Abstract
Electrical field stimulation of the mouse vas deferens (TO and C57/BL strains) caused the release of noradrenaline into the bathing medium. 2 Phenoxybenzamine (30 muM) or phentolamine (36 muM) plus cocaine (13 muM) caused a considerable increase in the noradrenaline output. 3 In the vasa deferentia from TO mice the output per pulse of noradrenaline was constant at frequencies of stimulation from 0.5 to 15 Hz whereas in the vasa deferentia from C57/BL mice the output per pulse of noradrenaline increased two-fold from 1.5 to 15 Hz. 4 Morphine (2 muM) inhibited the contractions of the vasa deferentia from TO mice. This effect was greater at low (0.1-1 Hz) than at high (10 Hz) frequencies of stimulation. Morphine (2 muM) did not inhibit the response of the tissue to exogenous noradrenaline. 5 Morphine (1 muM) reduced the noradrenaline output from the vasa deferentia of TO mice stimulated at 1.5 Hz but did not reduce the noradrenaline output at 15 Hz. At 1.5 Hz the reduction of noradrenaline output was reversed by naloxone (0.05 muM). 6 Morphine (5 muM) did not inhibit the uptake of [3H]-noradrenaline into the vasa deferentia from TO mice. 7 Only in high concentrations (ID50 30.88 muM) did morphine inhibit the contractions of the vasa deferentia from C57/BL mice. 8 Normorphine (100 muM) did not reduce the noradrenaline output from vasa deferentia of C57/BL mice.
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Selected References
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- Ambache N., Zar M. A. Evidence against adrenergic motor transmission in the guinea-pig vas deferens. J Physiol. 1971 Jul;216(2):359–389. doi: 10.1113/jphysiol.1971.sp009530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Furness J. B., Campbell G. R., Gillard S. M., Malmfors T., Cobb J. L., Burnstock G. Cellular studies of sympathetic denervation produced by 6-hydroxydopamine in the vas deferens. J Pharmacol Exp Ther. 1970 Jul;174(1):111–122. [PubMed] [Google Scholar]
- Furness J. B., Iwayama T. Terminal axons ensheathed in smooth muscle cells of the vas deferens. Z Zellforsch Mikrosk Anat. 1971;113(2):259–270. doi: 10.1007/BF00339420. [DOI] [PubMed] [Google Scholar]
- Greenberg R., Kosterlitz H. W., Waterfield A. A. The effects of hexamethonium, morphine and adrenaline on the output of acetylcholine from the myenteric plexus-longitudinal muscle preparation of the ileum. Br J Pharmacol. 1970 Nov;40(3):553P–554P. [PMC free article] [PubMed] [Google Scholar]
- 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]
- Henderson G., Hughes J., Kosterlitz H. W. The effects of morphine on the release of noradrenaline from the cat isolated nictitating membrane and the guinea-pig ileum myenteric plexus-longitudinal muscle preparation. Br J Pharmacol. 1975 Apr;53(4):505–512. doi: 10.1111/j.1476-5381.1975.tb07387.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Henderson G., Hughes J. Proceedings: Modulation of frequency-dependent noradrenaline release by calcium, angiotensin and morphine. Br J Pharmacol. 1974 Nov;52(3):455P–456P. [PMC free article] [PubMed] [Google Scholar]
- Hughes J. Evaluation of mechanisms controlling the release and inactivation of the adrenergic transmitter in the rabbit portal vein and vas deferens. Br J Pharmacol. 1972 Mar;44(3):472–491. doi: 10.1111/j.1476-5381.1972.tb07285.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hughes J. Inhibition of noradrenaline release by lysergic acid diethylamide. Br J Pharmacol. 1973 Dec;49(4):706–708. doi: 10.1111/j.1476-5381.1973.tb08549.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hughes J. Isolation of an endogenous compound from the brain with pharmacological properties similar to morphine. Brain Res. 1975 May 2;88(2):295–308. doi: 10.1016/0006-8993(75)90391-1. [DOI] [PubMed] [Google Scholar]
- 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]
- Hughes J., Roth R. H. Variation in noradrenaline output with changes in stimulus frequency and train length: role of different noradrenaline pools. Br J Pharmacol. 1974 Jul;51(3):373–381. doi: 10.1111/j.1476-5381.1974.tb10672.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hughes J., Smith T., Morgan B., Fothergill L. Purification and properties of enkephalin - the possible endogenous ligand for the morphine receptor. Life Sci. 1975 Jun 15;16(12):1753–1758. doi: 10.1016/0024-3205(75)90268-4. [DOI] [PubMed] [Google Scholar]
- Jones M. E., Spriggs T. L. Noradrenaline and motor transmission in the vas deferens of the mouse. Br J Pharmacol. 1975 Mar;53(3):323–331. [PMC free article] [PubMed] [Google Scholar]
- LANE B. P., RHODIN J. A. CELLULAR INTERRELATIONSHIPS AND ELECTRICAL ACTIVITY IN TWO TYPES OF SMOOTH MUSCLE. J Ultrastruct Res. 1964 Jun;10:470–488. doi: 10.1016/s0022-5320(64)80023-x. [DOI] [PubMed] [Google Scholar]
- Montel H., Starke K., Weber F. Influence of morphine and naloxone on the release of noradrenaline from rat brain cortex slices. Naunyn Schmiedebergs Arch Pharmacol. 1974;283(4):357–369. doi: 10.1007/BF00501109. [DOI] [PubMed] [Google Scholar]
- North R. A., Henderson G. Action of morphine on guinea-pig myenteric plexus and mouse vas deferens studied by intracellular recording. Life Sci. 1975 Jul 1;17(1):63–66. doi: 10.1016/0024-3205(75)90236-2. [DOI] [PubMed] [Google Scholar]
- O'Hanlon J. F., Jr, Campuzano H. C., Horvath S. M. A fluorometric assay for subnanogram concentrations of adrenaline and noradrenaline in plasma. Anal Biochem. 1970 Apr;34(2):568–581. doi: 10.1016/0003-2697(70)90142-9. [DOI] [PubMed] [Google Scholar]
- Waterfield A. A., Kosterlitz H. W. Stereospecific increase by narcotic antagonists of evoked acetylcholine output in guinea-pig ileum. Life Sci. 1975 Jun 15;16(12):1787–1792. doi: 10.1016/0024-3205(75)90275-1. [DOI] [PubMed] [Google Scholar]
- Yamauchi A., Burnstock G. Post-natal development of the innervation of the mouse vas deferens. A fine structural study. J Anat. 1969 Jan;104(Pt 1):17–32. [PMC free article] [PubMed] [Google Scholar]
