Department of Hematology-Oncology, School of Medicine, Pontificia Universidad Católica de Chile.
Platelets. 2011;22(8):596-601. doi: 10.3109/09537104.2011.578181. Epub 2011 Aug 2.
Cocaine abuse increases the risk of cardiac and cerebrovascular events, such as myocardial infarction and ischemic stroke. The underlying mechanisms leading to these complications are not fully understood although intravascular thrombus formation has been observed. The aim of this study was to investigate the existence of platelet activation and the effect of short-term abstinence in chronic cocaine consumers. We studied 23 cocaine dependent individuals (aged 20-54 years) who met DSM-IV criteria for cocaine dependence and 20 controls. Samples were obtained at baseline, within 72 h of last drug exposure and after 4 weeks of controlled abstinence. Monocyte-platelet aggregates (MPA) were measured by flow cytometry. Plasma levels of soluble CD40L (sCD40L), Neutrophil-Activating Peptide-2 (NAP-2) and regulated on activation normal T cells expressed and secreted (RANTES) were determined by ELISA. Levels of MPA, sCD40L, NAP-2 and RANTES were significantly higher (all p < 0.05) in cocaine addicts compared to controls at baseline. All the parameters returned to values similar to the control group after 4-weeks' abstinence. Levels of sCD40L and RANTES were associated with an index of intensity of drug consumption (p < 0.02). Our results demonstrate that cocaine use induces platelet activation which is a prominent finding after recent consumption. The persistence over time of this condition may contribute not only to acute thrombotic complications but also to the development of early-onset atherosclerotic process observed in cocaine abusers.
可卡因滥用会增加心脏和脑血管事件的风险,如心肌梗死和缺血性中风。虽然已经观察到血管内血栓形成,但导致这些并发症的潜在机制尚未完全了解。本研究旨在研究血小板活化的存在以及短期戒断对慢性可卡因使用者的影响。我们研究了 23 名符合 DSM-IV 可卡因依赖标准的可卡因依赖者(年龄 20-54 岁)和 20 名对照者。在基线、末次吸毒后 72 小时内和 4 周的控制戒断后采集样本。通过流式细胞术测量单核细胞-血小板聚集物(MPA)。通过 ELISA 测定血浆可溶性 CD40L(sCD40L)、中性粒细胞激活肽-2(NAP-2)和调节激活正常 T 细胞表达和分泌(RANTES)的水平。与对照组相比,基线时可卡因成瘾者的 MPA、sCD40L、NAP-2 和 RANTES 水平明显升高(均 p<0.05)。戒断 4 周后,所有参数均恢复至对照组相似水平。sCD40L 和 RANTES 水平与药物消耗强度指数相关(p<0.02)。我们的结果表明,可卡因使用会引起血小板活化,这是近期使用后的一个突出发现。这种情况随着时间的推移持续存在,不仅可能导致急性血栓并发症,还可能导致可卡因滥用者中观察到的早发性动脉粥样硬化过程的发展。