Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1980;71(1):195–200. doi: 10.1111/j.1476-5381.1980.tb10926.x

Inhibition of neuroeffector transmission by morphine in the vas deferens of naive and morphine-treated mice.

P Illes, R Schulz
PMCID: PMC2044430  PMID: 6258687

Abstract

1 The amplitude of excitatory junction potentials (e.j.ps) recorded intracellularly from smooth muscle cells of the mouse vas deferens varied with the strength of stimulation. Normorphine (0.4, 2 and 10 microM) shifted the stimulus-response curve to the right, without any change in slope. This shift of the curve was proportional to the concentration of the opiate in the bath. Naloxone (0.4 and 2 microM) antagonized this effect of normorphine. 2 The action of normorphine (2 and 10 microM) was studied in vasa deferentia prepared from control mice and mice that had been implanted with morphine pellets. Both groups of tissues were continuously exposed to a low concentration of normorphine (0.4 microM), to simulate the plasma concentration in the morphine-treated mice. Addition of 10 microM normorphine produced a parallel displacement of the curve in vasa deferentia from control animals, and a non-parallel displacement in tissues from morphine pellet-implanted mice. In the preparations from morphine-treated mice a pronounced degree of tolerance to normorphine was observed at a low stimulus strength. 3 Naloxone (0.4 and 2 microM) had a greater effect on vasa deferentia prepared from morphine-treated animals than on tissues from control mice, when both organs were continuously exposed to 0.4 microM normorphine. The difference in the effect of the antagonist in the two groups of preparations was absent when the incubating solution contained 2 microM normorphine. 4 It is concluded that a low intensity of stimulation the e.j.ps are more readily depressed by normorphine and also the degree of tolerance displayed is larger than at a high intensity of stimulation.

Full text

PDF
195

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. The transmission of excitation from autonomic nerve to smooth muscle. J Physiol. 1961 Jan;155:115–133. doi: 10.1113/jphysiol.1961.sp006617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cowie A. L., Kosterlitz H. W., Waterfield A. A. Factors influencing the release of acetylcholine from the myenteric plexus of the ileum of the guinea-pig and rabbit. Br J Pharmacol. 1978 Dec;64(4):565–580. doi: 10.1111/j.1476-5381.1978.tb17319.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cox B. M., Weinstock M. The effect of analgesic drugs on the release of acetylcholine from electrically stimulated guinea-pig ileum. Br J Pharmacol Chemother. 1966 May;27(1):81–92. doi: 10.1111/j.1476-5381.1966.tb01643.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Furness J. B. The excitatory input to a single smooth muscle cell. Pflugers Arch. 1970;314(1):1–13. doi: 10.1007/BF00587042. [DOI] [PubMed] [Google Scholar]
  5. Gibson R. D., Tingstad J. E. Formulation of a morphine implantation pellet suitable for tolerance-physical dependence studies in mice. J Pharm Sci. 1970 Mar;59(3):426–427. doi: 10.1002/jps.2600590338. [DOI] [PubMed] [Google Scholar]
  6. Gillan M. G., Kosterlitz H. W., Robson L. E., Waterfield A. A. The inhibitory effects of presynaptic alpha-adrenoceptor agonists on contractions of guinea-pig ileum and mouse vas deferens in the morphine-dependent and withdrawn states produced in vitro. Br J Pharmacol. 1979 Aug;66(4):601–608. doi: 10.1111/j.1476-5381.1979.tb13700.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hart S. L., Kitchen I., Waddell P. R. Different effects of current strength on inhibitory responses of the mouse vas deferens to methionine- and leucine-enkephalin. Br J Pharmacol. 1979 Jul;66(3):361–363. doi: 10.1111/j.1476-5381.1979.tb10838.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. 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]
  9. 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]
  10. 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]
  11. Illés P., Knoll J. Opiate and dopamine receptors in the isolated nictitating membrane of the cat. Pol J Pharmacol Pharm. 1978 Mar-Jun;30(2-3):293–304. [PubMed] [Google Scholar]
  12. 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]
  13. North R. A., Vitek L. V. The effect of chronic morphine treatment of excitatory junction potentials in the mouse vas deferens. Br J Pharmacol. 1980 Mar;68(3):399–405. doi: 10.1111/j.1476-5381.1980.tb14553.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. North R. A., Zieglgänsberger W. Opiate withdrawal signs in single myenteric neurones. Brain Res. 1978 Apr 7;144(1):208–211. doi: 10.1016/0006-8993(78)90453-5. [DOI] [PubMed] [Google Scholar]
  15. Schulz R., Herz A. Aspects of opiate dependence in the myenteric plexus of the guinea-pig. Life Sci. 1976 Oct 15;19(8):1117–1127. doi: 10.1016/0024-3205(76)90246-0. [DOI] [PubMed] [Google Scholar]

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

RESOURCES