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British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1993 Feb;108(2):393–397. doi: 10.1111/j.1476-5381.1993.tb12815.x

Interaction of selective compounds with muscarinic receptors at dispersed intestinal smooth muscle cells.

E Barocelli 1, M Chiavarini 1, V Ballabeni 1, F Bordi 1, M Impicciatore 1
PMCID: PMC1908000  PMID: 8448589

Abstract

1. The characterization of muscarinic receptors on single cells of the guinea-pig ileum longitudinal smooth muscle, devoid of neuronal elements, was functionally studied by estimating the affinities of muscarinic antagonists on acetylcholine-induced contractions. 2. Atropine (5 x 10(-11) to 5 x 10(-6) M), 4-diphenylacetoxy-N-methyl-piperidine methiodide (4-DAMP, 5 x 10(-8) to 5 x 10(-6) M), cyclohexyl(4-fluoro-phenyl) (3-piperidinopropyl) silanol (pFHHSiD, 5 x 10(-7) to 5 x 10(-5) M) as well as pirenzepine (5 x 10(-7) to 5 x 10(-5) M) competitively antagonized the acetylcholine-dependent contractions with different affinities (atropine > 4-DAMP > pFHHSiD > pirenzepine). 3. Methoctramine (5 x 10(-7) to 5 x 10(-5) M), and AF-DX 116 (5 x 10(-6) and 5 x 10(-5) M) also showed antagonist properties but these deviated from simple competition. These compounds, which discriminate between M2 and M3 receptors, showed a potency lower than that of pirenzepine, the rank order of potencies being pirenzepine > methoctramine > AF-DX 116. When concentrations of AF-DX 116, methoctramine and pirenzepine were increased an unspecific contractile effect occurred. 4. McN-A-343, a partial agonist on intact guinea-pig longitudinal smooth muscle strips, on this preparation induced a weak contraction (about 7% in comparison to control) that was not reversed by antimuscarinic agents. 5. These data indicate that M3 rather than M2 receptor sites are present on this tissue.

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Selected References

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  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. Barlow R. B., Berry K. J., Glenton P. A., Nilolaou N. M., Soh K. S. A comparison of affinity constants for muscarine-sensitive acetylcholine receptors in guinea-pig atrial pacemaker cells at 29 degrees C and in ileum at 29 degrees C and 37 degrees C. Br J Pharmacol. 1976 Dec;58(4):613–620. doi: 10.1111/j.1476-5381.1976.tb08631.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Barocelli E., Morini G., Ballabeni V., Lavezzo A., Impicciatore M. Effects of two new pirenzepine analogs on the contractile response of the guinea-pig oesophageal muscularis mucosae to acetylcholine, bethanechol, histamine and high potassium. Eur J Pharmacol. 1990 Apr 10;179(1-2):89–96. doi: 10.1016/0014-2999(90)90405-u. [DOI] [PubMed] [Google Scholar]
  4. Bitar K. N., Makhlouf G. M. Receptors on smooth muscle cells: characterization by contraction and specific antagonists. Am J Physiol. 1982 Apr;242(4):G400–G407. doi: 10.1152/ajpgi.1982.242.4.G400. [DOI] [PubMed] [Google Scholar]
  5. Bognar I. T., Altes U., Beinhauer C., Kessler I., Fuder H. A muscarinic receptor different from the M1, M2, M3 and M4 subtypes mediates the contraction of the rabbit iris sphincter. Naunyn Schmiedebergs Arch Pharmacol. 1992 Jun;345(6):611–618. doi: 10.1007/BF00164573. [DOI] [PubMed] [Google Scholar]
  6. Bognar I. T., Wesner M. T., Fuder H. Muscarine receptor types mediating autoinhibition of acetylcholine release and sphincter contraction in the guinea-pig iris. Naunyn Schmiedebergs Arch Pharmacol. 1990 Jan-Feb;341(1-2):22–29. doi: 10.1007/BF00195053. [DOI] [PubMed] [Google Scholar]
  7. Brown D. A., Forward A., Marsh S. Antagonist discrimination between ganglionic and ileal muscarinic receptors. Br J Pharmacol. 1980;71(2):362–364. doi: 10.1111/j.1476-5381.1980.tb10948.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Clague R. U., Eglen R. M., Strachan A. C., Whiting R. L. Action of agonists and antagonists at muscarinic receptors present on ileum and atria in vitro. Br J Pharmacol. 1985 Sep;86(1):163–170. doi: 10.1111/j.1476-5381.1985.tb09446.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Collins S. M., Crankshaw D. J. Dissociation of contraction and muscarinic receptor binding to isolated smooth muscle cells. Am J Physiol. 1986 Oct;251(4 Pt 1):G546–G552. doi: 10.1152/ajpgi.1986.251.4.G546. [DOI] [PubMed] [Google Scholar]
  10. Cost M., Majewski H. Evidence for facilitatory and inhibitory muscarinic receptors on postganglionic sympathetic nerves in mouse isolated atria. Br J Pharmacol. 1991 Apr;102(4):855–860. doi: 10.1111/j.1476-5381.1991.tb12266.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Delmendo R. E., Michel A. D., Whiting R. L. Affinity of muscarinic receptor antagonists for three putative muscarinic receptor binding sites. Br J Pharmacol. 1989 Feb;96(2):457–464. doi: 10.1111/j.1476-5381.1989.tb11838.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Doods H. N., Mathy M. J., Davidesko D., van Charldorp K. J., de Jonge A., van Zwieten P. A. Selectivity of muscarinic antagonists in radioligand and in vivo experiments for the putative M1, M2 and M3 receptors. J Pharmacol Exp Ther. 1987 Jul;242(1):257–262. [PubMed] [Google Scholar]
  13. Dörje F., Friebe T., Tacke R., Mutschler E., Lambrecht G. Novel pharmacological profile of muscarinic receptors mediating contraction of the guinea-pig uterus. Naunyn Schmiedebergs Arch Pharmacol. 1990 Sep;342(3):284–289. doi: 10.1007/BF00169439. [DOI] [PubMed] [Google Scholar]
  14. Eglen R. M., Kenny B. A., Michel A. D., Whiting R. L. Muscarinic activity of McN-A-343 and its value in muscarinic receptor classification. Br J Pharmacol. 1987 Apr;90(4):693–700. doi: 10.1111/j.1476-5381.1987.tb11222.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Eglen R. M., Michel A. D., Cornett C. M., Kunysz E. A., Whiting R. L. The interaction of hexamethonium with muscarinic receptor subtypes in vitro. Br J Pharmacol. 1989 Oct;98(2):499–506. doi: 10.1111/j.1476-5381.1989.tb12623.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Eglen R. M., Michel A. D., Whiting R. L. Characterization of the muscarinic receptor subtype mediating contractions of the guinea-pig uterus. Br J Pharmacol. 1989 Mar;96(3):497–499. doi: 10.1111/j.1476-5381.1989.tb11843.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Eglen R. M., Montgomery W. W., Dainty I. A., Dubuque L. K., Whiting R. L. The interaction of methoctramine and himbacine at atrial, smooth muscle and endothelial muscarinic receptors in vitro. Br J Pharmacol. 1988 Dec;95(4):1031–1038. doi: 10.1111/j.1476-5381.1988.tb11736.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Eltze M., Figala V. Affinity and selectivity of biperiden enantiomers for muscarinic receptor subtypes. Eur J Pharmacol. 1988 Dec 6;158(1-2):11–19. doi: 10.1016/0014-2999(88)90247-6. [DOI] [PubMed] [Google Scholar]
  19. Giachetti A., Micheletti R., Montagna E. Cardioselective profile of AF-DX 116, a muscarine M2 receptor antagonist. Life Sci. 1986 May 5;38(18):1663–1672. doi: 10.1016/0024-3205(86)90410-8. [DOI] [PubMed] [Google Scholar]
  20. Gilbert R., Rattan S., Goyal R. K. Pharmacologic identification, activation and antagonism of two muscarine receptor subtypes in the lower esophageal sphincter. J Pharmacol Exp Ther. 1984 Aug;230(2):284–291. [PubMed] [Google Scholar]
  21. Grider J. R., Bitar K. N., Makhlouf G. M. Identification of muscarinic M2 receptors on single muscle cells of the human and guinea pig intestine. Gastroenterology. 1987 Nov;93(5):951–957. doi: 10.1016/0016-5085(87)90556-7. [DOI] [PubMed] [Google Scholar]
  22. 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]
  23. Hulme E. C., Birdsall N. J., Buckley N. J. Muscarinic receptor subtypes. Annu Rev Pharmacol Toxicol. 1990;30:633–673. doi: 10.1146/annurev.pa.30.040190.003221. [DOI] [PubMed] [Google Scholar]
  24. Kilbinger H., Halim S., Lambrecht G., Weiler W., Wessler I. Comparison of affinities of muscarinic antagonists to pre- and postjunctional receptors in the guinea-pig ileum. Eur J Pharmacol. 1984 Aug 17;103(3-4):313–320. doi: 10.1016/0014-2999(84)90492-8. [DOI] [PubMed] [Google Scholar]
  25. Kilbinger H., Schneider R., Siefken H., Wolf D., D'Agostino G. Characterization of prejunctional muscarinic autoreceptors in the guinea-pig trachea. Br J Pharmacol. 1991 Jul;103(3):1757–1763. doi: 10.1111/j.1476-5381.1991.tb09859.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Lambrecht G., Feifel R., Forth B., Strohmann C., Tacke R., Mutschler E. p-fluoro-hexahydro-sila-difenidol: the first M2 beta-selective muscarinic antagonist. Eur J Pharmacol. 1988 Jul 26;152(1-2):193–194. doi: 10.1016/0014-2999(88)90856-4. [DOI] [PubMed] [Google Scholar]
  27. Lazareno S., Roberts F. F. Functional and binding studies with muscarinic M2-subtype selective antagonists. Br J Pharmacol. 1989 Sep;98(1):309–317. doi: 10.1111/j.1476-5381.1989.tb16896.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Melchiorre C., Cassinelli A., Quaglia W. Differential blockade of muscarinic receptor subtypes by polymethylene tetraamines. Novel class of selective antagonists of cardiac M-2 muscarinic receptors. J Med Chem. 1987 Jan;30(1):201–204. doi: 10.1021/jm00384a034. [DOI] [PubMed] [Google Scholar]
  29. Michel A. D., Whiting R. L. Methoctramine reveals heterogeneity of M2 muscarinic receptors in longitudinal ileal smooth muscle membranes. Eur J Pharmacol. 1988 Jan 19;145(3):305–311. doi: 10.1016/0014-2999(88)90434-7. [DOI] [PubMed] [Google Scholar]
  30. Mitchelson F. Muscarinic receptor differentiation. Pharmacol Ther. 1988;37(3):357–423. doi: 10.1016/0163-7258(88)90005-8. [DOI] [PubMed] [Google Scholar]
  31. Morini G., Barocelli E., Impicciatore M., Grider J. R., Makhlouf G. M. Receptor type for cholecystokinin on isolated intestinal muscle cells of the guinea pig. Regul Pept. 1990 May 21;28(3):313–321. doi: 10.1016/0167-0115(90)90029-v. [DOI] [PubMed] [Google Scholar]
  32. Nathanson N. M. Molecular properties of the muscarinic acetylcholine receptor. Annu Rev Neurosci. 1987;10:195–236. doi: 10.1146/annurev.ne.10.030187.001211. [DOI] [PubMed] [Google Scholar]
  33. O'Rourke S. T., Vanhoutte P. M. Subtypes of muscarinic receptors on adrenergic nerves and vascular smooth muscle of the canine saphenous vein. J Pharmacol Exp Ther. 1987 Apr;241(1):64–67. [PubMed] [Google Scholar]
  34. Pfeiffer A., Rochlitz H., Noelke B., Tacke R., Moser U., Mutschler E., Lambrecht G. Muscarinic receptors mediating acid secretion in isolated rat gastric parietal cells are of M3 type. Gastroenterology. 1990 Jan;98(1):218–222. doi: 10.1016/0016-5085(90)91314-v. [DOI] [PubMed] [Google Scholar]
  35. Schuurkes J. A., Van Bergen P. J., Van Nueten J. M. Prejunctional muscarinic (M1)-receptor interactions on guinea-pig ileum: lack of effect of cisapride. Br J Pharmacol. 1988 May;94(1):228–234. doi: 10.1111/j.1476-5381.1988.tb11519.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Souquet J. C., Grider J. R., Bitar K. N., Makhlouf G. M. Receptors for mammalian tachykinins on isolated intestinal smooth muscle cells. Am J Physiol. 1985 Oct;249(4 Pt 1):G533–G538. doi: 10.1152/ajpgi.1985.249.4.G533. [DOI] [PubMed] [Google Scholar]
  37. Verspohl E. J., Tacke R., Mutschler E., Lambrecht G. Muscarinic receptor subtypes in rat pancreatic islets: binding and functional studies. Eur J Pharmacol. 1990 Mar 27;178(3):303–311. doi: 10.1016/0014-2999(90)90109-j. [DOI] [PubMed] [Google Scholar]
  38. Waelbroeck M., Camus J., Tastenoy M., Mutschler E., Strohmann C., Tacke R., Lambrecht G., Christophe J. Stereoselectivity of (R)- and (S)-hexahydro-difenidol binding to neuroblastoma M1, cardiac M2, pancreatic M3, and striatum M4 muscarinic receptors. Chirality. 1991;3(2):118–123. doi: 10.1002/chir.530030207. [DOI] [PubMed] [Google Scholar]

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