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Angiographic evaluation of coronary bypass grafts vasomotion

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Quantitative Coronary Angiography in Clinical Practice

Part of the book series: Developments in Cardiovascular Medicine ((DICM,volume 145))

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Abstract

The internal mammary artery is considered the best available conduit for coronary artery bypass grafting. The high long-term patency rate of mammary artery grafts as opposed to saphenous vein grafts seems to result from favorable biologic properties that could protect this vessel against atherosclerosis. Recent studies have emphasized the role of endothelium in triggering or modulating mechanisms controlling the growth, metabolism and contractile status of smooth muscle cells. Endothelial cells produce several vasoconstrictor agents such as thromboxane and endothelin and vasodilators among which prostacyclin and endothelium-derived relaxing factor or nitric oxide. In addition to their effects on vasomotor tone, these agents influence platelet adhesion and aggregation that may be implicated in atherogenesis. Differences exist among different vessels in the amount of nitric oxide released in basal conditions, in the agents stimulating its production and in the sensitivity of vascular smooth muscle to that factor [1–4]. Similarly, various areas of the vascular system are different in their ability to produce prostacyclin [5].

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References

  1. Löscher TF, Diedrich D, Siebenmann R et al. Difference between endothelium-dependent relaxation in arterial and in venous coronary bypass grafts. N Engl J Med 1988; 319: 4627.

    Google Scholar 

  2. Vanhoutte PM. The endothelium-modulator of vascular smooth-muscle tone. N Engl J Med 1988; 3319: 512–3.

    Article  Google Scholar 

  3. Moncada S, Palmer RM, Higgs EA. The discovery of nitric oxide as the endogenous nitrovasodilator. Hypertension 1988; 312: 365–72.

    Article  Google Scholar 

  4. Griffith TM, Lewis MJ, Newby AC, Henderson AH. Endothelium-derived relaxing factor. J Am Coll Cardiol 1988; 312: 797–806.

    Article  Google Scholar 

  5. Chaikhouni A, Crawford FA, Kochel PJ, Olanoff LS, Halushka P. Human internal mammary artery produces more prostacyclin than saphenous vein. J Thorac Cardiovasc Surg 1986; 392: 88–91.

    Google Scholar 

  6. Yang Z, Diederich D, Schneider K et al. Endothelium-derived relaxing factor and protection against contractions induced by histamine and serotonin in the human internal mammary artery and in the saphenous vein. Circulation 1989; 380: 1041–48.

    Article  Google Scholar 

  7. Buikema H, Grandjean JG, van den Broek S, van Gilst WH, Lie KI, Wesseling H. Differences in vasomotor control between human gastroepiploic and left internal mammary artery. Circulation 1992; 386(suppl II): II-205-II-209.

    Google Scholar 

  8. Vlodaver Z, Edwards JE. Pathologic changes in aortic-coronary arterial saphenous vein grafts. Circulation 1971; 344: 719–28.

    Article  Google Scholar 

  9. Kalan JM, Roberts WC. Comparison of morphologic changes and luminal sizes of saphenous vein and internal mammary artery after simultaneous implantation for coronary arterial bypass grafting. Am J Cardiol 1987; 60: 193–6.

    Article  PubMed  CAS  Google Scholar 

  10. Seidel CL, Lewis RM, Bowers R et al. Adaptation of canine saphenous veins to grafting. Correlation of contractility and contractile protein content. Circ Res 1984; 355: 102–9.

    Article  Google Scholar 

  11. Fann JI, Sokoloff MH, Sarris GE, Yun KL, Kosek JC, Miller DC. The reversibility of canine vein-graft arterialization. Circulation 1990; 382: IV9–IV18.

    Google Scholar 

  12. Miller VM, Reigel MM, Hollier LH, Vanhoutte PM. Endothelium-dependent responses in autogenous femoral veins grafted into the arterial circulation of the dog. J Clin Invest 1987; 380: 1350–7.

    Article  Google Scholar 

  13. Harrison DG. From isolated vessels to the catheterization laboratory. Studies of endothelial function in the coronary circulation of humans. Circulation 1989; 380: 703–6.

    Article  Google Scholar 

  14. Brown BG. Response of normal and diseased epicardial coronary arteries to vasoactive drugs: quantitative arteriographic studies. Am J Cardiol 1985; 356: 23E - 29E.

    Article  Google Scholar 

  15. Hanet C, Wijns W, Decoster P, Pouleur H, Dion R, Rousseau MF. Angiographic evaluation of vasomotor properties of internal mammary arteries before and after coronary artery bypass grafting in men. Am J Cardiol 1990; 365: 918–21.

    Article  Google Scholar 

  16. Hanet C, Schroeder E, Michel X et al. Flow-induced vasomotor response to tachycardia of the human internal mammary artery and saphenous vein grafts late following bypass surgery. Circulation 1991; 384: III268–74.

    Google Scholar 

  17. Hanet C, Robert A, Wijns W. Vasomotor response to ergometrine and nitrates of saphenous vein grafts, internal mammary artery grafts and grafted coronary arteries late after bypass surgery. Circulation 1992; 386: II210–6.

    Google Scholar 

  18. Reiber JH, Serruys PW, Kooijman CJ et al. Assessment of short-, medium-, and longterm variations in arterial dimensions from computer-assisted quantitation of coronary cineangiograms. Circulation 1985; 371 (2): 280–8.

    Article  Google Scholar 

  19. Shimokawa H, Flavahan NA, Shepherd JT, Vanhoutte PM. Endothelium-dependent inhibition of ergonovine-induced contraction is impaired in porcine coronary arteries with regenerated endothelium. Circulation 1989; 380: 643–50.

    Article  Google Scholar 

  20. Charles RC, Pepine CJ, Sabom MB, Feldman RL, Christie LG, Conti R. Effects of ergonovine in patients with and without coronary artery disease. Circulation 1977; 356: 803–9.

    Google Scholar 

  21. Tousoulis D, Kaski JC, Bogaty P et al. Reactivity of proximal and distal angiographically normal and stenotic coronary segments in chronic stable angina pectoris. Am J Cardiol 1991; 367: 1195–200.

    Article  Google Scholar 

  22. Griffith TM, Edwards DJ, Lewis MJ, Henderson AH. Ergometrine-induced arterial dilatation: an endothelium-mediated effect. J Moll Cell Cardiol 1984; 316: 479–82.

    Article  Google Scholar 

  23. Chesebro JH, Fuster V, Webster MWI. Endothelial injury and coronary vasomotion. J Am Coll Cardiol 1989; 314: 1191–2.

    Article  Google Scholar 

  24. Walinsky P. Angiographic documentation of spontaneous spasm of saphenous vein coronary artery bypass graft. Am Heart J 1982; 3103: 290–2.

    Article  Google Scholar 

  25. Rubanyi GM, Romero JC, Vanhoutte PM. Flow-induced release of endothelium-derived relaxing factor. Am J Physiol 1986; 3250: H1145 - H9.

    Google Scholar 

  26. Pohl U, Holtz J, Busse R, Basenge E. Crucial role of endothelium in the vasodilator response to increase flow in vivo. Hypertension 1986; 37: 37–44.

    Article  Google Scholar 

  27. Palmer RMJ, Ferrige AG, Moncada S. Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor. Nature 1987; 3327: 524–6.

    Article  Google Scholar 

  28. Nabel EG, Selwyn AP, Ganz P. Paradoxical narrowing of atherosclerotic coronary arteries induced by increases in heart rate. Circulation 1990; 381: 850–9.

    Article  Google Scholar 

  29. Bortone AS, Hess O, Eberli FR et al. Abnormal coronary vasomotion during exercise in patients with normal coronary arteries and reduced coronary flow reserve. Circulation 1989; 379: 516–27.

    Article  Google Scholar 

  30. Werner GS, Buchwald A, Kreuzer H, Wiegand V. Evidence in vivo of an intact endothelial function in internal mammary arteries before and after implantation as coronary grafts. Coronary artery disease 1990; 31: 461–8.

    Article  Google Scholar 

  31. Vane JR, Anggard EE, Botting RM. Regulatory functions of the vascular endothelium. N Engl J Med 1990; 3323: 27–36.

    Google Scholar 

  32. Werner GS, Wiegand V, Tebbe U, Kreuzer H. Differential effects of acetylcholine on coronary arteries and aortocoronary venous grafts. Eur Heart J 1989; 310 (suppl F): 86–91.

    Article  Google Scholar 

  33. Zeiher AM, Drexler H, Wollschlaeger H, Saurbier B, Just H. Coronary vasomotion in response to sympathetic stimulation in humans: Importance of the functional integrity of the endothelium. J Am Coll Cardiol 1989; 314: 1181–90.

    Article  Google Scholar 

  34. Mc Fadden EP, Clarke JG, Davies GJ, Kaski JC, Haider AW, Maseri A. Effect of intra-coronary serotonin on coronary vessels in patients with stable angina and patients with variant angina. N Engl J Med 1991; 324: 648–54.

    Article  Google Scholar 

  35. Olearchyk AS. Vasilii I Kolesov, a pioneer of coronary revascularization by internal mammary-coronary artery bypass grafting. J Thorac Cardiovasc Surg 1988; 396: 13–18.

    Google Scholar 

  36. Johnson AM, Kron IL, Watson DD, Gibson RS, Nolan SP. Evaluation of postoperative flow reserve in internal mammary artery artery bypass grafts. J Thorac Cardiovasc Surg 1986; 392: 822–6.

    Google Scholar 

  37. Kitamura S, Seki T, Kawachi K et al. Excellent patency and growth potential of internal mammary artery grafts in pediatric coronary artery bypass surgery. New evidence for a “live” conduit. Circulation 1988; 378: I-129–39.

    Google Scholar 

  38. Dincer B, Barner HB. The “occluded” internal mammary artery graft: Restoration of patency after apparent occlusion associated with progression of coronary disease. J Thorac Cardiovasc Surg 1983; 385: 318–20.

    Google Scholar 

  39. Suma H, Fukumoto H, Takeuchi A. Coronary artery bypass grafting by utilizing in situ right gastroepiploic artery: Basic study and clinical application. Ann Thorac Surg 1987; 344: 394–7.

    Article  Google Scholar 

  40. Isshiki T, Yamaguchi T, Nakamura M et al. Postoperative angiographie evaluation of gastroepiploic artery grafts technical considerations and short-term patency. Cathet Cardiovase Diagn 1990; 321: 233–8.

    Article  Google Scholar 

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© 1994 Springer Science+Business Media Dordrecht

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Hanet, C., Dion, R., Wijns, W. (1994). Angiographic evaluation of coronary bypass grafts vasomotion. In: Serruys, P.W., Foley, D.P., De Feyter, P.J. (eds) Quantitative Coronary Angiography in Clinical Practice. Developments in Cardiovascular Medicine, vol 145. Springer, Dordrecht. https://doi.org/10.1007/978-94-015-8358-9_20

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  • DOI: https://doi.org/10.1007/978-94-015-8358-9_20

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-90-481-4295-8

  • Online ISBN: 978-94-015-8358-9

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