Thromb Haemost 1989; 62(03): 968-976
DOI: 10.1055/s-0038-1651037
Original Article
Schattauer GmbH Stuttgart

Effect of the Concentration of Ca2+ in the Suspending Medium on the Responses of Human and Rabbit Platelets to Aggregating Agents

M A Packham
The Department of Biochemistry, University of Toronto, Toronto, Canada, and the Department of Pathology, McMaster University, Hamilton, Canada
,
N L Bryant
The Department of Biochemistry, University of Toronto, Toronto, Canada, and the Department of Pathology, McMaster University, Hamilton, Canada
,
M A Guccione
The Department of Biochemistry, University of Toronto, Toronto, Canada, and the Department of Pathology, McMaster University, Hamilton, Canada
,
R L Kinlough-Rathbone
The Department of Biochemistry, University of Toronto, Toronto, Canada, and the Department of Pathology, McMaster University, Hamilton, Canada
,
J F Mustard
The Department of Biochemistry, University of Toronto, Toronto, Canada, and the Department of Pathology, McMaster University, Hamilton, Canada
› Author Affiliations
Further Information

Publication History

Received: 27 December 1988

Accepted after revision 19 June 1989

Publication Date:
30 June 2018 (online)

Summary

The effect of the concentration of Ca2+ in the suspending medium of human and rabbit platelets on aggregation, release of 14C-serotonin, and TXB2 formation in response to ADP, thrombin, l-0-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine (PAF), collagen and arachidonic acid was studied in either platelet-rich plasma anticoagulated with D-phenylalanyl-prolyl-arginyl chloromethylketone (PPACK) or citrate, or suspensions of washed platelets in modified Tyrode-albumin solutions containing 1 mM Mg2+ and concentrations of added Ca2+ ranging from 0 to 5 mM. In response to ADP, thrombin, or PAF, human platelets were stimulated to form TXA2 by close platelet contact in a low- Ca2+ medium; at physiological concentrations of Ca2+, TXB 2formation was much less and declined progressively as the concentration of Ca2+ was raised. When the formation of TXA 2was blocked with aspirin or indomethacin, aggregation and release by human platelets were strongest at physiological concentrations of Ca2+. Rabbit platelet responses differed markedly from those of human platelets because close contact of rabbit platelets in a low-Ca2+ medium did not promote TXA2 formation. Rabbit platelet responses were more strongly inhibited by the lack of added Ca2+ in the medium than the responses of human platelets, possibly because rabbit platelets do not contain releasable Ca2+.

In all studies of human platelets in media with low concentrations of Ca2+, the additional contribution to platelet responses of TXA2 formed because of close platelet contact should be considered because TXA2 formation is not usually stimulated in this way at physiological concentrations of Ca2+. When TXA2 formation is blocked, aggregation and release responses to all agonists are greatest at physiological concentrations of Ca2+. Thus, the responses of human platelets in media with low concentrations of Ca2+ (citrated platelet-rich plasma or artificial media to which no Ca2+ has been added) are abnormal in at least two ways, and do not correspond to the responses at physiological concentrations of Ca2+.

 
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