PDF herunterladen
Thromb Haemost 1993; 70(01): 129-134
DOI: 10.1055/s-0038-1646173
State-of-the-Art Lecture
Flow
Schattauer GmbH Stuttgart

The Effects of Flow on Blood Coagulation and Thrombosis

Steven M Slack
Department of Biomedical Engineering, Memphis State University, Memphis, TN, USA
,
Yingwen Cui
Department of Biomedical Engineering, Memphis State University, Memphis, TN, USA
,
Vincent T Turitto
Department of Biomedical Engineering, Memphis State University, Memphis, TN, USA
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
03. Juli 2018 (online)

Auch verfügbar auf
  als PDF herunterladen  Lizenzen und Reprints
 

  • References

  • 1 Cooke JP, Rossitch E, Andon NA, Loscalzo J, Brau VJ. Flow activates an endothelial potassium channel to release an endogenous nitrovasodilator. J Clin Invest 1991; 88: 1663-1671
    CrossrefPubMedGoogle Scholar
  • 2 Bird RB, Stewart WE, Lightfoot EN. Transport Phenomena. Wiley; New York: 1960
    Google Scholar
  • 3 Whitmore RL. Rheology of the Circulation. Pergamon Press; New York: 1968
    Google Scholar
  • 4 Middleman S. Transport Phenomena in the Cardiovascular System. John Wiley & Sons; New York: 1972
    Google Scholar
  • 5 Goldsmith HL, Turitto VT. Rheological aspects of thrombosis and haemostasis: Basic principles and applications. Thromb Haemostas 1986; 55: 415-435
    PubMedGoogle Scholar
  • 6 Lowe GDO. Nature and clinical importance of blood rheology. In: (Clinical Blood Rheology; Vol. 1.). Lowe GDO. (ed). CRC Press; Boca Raton: 1988. pp. 1-10
    Google Scholar
  • 7 Eckstein EC, Tilles AW, Millero FJ. Conditions for the occurrence of large near-wall excesses of small particles during blood flow. Microvasc Res 1988; 36: 31-39
    CrossrefPubMedGoogle Scholar
  • 8 Eckstein EC, Belgacem F. Model of platelet transport in flowing blood with drift and diffusion terms. Biophys J 1991; 60: 53-69
    CrossrefPubMedGoogle Scholar
  • 9 Brown CH, Leverett LB, Lewis CW, Alfrey CP, Heliums JD. Morphological, biochemical, and functional changes in human platelets subjected to shear stress. J Lab Clin Med 1975; 86: 462-471
    PubMedGoogle Scholar
  • 10 Moake JL, Turner NA, Stathopoulos NA, Nolasco LH, Heliums JD. Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear stress-induced platelet aggregation. J Clin Invest 1986; 78: 1456-1461
    CrossrefPubMedGoogle Scholar
  • 11 Moake JL, Turner NA, Stathopoulos NA, Nolasco LH, Heliums JD. Shear-induced platelet aggregation can be mediated by vWF released by platelets, as well as exogenous large or unusually large vWF multimers, requires adenosine diphosphate, and is resistant to aspirin. Blood 1988; 71: 1366-1374
    PubMedGoogle Scholar
  • 12 Ikeda Y, Handa M, Kawano K. et al.: The role of von Willebrand factor and fibrinogen in platelet aggregation under varying shear stress. J Clin Invest 1991; 87: 1234-1240
    CrossrefPubMedGoogle Scholar
  • 13 Nollert MU, Eskin SG, Mclntire LV. Shear stress increases inositol trisphosphate levels in human endothelial cells. Biochem Biophys Res Commun 1990; 170: 281-287
    CrossrefPubMedGoogle Scholar
  • 14 Diamond SL, Eskin SG, Mclntire LV. Fluid flow stimulates tissue plasminogen activator secretion by cultured human endothelial cells. Science 1989; 243: 1483-1485
    CrossrefPubMedGoogle Scholar
  • 15 Tesfamariam B, Cohen RA. Inhibition of adrenergic vasoconstriction by endothelial cell shear stress. Circ Res 1988; 63: 720-725
    CrossrefPubMedGoogle Scholar
  • 16 Cooke JP, Stamler J, Andon N, Davies PF, McKinley G, Loscalzo J. Flow stimulates endothelial cells to release a nitrovasodilator that is potentiated by reduced thiol. Am J Physiol 1990; 259: H804-H812
    PubMedGoogle Scholar
  • 17 Buga GM, Gold ME, Fukuto JM, Ignarro LJ. Shear stress-induced release of nitric oxide from endothelial cells grown on beads. Hypertension 1991; 17 (02) 187-193
    CrossrefPubMedGoogle Scholar
  • 18 Hsieh HJ, Li NQ, Frangos JA. Shear stress increases endothelial platelet-derived growth factor mRNA levels. Am J Physiol 1991; 260: H642-H646
    PubMedGoogle Scholar
  • 19 Jawien A, Bowen-Pope DF, Lindner V, Schwartz SM, Clowes AW. Platelet-derived growth factor promotes smooth muscle migration and intimal thickening in a rat model of balloon angioplasty. J Clin Invest 1992; 89: 507-511
    CrossrefPubMedGoogle Scholar
  • 20 Lassila R, Badimon JJ, Vallabhajosula S, Badimon L. Dynamic monitoring of platelet deposition on severely damaged vessel wall in flowing blood. Arteriosclerosis 1990; 10: 306-315
    CrossrefPubMedGoogle Scholar
  • 21 Weiss HJ, Turitto VT, Baumgartner HR. Role of shear rate and platelets in promoting fibrin formation on rabbit subendothelium. J Clin Invest 1986; 78: 1072-1082
    CrossrefPubMedGoogle Scholar
  • 22 Gemmell CH, Nemerson Y, Turitto VT. The effects of shear rate on the enzymatic activity of the tissue factor-factor Vila complex. Microvasc Res 1990; 40: 327-340
    CrossrefPubMedGoogle Scholar
  • 23 Goldsmith HL, Yu SS, Marlow J. Fluid mechanical stress and the platelet. Thromb Diath Haemorrh 1975; 34: 32-41
    PubMedGoogle Scholar
  • 24 Baumgartner HR. The role of blood flow in platelet adhesion, fibrin deposition, and formation of mural thrombi. Microvasc Res 1973; 5: 167-179
    CrossrefPubMedGoogle Scholar
  • 25 Weiss HJ, Turitto VT, Baumgartner HR. Effect of shear rate on platelet interaction with subendothelium in citrated and native blood. I. Shear-rate dependent decrease of adhesion in von Wille-brand's disease and the Bernard-Soulier syndrome. J Lab Clin Med 1978; 92: 750-764
    PubMedGoogle Scholar
  • 26 Baumgartner HR, Turitto VT, Weiss HJ. Effects of shear rate on platelet interaction with subendothelium in citrated and native blood. II. Relationships among platelet adhesion, thrombus dimensions, and fibrin formation. J Lab Clin Med 1980; 95: 208-221
    PubMedGoogle Scholar
  • 27 Baumgartner HR, Sakariassen K. Factors controlling thrombus formation on arterial lesions. Ann NY Acad Sci 1985; 454: 162-177
    CrossrefPubMedGoogle Scholar
  • 28 Turitto VT, Baumgartner HR. Platelet interaction with subendothelium in flowing rabbit blood: Effect of blood shear rate. Microvasc Res 1979; 17: 38-54
    CrossrefPubMedGoogle Scholar
  • 29 Baumgartner HR, Tschopp TB, Weiss HJ. Platelet interaction with collagen fibrils in flowing blood. II. Impaired adhesion-aggregation in bleeding disorders- a comparison with subendothelium. Thromb Haemostas 1977; 37: 17-28
    PubMedGoogle Scholar
  • 30 Firkin BG, Howard MA. On von Willebrand's disease. Br J Haemo-tol 1976; 32: 151-158
    CrossrefPubMedGoogle Scholar
  • 31 Tschopp TB, Weiss HJ, Baumgartner HR. Decreased adhesion of platelets to subendothelium in von Willebrand's disease. J Lab Clin Med 1974; 83: 296-300
    PubMedGoogle Scholar
  • 32 Baumgartner HR, Tschopp TB, Meyer D. Shear rate-dependent inhibition of platelet adhesion and aggregation on collagenous surfaces by antibodies to human factor VIII/von Willebrand factor. Br J Haemotol 1980; 44: 127-139
    CrossrefPubMedGoogle Scholar
  • 33 Badimon L, Badimon JJ, Turitto VT, Fuster V. Role of von Willebrand factor in mediating platelet-vessel wall interaction at low shear rates: The importance of perfusion conditions. Blood 1989; 73: 961-967
    PubMedGoogle Scholar
  • 34 Weiss HJ, Baumgartner HR, Tschopp TB, Turitto VT, Cohen D. Correction by factor VIII of the impaired platelet adhesion to subendothelium in von Willebrand's disease. Blood 1978; 51: 267-279
    PubMedGoogle Scholar
  • 35 Sakariassen KS, Bolhuis PA, Sixma JJ. Human blood platelet adhesion to artery subendothelium is mediated by factor VIII-Von Willebrand factor bound to the subendothelium. Nature 1979; 279: 636-638
    CrossrefPubMedGoogle Scholar
  • 36 Bolhuis PA, Sakariassen KS, Sander HJ, Bouma BN, Sixma JJ. Binding of factor VIII-von Willebrand factor to human arterial subendothelium precedes increased platelet adhesion and enhances platelet spreading. J Lab Clin Med 1981; 97: 568-576
    PubMedGoogle Scholar
  • 37 Turitto VT, Weiss HJ, Baumgartner HR. Decreased platelet adhesion on vessel segments in von Willebrand's disease: A defect in initial platelet attachment. J Lab Clin Med 1983; 102: 551-564
    PubMedGoogle Scholar
  • 38 Rand JH, Patel ND, Schwartz E, Zhou SL, Potter BJ. 150 KD von Willebrand factor binding protein extracted from human vascular subendothelium is type VI collagen. J Clin Invest 1991; 88: 253-259
    CrossrefPubMedGoogle Scholar
  • 39 Nieuwenhuis HK, Sakariassen KS, Houdijk WPM. et al.: Deficiency of platelet membrane glycoprotein Iassociated with a decreased platelet adhesion to subendothelium: A defect in platelet spreading. Blood 1986; 68: 692-695
    PubMedGoogle Scholar
  • 40 Jenkins CSP, Phillips DR, Clemetson KJ, et al. Platelet membrane glycoproteins implicated in ristocetin-induced aggregation: Studies of the proteins on platelets from patients with Bernard-Soulier syndrome and von Willebrand's disease. J Clin Invest 1976; 57: 112-124
    CrossrefPubMedGoogle Scholar
  • 41 Roth GJ. Developing relationships: Arterial platelet adhesion, glycoprotein lb and leucine-rich glycoproteins. Blood 1991; 77: 5-19
    PubMedGoogle Scholar
  • 42 Fujimura Y, Ruggeri ZM, Zimmerman TS. Structure and function of human von Willebrand factor. In: Coagulation and Bleeding Disorders: The Role of Factor VIII and von Willebrand Factor. Zimmerman TS, Ruggeri Z. (eds). Marcel Dekker; New York: 1989. p. 77
    Google Scholar
  • 43 Girma JP, Meyer D, Verweij CL, Pannekoek H, Sixma JJ. Structure-function relationship of human von Willebrand factor. Blood 1987; 70: 605-611
    PubMedGoogle Scholar
  • 44 Turitto VT, Weiss HJ, Baumgartner HR. Platelet interaction with rabbit subendothelium in von Willebrand's disease: Altered thrombus formation distinct from defective platelet adhesion. J Clin Invest 1984; 74: 1730-1741
    CrossrefPubMedGoogle Scholar
  • 45 Peterson DM, Stathopoulos NA, Giorgio TD, Heliums JD, Moake JL. Shear-induced platelet aggregation requires von Willebrand factor and platelet membrane glycoproteins lb and IIb-IIIa. Blood 1987; 69: 625-628
    PubMedGoogle Scholar
  • 46 Ikeda Y, Murata M, Araki Y. et al.: Importance of fibrinogen and platelet membrane glycoprotein IIb/IIIa in shear-induced platelet aggregation. Thromb Res 1988; 51: 157-163
    CrossrefPubMedGoogle Scholar
  • 47 Timmons S, Hawiger J. von Willebrand factor can substitute for plasma fibrinogen in ADP-induced platelet aggregation. Trans Assoc Am Physicians 1986; 99: 226-235
    PubMedGoogle Scholar
  • 48 Packham MA, Mustard JF. The role of platelets in the development and complications of atherosclerosis. Semin Hematol 1986; 23: 8-26
    PubMedGoogle Scholar
  • 49 Woolf N, Davies MJ. Interrelationship between atherosclerosis and thrombosis. In: Thrombosis in Cardiovascular Disorders. Fuster V, Verstraete M. (eds). W.B. Saunders; Philadelphia: 1992. pp. 41-78
    Google Scholar
  • 50 Ross R, Glomset J, Kariya B. et al.: A platelet dependent serum factor that stimulates the proliferation of arterial smooth muscle cells in vitro. Proc Natl Acad Sci USA 1974; 71: 1207-1210
    CrossrefPubMedGoogle Scholar
  • 51 Badimon L, Badimon JJ. Mechanisms of arterial thrombosis in non-parallel streamlines: Platelet thrombi grow on the apex of stenotic severely injured vessel wall. J Clin Invest 1989; 84: 1134-1144
    CrossrefPubMedGoogle Scholar
  • 52 Cui Y. Simulation of velocity and shear rate profiles for investigating the influence of stenotic geometry and thrombosis. Masters Thesis, Memphis State University; 1992
    Google Scholar