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. 1986 Jan 15;233(2):309–319. doi: 10.1042/bj2330309

Extracellular ATP: effects, sources and fate.

J L Gordon
PMCID: PMC1153029  PMID: 3006665

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Selected References

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  1. Akasu T., Hirai K., Koketsu K. Modulatory actions of ATP on membrane potentials of bullfrog sympathetic ganglion cells. Brain Res. 1983 Jan 10;258(2):313–317. doi: 10.1016/0006-8993(83)91157-5. [DOI] [PubMed] [Google Scholar]
  2. BERNE R. M. REGULATION OF CORONARY BLOOD FLOW. Physiol Rev. 1964 Jan;44:1–29. doi: 10.1152/physrev.1964.44.1.1. [DOI] [PubMed] [Google Scholar]
  3. BINET L., BURSTEIN M. Poumon et action vasculaire de l'adénosinetriphosphate. Presse Med. 1950 Oct 28;58(68):1201–1203. [PubMed] [Google Scholar]
  4. BORN G. V. Aggregation of blood platelets by adenosine diphosphate and its reversal. Nature. 1962 Jun 9;194:927–929. doi: 10.1038/194927b0. [DOI] [PubMed] [Google Scholar]
  5. Baer H. P., Drummond G. I. Catabolism of adenine nucleotides by the isolated perfused rat heart. Proc Soc Exp Biol Med. 1968 Jan;127(1):33–36. doi: 10.3181/00379727-127-32614. [DOI] [PubMed] [Google Scholar]
  6. Berne R. M. The role of adenosine in the regulation of coronary blood flow. Circ Res. 1980 Dec;47(6):807–813. doi: 10.1161/01.res.47.6.807. [DOI] [PubMed] [Google Scholar]
  7. Black P. H. Shedding from the cell surface of normal and cancer cells. Adv Cancer Res. 1980;32:75–199. doi: 10.1016/s0065-230x(08)60361-9. [DOI] [PubMed] [Google Scholar]
  8. Boeynaems J. M., Galand N. Stimulation of vascular prostacyclin synthesis by extracellular ADP and ATP. Biochem Biophys Res Commun. 1983 Apr 15;112(1):290–296. doi: 10.1016/0006-291x(83)91829-6. [DOI] [PubMed] [Google Scholar]
  9. Born G. V., Kratzer M. A. Source and concentration of extracellular adenosine triphosphate during haemostasis in rats, rabbits and man. J Physiol. 1984 Sep;354:419–429. doi: 10.1113/jphysiol.1984.sp015385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Born G. V. Observations on the change in shape of blood platelets brought about by adenosine diphosphate. J Physiol. 1970 Aug;209(2):487–511. doi: 10.1113/jphysiol.1970.sp009176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Born G. V., Richardson P. D. Activation time of blood platelets. J Membr Biol. 1980 Dec 15;57(2):87–90. doi: 10.1007/BF01868994. [DOI] [PubMed] [Google Scholar]
  12. Brown C. M., Burnstock G. The structural conformation of the polyphosphate chain of the ATP molecule is critical for its promotion of prostaglandin biosynthesis. Eur J Pharmacol. 1981 Jan 5;69(1):81–86. doi: 10.1016/0014-2999(81)90604-x. [DOI] [PubMed] [Google Scholar]
  13. Brown C., Burnstock G., Cocks T. Effects of adenosine 5'-triphosphate (ATP) and beta-gamma-methylene ATP on the rat urinary bladder. Br J Pharmacol. 1979 Jan;65(1):97–102. doi: 10.1111/j.1476-5381.1979.tb17337.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Burgess G. M., Claret M., Jenkinson D. H. Effects of catecholamines, ATP and ionophore A23187 on potassium and calcium movements in isolated hepatocytes. Nature. 1979 Jun 7;279(5713):544–546. doi: 10.1038/279544a0. [DOI] [PubMed] [Google Scholar]
  15. Burgess G. M., Claret M., Jenkinson D. H. Effects of quinine and apamin on the calcium-dependent potassium permeability of mammalian hepatocytes and red cells. J Physiol. 1981 Aug;317:67–90. doi: 10.1113/jphysiol.1981.sp013814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Burnstock G. Comparative studies of purinergic nerves. J Exp Zool. 1975 Oct;194(1):103–133. doi: 10.1002/jez.1401940108. [DOI] [PubMed] [Google Scholar]
  17. Burnstock G., Cusack N. J., Hills J. M., MacKenzie I., Meghji P. Studies on the stereoselectivity of the P2-purinoceptor. Br J Pharmacol. 1983 Aug;79(4):907–913. doi: 10.1111/j.1476-5381.1983.tb10535.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Burnstock G., Cusack N. J., Meldrum L. A. Effects of phosphorothioate analogues of ATP, ADP and AMP on guinea-pig taenia coli and urinary bladder. Br J Pharmacol. 1984 Jun;82(2):369–374. doi: 10.1111/j.1476-5381.1984.tb10771.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Burnstock G., Cusack N. J., Meldrum L. A. Studies on the stereoselectivity of the P2-purinoceptor on the guinea-pig vas deferens. Br J Pharmacol. 1985 Feb;84(2):431–434. doi: 10.1111/j.1476-5381.1985.tb12927.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Burnstock G., Kennedy C. Is there a basis for distinguishing two types of P2-purinoceptor? Gen Pharmacol. 1985;16(5):433–440. doi: 10.1016/0306-3623(85)90001-1. [DOI] [PubMed] [Google Scholar]
  21. Burnstock G., Meghji P. Distribution of P1- and P2-purinoceptors in the guinea-pig and frog heart. Br J Pharmacol. 1981 Aug;73(4):879–885. doi: 10.1111/j.1476-5381.1981.tb08741.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Burnstock G. Neural nomenclature. Nature. 1971 Jan 22;229(5282):282–283. doi: 10.1038/229282d0. [DOI] [PubMed] [Google Scholar]
  23. Burnstock G. Purinergic nerves. Pharmacol Rev. 1972 Sep;24(3):509–581. [PubMed] [Google Scholar]
  24. Cameron D. J. Inhibition of macrophage mediated cytotoxicity by exogenous adenosine 5'-triphosphate. J Clin Lab Immunol. 1984 Dec;15(4):215–218. [PubMed] [Google Scholar]
  25. Chapal J., Loubatieres-Mariani M. M. Evidence for purinergic receptors on vascular smooth muscle in rat pancreas. Eur J Pharmacol. 1983 Mar 4;87(4):423–430. doi: 10.1016/0014-2999(83)90081-x. [DOI] [PubMed] [Google Scholar]
  26. Chaudry I. H., Sayeed M. M., Baue A. E. Effect of adenosine triphosphate-magnesium chloride administration in shock. Surgery. 1974 Feb;75(2):220–227. [PubMed] [Google Scholar]
  27. Clemens M. G., Forrester T. Appearance of adenosine triphosphate in the coronary sinus effluent from isolated working rat heart in response to hypoxia. J Physiol. 1981 Mar;312:143–158. doi: 10.1113/jphysiol.1981.sp013621. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Cockcroft S., Gomperts B. D. Activation and inhibition of calcium-dependent histamine secretion by ATP ions applied to rat mast cells. J Physiol. 1979 Nov;296:229–243. doi: 10.1113/jphysiol.1979.sp013002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Cockcroft S., Gomperts B. D. The ATP4- receptor of rat mast cells. Biochem J. 1980 Jun 15;188(3):789–798. doi: 10.1042/bj1880789. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Collis M. G., Pettinger S. J. Can ATP stimulate P1-receptors in guinea-pig atrium without conversion to adenosine? Eur J Pharmacol. 1982 Jul 30;81(4):521–529. doi: 10.1016/0014-2999(82)90341-7. [DOI] [PubMed] [Google Scholar]
  31. Cooper D. R., Lewis G. P., Lieberman G. E., Webb H., Westwick J. ADP metabolism in vascular tissue, a possible thrombo-regulatory mechanism. Thromb Res. 1979;14(6):901–914. doi: 10.1016/0049-3848(79)90008-2. [DOI] [PubMed] [Google Scholar]
  32. Crutchley D. J., Eling T. E., Anderson M. W. ADPase activity of isolated perfused rat lung. Life Sci. 1978 Apr 24;22(16):1413–1420. doi: 10.1016/0024-3205(78)90635-5. [DOI] [PubMed] [Google Scholar]
  33. Crutchley D. J., Ryan U. S., Ryan J. W. Effects of aspirin and dipyridamole on the degradation of adenosine diphosphate by cultured cells derived from bovine pulmonary artery. J Clin Invest. 1980 Jul;66(1):29–35. doi: 10.1172/JCI109831. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Cusack N. J., Hickman M. E., Born G. V. Effects of D- and L- enantiomers of adenosine, AMP and ADP and their 2-chloro- and 2-azido- analogues on human platelets. Proc R Soc Lond B Biol Sci. 1979 Nov 30;206(1163):139–144. doi: 10.1098/rspb.1979.0097. [DOI] [PubMed] [Google Scholar]
  35. Cusack N. J., Hourani S. M. Effects of RP and SP diastereoisomers of adenosine 5'-O-(1-thiodiphosphate) on human platelets. Br J Pharmacol. 1981 Jun;73(2):409–412. doi: 10.1111/j.1476-5381.1981.tb10437.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Cusack N. J., Hourani S. M. Some pharmacological and biochemical interactions of the enantiomers of adenylyl 5'-(beta, gamma-methylene)-diphosphonate with the guinea-pig urinary bladder. Br J Pharmacol. 1984 May;82(1):155–159. doi: 10.1111/j.1476-5381.1984.tb16453.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Cusack N. J., Pearson J. D., Gordon J. L. Stereoselectivity of ectonucleotidases on vascular endothelial cells. Biochem J. 1983 Sep 15;214(3):975–981. doi: 10.1042/bj2140975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Cusack N. J., Planker M. Relaxation of isolated taenia coli of guinea-pig by enantiomers of 2-azido analogues of adenosine and adenine nucleotides. Br J Pharmacol. 1979 Sep;67(1):153–158. [PMC free article] [PubMed] [Google Scholar]
  39. DUFF F., PATTERSON G. C., SHEPHERD J. T. A quantitative study of the response to adenosine triphosphate of the blood vessels of the human hand and forearm. J Physiol. 1954 Sep 28;125(3):581–589. doi: 10.1113/jphysiol.1954.sp005182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Dahlquist R., Diamant B. Interaction of ATP and calcium on the rat mast cell: effect on histamine release. Acta Pharmacol Toxicol (Copenh) 1974 May;34(5):368–384. doi: 10.1111/j.1600-0773.1974.tb03533.x. [DOI] [PubMed] [Google Scholar]
  41. Dahlén S. E., Hedqvist P. ATP, beta-gamma-methylene-ATP, and adenosine inhibit non-cholinergic non-adrenergic transmission in rat urinary bladder. Acta Physiol Scand. 1980 Jun;109(2):137–142. doi: 10.1111/j.1748-1716.1980.tb06578.x. [DOI] [PubMed] [Google Scholar]
  42. Dicker P., Heppel L. A., Rozengurt E. Control of membrane permeability by external and internal ATP in 3T6 cells grown in serum-free medium. Proc Natl Acad Sci U S A. 1980 Apr;77(4):2103–2107. doi: 10.1073/pnas.77.4.2103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Dosne A. M., Legrand C., Bauvois B., Bodevin E., Caen J. P. Comparative degradation of adenylnucleotides by cultured endothelial cells and fibroblasts. Biochem Biophys Res Commun. 1978 Nov 14;85(1):183–189. doi: 10.1016/s0006-291x(78)80027-8. [DOI] [PubMed] [Google Scholar]
  44. Drury A. N., Szent-Györgyi A. The physiological activity of adenine compounds with especial reference to their action upon the mammalian heart. J Physiol. 1929 Nov 25;68(3):213–237. doi: 10.1113/jphysiol.1929.sp002608. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Dvorak H. F., Quay S. C., Orenstein N. S., Dvorak A. M., Hahn P., Bitzer A. M., Carvalho A. C. Tumor shedding and coagulation. Science. 1981 May 22;212(4497):923–924. doi: 10.1126/science.7195067. [DOI] [PubMed] [Google Scholar]
  46. Ellison J. P., Hibbs R. G. An ultrastructural study of mammalian cardiac ganglia. J Mol Cell Cardiol. 1976 Feb;8(2):89–101. doi: 10.1016/0022-2828(76)90023-7. [DOI] [PubMed] [Google Scholar]
  47. Fedan J. S., Hogaboom G. K., Westfall D. P., O'Donnell J. P. Comparison of contractions of the smooth muscle of the guinea-pig vas deferens induced by ATP and related nucleotides. Eur J Pharmacol. 1982 Jul 9;81(2):193–204. doi: 10.1016/0014-2999(82)90437-x. [DOI] [PubMed] [Google Scholar]
  48. Forrester T. An estimate of adenosine triphosphate release into the venous effluent from exercising human forearm muscle. J Physiol. 1972 Aug;224(3):611–628. doi: 10.1113/jphysiol.1972.sp009915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Forrester T., Harper A. M., MacKenzie E. T., Thomson E. M. Effect of adenosine triphosphate and some derivatives on cerebral blood flow and metabolism. J Physiol. 1979 Nov;296:343–355. doi: 10.1113/jphysiol.1979.sp013009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Forrester T., Lind A. R. Identification of adenosine triphosphate in human plasma and the concentration in the venous effluent of forearm muscles before, during and after sustained contractions. J Physiol. 1969 Oct;204(2):347–364. doi: 10.1113/jphysiol.1969.sp008917. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Forrester T., Williams C. A. Release of adenosine triphosphate from isolated adult heart cells in response to hypoxia. J Physiol. 1977 Jun;268(2):371–390. doi: 10.1113/jphysiol.1977.sp011862. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Fredholm B. B., Hedqvist P., Lindström K., Wennmalm M. Release of nucleosides and nucleotides from the rabbit heart by sympathetic nerve stimulation. Acta Physiol Scand. 1982 Nov;116(3):285–295. doi: 10.1111/j.1748-1716.1982.tb07142.x. [DOI] [PubMed] [Google Scholar]
  53. Furchgott R. F., Zawadzki J. V. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. Nature. 1980 Nov 27;288(5789):373–376. doi: 10.1038/288373a0. [DOI] [PubMed] [Google Scholar]
  54. Furness J. B., Costa M. The nervous release and the action of substances which affect intestinal muscle through neither adrenoreceptors nor cholinoreceptors. Philos Trans R Soc Lond B Biol Sci. 1973 Mar 15;265(867):123–133. doi: 10.1098/rstb.1973.0015. [DOI] [PubMed] [Google Scholar]
  55. Fyffe R. E., Perl E. R. Is ATP a central synaptic mediator for certain primary afferent fibers from mammalian skin? Proc Natl Acad Sci U S A. 1984 Nov;81(21):6890–6893. doi: 10.1073/pnas.81.21.6890. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Gallacher D. V. Are there purinergic receptors on parotid acinar cells? Nature. 1982 Mar 4;296(5852):83–86. doi: 10.1038/296083a0. [DOI] [PubMed] [Google Scholar]
  57. George J. N., Thoi L. L., McManus L. M., Reimann T. A. Isolation of human platelet membrane microparticles from plasma and serum. Blood. 1982 Oct;60(4):834–840. [PubMed] [Google Scholar]
  58. Glasgow J. G., Schade R., Pitlick F. A. Evidence that ADP hydrolysis by human cells is related to thrombogenic potential1. Thromb Res. 1978 Aug;13(2):255–266. doi: 10.1016/0049-3848(78)90013-0. [DOI] [PubMed] [Google Scholar]
  59. Gordon J. L., Martin W. Endothelium-dependent relaxation of the pig aorta: relationship to stimulation of 86Rb efflux from isolated endothelial cells. Br J Pharmacol. 1983 Jun;79(2):531–541. doi: 10.1111/j.1476-5381.1983.tb11028.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Gough G. R., Maguire M. H., Satchell D. G. Three new adenosine triphosphate analogs. Synthesis and effects on isolated gut. J Med Chem. 1973 Oct;16(10):1188–1190. doi: 10.1021/jm00268a028. [DOI] [PubMed] [Google Scholar]
  61. Gough G., Maguire M. H., Penglis F. Analogues of adenosine 5'-diphosphate-new platelet aggregators. Influence of purine ring and and phosphate chain substitutions on the platelet-aggregating potency of adenosine 5'-diphosphate. Mol Pharmacol. 1972 Mar;8(2):170–177. [PubMed] [Google Scholar]
  62. Gregory S., Kern M. Adenosine and adenine nucleotides are mitogenic for mouse thymocytes. Biochem Biophys Res Commun. 1978 Aug 14;83(3):1111–1116. doi: 10.1016/0006-291x(78)91510-3. [DOI] [PubMed] [Google Scholar]
  63. Griffith T. M., Edwards D. H., Lewis M. J., Newby A. C., Henderson A. H. The nature of endothelium-derived vascular relaxant factor. Nature. 1984 Apr 12;308(5960):645–647. doi: 10.1038/308645a0. [DOI] [PubMed] [Google Scholar]
  64. Guccione M. A., Packham M. A., Kinlough-Rathbone R. L., Mustard J. F. Reactions of 14C-ADP and 14C-ATP with washed platelets from rabbits. Blood. 1971 May;37(5):542–555. [PubMed] [Google Scholar]
  65. HILLARP N. A. The release of catechol amines from the amine containing granules of the adrenal medulla. Acta Physiol Scand. 1958 Oct 8;43(3-4):292–302. doi: 10.1111/j.1748-1716.1958.tb01596.x. [DOI] [PubMed] [Google Scholar]
  66. HOLTON P. The liberation of adenosine triphosphate on antidromic stimulation of sensory nerves. J Physiol. 1959 Mar 12;145(3):494–504. doi: 10.1113/jphysiol.1959.sp006157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Haslam R. J. Interactions of the pharmacological receptors of blood platelets with adenylate cyclase. Ser Haematol. 1973;6(3):333–350. [PubMed] [Google Scholar]
  68. Henon B. K., McAfee D. A. The ionic basis of adenosine receptor actions on post-ganglionic neurones in the rat. J Physiol. 1983 Mar;336:607–620. doi: 10.1113/jphysiol.1983.sp014600. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Hogaboom G. K., O'Donnell J. P., Fedan J. S. Purinergic receptors: photoaffinity analog of adenosine triphosphate is a specific adenosine triphosphate antagonist. Science. 1980 Jun 13;208(4449):1273–1276. doi: 10.1126/science.6103581. [DOI] [PubMed] [Google Scholar]
  70. Hourani S. M., Welford L. A., Cusack N. J. L-AMP-PCP, an ATP receptor agonist in guinea-pig bladder, is inactive on taenia coli. Eur J Pharmacol. 1985 Jan 22;108(2):197–200. doi: 10.1016/0014-2999(85)90726-5. [DOI] [PubMed] [Google Scholar]
  71. Hugues M., Romey G., Duval D., Vincent J. P., Lazdunski M. Apamin as a selective blocker of the calcium-dependent potassium channel in neuroblastoma cells: voltage-clamp and biochemical characterization of the toxin receptor. Proc Natl Acad Sci U S A. 1982 Feb;79(4):1308–1312. doi: 10.1073/pnas.79.4.1308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Ikehara S., Pahwa R. N., Lunzer D. G., Good R. A., Modak M. J. Adenosine-5'-triphosphate-(ATP) mediated stimulation and suppression of DNA synthesis in lymphoid cells. I. Characterization of ATP responsive cells in mouse lymphoid organs. J Immunol. 1981 Nov;127(5):1834–1838. [PubMed] [Google Scholar]
  73. Ingerman C. M., Smith J. B., Silver M. J. Direct measurement of platelet secretion in whole blood. Thromb Res. 1979;16(3-4):335–344. doi: 10.1016/0049-3848(79)90081-1. [DOI] [PubMed] [Google Scholar]
  74. Israël M., Lesbats B., Meunier F. M., Stinnakre J. Postsynaptic release of adenosine triphosphate induced by single impulse transmitter action. Proc R Soc Lond B Biol Sci. 1976 Jun 30;193(1113):461–468. doi: 10.1098/rspb.1976.0058. [DOI] [PubMed] [Google Scholar]
  75. Jahr C. E., Jessell T. M. ATP excites a subpopulation of rat dorsal horn neurones. Nature. 1983 Aug 25;304(5928):730–733. doi: 10.1038/304730a0. [DOI] [PubMed] [Google Scholar]
  76. Jenkinson D. H., Haylett D. G., Cook N. S. Calcium-activated potassium channels in liver cells. Cell Calcium. 1983 Dec;4(5-6):429–437. doi: 10.1016/0143-4160(83)90019-2. [DOI] [PubMed] [Google Scholar]
  77. Johnson V. E., Hilton P. J. Frusemide-sensitive sodium and potassium transport by human leucocytes. Clin Sci (Lond) 1985 Jan;68(1):89–91. doi: 10.1042/cs0680089. [DOI] [PubMed] [Google Scholar]
  78. Kang E. S., Gates R. E., Chiang T. M., Kang A. H. Ectoprotein kinase activity of the isolated rat adipocyte. Biochem Biophys Res Commun. 1979 Feb 14;86(3):769–778. doi: 10.1016/0006-291x(79)91779-0. [DOI] [PubMed] [Google Scholar]
  79. Kennedy C., Burnstock G. ATP produces vasodilation via P1 purinoceptors and vasoconstriction via P2 purinoceptors in the isolated rabbit central ear artery. Blood Vessels. 1985;22(3):145–155. doi: 10.1159/000158592. [DOI] [PubMed] [Google Scholar]
  80. Kennedy C., Burnstock G. Evidence for two types of P2-purinoceptor in longitudinal muscle of the rabbit portal vein. Eur J Pharmacol. 1985 Apr 23;111(1):49–56. doi: 10.1016/0014-2999(85)90112-8. [DOI] [PubMed] [Google Scholar]
  81. Kennedy C., Delbro D., Burnstock G. P2-purinoceptors mediate both vasodilation (via the endothelium) and vasoconstriction of the isolated rat femoral artery. Eur J Pharmacol. 1985 Jan 2;107(2):161–168. doi: 10.1016/0014-2999(85)90055-x. [DOI] [PubMed] [Google Scholar]
  82. Kreutzberg G. W., Barron K. D., Schubert P. Cytochemical localization of 5'-nucleotidase in glial plasma membranes. Brain Res. 1978 Dec 15;158(2):247–257. doi: 10.1016/0006-8993(78)90672-8. [DOI] [PubMed] [Google Scholar]
  83. Ku D. D. Coronary vascular reactivity after acute myocardial ischemia. Science. 1982 Nov 5;218(4572):576–578. doi: 10.1126/science.7123259. [DOI] [PubMed] [Google Scholar]
  84. Kübler D., Pyerin W., Kinzel V. Protein kinase activity and substrates at the surface of intact HeLa cells. J Biol Chem. 1982 Jan 10;257(1):322–329. [PubMed] [Google Scholar]
  85. LeRoy E. C., Ager A., Gordon J. L. Effects of neutrophil elastase and other proteases on porcine aortic endothelial prostaglandin I2 production, adenine nucleotide release, and responses to vasoactive agents. J Clin Invest. 1984 Sep;74(3):1003–1010. doi: 10.1172/JCI111467. [DOI] [PMC free article] [PubMed] [Google Scholar]
  86. Lieberman G. E., Lewis G. P., Peters T. J. A membrane-bound enzyme in rabbit aorta capable of inhibiting adenosine-diphosphate-induced platelet aggregation. Lancet. 1977 Aug 13;2(8033):330–332. doi: 10.1016/s0140-6736(77)91488-x. [DOI] [PubMed] [Google Scholar]
  87. Lollar P., Owen W. G. Active-site-dependent, thrombin-induced release of adenine nucleotides from cultured human endothelial cells. Ann N Y Acad Sci. 1981;370:51–56. doi: 10.1111/j.1749-6632.1981.tb29720.x. [DOI] [PubMed] [Google Scholar]
  88. Loubatieres-Mariani M. M., Chapal J., Lignon F., Valette G. Structural specificity of nucleotides for insulin secretory action from the isolated perfused rat pancreas. Eur J Pharmacol. 1979 Nov 16;59(3-4):277–286. doi: 10.1016/0014-2999(79)90291-7. [DOI] [PubMed] [Google Scholar]
  89. Lush D. J., Munday K. A., Noble A. R. Furosemide fails to alter plasma active or inactive renin in conscious sheep but does so in anaesthetized animals. J Physiol. 1983 Jul;340:57–75. doi: 10.1113/jphysiol.1983.sp014749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  90. Macfarlane D. E., Mills D. C. The effects of ATP on platelets: evidence against the central role of released ADP in primary aggregation. Blood. 1975 Sep;46(3):309–320. [PubMed] [Google Scholar]
  91. Macfarlane D. E., Srivastava P. C., Mills D. C. 2-Methylthioadenosine[beta-32P]diphosphate. An agonist and radioligand for the receptor that inhibits the accumulation of cyclic AMP in intact blood platelets. J Clin Invest. 1983 Mar;71(3):420–428. doi: 10.1172/JCI110786. [DOI] [PMC free article] [PubMed] [Google Scholar]
  92. Maguire M. H., Satchell D. G. The contribution of adenosine to the inhibitory actions of adenine nucleotides on the guinea-pig taenia coli: studies with phosphate-modified adenine nucleotide analogs and dipyridamole. J Pharmacol Exp Ther. 1979 Dec;211(3):626–631. [PubMed] [Google Scholar]
  93. Martin W., Cusack N. J., Carleton J. S., Gordon J. L. Specificity of P2-purinoceptor that mediates endothelium-dependent relaxation of the pig aorta. Eur J Pharmacol. 1985 Feb 5;108(3):295–299. doi: 10.1016/0014-2999(85)90452-2. [DOI] [PubMed] [Google Scholar]
  94. Meghji P., Burnstock G. The effects of adenyl compounds on the heart of the axolotl (Ambystoma mexicanum). Comp Biochem Physiol C. 1983;76(2):319–326. doi: 10.1016/0742-8413(83)90085-3. [DOI] [PubMed] [Google Scholar]
  95. Moody C. J., Meghji P., Burnstock G. Stimulation of P1-purinoceptors by ATP depends partly on its conversion to AMP and adenosine and partly on direct action. Eur J Pharmacol. 1984 Jan 13;97(1-2):47–54. doi: 10.1016/0014-2999(84)90511-9. [DOI] [PubMed] [Google Scholar]
  96. Needleman P., Minkes M. S., Douglas J. R., Jr Stimulation of prostaglandin biosynthesis by adenine nucleotides. Profile of prostaglandin release by perfused organs. Circ Res. 1974 Apr;34(4):455–460. doi: 10.1161/01.res.34.4.455. [DOI] [PubMed] [Google Scholar]
  97. Ohkawa M., Chaudry I. H., Clemens M. G., Baue A. E. ATP-MgCl2 produces sustained improvement in hepatic mitochondrial function and blood flow after hepatic ischemia. J Surg Res. 1984 Sep;37(3):226–234. doi: 10.1016/0022-4804(84)90183-5. [DOI] [PubMed] [Google Scholar]
  98. Paddle B. M., Burnstock G. Release of ATP from perfused heart during coronary vasodilatation. Blood Vessels. 1974;11(3):110–119. doi: 10.1159/000158005. [DOI] [PubMed] [Google Scholar]
  99. Pearson J. D., Carleton J. S., Gordon J. L. Metabolism of adenine nucleotides by ectoenzymes of vascular endothelial and smooth-muscle cells in culture. Biochem J. 1980 Aug 15;190(2):421–429. doi: 10.1042/bj1900421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  100. Pearson J. D., Cusack N. J. Investigation of the preferred Mg(II)-adenine-nucleotide complex at the active site of ectonucleotidases in intact vascular cells using phosphorothioate analogues of ADP and ATP. Eur J Biochem. 1985 Sep 2;151(2):373–375. doi: 10.1111/j.1432-1033.1985.tb09111.x. [DOI] [PubMed] [Google Scholar]
  101. Pearson J. D., Gordon J. L. Nucleotide metabolism by endothelium. Annu Rev Physiol. 1985;47:617–627. doi: 10.1146/annurev.ph.47.030185.003153. [DOI] [PubMed] [Google Scholar]
  102. Pearson J. D., Gordon J. L. Vascular endothelial and smooth muscle cells in culture selectively release adenine nucleotides. Nature. 1979 Oct 4;281(5730):384–386. doi: 10.1038/281384a0. [DOI] [PubMed] [Google Scholar]
  103. Pearson J. D., Slakey L. L., Gordon J. L. Stimulation of prostaglandin production through purinoceptors on cultured porcine endothelial cells. Biochem J. 1983 Jul 15;214(1):273–276. doi: 10.1042/bj2140273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  104. Penttila A., Trump B. F. Extracellular acidosis protects Ehrlich ascites tumor cells and rat renal cortex against anoxic injury. Science. 1974 Jul 19;185(4147):277–278. doi: 10.1126/science.185.4147.277. [DOI] [PubMed] [Google Scholar]
  105. Potter D. D., Furshpan E. J., Landis S. C. Transmitter status in cultured rat sympathetic neurons: plasticity and multiple function. Fed Proc. 1983 Apr;42(6):1626–1632. [PubMed] [Google Scholar]
  106. Rapoport R. M., Murad F. Agonist-induced endothelium-dependent relaxation in rat thoracic aorta may be mediated through cGMP. Circ Res. 1983 Mar;52(3):352–357. doi: 10.1161/01.res.52.3.352. [DOI] [PubMed] [Google Scholar]
  107. Remold-O'Donnell E. Protein kinase activity associated with the surface of guinea pig macrophages. J Exp Med. 1978 Oct 1;148(4):1099–1104. doi: 10.1084/jem.148.4.1099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  108. Rozengurt E., Heppel L. A. Reciprocal control of membrane permeability of transformed cultures of mouse cell lines by external and internal ATP. J Biol Chem. 1979 Feb 10;254(3):708–714. [PubMed] [Google Scholar]
  109. Rutherford A., Burnstock G. Neuronal and non-neuronal components in the overflow of labelled adenyl compounds from guinea-pig taenia coli. Eur J Pharmacol. 1978 Mar 15;48(2):195–202. doi: 10.1016/0014-2999(78)90328-x. [DOI] [PubMed] [Google Scholar]
  110. Ryan J. W., Smith U. Metabolism of adenosine 5'-monophosphate during circulation through the lungs. Trans Assoc Am Physicians. 1971;84:297–306. [PubMed] [Google Scholar]
  111. Ryan U. S. Structural bases for metabolic activity. Annu Rev Physiol. 1982;44:223–239. doi: 10.1146/annurev.ph.44.030182.001255. [DOI] [PubMed] [Google Scholar]
  112. Salt T. E., Hill R. G. Excitation of single sensory neurones in the rat caudal trigeminal nucleus by iontophoretically applied adenosine 5'-triphosphate. Neurosci Lett. 1983 Jan 31;35(1):53–57. doi: 10.1016/0304-3940(83)90526-8. [DOI] [PubMed] [Google Scholar]
  113. Satchell D. G., Burnstock G. Comparison of the inhibitory effects on the guinea-pig taenia coli of adenine nucleotides and adenosine in the presence and absence of dipyridamole. Eur J Pharmacol. 1975 Jun-Jul;32(02):324–328. doi: 10.1016/0014-2999(75)90299-x. [DOI] [PubMed] [Google Scholar]
  114. Satchell D. G., Maguire M. H. Inhibitory effects of adenine nucleotide analogs on the isolated guinea-pig taenia coli. J Pharmacol Exp Ther. 1975 Dec;195(3):540–548. [PubMed] [Google Scholar]
  115. Schmidt A., Ortaldo J. R., Herberman R. B. Inhibition of human natural killer cell reactivity by exogenous adenosine 5'-triphosphate. J Immunol. 1984 Jan;132(1):146–150. [PubMed] [Google Scholar]
  116. Schwartzman M., Pinkas R., Raz A. Evidence for different purinergic receptors for ATP and ADP in rabbit kidney and heart. Eur J Pharmacol. 1981 Sep 11;74(2-3):167–173. doi: 10.1016/0014-2999(81)90527-6. [DOI] [PubMed] [Google Scholar]
  117. Silinsky E. M., Ginsborg B. L. Inhibition of acetylcholine release from preganglionic frog nerves by ATP but not adenosine. Nature. 1983 Sep 22;305(5932):327–328. doi: 10.1038/305327a0. [DOI] [PubMed] [Google Scholar]
  118. Smith U., Ryan J. W. Electron microscopy of endothelial and epithelial components of the lungs: correlations of structure and function. Fed Proc. 1973 Sep;32(9):1957–1966. [PubMed] [Google Scholar]
  119. Sneddon P., Burnstock G. ATP as a co-transmitter in rat tail artery. Eur J Pharmacol. 1984 Oct 30;106(1):149–152. doi: 10.1016/0014-2999(84)90688-5. [DOI] [PubMed] [Google Scholar]
  120. Sneddon P., Burnstock G. Inhibition of excitatory junction potentials in guinea-pig vas deferens by alpha, beta-methylene-ATP: further evidence for ATP and noradrenaline as cotransmitters. Eur J Pharmacol. 1984 Apr 13;100(1):85–90. doi: 10.1016/0014-2999(84)90318-2. [DOI] [PubMed] [Google Scholar]
  121. Sommarin M., Henriksson T., Jergil B. Cyclic AMP-dependent protein phosphorylation on the surface of rat hepatocytes. FEBS Lett. 1981 May 18;127(2):285–289. doi: 10.1016/0014-5793(81)80225-6. [DOI] [PubMed] [Google Scholar]
  122. Stanley K. K., Edwards M. R., Luzio J. P. Subcellular distribution and movement of 5'-nucleotidase in rat cells. Biochem J. 1980 Jan 15;186(1):59–69. doi: 10.1042/bj1860059. [DOI] [PMC free article] [PubMed] [Google Scholar]
  123. Stone T. W. Physiological roles for adenosine and adenosine 5'-triphosphate in the nervous system. Neuroscience. 1981;6(4):523–555. doi: 10.1016/0306-4522(81)90145-7. [DOI] [PubMed] [Google Scholar]
  124. Stone T. W., Taylor D. A. Antagonism by clonidine of neuronal depressant responses to adenosine, adenosine-5'-monophosphate and adenosine triphosphate. Br J Pharmacol. 1978 Nov;64(3):369–374. doi: 10.1111/j.1476-5381.1978.tb08659.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  125. Trams E. G. A proposal for the role of ecto-enzymes and adenylates in traumatic shock. J Theor Biol. 1980 Dec 7;87(3):609–621. doi: 10.1016/0022-5193(80)90239-8. [DOI] [PubMed] [Google Scholar]
  126. Trams E. G. Evidence for ATP action on the cell surface. Nature. 1974 Dec 6;252(5483):480–482. doi: 10.1038/252480a0. [DOI] [PubMed] [Google Scholar]
  127. Trams E. G., Lauter C. J. On the sidedness of plasma membrane enzymes. Biochim Biophys Acta. 1974 Apr 29;345(2):180–197. doi: 10.1016/0005-2736(74)90257-0. [DOI] [PubMed] [Google Scholar]
  128. Van Coevorden A., Boeynaems J. M. Physiological concentrations of ADP stimulate the release of prostacyclin from bovine aortic endothelial cells. Prostaglandins. 1984 Apr;27(4):615–626. doi: 10.1016/0090-6980(84)90097-2. [DOI] [PubMed] [Google Scholar]
  129. WILLIAMSON J. R., DIPIETRO D. L. EVIDENCE FOR EXTRACELLULAR ENZYMIC ACTIVITY OF THE ISOLATED PERFUSED RAT HEART. Biochem J. 1965 Apr;95:226–232. doi: 10.1042/bj0950226. [DOI] [PMC free article] [PubMed] [Google Scholar]
  130. WOLF M. M., BERNE R. M. Coronary vasodilator properties of purine and pyrimidine derivatives. Circ Res. 1956 May;4(3):343–348. doi: 10.1161/01.res.4.3.343. [DOI] [PubMed] [Google Scholar]
  131. Weisman G. A., Dunn S. D., De B. K., Kitagawa T., Friedberg I. On the role of protein phosphorylation in the ATP-dependent permeabilization of transformed cells. J Cell Physiol. 1984 Feb;118(2):124–132. doi: 10.1002/jcp.1041180204. [DOI] [PubMed] [Google Scholar]
  132. Westfall D. P., Stitzel R. E., Rowe J. N. The postjunctional effects and neural release of purine compounds in the guinea-pig vas deferens. Eur J Pharmacol. 1978 Jul 1;50(1):27–38. doi: 10.1016/0014-2999(78)90250-9. [DOI] [PubMed] [Google Scholar]
  133. Woo Y. T., Manery J. F. 5'-nucleotidase: an ecto-enzyme of frog skeletal muscle. Biochim Biophys Acta. 1975 Jul 27;397(1):144–152. doi: 10.1016/0005-2744(75)90188-6. [DOI] [PubMed] [Google Scholar]

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