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. 1986 May;374:153–164. doi: 10.1113/jphysiol.1986.sp016072

Non-cholinergic excitatory and inhibitory junction potentials in the circular smooth muscle of the guinea-pig ileum.

R A Bywater, G S Taylor
PMCID: PMC1182713  PMID: 3746685

Abstract

Intracellular micro-electrodes have been used to record evoked non-cholinergic junction potentials from the muscle layers of strips of guinea-pig ileum cut parallel to the longitudinal muscle. Transmural stimulation with single pulses, 0.6 ms duration produced inhibitory junction potentials (i.j.p.s) in the circular muscle layer. In the circular muscle layer, transmural stimulation with repetitive volleys (e.g. three pulses, 0.6 ms, 50 Hz delivered every 4 s) at low stimulus strengths (25-40 mA) produced non-cholinergic excitatory junction potentials (e.j.p.s) after an initial i.j.p. At higher stimulus strengths (greater than 40 mA) i.j.p.s occurred following each volley but were superimposed on a prolonged depolarization. Following repetitive volley stimulation every four seconds in the presence of apamin (0.25 microM), the i.j.p.s. were abolished and the non-cholinergic e.j.p.s clearly showed facilitation. At higher stimulus strengths (and at volley repetition rates of less than 0.1 Hz) volley stimulation now produced an apamin-resistant slow hyperpolarization followed by a distinct slow depolarization. Electrotonic potentials were readily recorded from the superficially located longitudinal muscle cells: in this muscle layer transmural stimulation produced small, slow changes in membrane potential. These results suggest that non-cholinergic excitatory and inhibitory nerve fibres primarily supply the circular rather than the longitudinal muscle layer in the guinea-pig ileum.

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Selected References

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

  1. Abe Y., Tomita T. Cable properties of smooth muscle. J Physiol. 1968 May;196(1):87–100. doi: 10.1113/jphysiol.1968.sp008496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bauer V., Kuriyama H. Evidence for non-cholinergic, non-adrenergic transmission in the guinea-pig ileum. J Physiol. 1982 Sep;330:95–110. doi: 10.1113/jphysiol.1982.sp014331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Björkroth U. Inhibition of smooth muscle contractions induced by capsaicin and electrical transmural stimulation by a substance P antagonist. Acta Physiol Scand Suppl. 1983;515:11–16. [PubMed] [Google Scholar]
  4. Bywater R. A., Holman M. E., Taylor G. S. Atropine-resistant depolarization in the guinea-pig small intestine. J Physiol. 1981 Jul;316:369–378. doi: 10.1113/jphysiol.1981.sp013794. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bywater R. A., Taylor G. S. Non-cholinergic fast and slow post-stimulus depolarization in the guinea-pig ileum. J Physiol. 1983 Jul;340:47–56. doi: 10.1113/jphysiol.1983.sp014748. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bywater R. A., Taylor G. S. The passive membrane properties and excitatory junction potentials of the guinea pig deferens. J Physiol. 1980 Mar;300:303–316. doi: 10.1113/jphysiol.1980.sp013163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Costa M., Furness J. B., Pullin C. O., Bornstein J. Substance P enteric neurons mediate non-cholinergic transmission to the circular muscle of the guinea-pig intestine. Naunyn Schmiedebergs Arch Pharmacol. 1985 Feb;328(4):446–453. doi: 10.1007/BF00692914. [DOI] [PubMed] [Google Scholar]
  8. Franco R., Costa M., Furness J. B. Evidence for the release of endogenous substance P from intestinal nerves. Naunyn Schmiedebergs Arch Pharmacol. 1979 Apr;306(3):195–201. doi: 10.1007/BF00507103. [DOI] [PubMed] [Google Scholar]
  9. Gintzler A. R., Hyde D. A specific substance P antagonist attenuates non-cholinergic electrically induced contractures of the guinea pig isolated ileum. Neurosci Lett. 1983 Sep 19;40(1):75–79. doi: 10.1016/0304-3940(83)90095-2. [DOI] [PubMed] [Google Scholar]
  10. Habermann E. Apamin. Pharmacol Ther. 1984;25(2):255–270. doi: 10.1016/0163-7258(84)90046-9. [DOI] [PubMed] [Google Scholar]
  11. Maas A. J., Den Hertog A. The effect of apamin on the smooth muscle cells of the guinea-pig taenia coli. Eur J Pharmacol. 1979 Sep 15;58(2):151–156. doi: 10.1016/0014-2999(79)90006-2. [DOI] [PubMed] [Google Scholar]
  12. Maas A. J. The effects of apamin on responses evoked by field stimulation in guinea-pig taenia caeci. Eur J Pharmacol. 1981 Jul 17;73(1):1–9. doi: 10.1016/0014-2999(81)90139-4. [DOI] [PubMed] [Google Scholar]
  13. Muller M. J., Baer H. P. Apamin, a nonspecific antagonist of smooth muscle relaxants. Naunyn Schmiedebergs Arch Pharmacol. 1980 Feb;311(1):105–107. doi: 10.1007/BF00500310. [DOI] [PubMed] [Google Scholar]
  14. Niel J. P., Bywater R. A., Taylor G. S. Apamin-resistant post-stimulus hyperpolarization in the circular muscle of the guinea-pig ileum. J Auton Nerv Syst. 1983 Nov;9(2-3):565–569. doi: 10.1016/0165-1838(83)90014-0. [DOI] [PubMed] [Google Scholar]
  15. Niel J. P., Bywater R. A., Taylor G. S. Effect of substance P on non-cholinergic fast and slow post-stimulus depolarization in the guinea-pig ileum. J Auton Nerv Syst. 1983 Dec;9(4):573–584. doi: 10.1016/0165-1838(83)90114-5. [DOI] [PubMed] [Google Scholar]
  16. Shuba M. F., Vladimirova I. A. Effect of apamin on the electrical responses of smooth muscle to adenosine 5'-triphosphate and to non-adrenergic, non-cholinergic nerve stimulation. Neuroscience. 1980;5(5):853–859. doi: 10.1016/0306-4522(80)90154-2. [DOI] [PubMed] [Google Scholar]
  17. Tonini M., Frigo G., Lecchini S., D'Angelo L., Crema A. Hyoscine-resistant peristalsis in guinea-pig ileum. Eur J Pharmacol. 1981 May 22;71(4):375–381. doi: 10.1016/0014-2999(81)90181-3. [DOI] [PubMed] [Google Scholar]

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