Subscribe to RSS
DOI: 10.1055/s-0038-1661316
Epinephrine-Induced Aggregation of Rabbit Platelets Refractory to ADP
Publication History
Received 26 February 1985
Accepted 15 March 1985
Publication Date:
18 July 2018 (online)
Summary
The mechanisms involved in platelet aggregation induced by epinephrine are unclear. Although epinephrine does not aggregate washed rabbit platelets, platelets made refractory to ADP will aggregate in response to epinephrine in the presence of ADP. We have examined whether the mechanism(s) by which epinephrine induces aggregation of refractory platelets involves fibrinogen binding and Ca2+ association. With normal platelets, ADP causes aggregation, fibrinogen binding and Ca2+ association in a medium containing 0.2 mM 45Ca2+. After 3 min of incubation with ADP, fibrinogen dissociates from platelets, but 45Ca2+ does not. Epinephrine alone does not cause aggregation, fibrinogen binding or 45Ca2+ association. Platelets that are refractory to ADP do not aggregate and bind fibrinogen upon addition of ADP, but aggregate and bind fibrinogen in response to epinephrine, provided ADP is still present. These effects of epinephrine are mediated by the α-adrenergic receptor since they are blocked by phentolamine or verapamil and potentiated by propranolol. However, epinephrine-induced aggregation of platelets refractory to ADP does not involve further detectable increase in the amount of 45Ca2+ associated with the platelets.
-
References
- 1 O’Brien JR. Changes in platelet membranes possibly associated with platelet stickiness. Nature 1966; 212: 1057-1058
- 2 Drummond AH. Interactions of blood platelets with biogenic amines: uptake, stimulation and receptor binding. In: Platelets in Biology and Pathology. Vol 1. Gordon JL. (Ed) Elsevier/North-Holland Biomedical Press; New York: 1976. pp 203-239
- 3 Hallam TJ, Scrutton MC, Wallis RB. Responses of rabbit platelets to adrenaline induced by other agonists. Thromb Res 1981; 21: 413-424
- 4 Bennett JS, Vilaire G. Exposure of platelet fibrinogen receptors by ADP and epinephrine. J Clin Invest 1979; 64: 1393-1401
- 5 Peerschke EI. Induction of human platelet fibrinogen receptors by epinephrine in the absence of released ADP. Blood 1982; 60: 71-77
- 6 Di Minno G, Capitanio AM, Thiagarajan P, Martinez J, Murphy S. Exposure of fibrinogen receptors on fresh and stored platelets by ADP and epinephrine as single agents and as a pair. Blood 1983; 61: 1054-1059
- 7 Haslam RJ. Mechanisms of blood platelet aggregation. In: Physiology of Hemostasis and Thrombosis. Johnson SA, Seegers WH. (Eds) C C Thomas, Springfield; Illinois: 1967. pp 88-112
- 8 Plow EF, Marguerie GA. Induction of the fibrinogen receptor on human platelets by epinephrine and the combination of epinephrine and ADP. J Biol Chem 1980; 255: 10971-10977
- 9 Owen NE, Feinberg H, Le Breton GC. Epinephrine induces Ca2+ uptake in human blood platelets. Am J Physiol 1980; 239: H483-H488
- 10 Owen NE, Le Breton CG. The involvement of calcium in epinephrine or ADP potentiation of human platelet aggregation. Thromb Res 1980; 17: 855-863
- 11 Brass LF, Shattil SJ. Changes in surface-bound and exchangeable calcium during platelet activation. J Biol Chem 1982; 257: 14000-14005
- 12 Clare KA, Scrutton MC. The role of Ca2+ uptake in the response of human platelets to adrenaline and to 1-0-alkyl-2-acetyl-sn-glycerol-3- phosphocholine (platelet-activating factor). Eur J Biochem 1984; 140: 129-136
- 13 Molnar J, Lorand L. Studies on apyrases. Arch Biochem Biophys 1961; 93: 353-363
- 14 Mustard JF, Perry DW, Kinlough-Rathbone RL, Packham MA. Factors responsible for ADP-induced release reaction of human platelets. Am J Physiol 1975; 228: 1757-1765
- 15 Lawrie JS, Ross J, Kemp GD. Purification of fibrinogen and the separation of its degradation products in the presence of calcium ions. Biochem Soc Trans 1979; 7: 693-694
- 16 Ardlie NG, Perry DW, Packham MA, Mustard JF. Influence of apyrase on stability of suspensions of washed rabbit platelets. Proc Soc Exp Biol Med 1971; 136: 1021-1023
- 17 Greenberg J, Packham MA, Cazenave J-P, Reimers H-J, Mustard JF. Effects on platelet function of removal of platelet sialic acid by neuraminidase. Lab Invest 1975; 32: 476-484
- 18 McFarlane AS. Efficient trace-labelling of proteins with iodine. Nature 1958; 182: 53
- 19 Mustard JF, Packham MA, Kinlough-Rathbone RL, Perry DW, Regoeczi E. Fibrinogen and ADP-induced platelet aggregation. Blood 1978; 52: 453-466
- 20 Harfenist EJ, Packham MA, Mustard JF. Reversibility of the association of fibrinogen with rabbit platelets exposed to ADP. Blood 1980; 56: 189-198
- 21 Evans RJ, Gordon JL. Refractoriness in blood platelets: effect of prior exposure to aggregating agents on subsequent aggregation responses. Br J Pharmacol 1974; 51: 123 P
- 22 Holme S, Holmsen H. ADP-induced refractory state of platelets in vitro. I. Methodological studies on aggregation in platelet rich plasma. Scand J Haematol 1975; 15: 96-103
- 23 Hallam TJ, Ruggles PA, Scrutton MC, Wallis RB. Desensitisation in human and rabbit blood platelets. Thromb Haemostas 1982; 47: 278-284
- 24 Massini P, Lüscher EF. On the significance of the influx of calcium ions into stimulated human blood platelets. Biochim Biophys Acta 1976; 436: 652-663
- 25 Barnathan ES, Addonizio VP, Shattil SJ. Interaction of verapamil with human platelet adrenergic receptors. Am J Physiol 1982; 242: H19-H23
- 26 Scrutton MC, Wallis RB. Catecholamine receptors. In: Platelets in Biology and Pathology. Vol 2. Gordon JL. (Ed) Elsevier/North- Holland Biochemical Press; New York: 1981. pp 179-210
- 27 Abdulla YH. β-Adrenergic receptors in human platelets. J Athero- scler Res 1969; 9: 171-177
- 28 Kerry R, Scrutton MC. Platelet β-adrenoceptors. Br J Pharmacol 1983; 79: 681-691
- 29 Yu SK, Latour JG. Potentiation by α- and inhibition by β-adrenergic stimulations of rat platelet aggregation. A comparative study with human and rabbit platelets Thromb Haemostas 1977; 37: 413-422
- 30 Figures WR, Strimpler AM, Scearce M, Mills JK, Wachtfogel YT, Colman RF, Colman RW. Role of ADP receptors in epinephrine- induced platelet activation. Fed Proc 1984; 43: 660 (Abstr.)