. Thoa, N. B., Wooten, F., Axelrod, J., andKoplin, I. J. 1975. On the mechanism of release of norepinephrine from sympathetic nerves induced by depolarizing agents and sympathomimetic drugs. Mol. Pharmacol. 11:10–18.

    Google Scholar 

  21. Wakade, A. R., andKirpekar, S. M. 1974. Calcium-independent release of3H-norepinephrine from reserpine-pretreated guinea-pig vas deferens and seminal vesicle. J. Pharmacol. Exp. Ther. 190:451–458.

    Google Scholar 

  22. Bustos, G., andRoth, R. H. 1972. Release of monoamines from the striatum and hypothalamus effect of α-hydroxybutyrate. Br. J. Pharmacol. 46:101–115.

    Google Scholar 

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

    Google Scholar 

  24. Thoenen, H., Huerlimann, A., andHaefely, W. 1969. Cation dependence of the noradrenaline-releasing action of tyramine. Eur. J. Pharmacol. 6:29–37.

    Google Scholar 

  25. Keen, P. M., andBogdanski, D. F. 1970. Sodium and calcium ions in uptake and release of norepinephrine by nerve endings. J. Physiol. 219:677–682.

    Google Scholar 

  26. Orrego, F., Jankelevich, J., Ceruti, L., andFerrera, E. 1974. Differential effects of electrical stimulation on the release of3H-noradrenaline and14C-α-aminoisobutyrate from brain slices. Nature 251:55–57.

    Google Scholar 

  27. Boulton, A. A. 1976. Identification, metabolism and function of meta-and paratyramine, phenylethylamine and tryptamine in brain. Adv. Biochem. Psychopharmacol. 15:56–67.

    Google Scholar 

  28. Boulton, A. A., andBaker, G. B. 1975. The subcellular distribution of β-phenylethylamine,p-tyramine and tryptamine in rat brain. J. Neurochem. 25:477–481.

    Google Scholar 

  29. Boulton, A. A., Juorio, A. V., andWu, P. H. 1977. The effects of reserpine and 6-hydroxydopamine on the concentrations of some arylalkylamines in rat brain. Br. J. Pharmacol. 59:209–214.

    Google Scholar 

  30. Matthaei, H., Lentzen, H., andPhillipu, A. 1976. Competition of some biogenic amines for uptake into synaptic vesicles of the striatum. N. S. Arch. Pharmacol. 293:89–96.

    Google Scholar 

  31. De Belleroche, J. S., andBradford, H. F. 1977. On the site of origin of transmitter amino acids released by depolarization of nerve terminals in vitro. J. Neurochem. 29:335–343.

    Google Scholar 

  32. Israel, M., Lesbats, B., Manaranche, R., Marsal, J., Mastour-Frachon, P., andMeunier, F. M. 1977. Related changes in amounts of Ach and ATP in resting and activeTorpedo nerve electroplaque synapses. J. Neurochem. 28:1259–1267.

    Google Scholar 

  33. Wirz-Justice, A. 1972. The influence of various amines and amino acids on K+-stimulated release of dopamine and serotonin from rat striatum. Eur. J. Pharmacol. 19:281–284.

    Google Scholar 

  34. Fillenz, M. 1977. The factors which provide short-term and long-term control of transmitter release. Prog. Neurobiol. 8:251–278.

    Google Scholar 

  35. Boulton, A. A. 1976. Cerebral Aryl Alkyl Aminergic Mechanisms. Vol. I, Psychopharmacology Series. Pages 22–39,in Usdin, E., and Sandler, M. (eds.), Trace Amines in the Brain, Marcel Dekker, New York.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dyck, L.E. Uptake and release ofmeta-tyramine,para-tyramine, and dopamine in rat striatal slices. Neurochem Res 3, 775–791 (1978). https://doi.org/10.1007/BF00966000

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00966000

Keywords

Navigation