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1990 | 41 | 1-3 |

Tytuł artykułu

Quantification of the potencies of EDRF-releases from isolated rabbit aortic strips

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Trybulec M., Dudek R., Radziszewski W., Świerkosz T, Zembowicz A.: Quantification of the potencies of EDRF-releasers from isolated rabbit aortic strips. Acta Physiol. Pol. 1990, 41(1-3): 78-86. We have compared several known releasers of endothelium-derived relaxing factor (EDRF)(13) in respect to their potencies to generate EDRF by endothelium of rabbit aortic strips (RbA) superfused with Krebs’ buffer. The vasorelaxation by EDRF which is equivalent to 10 pmoles of GTN was evoked by 0.7 pmoles of substance P(SP), 50 pmoles of acetylcholine (Ach), 521 pmoles of calcium ionophore A 23187, 2720 pmoles of ADP. Threshold potencies of these agonists are inversely proportional to the maximum amount of EDRF released. Phospholipase C (PLC) from Clostridium perfringens at a dose of 0.1 U caused the relaxation of a similar magnitude. Phospholipase A2 (1 U), thrombin (1 U), bradykinin (30 nmoles) and serotonin (10 pmoles) did not release EDRF. It is concluded that endothelial cells of RbA differ from endothelial cells of other species in their susceptibility to release EDRF in response to various agonists.

Wydawca

-

Rocznik

Tom

41

Numer

1-3

Opis fizyczny

p.79-86,fig.,ref.

Twórcy

autor
  • Department of Pharmacology, Copernicus Academy of Medicine, Krakow, Poland
autor
  • Department of Pharmacology, Copernicus Academy of Medicine, Krakow, Poland
  • Department of Pharmacology, Copernicus Academy of Medicine, Krakow, Poland
autor
  • Department of Pharmacology, Copernicus Academy of Medicine, Krakow, Poland
autor
  • Department of Pharmacology, Copernicus Academy of Medicine, Krakow, Poland

Bibliografia

  • 1. Angus J. A., Campbell G. R., Cooks T. M., Manderson J. A. (1983). Vasodilatation by acetylcholine is endothelium-dependent; a study by sonomicrometry in canine femoral artery in vivo. J. Physiol., 344, 209-222.
  • 2. Azuma H., Ishikawa M., Sekizaki S. (1986). Endothelium-dependent inhibition of platelet aggregation. Br. J. Pharmacol., 88, 411-415.
  • 3. Berridge M. J., Irvine R. F. (1984). Inositol triphosphate a novel second messenger in cellular signal transduction. Nature, 312, 315-321.
  • 4. Bunting S., Gryglewski R., Moncada S., Vane J. R. (1976). Arterial walls generate from prostaglandin endoperoxides a substance (prostaglandin X) which relaxes strips of mesenteric and coeliac arteries and inhibits platelet aggregation. Prostaglandins, 12, 897-913.
  • 5. Chand N., Altura B. M. (1981). Acetylcholine and bradykinin relax intrapulmonary arteries by acting on endothelial cells: role in lung vascular diseases. Science, 213, 1376-1379.
  • 6. Cherry P. D., Furchgott R., Zawadzki J., Jothianadan J. (1982). The role of endothelial cells in the relaxation of isolated arteries by bradykinin. Proc. Natl. Acad. Sci. USA, 79, 106-110.
  • 7. Cherry P., Furchgott R., Zawadzki J. (1983). The endothelium-dependent relaxation of vascular smooth muscle by unsaturated fatty acid. Fed. Proc., 42, 619.
  • 8. Choen R., Shepherd J., Vanhoutte P. (1984). Endothelium and asymetrie responses of the coronary arterial wall. Am. J. Physiol., 247, H402-H408.
  • 9. Cocks T. M., Angus J. A. (1983). Endothelium-dependent relaxation of coronary arteries by noradrenaline and serotonin. Nature, 305, 627-630.
  • 10. Cocks T. M., Angus J. A., Campbell J. H., Campbell G. R. (1985). Release and properties of endothelium-derived relaxing factor (EDRF) from endothelial cells in culture. J. Cell. Physiology, 23, 310-320.
  • 11. Förstermann U., Hertting G., Neufang В. (1984). The importance of endogenous prostaglandins other than prostacyclin for the modulation of contractility of some rabbit blood vessels. Br. J. Pharmacol., 81, 623-630.
  • 12. Förstermann U., Trogisch G., Busse R. (1985). Species-dependent differences in the nature of endothelium-derived vascular relaxing factor. Eur. J. Pharmacol., 106; 639-643.1
  • 13. Furchgott R., Zawadzki J. (1980). The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. Nature, 288, 373-376.
  • 14. Furchgott R. F. (1984). The role of endothelium in the responses of vascular smooth muscle to drugs. Ann. Rev. Pharmacol. Toxicol., 24, 175-197.
  • 15. Gordon J. L., Martin W. (1983). Endothelium-dependent relaxation of the pig aorta: relationship to stimulation of Rb efflux from isolated endothelial cells. Br. J. Pharmacol., 183, 1376-1379.16.
  • 16. Griffith T. M., Edwards D. H., Lewis M. J., Newby A. C., Henderson A. H. (1984). The nature of endothelium-derived vascular factor. Nature, 308, 645-647.
  • 17. Gruetter C. A., Barry B. K., Mcnamara D. B., Gruetter D. Y., Kadowitz P. J., Ignarro L. J. (1979). Relaxation of bovine coronary arteries and activation of coronary arterial guanylate cyclase by nitric oxide, nitroprusside and a carcinogenic nitrosamine. J. Cyclic. Nucl. Res., 5, 211-224.
  • 18. Gryglewski R. J., Palmer R. M. J., Moncada S. (1986). Superoxide anion is involved in the breakdown of endothelium-derived vascular relaxing factor. Nature, 320, 454-456.
  • 19. Gryglewski R. J., Moncada S., Palmer R. M. J. (1986). Bioassay of prostacyclin and endothelium-derived relaxing factor (EDRF) from porcine aortic endothelial cells. Br. J. Pharmacol., 87, 685-694.
  • 20. Gryglewski R. J., de Nucci G., Warner T., Bearpack T., Vane J. R. (1988). Phospholipase C releases endothelium-derived relaxing factor from bovine aortic endothelial cells. Br. J. Pharmacol., 93, 106 P.
  • 21. Ignarro L. J., Byrns R. E., Buga G. M., Wood K. S. (1987). Endothelium-derived relaxing factor from pulmonary artery and vein possesses pharmacologic and chemical properties identical to those of nitric oxide radical. Circ. Res., 61, 866-879.
  • 22. Ito T. T., Ogawa K., Enomoto J., Hasimoto H., Kai J., Satake T. (1980). Comparison of effects of PGI2 and PGE, on coronary and systemic haemodynamics and on coronary cyclic nucleotide levels in dogs. Adv. Prostagl. Thromb. Res., vol. 7, 64.23
  • 23. Ku D. (1982). Coronary vascular reactivity after acute myocardial ischemia. Science, 218, 576-578.
  • 24. Lambert T., Kent R., Whorton R. (1986). Bradykinin stimulation of inositol polyphoshate production in porcine aortic endothelial cells. J. Biol. Chem., 261, 15288-15293.
  • 25. Martin W., Villani G. M., Jothianadan D., Furchgott R. F. (1985). Selective blockade of endothelium-dependent and glyceryl trinitrate induced relaxation by hemoglobin and methylene blue in the rabbit aorta. J. Pharmacol. Exp. Ther., 232, 708-716.
  • 26. Martin W., Cusack N., Carleton J., Gordon J. (1985). Specificity of P2-purinoceptor that mediates endothelium-dependent relaxation of the pig aorta. Eur. J. Pharmacol., 108, 295-299.
  • 27. Miller V. W., Vanhoutte P. M. (1986). Endothelium-dependent responses in isolated blood vessels of lower vertebrates. Blood Vessels, 23, 255-235.
  • 28. Moncada S., Gryglewski R., Bunting S., Vane J. R. (1976). An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregation. Nature, 263, 663-665.
  • 29. Nedham L., Cusack N., Pearson J., Gordon J. (1987). Characteristics of the P2-purinoceptors that mediates prostacyclin production by pig aorta endothelial cells. Eur. J. Pharmacol., 134, 193-209.
  • 30. Nitz R. E., Fiedler V. B. (1987). Molsidomine: alternative approach to treat myocardial ischemia. Pharmacotherapy, 7, 28-37.
  • 31. Palmer R. M. J,, Ferridge A. G., Moncada S. (1987). Release of nitric oxide accounts for the biological activity of endothelium-derived relaxing factor. Nature, 327, 524-526.
  • 32. Radomski M. W., Palmer R. M. J., Moncada S. (1987). The anti-aggregating properties of vascular endothelium: interactions between prostacyclin and nitric oxide. Br. J. Pharmacol., 92, 639-646.
  • 33. Schröder H., Schrör K. (1988). Organische Nitrate und Thrombozytenfunktion. Haemo- staseologie, 8, 90-99.
  • 34. Vane J. R. (1964). The use of isolated organs for detecting active substances in the circulating blood. Br. J. Pharmacol. Chemother., 23, 360.

Typ dokumentu

Bibliografia

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Identyfikator YADDA

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