Cocaine activates platelets and increases the formation of circulating platelet containing microaggregates in humans

Citation
Cm. Heesch et al., Cocaine activates platelets and increases the formation of circulating platelet containing microaggregates in humans, HEART, 83(6), 2000, pp. 688-695
Citations number
42
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
HEART
ISSN journal
13556037 → ACNP
Volume
83
Issue
6
Year of publication
2000
Pages
688 - 695
Database
ISI
SICI code
1355-6037(200006)83:6<688:CAPAIT>2.0.ZU;2-4
Abstract
Objective-To determine whether there is evidence of platelet activation fol lowing in vivo cocaine administration in humans, as cocaine abuse is associ ated with myocardial infarction and stroke, and platelet activation leading to thrombosis is a possible mechanism. Setting-University hospital. Design and subjects-Following a randomised, double blind crossover design, 14 healthy volunteers were studied twice, receiving cocaine (2 mg/kg intran asally) once and placebo once. Flow cytometric analysis of P-selectin expre ssion (an alpha granule membrane protein found on the surface of activated platelets), quantification of the platelet specific proteins platelet facto r 4 and beta thromboglobulin, and measurement of platelet containing microa ggregate and platelet microparticle (fragment) formation were used to asses s platelet activation. Circulating von Willebrand factor antigen (VWF) was measured to evaluate a possible role of endothelial stimulation concurrent with platelet activation. Results-There was an increase in both platelet factor 4 (mean (SD), 16 (7) to 39 (22) IU/ml, p = 0.04) and beta thromboglobulin (70 (20) to 98 (26) IU /ml, p < 0.01) at 120 minutes following cocaine administration. Platelet co ntaining microaggregate formation was increased at 40 minutes (from 47 (3.2 )% to 54 (2.0)%, p < 0.001) and 80 minutes (55 (2.5)%, p = 0.04). Bleeding time decreased following cocaine from 10 (1) to 9 (1) minutes (p = 0.07). N o changes in any of the measured variables were noted following placebo adm inistration. Conclusions-Cocaine exposure causes platelet activation, alpha granule rele ase, and platelet containing microaggregate formation. These data support t he view that cocaine, even at the relatively low doses commonly self admini stered by occasional abusers, may promote thrombosis and predispose healthy individuals to ischaemic events. Platelet inhibitors should be considered early in any patient with suspected cocaine related ischaemia.