Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1982 Apr;75(4):599–604. doi: 10.1111/j.1476-5381.1982.tb09179.x

Effects of divalent cations and normorphine on spontaneous excitatory junction potentials in the mouse vas deferens.

P Illes, R A North
PMCID: PMC2071523  PMID: 7066607

Abstract

1 Excitatory junction potentials (e.j.ps) occurring spontaneously or evoked by nerve stimulation were recorded intracellularly from smooth muscle cells of the mouse isolated vas deferens. 2 The amplitude of the evoked e.j.ps and the amplitude and frequency of spontaneous e.j.ps were measured before and during application of normorphine or solutions which might be expected change the influx of calcium ions into the nerve terminals. 3 Spontaneous e.j.ps could be recorded even in solutins which contained tetrodotoxin (1 microM), no added calcium an EGTA (1mM). A four fold increase in calcium concentration from 1.25 to 5 mM greatly increased the amplitude of the evoked e.j.ps but had no effect on the amplitude or frequency of the spontaneous e.j.ps. 4 Magnesium (12mM) and cobalt (4mM) both greatly reduced the evoked e.j.ps and also reduced the frequency of spontaneous e.j.ps. 5 Normorphine (2 microM) reduced the amplitude of the evoked e.j.p by 70% but had no effect on the amplitude or frequency of spontaneous e.j.ps. 6 It is suggested that normorphine inhibits noradrenaline secretion from nerve varicosities by a mechanism different from that of magnesium and cobalt. One possibility is a block of action potential propagation along varicose fibers.

Full text

PDF
599

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BURNSTOCK G., HOLMAN M. E. Spontaneous potential at sympathetic nerve endings in smooth muscle. J Physiol. 1962 Mar;160:446–460. doi: 10.1113/jphysiol.1962.sp006858. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bennett M. R., Lavidis N. A. An electrophysiological analysis of the effects of morphine on the calcium dependence of neuromuscular transmission in the mouse vas deferens. Br J Pharmacol. 1980 Jun;69(2):185–191. doi: 10.1111/j.1476-5381.1980.tb07889.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Dodge F. A., Jr, Rahamimoff R. Co-operative action a calcium ions in transmitter release at the neuromuscular junction. J Physiol. 1967 Nov;193(2):419–432. doi: 10.1113/jphysiol.1967.sp008367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Furness J. B. The effect of external potassium ion concentration on autonomic neuro-muscular transmission. Pflugers Arch. 1970;317(4):310–326. doi: 10.1007/BF00586580. [DOI] [PubMed] [Google Scholar]
  5. Guerrero-Munoz F., Cerreta K. V., Guerrero M. L., Way E. L. Effect of morphine on synaptosomal Ca++ uptake. J Pharmacol Exp Ther. 1979 Apr;209(1):132–136. [PubMed] [Google Scholar]
  6. HUBBARD J. I. The effect of calcium and magnesium on the spontaneous release of transmitter from mammalian motor nerve endings. J Physiol. 1961 Dec;159:507–517. doi: 10.1113/jphysiol.1961.sp006824. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hagiwara S., Byerly L. Calcium channel. Annu Rev Neurosci. 1981;4:69–125. doi: 10.1146/annurev.ne.04.030181.000441. [DOI] [PubMed] [Google Scholar]
  8. Henderson G. Effect of normorphine and enkephalin on spontaneous potentials in the vas deferens. Eur J Pharmacol. 1976 Oct;39(2):409–412. doi: 10.1016/0014-2999(76)90153-9. [DOI] [PubMed] [Google Scholar]
  9. Henderson G., Hughes J., Kosterlitz H. W. A new example of a morphine-sensitive neuro-effector junction: adrenergic transmission in the mouse vas deferens. Br J Pharmacol. 1972 Dec;46(4):764–766. doi: 10.1111/j.1476-5381.1972.tb06901.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Henderson G., North R. A. Depression by morphine of excitatory junction potentials in the vas deferens of the mouse. Br J Pharmacol. 1976 Jul;57(3):341–346. [PMC free article] [PubMed] [Google Scholar]
  11. Hubbard J. I., Jones S. F., Landau E. M. On the mechanism by which calcium and magnesium affect the spontaneous release of transmitter from mammalian motor nerve terminals. J Physiol. 1968 Feb;194(2):355–380. doi: 10.1113/jphysiol.1968.sp008413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hughes J., Kosterlitz H. W., Leslie F. M. Effect of morphine on adrenergic transmission in the mouse vas deferens. Assessment of agonist and antogonist potencies of narcotic analgesics. Br J Pharmacol. 1975 Mar;53(3):371–381. doi: 10.1111/j.1476-5381.1975.tb07373.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Ito Y., Tajima K. Action of morphine on the neuro-effector transmission in the guinea-pig ileum and in the mouse vas deferens. J Physiol. 1980 Oct;307:367–383. doi: 10.1113/jphysiol.1980.sp013440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. JENKINSON D. H. The nature of the antagonism between calcium and magnesium ions at the neuromuscular junction. J Physiol. 1957 Oct 30;138(3):434–444. doi: 10.1113/jphysiol.1957.sp005860. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kharasch E. D., Mellow A. M., Silinsky E. M. Intracellular magnesium does not antagonize calcium-dependent acetylcholine secretion. J Physiol. 1981 May;314:255–263. doi: 10.1113/jphysiol.1981.sp013705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Morita K., North R. A. Opiates and enkephalin reduce the excitability of neuronal processes. Neuroscience. 1981;6(10):1943–1951. doi: 10.1016/0306-4522(81)90034-8. [DOI] [PubMed] [Google Scholar]
  17. North R. A., Tonini M. The mechanism of action of narcotic analgesics in the guinea-pig ileum. Br J Pharmacol. 1977 Dec;61(4):541–549. doi: 10.1111/j.1476-5381.1977.tb07546.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Tokimasa T., Morita K., North A. Opiates and clonidine prolong calcium-dependent after-hyperpolarizations. Nature. 1981 Nov 12;294(5837):162–163. doi: 10.1038/294162a0. [DOI] [PubMed] [Google Scholar]
  19. Weakly J. N. The action of cobalt ions on neuromuscular transmission in the frog. J Physiol. 1973 Nov;234(3):597–612. doi: 10.1113/jphysiol.1973.sp010363. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES