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. 1991 Mar;65(3):116–125. doi: 10.1136/hrt.65.3.116

St Cyres lecture. Endothelium in control.

A H Henderson 1
PMCID: PMC1024532  PMID: 2015118

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Selected References

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

  1. Abell T. J., Richards A. M., Ikram H., Espiner E. A., Yandle T. Atrial natriuretic factor inhibits proliferation of vascular smooth muscle cells stimulated by platelet-derived growth factor. Biochem Biophys Res Commun. 1989 May 15;160(3):1392–1396. doi: 10.1016/s0006-291x(89)80158-5. [DOI] [PubMed] [Google Scholar]
  2. Amezcua J. L., Palmer R. M., de Souza B. M., Moncada S. Nitric oxide synthesized from L-arginine regulates vascular tone in the coronary circulation of the rabbit. Br J Pharmacol. 1989 Aug;97(4):1119–1124. doi: 10.1111/j.1476-5381.1989.tb12569.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Andrews H. E., Bruckdorfer K. R., Dunn R. C., Jacobs M. Low-density lipoproteins inhibit endothelium-dependent relaxation in rabbit aorta. Nature. 1987 May 21;327(6119):237–239. doi: 10.1038/327237a0. [DOI] [PubMed] [Google Scholar]
  4. Angelini G. D., Christie M. I., Bryan A. J., Lewis M. J. Surgical preparation impairs release of endothelium-derived relaxing factor from human saphenous vein. Ann Thorac Surg. 1989 Sep;48(3):417–420. doi: 10.1016/s0003-4975(10)62869-x. [DOI] [PubMed] [Google Scholar]
  5. Angus J. A., Campbell G. R., Cocks T. M., Manderson J. A. Vasodilatation by acetylcholine is endothelium-dependent: a study by sonomicrometry in canine femoral artery in vivo. J Physiol. 1983 Nov;344:209–222. doi: 10.1113/jphysiol.1983.sp014934. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Angus J. A., Cocks T. M. Endothelium-derived relaxing factor. Pharmacol Ther. 1989;41(1-2):303–352. doi: 10.1016/0163-7258(89)90112-5. [DOI] [PubMed] [Google Scholar]
  7. Asakura T., Karino T. Flow patterns and spatial distribution of atherosclerotic lesions in human coronary arteries. Circ Res. 1990 Apr;66(4):1045–1066. doi: 10.1161/01.res.66.4.1045. [DOI] [PubMed] [Google Scholar]
  8. Barrett M. L., Willis A. L., Vane J. R. Inhibition of platelet-derived mitogen release by nitric oxide (EDRF). Agents Actions. 1989 Jun;27(3-4):488–491. doi: 10.1007/BF01972860. [DOI] [PubMed] [Google Scholar]
  9. Booth R. F., Martin J. F., Honey A. C., Hassall D. G., Beesley J. E., Moncada S. Rapid development of atherosclerotic lesions in the rabbit carotid artery induced by perivascular manipulation. Atherosclerosis. 1989 Apr;76(2-3):257–268. doi: 10.1016/0021-9150(89)90109-3. [DOI] [PubMed] [Google Scholar]
  10. Bredt D. S., Snyder S. H. Isolation of nitric oxide synthetase, a calmodulin-requiring enzyme. Proc Natl Acad Sci U S A. 1990 Jan;87(2):682–685. doi: 10.1073/pnas.87.2.682. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Brutsaert D. L., Meulemans A. L., Sipido K. R., Sys S. U. Effects of damaging the endocardial surface on the mechanical performance of isolated cardiac muscle. Circ Res. 1988 Feb;62(2):358–366. doi: 10.1161/01.res.62.2.358. [DOI] [PubMed] [Google Scholar]
  12. Brutsaert D. L. The endocardium. Annu Rev Physiol. 1989;51:263–273. doi: 10.1146/annurev.ph.51.030189.001403. [DOI] [PubMed] [Google Scholar]
  13. Bult H., Boeckxstaens G. E., Pelckmans P. A., Jordaens F. H., Van Maercke Y. M., Herman A. G. Nitric oxide as an inhibitory non-adrenergic non-cholinergic neurotransmitter. Nature. 1990 May 24;345(6273):346–347. doi: 10.1038/345346a0. [DOI] [PubMed] [Google Scholar]
  14. Byrne J. V., Griffith T. M., Edwards D. H., Harrison T. J., Johnston K. R. Investigation of the vasoconstrictor action of subarachnoid haemoglobin in the pig cerebral circulation in vivo. Br J Pharmacol. 1989 Jul;97(3):669–674. doi: 10.1111/j.1476-5381.1989.tb12002.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Cannon R. O., 3rd, Watson R. M., Rosing D. R., Epstein S. E. Angina caused by reduced vasodilator reserve of the small coronary arteries. J Am Coll Cardiol. 1983 Jun;1(6):1359–1373. doi: 10.1016/s0735-1097(83)80037-0. [DOI] [PubMed] [Google Scholar]
  16. Carden D. L., Smith J. K., Korthuis R. J. Neutrophil-mediated microvascular dysfunction in postischemic canine skeletal muscle. Role of granulocyte adherence. Circ Res. 1990 May;66(5):1436–1444. doi: 10.1161/01.res.66.5.1436. [DOI] [PubMed] [Google Scholar]
  17. Caro C. G., Lever M. J. The mass transport of the arterial wall: effect of mechanical stresses and vasoactive agents, including nitrates. Z Kardiol. 1983;72 (Suppl 3):178–181. [PubMed] [Google Scholar]
  18. Chilian W. M., Dellsperger K. C., Layne S. M., Eastham C. L., Armstrong M. A., Marcus M. L., Heistad D. D. Effects of atherosclerosis on the coronary microcirculation. Am J Physiol. 1990 Feb;258(2 Pt 2):H529–H539. doi: 10.1152/ajpheart.1990.258.2.H529. [DOI] [PubMed] [Google Scholar]
  19. Christie M. I., Griffith T. M., Lewis M. J. A comparison of basal and agonist-stimulated release of endothelium-derived relaxing factor from different arteries. Br J Pharmacol. 1989 Oct;98(2):397–406. doi: 10.1111/j.1476-5381.1989.tb12610.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Christie M. I., Lewis M. J. Vascular smooth muscle sensitivity to endothelium-derived relaxing factor is different in different arteries. Br J Pharmacol. 1988 Oct;95(2):630–636. doi: 10.1111/j.1476-5381.1988.tb11685.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Cohen R. A., Zitnay K. M., Haudenschild C. C., Cunningham L. D. Loss of selective endothelial cell vasoactive functions caused by hypercholesterolemia in pig coronary arteries. Circ Res. 1988 Nov;63(5):903–910. doi: 10.1161/01.res.63.5.903. [DOI] [PubMed] [Google Scholar]
  22. Colden-Stanfield M., Schilling W. P., Ritchie A. K., Eskin S. G., Navarro L. T., Kunze D. L. Bradykinin-induced increases in cytosolic calcium and ionic currents in cultured bovine aortic endothelial cells. Circ Res. 1987 Nov;61(5):632–640. doi: 10.1161/01.res.61.5.632. [DOI] [PubMed] [Google Scholar]
  23. Collins P., Chappell S. P., Griffith T. M., Lewis M. J., Henderson A. H. Differences in basal endothelium-derived relaxing factor activity in different artery types. J Cardiovasc Pharmacol. 1986 Nov-Dec;8(6):1158–1162. doi: 10.1097/00005344-198611000-00010. [DOI] [PubMed] [Google Scholar]
  24. Collins P., Griffith T. M., Henderson A. H., Lewis M. J. Endothelium-derived relaxing factor alters calcium fluxes in rabbit aorta: a cyclic guanosine monophosphate-mediated effect. J Physiol. 1986 Dec;381:427–437. doi: 10.1113/jphysiol.1986.sp016336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Collins P., Henderson A. H., Lang D., Lewis M. J. Endothelium-derived relaxing factor and nitroprusside compared in noradrenaline- and K+-contracted rabbit and rat aortae. J Physiol. 1988 Jun;400:395–404. doi: 10.1113/jphysiol.1988.sp017127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Cox D. A., Vita J. A., Treasure C. B., Fish R. D., Alexander R. W., Ganz P., Selwyn A. P. Atherosclerosis impairs flow-mediated dilation of coronary arteries in humans. Circulation. 1989 Sep;80(3):458–465. doi: 10.1161/01.cir.80.3.458. [DOI] [PubMed] [Google Scholar]
  27. Cronstein B. N., Levin R. I., Belanoff J., Weissmann G., Hirschhorn R. Adenosine: an endogenous inhibitor of neutrophil-mediated injury to endothelial cells. J Clin Invest. 1986 Sep;78(3):760–770. doi: 10.1172/JCI112638. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Curmi P. A., Juan L., Tedgui A. Effect of transmural pressure on low density lipoprotein and albumin transport and distribution across the intact arterial wall. Circ Res. 1990 Jun;66(6):1692–1702. doi: 10.1161/01.res.66.6.1692. [DOI] [PubMed] [Google Scholar]
  29. Dauber I. M., VanBenthuysen K. M., McMurtry I. F., Wheeler G. S., Lesnefsky E. J., Horwitz L. D., Weil J. V. Functional coronary microvascular injury evident as increased permeability due to brief ischemia and reperfusion. Circ Res. 1990 Apr;66(4):986–998. doi: 10.1161/01.res.66.4.986. [DOI] [PubMed] [Google Scholar]
  30. De Mey J. G., Vanhoutte P. M. Heterogeneous behavior of the canine arterial and venous wall. Importance of the endothelium. Circ Res. 1982 Oct;51(4):439–447. doi: 10.1161/01.res.51.4.439. [DOI] [PubMed] [Google Scholar]
  31. Derian C. K., Moskowitz M. A. Polyphosphoinositide hydrolysis in endothelial cells and carotid artery segments. Bradykinin-2 receptor stimulation is calcium-independent. J Biol Chem. 1986 Mar 15;261(8):3831–3837. [PubMed] [Google Scholar]
  32. Drexler H., Zeiher A. M., Wollschläger H., Meinertz T., Just H., Bonzel T. Flow-dependent coronary artery dilatation in humans. Circulation. 1989 Sep;80(3):466–474. doi: 10.1161/01.cir.80.3.466. [DOI] [PubMed] [Google Scholar]
  33. Dreyer W. J., Smith C. W., Michael L. H., Rossen R. D., Hughes B. J., Entman M. L., Anderson D. C. Canine neutrophil activation by cardiac lymph obtained during reperfusion of ischemic myocardium. Circ Res. 1989 Dec;65(6):1751–1762. doi: 10.1161/01.res.65.6.1751. [DOI] [PubMed] [Google Scholar]
  34. Edwards D. H., Griffith T. M., Ryley H. C., Henderson A. H. Haptoglobin-haemoglobin complex in human plasma inhibits endothelium dependent relaxation: evidence that endothelium derived relaxing factor acts as a local autocoid. Cardiovasc Res. 1986 Aug;20(8):549–556. doi: 10.1093/cvr/20.8.549. [DOI] [PubMed] [Google Scholar]
  35. Evans H. G., Ryley H. C., Hallett I., Lewis M. J. Human red blood cells inhibit endothelium-derived relaxing factor (EDRF) activity. Eur J Pharmacol. 1989 Apr 25;163(2-3):361–364. doi: 10.1016/0014-2999(89)90207-0. [DOI] [PubMed] [Google Scholar]
  36. Evans H. G., Smith J. A., Lewis M. J. Release of endothelium-derived relaxing factor is inhibited by 8-bromo-cyclic guanosine monophosphate. J Cardiovasc Pharmacol. 1988 Dec;12(6):672–677. doi: 10.1097/00005344-198812000-00008. [DOI] [PubMed] [Google Scholar]
  37. Factor S. M., Sonnenblick E. H. The pathogenesis of clinical and experimental congestive cardiomyopathies: recent concepts. Prog Cardiovasc Dis. 1985 May-Jun;27(6):395–420. doi: 10.1016/0033-0620(85)90002-7. [DOI] [PubMed] [Google Scholar]
  38. Freiman P. C., Mitchell G. G., Heistad D. D., Armstrong M. L., Harrison D. G. Atherosclerosis impairs endothelium-dependent vascular relaxation to acetylcholine and thrombin in primates. Circ Res. 1986 Jun;58(6):783–789. doi: 10.1161/01.res.58.6.783. [DOI] [PubMed] [Google Scholar]
  39. Fry D. L. Mass transport, atherogenesis, and risk. Arteriosclerosis. 1987 Jan-Feb;7(1):88–100. doi: 10.1161/01.atv.7.1.88. [DOI] [PubMed] [Google Scholar]
  40. Furchgott R. F. Role of endothelium in responses of vascular smooth muscle. Circ Res. 1983 Nov;53(5):557–573. doi: 10.1161/01.res.53.5.557. [DOI] [PubMed] [Google Scholar]
  41. Furchgott R. F. The role of endothelium in the responses of vascular smooth muscle to drugs. Annu Rev Pharmacol Toxicol. 1984;24:175–197. doi: 10.1146/annurev.pa.24.040184.001135. [DOI] [PubMed] [Google Scholar]
  42. 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]
  43. Furlong B., Henderson A. H., Lewis M. J., Smith J. A. Endothelium-derived relaxing factor inhibits in vitro platelet aggregation. Br J Pharmacol. 1987 Apr;90(4):687–692. doi: 10.1111/j.1476-5381.1987.tb11221.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Förstermann U., Mülsch A., Böhme E., Busse R. Stimulation of soluble guanylate cyclase by an acetylcholine-induced endothelium-derived factor from rabbit and canine arteries. Circ Res. 1986 Apr;58(4):531–538. doi: 10.1161/01.res.58.4.531. [DOI] [PubMed] [Google Scholar]
  45. Galle J., Bassenge E., Busse R. Oxidized low density lipoproteins potentiate vasoconstrictions to various agonists by direct interaction with vascular smooth muscle. Circ Res. 1990 May;66(5):1287–1293. doi: 10.1161/01.res.66.5.1287. [DOI] [PubMed] [Google Scholar]
  46. Garg U. C., Hassid A. Nitric oxide-generating vasodilators and 8-bromo-cyclic guanosine monophosphate inhibit mitogenesis and proliferation of cultured rat vascular smooth muscle cells. J Clin Invest. 1989 May;83(5):1774–1777. doi: 10.1172/JCI114081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Garthwaite J., Charles S. L., Chess-Williams R. Endothelium-derived relaxing factor release on activation of NMDA receptors suggests role as intercellular messenger in the brain. Nature. 1988 Nov 24;336(6197):385–388. doi: 10.1038/336385a0. [DOI] [PubMed] [Google Scholar]
  48. Gebremedhin D., Koltai M. Z., Pogátsa G., Magyar K., Hadházy P. Influence of experimental diabetes on the mechanical responses of canine coronary arteries: role of endothelium. Cardiovasc Res. 1988 Aug;22(8):537–544. doi: 10.1093/cvr/22.8.537. [DOI] [PubMed] [Google Scholar]
  49. Gillespie J. S., Liu X. R., Martin W. The effects of L-arginine and NG-monomethyl L-arginine on the response of the rat anococcygeus muscle to NANC nerve stimulation. Br J Pharmacol. 1989 Dec;98(4):1080–1082. doi: 10.1111/j.1476-5381.1989.tb12650.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Gisclard V., Miller V. M., Vanhoutte P. M. Effect of 17 beta-estradiol on endothelium-dependent responses in the rabbit. J Pharmacol Exp Ther. 1988 Jan;244(1):19–22. [PubMed] [Google Scholar]
  51. Goodnight S. H., Jr The vascular effects of omega-3 fatty acids. J Invest Dermatol. 1989 Aug;93(2 Suppl):102S–106S. doi: 10.1111/1523-1747.ep12581218. [DOI] [PubMed] [Google Scholar]
  52. Gordon J. B., Ganz P., Nabel E. G., Fish R. D., Zebede J., Mudge G. H., Alexander R. W., Selwyn A. P. Atherosclerosis influences the vasomotor response of epicardial coronary arteries to exercise. J Clin Invest. 1989 Jun;83(6):1946–1952. doi: 10.1172/JCI114103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Griffith T. M., Edwards D. H. Basal EDRF activity helps to keep the geometrical configuration of arterial bifurcations close to the Murray optimum. J Theor Biol. 1990 Oct 21;146(4):545–573. doi: 10.1016/s0022-5193(05)80378-9. [DOI] [PubMed] [Google Scholar]
  54. Griffith T. M., Edwards D. H., Davies R. L., Harrison T. J., Evans K. T. EDRF coordinates the behaviour of vascular resistance vessels. Nature. 1987 Oct 1;329(6138):442–445. doi: 10.1038/329442a0. [DOI] [PubMed] [Google Scholar]
  55. Griffith T. M., Edwards D. H., Davies R. L., Harrison T. J., Evans K. T. Endothelium-derived relaxing factor (EDRF) and resistance vessels in an intact vascular bed: a microangiographic study of the rabbit isolated ear. Br J Pharmacol. 1988 Mar;93(3):654–662. doi: 10.1111/j.1476-5381.1988.tb10323.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Griffith T. M., Edwards D. H., Davies R. L., Henderson A. H. The role of EDRF in flow distribution: a microangiographic study of the rabbit isolated ear. Microvasc Res. 1989 Mar;37(2):162–177. doi: 10.1016/0026-2862(89)90035-6. [DOI] [PubMed] [Google Scholar]
  57. Griffith T. M., Edwards D. H., Lewis M. J., Henderson A. H. Ergometrine-induced arterial dilatation: an endothelium-mediated effect. J Mol Cell Cardiol. 1984 May;16(5):479–482. doi: 10.1016/s0022-2828(84)80619-7. [DOI] [PubMed] [Google Scholar]
  58. Griffith T. M., Edwards D. H., Lewis M. J., Henderson A. H. Evidence that cyclic guanosine monophosphate (cGMP) mediates endothelium-dependent relaxation. Eur J Pharmacol. 1985 Jun 7;112(2):195–202. doi: 10.1016/0014-2999(85)90496-0. [DOI] [PubMed] [Google Scholar]
  59. 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]
  60. Griffith T. M., Edwards D. H., Newby A. C., Lewis M. J., Henderson A. H. Production of endothelium derived relaxant factor is dependent on oxidative phosphorylation and extracellular calcium. Cardiovasc Res. 1986 Jan;20(1):7–12. doi: 10.1093/cvr/20.1.7. [DOI] [PubMed] [Google Scholar]
  61. Griffith T. M., Henderson A. H. EDRF and the regulation of vascular tone. Int J Microcirc Clin Exp. 1989 Nov;8(4):383–396. [PubMed] [Google Scholar]
  62. Griffith T. M., Henderson A. H., Edwards D. H., Lewis M. J. Isolated perfused rabbit coronary artery and aortic strip preparations: the role of endothelium-derived relaxant factor. J Physiol. 1984 Jun;351:13–24. doi: 10.1113/jphysiol.1984.sp015228. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Griffith T. M., Lewis M. J., Newby A. C., Henderson A. H. Endothelium-derived relaxing factor. J Am Coll Cardiol. 1988 Sep;12(3):797–806. doi: 10.1016/0735-1097(88)90324-5. [DOI] [PubMed] [Google Scholar]
  64. Gryglewski R. J., Palmer R. M., Moncada S. Superoxide anion is involved in the breakdown of endothelium-derived vascular relaxing factor. Nature. 1986 Apr 3;320(6061):454–456. doi: 10.1038/320454a0. [DOI] [PubMed] [Google Scholar]
  65. Hallam T. J., Pearson J. D. Exogenous ATP raises cytoplasmic free calcium in fura-2 loaded piglet aortic endothelial cells. FEBS Lett. 1986 Oct 20;207(1):95–99. doi: 10.1016/0014-5793(86)80019-9. [DOI] [PubMed] [Google Scholar]
  66. Harris K. H., MacLeod K. M. Influence of the endothelium on contractile responses of arteries from diabetic rats. Eur J Pharmacol. 1988 Aug 9;153(1):55–64. doi: 10.1016/0014-2999(88)90587-0. [DOI] [PubMed] [Google Scholar]
  67. Heistad D. D., Mark A. L., Marcus M. L., Piegors D. J., Armstrong M. L. Dietary treatment of atherosclerosis abolishes hyperresponsiveness to serotonin: implications for vasospasm. Circ Res. 1987 Sep;61(3):346–351. doi: 10.1161/01.res.61.3.346. [DOI] [PubMed] [Google Scholar]
  68. Henderson A. H. Syndrome X. Cardiovasc Drugs Ther. 1989 Jun;3 (Suppl 1):271–274. doi: 10.1007/BF00148471. [DOI] [PubMed] [Google Scholar]
  69. Hibbs J. B., Jr, Vavrin Z., Taintor R. R. L-arginine is required for expression of the activated macrophage effector mechanism causing selective metabolic inhibition in target cells. J Immunol. 1987 Jan 15;138(2):550–565. [PubMed] [Google Scholar]
  70. Hogan J. C., Lewis M. J., Henderson A. H. In vivo EDRF activity influences platelet function. Br J Pharmacol. 1988 Aug;94(4):1020–1022. doi: 10.1111/j.1476-5381.1988.tb11616.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Hogan J. C., Smith J. A., Richards A. C., Lewis M. J. Atrial natriuretic peptide inhibits the release of endothelium-derived relaxing factor from blood vessels of the rabbit. Eur J Pharmacol. 1989 Jun 8;165(1):129–134. doi: 10.1016/0014-2999(89)90778-4. [DOI] [PubMed] [Google Scholar]
  72. Horio Y., Yasue H., Rokutanda M., Nakamura N., Ogawa H., Takaoka K., Matsuyama K., Kimura T. Effects of intracoronary injection of acetylcholine on coronary arterial diameter. Am J Cardiol. 1986 Apr 15;57(11):984–989. doi: 10.1016/0002-9149(86)90743-5. [DOI] [PubMed] [Google Scholar]
  73. Ignarro L. J. Biological actions and properties of endothelium-derived nitric oxide formed and released from artery and vein. Circ Res. 1989 Jul;65(1):1–21. doi: 10.1161/01.res.65.1.1. [DOI] [PubMed] [Google Scholar]
  74. Ignarro L. J., Burke T. M., Wood K. S., Wolin M. S., Kadowitz P. J. Association between cyclic GMP accumulation and acetylcholine-elicited relaxation of bovine intrapulmonary artery. J Pharmacol Exp Ther. 1984 Mar;228(3):682–690. [PubMed] [Google Scholar]
  75. Ignarro L. J., Byrns R. E., Buga G. M., Wood K. S. Endothelium-derived relaxing factor from pulmonary artery and vein possesses pharmacologic and chemical properties identical to those of nitric oxide radical. Circ Res. 1987 Dec;61(6):866–879. doi: 10.1161/01.res.61.6.866. [DOI] [PubMed] [Google Scholar]
  76. Jacob R., Merritt J. E., Hallam T. J., Rink T. J. Repetitive spikes in cytoplasmic calcium evoked by histamine in human endothelial cells. Nature. 1988 Sep 1;335(6185):40–45. doi: 10.1038/335040a0. [DOI] [PubMed] [Google Scholar]
  77. Jayakody L., Senaratne M., Thomson A., Kappagoda T. Endothelium-dependent relaxation in experimental atherosclerosis in the rabbit. Circ Res. 1987 Feb;60(2):251–264. doi: 10.1161/01.res.60.2.251. [DOI] [PubMed] [Google Scholar]
  78. Kaiser L., Spickard R. C., Olivier N. B. Heart failure depresses endothelium-dependent responses in canine femoral artery. Am J Physiol. 1989 Apr;256(4 Pt 2):H962–H967. doi: 10.1152/ajpheart.1989.256.4.H962. [DOI] [PubMed] [Google Scholar]
  79. Kalan J. M., Roberts W. C. Significance of cardiac weight in patients having coronary artery bypass grafting for angina pectoris. Am J Cardiol. 1988 Jul 1;62(1):36–40. doi: 10.1016/0002-9149(88)91361-6. [DOI] [PubMed] [Google Scholar]
  80. Kamata K., Miyata N., Kasuya Y. Impairment of endothelium-dependent relaxation and changes in levels of cyclic GMP in aorta from streptozotocin-induced diabetic rats. Br J Pharmacol. 1989 Jun;97(2):614–618. doi: 10.1111/j.1476-5381.1989.tb11993.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  81. Kassell N. F., Sasaki T., Colohan A. R., Nazar G. Cerebral vasospasm following aneurysmal subarachnoid hemorrhage. Stroke. 1985 Jul-Aug;16(4):562–572. doi: 10.1161/01.str.16.4.562. [DOI] [PubMed] [Google Scholar]
  82. Katsuki S., Arnold W., Mittal C., Murad F. Stimulation of guanylate cyclase by sodium nitroprusside, nitroglycerin and nitric oxide in various tissue preparations and comparison to the effects of sodium azide and hydroxylamine. J Cyclic Nucleotide Res. 1977 Feb;3(1):23–35. [PubMed] [Google Scholar]
  83. Kawamoto J. H., McLaughlin B. E., Brien J. F., Marks G. S., Nakatsu K. Biotransformation of glyceryl trinitrate and elevation of cyclic GMP precede glyceryl trinitrate-induced vasodilation. J Cardiovasc Pharmacol. 1990 May;15(5):714–719. doi: 10.1097/00005344-199005000-00005. [DOI] [PubMed] [Google Scholar]
  84. Kelm M., Schrader J. Control of coronary vascular tone by nitric oxide. Circ Res. 1990 Jun;66(6):1561–1575. doi: 10.1161/01.res.66.6.1561. [DOI] [PubMed] [Google Scholar]
  85. Knowles R. G., Palacios M., Palmer R. M., Moncada S. Formation of nitric oxide from L-arginine in the central nervous system: a transduction mechanism for stimulation of the soluble guanylate cyclase. Proc Natl Acad Sci U S A. 1989 Jul;86(13):5159–5162. doi: 10.1073/pnas.86.13.5159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  86. Kolodgie F. D., Virmani R., Rice H. E., Mergner W. J. Vascular reactivity during the progression of atherosclerotic plaque. A study in Watanabe heritable hyperlipidemic rabbits. Circ Res. 1990 Apr;66(4):1112–1126. doi: 10.1161/01.res.66.4.1112. [DOI] [PubMed] [Google Scholar]
  87. Komori K., Shimokawa H., Vanhoutte P. M. Endothelium-dependent relaxation in response to aggregating platelets in porcine femoral veins and its modulation by diet. Circulation. 1989 Aug;80(2):401–409. doi: 10.1161/01.cir.80.2.401. [DOI] [PubMed] [Google Scholar]
  88. Kugiyama K., Kerns S. A., Morrisett J. D., Roberts R., Henry P. D. Impairment of endothelium-dependent arterial relaxation by lysolecithin in modified low-density lipoproteins. Nature. 1990 Mar 8;344(6262):160–162. doi: 10.1038/344160a0. [DOI] [PubMed] [Google Scholar]
  89. Lambert T. L., Kent R. S., Whorton A. R. Bradykinin stimulation of inositol polyphosphate production in porcine aortic endothelial cells. J Biol Chem. 1986 Nov 15;261(32):15288–15293. [PubMed] [Google Scholar]
  90. Lamping K. G., Dole W. P. Acute hypertension selectively potentiates constrictor responses of large coronary arteries to serotonin by altering endothelial function in vivo. Circ Res. 1987 Dec;61(6):904–913. doi: 10.1161/01.res.61.6.904. [DOI] [PubMed] [Google Scholar]
  91. Lang D., Lewis M. J. Endothelium-derived relaxing factor inhibits the formation of inositol trisphosphate by rabbit aorta. J Physiol. 1989 Apr;411:45–52. doi: 10.1113/jphysiol.1989.sp017558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  92. Lansman J. B. Endothelial mechanosensors. Going with the flow. Nature. 1988 Feb 11;331(6156):481–482. doi: 10.1038/331481a0. [DOI] [PubMed] [Google Scholar]
  93. Lansman J. B., Hallam T. J., Rink T. J. Single stretch-activated ion channels in vascular endothelial cells as mechanotransducers? 1987 Feb 26-Mar 4Nature. 325(6107):811–813. doi: 10.1038/325811a0. [DOI] [PubMed] [Google Scholar]
  94. Lewis M. J., Shah A. M., Smith J. A., Henderson A. H. Does endocardium modulate myocardial contractile performance? Cardioscience. 1990 Jun;1(2):83–87. [PubMed] [Google Scholar]
  95. Ludmer P. L., Selwyn A. P., Shook T. L., Wayne R. R., Mudge G. H., Alexander R. W., Ganz P. Paradoxical vasoconstriction induced by acetylcholine in atherosclerotic coronary arteries. N Engl J Med. 1986 Oct 23;315(17):1046–1051. doi: 10.1056/NEJM198610233151702. [DOI] [PubMed] [Google Scholar]
  96. Lüscher T. F., Diederich D., Siebenmann R., Lehmann K., Stulz P., von Segesser L., Yang Z. H., Turina M., Grädel E., Weber E. Difference between endothelium-dependent relaxation in arterial and in venous coronary bypass grafts. N Engl J Med. 1988 Aug 25;319(8):462–467. doi: 10.1056/NEJM198808253190802. [DOI] [PubMed] [Google Scholar]
  97. Marletta M. A., Yoon P. S., Iyengar R., Leaf C. D., Wishnok J. S. Macrophage oxidation of L-arginine to nitrite and nitrate: nitric oxide is an intermediate. Biochemistry. 1988 Nov 29;27(24):8706–8711. doi: 10.1021/bi00424a003. [DOI] [PubMed] [Google Scholar]
  98. Martin S. E., Chenoweth D. E., Engler R. L., Roth D. M., Longhurst J. C. C5a decreases regional coronary blood flow and myocardial function in pigs: implications for a granulocyte mechanism. Circ Res. 1988 Aug;63(2):483–491. doi: 10.1161/01.res.63.2.483. [DOI] [PubMed] [Google Scholar]
  99. Martin W., Smith J. A., White D. G. The mechanisms by which haemoglobin inhibits the relaxation of rabbit aorta induced by nitrovasodilators, nitric oxide, or bovine retractor penis inhibitory factor. Br J Pharmacol. 1986 Nov;89(3):563–571. doi: 10.1111/j.1476-5381.1986.tb11157.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  100. Martin W., Villani G. M., Jothianandan D., Furchgott R. F. Selective blockade of endothelium-dependent and glyceryl trinitrate-induced relaxation by hemoglobin and by methylene blue in the rabbit aorta. J Pharmacol Exp Ther. 1985 Mar;232(3):708–716. [PubMed] [Google Scholar]
  101. McCall T. B., Boughton-Smith N. K., Palmer R. M., Whittle B. J., Moncada S. Synthesis of nitric oxide from L-arginine by neutrophils. Release and interaction with superoxide anion. Biochem J. 1989 Jul 1;261(1):293–296. doi: 10.1042/bj2610293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  102. Melkumyants A. M., Balashov S. A. Effect of blood viscocity on arterial flow induced dilator response. Cardiovasc Res. 1990 Feb;24(2):165–168. doi: 10.1093/cvr/24.2.165. [DOI] [PubMed] [Google Scholar]
  103. Miller V. M., Aarhus L. L., Vanhoutte P. M. Modulation of endothelium-dependent responses by chronic alterations of blood flow. Am J Physiol. 1986 Sep;251(3 Pt 2):H520–H527. doi: 10.1152/ajpheart.1986.251.3.H520. [DOI] [PubMed] [Google Scholar]
  104. Moore S., Friedman R. J., Singal D. P., Gauldie J., Blajchman M. A., Roberts R. S. Inhibition of injury induced thromboatherosclerotic lesions by anti-platelet serum in rabbits. Thromb Haemost. 1976 Feb 29;35(1):70–81. [PubMed] [Google Scholar]
  105. Morgan J. P., Morgan K. G. Alteration of cytoplasmic ionized calcium levels in smooth muscle by vasodilators in the ferret. J Physiol. 1984 Dec;357:539–551. doi: 10.1113/jphysiol.1984.sp015516. [DOI] [PMC free article] [PubMed] [Google Scholar]
  106. Moritoki H., Tanioka A., Maeshiba Y., Iwamoto T., Ishida Y., Araki H. Age-associated decrease in histamine-induced vasodilation may be due to reduction of cyclic GMP formation. Br J Pharmacol. 1988 Dec;95(4):1015–1022. doi: 10.1111/j.1476-5381.1988.tb11734.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  107. Myers P. R., Minor R. L., Jr, Guerra R., Jr, Bates J. N., Harrison D. G. Vasorelaxant properties of the endothelium-derived relaxing factor more closely resemble S-nitrosocysteine than nitric oxide. Nature. 1990 May 10;345(6271):161–163. doi: 10.1038/345161a0. [DOI] [PubMed] [Google Scholar]
  108. Nabel E. G., Ganz P., Gordon J. B., Alexander R. W., Selwyn A. P. Dilation of normal and constriction of atherosclerotic coronary arteries caused by the cold pressor test. Circulation. 1988 Jan;77(1):43–52. doi: 10.1161/01.cir.77.1.43. [DOI] [PubMed] [Google Scholar]
  109. Nakagomi T., Kassell N. F., Sasaki T., Fujiwara S., Lehman R. M., Torner J. C. Impairment of endothelium-dependent vasodilation induced by acetylcholine and adenosine triphosphate following experimental subarachnoid hemorrhage. Stroke. 1987 Mar-Apr;18(2):482–489. doi: 10.1161/01.str.18.2.482. [DOI] [PubMed] [Google Scholar]
  110. Newby A. C., Henderson A. H. Stimulus-secretion coupling in vascular endothelial cells. Annu Rev Physiol. 1990;52:661–674. doi: 10.1146/annurev.ph.52.030190.003305. [DOI] [PubMed] [Google Scholar]
  111. Ohlstein E. H., Nichols A. J. Rabbit polymorphonuclear neutrophils elicit endothelium-dependent contraction in vascular smooth muscle. Circ Res. 1989 Oct;65(4):917–924. doi: 10.1161/01.res.65.4.917. [DOI] [PubMed] [Google Scholar]
  112. Olafsson B., Forman M. B., Puett D. W., Pou A., Cates C. U., Friesinger G. C., Virmani R. Reduction of reperfusion injury in the canine preparation by intracoronary adenosine: importance of the endothelium and the no-reflow phenomenon. Circulation. 1987 Nov;76(5):1135–1145. doi: 10.1161/01.cir.76.5.1135. [DOI] [PubMed] [Google Scholar]
  113. Olesen S. P., Clapham D. E., Davies P. F. Haemodynamic shear stress activates a K+ current in vascular endothelial cells. Nature. 1988 Jan 14;331(6152):168–170. doi: 10.1038/331168a0. [DOI] [PubMed] [Google Scholar]
  114. Palacios M., Knowles R. G., Palmer R. M., Moncada S. Nitric oxide from L-arginine stimulates the soluble guanylate cyclase in adrenal glands. Biochem Biophys Res Commun. 1989 Dec 15;165(2):802–809. doi: 10.1016/s0006-291x(89)80037-3. [DOI] [PubMed] [Google Scholar]
  115. Palmer R. M., Ashton D. S., Moncada S. Vascular endothelial cells synthesize nitric oxide from L-arginine. Nature. 1988 Jun 16;333(6174):664–666. doi: 10.1038/333664a0. [DOI] [PubMed] [Google Scholar]
  116. Palmer R. M., Ferrige A. G., Moncada S. Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor. Nature. 1987 Jun 11;327(6122):524–526. doi: 10.1038/327524a0. [DOI] [PubMed] [Google Scholar]
  117. Panza J. A., Quyyumi A. A., Brush J. E., Jr, Epstein S. E. Abnormal endothelium-dependent vascular relaxation in patients with essential hypertension. N Engl J Med. 1990 Jul 5;323(1):22–27. doi: 10.1056/NEJM199007053230105. [DOI] [PubMed] [Google Scholar]
  118. Pearson P. J., Schaff H. V., Vanhoutte P. M. Long-term impairment of endothelium-dependent relaxations to aggregating platelets after reperfusion injury in canine coronary arteries. Circulation. 1990 Jun;81(6):1921–1927. doi: 10.1161/01.cir.81.6.1921. [DOI] [PubMed] [Google Scholar]
  119. Pelc L. R., Garancis J. C., Gross G. J., Warltier D. C. Alteration of endothelium-dependent distribution of myocardial blood flow after coronary occlusion and reperfusion. Circulation. 1990 Jun;81(6):1928–1937. doi: 10.1161/01.cir.81.6.1928. [DOI] [PubMed] [Google Scholar]
  120. Pentikäinen P. J., Halinen M. O., Helin M. J. Pharmacokinetics of intravenous mexiletine in patients with acute myocardial infarction. J Cardiovasc Pharmacol. 1984 Jan-Feb;6(1):1–6. [PubMed] [Google Scholar]
  121. Pohl U., Busse R. EDRF increases cyclic GMP in platelets during passage through the coronary vascular bed. Circ Res. 1989 Dec;65(6):1798–1803. doi: 10.1161/01.res.65.6.1798. [DOI] [PubMed] [Google Scholar]
  122. Pollock W. K., Wreggett K. A., Irvine R. F. Inositol phosphate production and Ca2+ mobilization in human umbilical-vein endothelial cells stimulated by thrombin and histamine. Biochem J. 1988 Dec 1;256(2):371–376. doi: 10.1042/bj2560371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  123. Radomski M. W., Palmer R. M., Moncada S. An L-arginine/nitric oxide pathway present in human platelets regulates aggregation. Proc Natl Acad Sci U S A. 1990 Jul;87(13):5193–5197. doi: 10.1073/pnas.87.13.5193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  124. Radomski M. W., Palmer R. M., Moncada S. The role of nitric oxide and cGMP in platelet adhesion to vascular endothelium. Biochem Biophys Res Commun. 1987 Nov 13;148(3):1482–1489. doi: 10.1016/s0006-291x(87)80299-1. [DOI] [PubMed] [Google Scholar]
  125. Rapoport R. M. Cyclic guanosine monophosphate inhibition of contraction may be mediated through inhibition of phosphatidylinositol hydrolysis in rat aorta. Circ Res. 1986 Mar;58(3):407–410. doi: 10.1161/01.res.58.3.407. [DOI] [PubMed] [Google Scholar]
  126. Rapoport R. M., Draznin M. B., Murad F. Endothelium-dependent relaxation in rat aorta may be mediated through cyclic GMP-dependent protein phosphorylation. Nature. 1983 Nov 10;306(5939):174–176. doi: 10.1038/306174a0. [DOI] [PubMed] [Google Scholar]
  127. Rees D. D., Palmer R. M., Moncada S. Role of endothelium-derived nitric oxide in the regulation of blood pressure. Proc Natl Acad Sci U S A. 1989 May;86(9):3375–3378. doi: 10.1073/pnas.86.9.3375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  128. Reidy M. A., Silver M. Endothelial regeneration. VII. Lack of intimal proliferation after defined injury to rat aorta. Am J Pathol. 1985 Feb;118(2):173–177. [PMC free article] [PubMed] [Google Scholar]
  129. Ross R. The pathogenesis of atherosclerosis--an update. N Engl J Med. 1986 Feb 20;314(8):488–500. doi: 10.1056/NEJM198602203140806. [DOI] [PubMed] [Google Scholar]
  130. Rubanyi G. M., Vanhoutte P. M. Superoxide anions and hyperoxia inactivate endothelium-derived relaxing factor. Am J Physiol. 1986 May;250(5 Pt 2):H822–H827. doi: 10.1152/ajpheart.1986.250.5.H822. [DOI] [PubMed] [Google Scholar]
  131. Rösen R., König E., Klaus W. Different sensitivities of arteries and veins to glyceryltrinitrate-induced relaxation and tolerance: an "in vitro" study on isolated vessels from rabbits. Arch Int Pharmacodyn Ther. 1987 Feb;285(2):226–237. [PubMed] [Google Scholar]
  132. Saenz de Tejada I., Goldstein I., Azadzoi K., Krane R. J., Cohen R. A. Impaired neurogenic and endothelium-mediated relaxation of penile smooth muscle from diabetic men with impotence. N Engl J Med. 1989 Apr 20;320(16):1025–1030. doi: 10.1056/NEJM198904203201601. [DOI] [PubMed] [Google Scholar]
  133. Salvemini D., Korbut R., Anggård E., Vane J. Immediate release of a nitric oxide-like factor from bovine aortic endothelial cells by Escherichia coli lipopolysaccharide. Proc Natl Acad Sci U S A. 1990 Apr;87(7):2593–2597. doi: 10.1073/pnas.87.7.2593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  134. Salvemini D., Masini E., Anggard E., Mannaioni P. F., Vane J. Synthesis of a nitric oxide-like factor from L-arginine by rat serosal mast cells: stimulation of guanylate cyclase and inhibition of platelet aggregation. Biochem Biophys Res Commun. 1990 Jun 15;169(2):596–601. doi: 10.1016/0006-291x(90)90372-t. [DOI] [PubMed] [Google Scholar]
  135. Sassen L. M., Hartog J. M., Lamers J. M., Klompe M., Van Woerkens L. J., Verdouw P. D. Mackerel oil and atherosclerosis in pigs. Eur Heart J. 1989 Sep;10(9):838–846. doi: 10.1093/oxfordjournals.eurheartj.a059579. [DOI] [PubMed] [Google Scholar]
  136. Seidel C. L., LaRochelle J. Venous and arterial endothelia: different dilator abilities in dog vessels. Circ Res. 1987 Apr;60(4):626–630. doi: 10.1161/01.res.60.4.626. [DOI] [PubMed] [Google Scholar]
  137. Sellke F. W., Armstrong M. L., Harrison D. G. Endothelium-dependent vascular relaxation is abnormal in the coronary microcirculation of atherosclerotic primates. Circulation. 1990 May;81(5):1586–1593. doi: 10.1161/01.cir.81.5.1586. [DOI] [PubMed] [Google Scholar]
  138. Shimokawa H., Aarhus L. L., Vanhoutte P. M. Porcine coronary arteries with regenerated endothelium have a reduced endothelium-dependent responsiveness to aggregating platelets and serotonin. Circ Res. 1987 Aug;61(2):256–270. doi: 10.1161/01.res.61.2.256. [DOI] [PubMed] [Google Scholar]
  139. Shimokawa H., Flavahan N. A., Shepherd J. T., Vanhoutte P. M. Endothelium-dependent inhibition of ergonovine-induced contraction is impaired in porcine coronary arteries with regenerated endothelium. Circulation. 1989 Sep;80(3):643–650. doi: 10.1161/01.cir.80.3.643. [DOI] [PubMed] [Google Scholar]
  140. Shimokawa H., Flavahan N. A., Vanhoutte P. M. Natural course of the impairment of endothelium-dependent relaxations after balloon endothelium removal in porcine coronary arteries. Possible dysfunction of a pertussis toxin-sensitive G protein. Circ Res. 1989 Sep;65(3):740–753. doi: 10.1161/01.res.65.3.740. [DOI] [PubMed] [Google Scholar]
  141. Shimokawa H., Kim P., Vanhoutte P. M. Endothelium-dependent relaxation to aggregating platelets in isolated basilar arteries of control and hypercholesterolemic pigs. Circ Res. 1988 Sep;63(3):604–612. doi: 10.1161/01.res.63.3.604. [DOI] [PubMed] [Google Scholar]
  142. Shimokawa H., Vanhoutte P. M. Dietary omega 3 fatty acids and endothelium-dependent relaxations in porcine coronary arteries. Am J Physiol. 1989 Apr;256(4 Pt 2):H968–H973. doi: 10.1152/ajpheart.1989.256.4.H968. [DOI] [PubMed] [Google Scholar]
  143. Spekhorst H., SippensGroenewegen A., David G. K., Janse M. J., Dunning A. J. Body surface mapping during percutaneous transluminal coronary angioplasty. QRS changes indicating regional myocardial conduction delay. Circulation. 1990 Mar;81(3):840–849. doi: 10.1161/01.cir.81.3.840. [DOI] [PubMed] [Google Scholar]
  144. Steinberg D., Parthasarathy S., Carew T. E., Khoo J. C., Witztum J. L. Beyond cholesterol. Modifications of low-density lipoprotein that increase its atherogenicity. N Engl J Med. 1989 Apr 6;320(14):915–924. doi: 10.1056/NEJM198904063201407. [DOI] [PubMed] [Google Scholar]
  145. Takahashi M., Yui Y., Yasumoto H., Aoyama T., Morishita H., Hattori R., Kawai C. Lipoproteins are inhibitors of endothelium-dependent relaxation of rabbit aorta. Am J Physiol. 1990 Jan;258(1 Pt 2):H1–H8. doi: 10.1152/ajpheart.1990.258.1.H1. [DOI] [PubMed] [Google Scholar]
  146. Thom S., Hughes A., Martin G., Sever P. S. Endothelium-dependent relaxation in isolated human arteries and veins. Clin Sci (Lond) 1987 Nov;73(5):547–552. doi: 10.1042/cs0730547. [DOI] [PubMed] [Google Scholar]
  147. Tomita T., Ezaki M., Miwa M., Nakamura K., Inoue Y. Rapid and reversible inhibition by low density lipoprotein of the endothelium-dependent relaxation to hemostatic substances in porcine coronary arteries. Heat and acid labile factors in low density lipoprotein mediate the inhibition. Circ Res. 1990 Jan;66(1):18–27. doi: 10.1161/01.res.66.1.18. [DOI] [PubMed] [Google Scholar]
  148. Treasure C. B., Vita J. A., Cox D. A., Fish R. D., Gordon J. B., Mudge G. H., Colucci W. S., Sutton M. G., Selwyn A. P., Alexander R. W. Endothelium-dependent dilation of the coronary microvasculature is impaired in dilated cardiomyopathy. Circulation. 1990 Mar;81(3):772–779. doi: 10.1161/01.cir.81.3.772. [DOI] [PubMed] [Google Scholar]
  149. Vallance P., Collier J., Moncada S. Effects of endothelium-derived nitric oxide on peripheral arteriolar tone in man. Lancet. 1989 Oct 28;2(8670):997–1000. doi: 10.1016/s0140-6736(89)91013-1. [DOI] [PubMed] [Google Scholar]
  150. Van de Voorde J., Leusen I. Endothelium-dependent and independent relaxation of aortic rings from hypertensive rats. Am J Physiol. 1986 May;250(5 Pt 2):H711–H717. doi: 10.1152/ajpheart.1986.250.5.H711. [DOI] [PubMed] [Google Scholar]
  151. VanBenthuysen K. M., McMurtry I. F., Horwitz L. D. Reperfusion after acute coronary occlusion in dogs impairs endothelium-dependent relaxation to acetylcholine and augments contractile reactivity in vitro. J Clin Invest. 1987 Jan;79(1):265–274. doi: 10.1172/JCI112793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  152. Verbeuren T. J., Jordaens F. H., Zonnekeyn L. L., Van Hove C. E., Coene M. C., Herman A. G. Effect of hypercholesterolemia on vascular reactivity in the rabbit. I. Endothelium-dependent and endothelium-independent contractions and relaxations in isolated arteries of control and hypercholesterolemic rabbits. Circ Res. 1986 Apr;58(4):552–564. doi: 10.1161/01.res.58.4.552. [DOI] [PubMed] [Google Scholar]
  153. Vita J. A., Treasure C. B., Nabel E. G., McLenachan J. M., Fish R. D., Yeung A. C., Vekshtein V. I., Selwyn A. P., Ganz P. Coronary vasomotor response to acetylcholine relates to risk factors for coronary artery disease. Circulation. 1990 Feb;81(2):491–497. doi: 10.1161/01.cir.81.2.491. [DOI] [PubMed] [Google Scholar]
  154. Wei E. P., Kontos H. A., Christman C. W., DeWitt D. S., Povlishock J. T. Superoxide generation and reversal of acetylcholine-induced cerebral arteriolar dilation after acute hypertension. Circ Res. 1985 Nov;57(5):781–787. doi: 10.1161/01.res.57.5.781. [DOI] [PubMed] [Google Scholar]
  155. Weidinger F. F., McLenachan J. M., Cybulsky M. I., Gordon J. B., Rennke H. G., Hollenberg N. K., Fallon J. T., Ganz P., Cooke J. P. Persistent dysfunction of regenerated endothelium after balloon angioplasty of rabbit iliac artery. Circulation. 1990 May;81(5):1667–1679. doi: 10.1161/01.cir.81.5.1667. [DOI] [PubMed] [Google Scholar]
  156. White D. G., Lewis M. J., Griffith T. M., Edwards D. H., Henderson A. H. Influence of endothelium on drug-induced relaxation of the rabbit aorta. Eur J Pharmacol. 1986 Feb 11;121(1):19–23. doi: 10.1016/0014-2999(86)90387-0. [DOI] [PubMed] [Google Scholar]
  157. White D. G., Martin W. Differential control and calcium-dependence of production of endothelium-derived relaxing factor and prostacyclin by pig aortic endothelial cells. Br J Pharmacol. 1989 Jul;97(3):683–690. doi: 10.1111/j.1476-5381.1989.tb12004.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  158. Yamamoto Y., Tomoike H., Egashira K., Kobayashi T., Kawasaki T., Nakamura M. Pathogenesis of coronary artery spasm in miniature swine with regional intimal thickening after balloon denudation. Circ Res. 1987 Jan;60(1):113–121. doi: 10.1161/01.res.60.1.113. [DOI] [PubMed] [Google Scholar]
  159. Yasue H., Matsuyama K., Matsuyama K., Okumura K., Morikami Y., Ogawa H. Responses of angiographically normal human coronary arteries to intracoronary injection of acetylcholine by age and segment. Possible role of early coronary atherosclerosis. Circulation. 1990 Feb;81(2):482–490. doi: 10.1161/01.cir.81.2.482. [DOI] [PubMed] [Google Scholar]

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