Naunyn-Schmiedeberg's Archives of Pharmacology

, Volume 310, Issue 1, pp 21–24 | Cite as

Differential depression by apomorphine of the dorsal root potentials spreading caudally and cranially in the cat spinal cord

  • Krystyna Lupa
  • Grażyna Wójcik
  • Andrzej Niechaj
Article

Summary

The effect of apomorphine on bilateral dorsal root potentials (DRPs) spreading caudally and cranially along three segments of the lower spinal cord was studied in spinal cats anaesthetized with thiamylal sodium. The DRPs were produced by single impulses at 4 times the threshold strength. Apomorphine in a dose of 5 mg/kg, i.v., depressed ipsilateral DRPs spreading caudally to 77% of their initial amplitude and the period of depression was 50 min. Depression of DRPs spreading cranially was significantly greater (maximum reduction to 59%) and lasted about 60 min. Contralateral DRPs spreading cranially were also more depressed than those spreading caudally. These effects were not due to differences in the level of the spinal cord segments investigated. Increase in strength of stimulation to 40 times threshold did not significantly change the depression of DRPs produced by apomorphine. Depression of DRPs depended on the dose of apomorphine. Pimozide and haloperidol blocked the apomorphine-induced depression of the DRPs. It is suggested that differences in the depression of the DRPs spreading caudally and cranially result from different numbers of dopaminergic neurons terminating on interneurons transmitting depolarization cranially or caudally, respectively.

Key words

Apomorphine Dorsal root potentials Presynaptic inhibition Spinal cord 

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References

  1. Andén, N. E., Rubenson, A., Fuxe, K., Hokfelt, T.: Evidence for dopamine receptor stimulation by apomorphine. J. Pharm. Pharmacol. 19, 626–629 (1967)Google Scholar
  2. Andén, N. E., Butcher, S. G., Corrodi, H., Fuxe, K., Ungerstedt, U.: Receptor activity and turnover of dopamine and noradrenaline after neuroleptics. Eur. J. Pharmacol. 11, 303–314 (1970)Google Scholar
  3. Andén, N. E., Bédard, P., Fuxe, K., Ungerstedt, U.: Early and selective increase in brain dopamine after axotomy. Experientia (Basel) 28, 300–301 (1972)Google Scholar
  4. Barron, D. H., Matthews, B. H. C.: The interpretation of potential changes in the spinal cord. J. Physiol. (Lond.) 92, 276–321 (1938)Google Scholar
  5. Bingham, W. G., Ruffolo, R., Goodman, J. H., Knofel, J., Friedman, S.: Norepinephrine and dopamine levels in normal dog and monkey spinal cord. Life Sci. 16, 1521–1526 (1975)Google Scholar
  6. Casey, K. L., Oakley, B.: Intraspinal latency, cutaneous fiber composition, and afferent control of the dorsal root reflex in cat. Brain Res. 47, 353–369 (1972)Google Scholar
  7. Commissiong, J. W., Galli, C. L., Neff, N. H.: Differentiation of dopaminergic and noradrenergic neurons in rat spinal cord. J. Neurochem. 30, 1095–1099 (1978)Google Scholar
  8. Devor, M., Merrill, E. G., Wall, P. D.: Dorsal horn cells that respond to stimulation of distant dorsal roots. J. Physiol. (Lond.) 270, 519–531 (1977)Google Scholar
  9. Ernst, A. M.: Mode of action of apomorphine and dexamphetamine on gnawing compulsion in rats. Psychopharmacologia (Berl.) 10, 316–323 (1967)Google Scholar
  10. Kebabian, J. W., Petzold, G. L., Greengard, P.: Dopamine-sensitive adenylate cyclase in caudate nucleus of rat brain, and its similarity to the “dopamine receptor”. Proc. Natl. Acad. Sci. USA 69, 2145–2149 (1972)Google Scholar
  11. Lupa, K., Niechaj, A.: Bilateral dorsal root potentials in the lower sacral spinal cord. Pflügers Arch. 369, 187–192 (1977)Google Scholar
  12. Lupa, K., Wójcik, G., Ożóg, M., Niechaj, A.: Spread of the dorsal root potentials in lower lumbar, sacral and upper caudal spinal cord. Pflügers Arch. 381, 201–207 (1979)Google Scholar
  13. Magnusson, T.: Effect of chronic transection on dopamine, noradrenaline and 5-hydroxytryptamine in the rat spinal cord. Naunyn-Schmiedeberg's Arch. Pharmacol. 278, 13–22 (1973)Google Scholar
  14. Nygren, L. G., Olson, L.: On spinal noradrenaline receptor supersensitivity: correlation between nerve terminal densities and flexor reflexes various times after intracisternal 6-hydroxydopamine. Brain Res. 116, 455–470 (1976)Google Scholar
  15. Reid, J. L., Zivin, J. A., Foppen, F. H., Kopin, I. J.: Catecholamine neurotransmitters and synthetic enzymes in the spinal cord of the rat. Life Sci. 16, 975–984 (1975)Google Scholar
  16. Roos, B. E.: Decrease in homovanillic acid as evidence for dopamine receptor stimulation in the neostriatum of the rat. J. Pharm. Pharmacol. 21, 263–264 (1969)Google Scholar
  17. Schlosser, W., Horst, W. D., Spiegel, H. E., Sigg, W. B.: Apomorphine and its effects on the spinal cord. Neuropharmacology 11, 417–426 (1972)Google Scholar
  18. Szentágothai, J.: Neuronal and synaptic arrangement in the substantia gelatinosa Rolandi. J. Comp. Neurol. 122, 219–239 (1964)Google Scholar
  19. Wall, P. D.: The origin of a spinal cord slow potential. J. Physiol. (Lond.) 164, 508–526 (1962)Google Scholar

Copyright information

© Springer-Verlag 1979

Authors and Affiliations

  • Krystyna Lupa
    • 1
  • Grażyna Wójcik
    • 1
  • Andrzej Niechaj
    • 1
  1. 1.Department of Human PhysiologyMedical SchoolLublinPoland

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