Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1988 Jul;401:277–293. doi: 10.1113/jphysiol.1988.sp017162

Short- and long-latency muscarinic inhibition of noradrenaline release from rabbit atria induced by vagal stimulation.

A Habermeier-Muth 1, E Muscholl 1
PMCID: PMC1191849  PMID: 3171988

Abstract

1. The influence of the time interval between vagal and sympathetic nerve stimuli on the magnitude of muscarinic inhibition of noradrenaline release was studied in the isolated perfused rabbit atria preparation. The transmitter stores were labelled with [14C]choline and [3H]noradrenaline. 2. The right cardiac postganglionic sympathetic nerves were stimulated at 3 Hz for 3 min three times at intervals of 10 min. The [3H]noradrenaline outflow evoked by the second stimulation equalled the averaged means of the log values of amine outflows evoked by the first and third stimulations. 3. During the second sympathetic stimulation the right vagus nerve was stimulated (3 Hz, 3 min) in such a way that the impulses preceded the sympathetic stimuli by a fixed time interval varying within the range 0.3-283 ms. Outflow of [3H]noradrenaline was then compared with the individual 'expected value' calculated from the first and the third nerve stimulations. 4. [3H]Noradrenaline outflow was significantly decreased when the sympathetic impulses were delayed for between 3 and 10 ms or between 200 and 283 ms with respect to the vagus impulses. No significant inhibition of [3H]noradrenaline outflow occurred with delay times between 0.3 and 1.7 or 30 and 167 ms. Acetylcholine release was unaffected by varying the impulse delay time. 5. Atropine (1-300 nM) decreased and eventually abolished vagally mediated inhibition of [3H]noradrenaline outflow at both the 3 and 233 ms impulse delay periods and the evoked outflow of [14C]choline and [14C]acetylcholine was then approximately doubled. No enhancement of [3H]noradrenaline outflow was observed at an intermediate impulse delay time (100 ms) in the presence of atropine. 6. In the presence of (+)-tubocurarine (10 microM) [3H]noradrenaline outflow was unaffected by vagal stimulation at either the short or the long impulse delay time whereas that of [14C]choline and [14C]acetylcholine dropped to 3.4% (short) and 4.6% (long) of the control values. 7. Allowing for estimated conduction times in the vagal and sympathetic nerve pathways, the initial peak of muscarinic inhibition of noradrenaline release corresponds with excitation of the terminal cholinergic fibres occurring 20 ms before their adrenergic counterparts. A 'silent period' follows and then a second phase of muscarinic presynaptic inhibition occurs, peaking 250 ms after excitation of the cholinergic nerve terminals and levelling off completely within 100 ms. 8. It is concluded that both inhibitory peak responses are caused by a single volley of acetylcholine that affects two separate populations of muscarinic receptors.(ABSTRACT TRUNCATED AT 400 WORDS)

Full text

PDF
277

Images in this article

Selected References

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

  1. ARUNLAKSHANA O., SCHILD H. O. Some quantitative uses of drug antagonists. Br J Pharmacol Chemother. 1959 Mar;14(1):48–58. doi: 10.1111/j.1476-5381.1959.tb00928.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Blackman J. G., Gauldie R. W., Milne R. J. Interaction of competitive antagonists: the anti-curare action of hexamethonium and other antagonists at the skeletal neuromuscular junction. Br J Pharmacol. 1975 May;54(1):91–100. doi: 10.1111/j.1476-5381.1975.tb07414.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bolton T. B. Mechanisms of action of transmitters and other substances on smooth muscle. Physiol Rev. 1979 Jul;59(3):606–718. doi: 10.1152/physrev.1979.59.3.606. [DOI] [PubMed] [Google Scholar]
  4. Chassaing C., Duchene-Marullaz P., Veyrac M. J. Effects of catecholamines on cardiac chronotropic response to vagal stimulation in the dog. Am J Physiol. 1983 Nov;245(5 Pt 1):H721–H724. doi: 10.1152/ajpheart.1983.245.5.H721. [DOI] [PubMed] [Google Scholar]
  5. Ehinger B., Falck B., Sporrong B. Possible axo-axonal synapses between peripheral adrenergic and cholinergic nerve terminals. Z Zellforsch Mikrosk Anat. 1970;107(4):508–521. doi: 10.1007/BF00335438. [DOI] [PubMed] [Google Scholar]
  6. Fozard J. R., Muscholl E. Effects of several muscarinic agonists on cardiac performance and the release of noradrenaline from sympathetic nerves of the perfused rabbit heart. Br J Pharmacol. 1972 Aug;45(4):616–629. doi: 10.1111/j.1476-5381.1972.tb08119.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Fuder H., Meiser C., Wormstall H., Muscholl E. The effects of several muscarinic antagonists on pre- and postsynaptic receptors in the isolated rabbit heart. Naunyn Schmiedebergs Arch Pharmacol. 1981 Feb;316(1):31–37. doi: 10.1007/BF00507223. [DOI] [PubMed] [Google Scholar]
  8. Graffe K. H., Stefano F. J., Langer S. Z. Preferential metabolism of (-) 3 H-norepinephrine through the deaminated glycol in the rat vas deferens. Biochem Pharmacol. 1973 May 15;22(10):1147–1160. doi: 10.1016/0006-2952(73)90231-1. [DOI] [PubMed] [Google Scholar]
  9. Hammer R., Giachetti A. Muscarinic receptor subtypes: M1 and M2 biochemical and functional characterization. Life Sci. 1982 Dec 27;31(26):2991–2998. doi: 10.1016/0024-3205(82)90066-2. [DOI] [PubMed] [Google Scholar]
  10. Hedqvist P., Wennmalm A. Comparison of the effects of prostaglandins E 1, E 2 and F 2 alpha on the sympathetically stimulated rabbit heart. Acta Physiol Scand. 1971 Oct;83(2):156–162. doi: 10.1111/j.1748-1716.1971.tb05064.x. [DOI] [PubMed] [Google Scholar]
  11. Hill-Smith I., Purves R. D. Synaptic delay in the heart: an ionophoretic study. J Physiol. 1978 Jun;279:31–54. doi: 10.1113/jphysiol.1978.sp012329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Illes P. Mechanisms of receptor-mediated modulation of transmitter release in noradrenergic, cholinergic and sensory neurones. Neuroscience. 1986 Apr;17(4):909–928. doi: 10.1016/0306-4522(86)90071-0. [DOI] [PubMed] [Google Scholar]
  13. Junstad M., Wennmalm A. Release of prostaglandin from the rabbit isolated heart following vagal nerve stimulation or acetylcholine infusion. Br J Pharmacol. 1974 Nov;52(3):375–379. doi: 10.1111/j.1476-5381.1974.tb08605.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Lavallée M., de Champlain J., Nadeau R. A., Yamaguchi N. Muscarinic inhibition of endogenous myocardial catecholamine liberation in the dog. Can J Physiol Pharmacol. 1978 Aug;56(4):642–649. doi: 10.1139/y78-102. [DOI] [PubMed] [Google Scholar]
  15. Levy M. N., Blattberg B. Effect of vagal stimulation on the overflow of norepinephrine into the coronary sinus during cardiac sympathetic nerve stimulation in the dog. Circ Res. 1976 Feb;38(2):81–84. doi: 10.1161/01.res.38.2.81. [DOI] [PubMed] [Google Scholar]
  16. Lindmar R., Löffelholz K., Weide W., Witzke J. Neuronal uptake of choline following release of acetylcholine in the perfused heart. J Pharmacol Exp Ther. 1980 Dec;215(3):710–715. [PubMed] [Google Scholar]
  17. Loiacono R. E., Story D. F. Effect of alpha-adrenoceptor agonists and antagonists on cholinergic transmission in guinea-pig isolated atria. Naunyn Schmiedebergs Arch Pharmacol. 1986 Sep;334(1):40–47. doi: 10.1007/BF00498738. [DOI] [PubMed] [Google Scholar]
  18. Löffelholz K., Muscholl E. Inhibition by parasympathetic nerve stimulation of the release of the adrenergic transmitter. Naunyn Schmiedebergs Arch Pharmakol. 1970;267(2):181–184. doi: 10.1007/BF00999400. [DOI] [PubMed] [Google Scholar]
  19. Löffelholz K., Pappano A. J. The parasympathetic neuroeffector junction of the heart. Pharmacol Rev. 1985 Mar;37(1):1–24. [PubMed] [Google Scholar]
  20. Manber L., Gershon M. D. A reciprocal adrenergic-cholinergic axoaxonic synapse in the mammalian gut. Am J Physiol. 1979 Jun;236(6):E738–E745. doi: 10.1152/ajpendo.1979.236.6.E738. [DOI] [PubMed] [Google Scholar]
  21. Martin P. J., Levy J. R., Wexberg S., Levy M. N. Phasic effects of repetitive vagal stimulation on atrial contraction. Circ Res. 1983 Jun;52(6):657–663. doi: 10.1161/01.res.52.6.657. [DOI] [PubMed] [Google Scholar]
  22. Morita K., North R. A., Tokimasa T. Muscarinic agonists inactivate potassium conductance of guinea-pig myenteric neurones. J Physiol. 1982 Dec;333:125–139. doi: 10.1113/jphysiol.1982.sp014443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Muscholl E., Muth A. The effect of physostigmine on the vagally induced muscarinic inhibition of noradrenaline release from the isolated perfused rabbit atria. Naunyn Schmiedebergs Arch Pharmacol. 1982 Aug;320(2):160–169. doi: 10.1007/BF00506316. [DOI] [PubMed] [Google Scholar]
  24. Muscholl E. Peripheral muscarinic control of norepinephrine release in the cardiovascular system. Am J Physiol. 1980 Dec;239(6):H713–H720. doi: 10.1152/ajpheart.1980.239.6.H713. [DOI] [PubMed] [Google Scholar]
  25. North R. A. Receptors on individual neurones. Neuroscience. 1986 Apr;17(4):899–907. doi: 10.1016/0306-4522(86)90070-9. [DOI] [PubMed] [Google Scholar]
  26. Paton W. D., Vizi E. S. The inhibitory action of noradrenaline and adrenaline on acetylcholine output by guinea-pig ileum longitudinal muscle strip. Br J Pharmacol. 1969 Jan;35(1):10–28. doi: 10.1111/j.1476-5381.1969.tb07964.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Pott L. On the time course of the acetylcholine-induced hyperpolarization in quiescent guinea-pig atria. Pflugers Arch. 1979 May 15;380(1):71–77. doi: 10.1007/BF00582615. [DOI] [PubMed] [Google Scholar]
  28. Starke K. Alpha sympathomimetic inhibition of adrenergic and cholinergic transmission in the rabbit heart. Naunyn Schmiedebergs Arch Pharmacol. 1972;274(1):18–45. doi: 10.1007/BF00501004. [DOI] [PubMed] [Google Scholar]
  29. Wetzel G. T., Brown J. H. Presynaptic modulation of acetylcholine release from cardiac parasympathetic neurons. Am J Physiol. 1985 Jan;248(1 Pt 2):H33–H39. doi: 10.1152/ajpheart.1985.248.1.H33. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES