Casartelli Alessandro, Dacome Lisa, Tessari Michela, Pascali Jennifer, Bortolotti Federica, Trevisan Maria Teresa, Bosco Oliviero, Cristofori Patrizia, Tagliaro Franco
Toxicology and Pathology Department, Aptuit Medicine Research centre, Verona, Italy; Faculty of Medicine and Surgery, Public Health and Community Medicine Department, University of Verona, Verona, Italy.
Toxicology and Pathology Department , Aptuit Medicine Research centre , Verona , Italy.
Heart Asia. 2014 Jul 8;6(1):100-7. doi: 10.1136/heartasia-2013-010482. eCollection 2014.
Cocaine is known to produce life-threatening cardiovascular complications, and the investigation of the causes of death may be challenging in forensic medicine. The increasing knowledge of the cardiac function biomarkers and the increasing sensitivity of assays provide new tools in monitoring the cardiac life-threatening pathological conditions and in the sudden death investigation in chronic abusers. In this work, cardiac dysfunction was assessed in an animal model by measuring troponin I and natriuretic peptides as biomarkers, and considering other standard endpoints used in preclinical toxicology studies.
Lister Hooded rats were treated with cocaine in chronic self-administration studies. Troponin I (cTnI) and atrial natriuretic peptide (ANP) were evaluated at different time points and heart weight and histopathology were assessed at the end of the treatment period. Furthermore, cocaine and its main metabolites were measured in the rat fur to assess rats' cocaine exposure. All the procedures and endpoints considered were designed to allow an easy and complete translation from the laboratory animals to human beings, and the same approach was also adopted with a group of 10 healthy cocaine abuse volunteers with no cardiac pathologies.
Cardiac troponin I values were unaffected, and ANP showed an increasing trend with time in all cocaine-treated animals considered. Similarly, in the healthy volunteers, no changes were observed in troponin serum levels, whereas the N-terminal brain natriuretic pro-peptide (NT proBNP) showed variations comparable with the changes observed in rats.
In conclusion, natriuretic peptides could represent an early indicator of heart dysfunction liability in chronic cocaine abusers.
可卡因已知会引发危及生命的心血管并发症,在法医学中,死因调查可能具有挑战性。对心脏功能生物标志物的了解不断增加以及检测方法的灵敏度不断提高,为监测危及心脏生命的病理状况和慢性滥用者猝死调查提供了新工具。在本研究中,通过测量肌钙蛋白I和利钠肽作为生物标志物,并考虑临床前毒理学研究中使用的其他标准终点,在动物模型中评估心脏功能障碍。
在慢性自我给药研究中,用可卡因处理利斯特戴帽大鼠。在不同时间点评估肌钙蛋白I(cTnI)和心房利钠肽(ANP),并在治疗期结束时评估心脏重量和组织病理学。此外,测量大鼠毛发中的可卡因及其主要代谢物,以评估大鼠的可卡因暴露情况。所有考虑的程序和终点均旨在便于从实验动物完整地转化到人类,并且对一组10名无心脏疾病的健康可卡因滥用志愿者也采用了相同的方法。
在所有考虑的可卡因处理动物中,心脏肌钙蛋白I值未受影响,ANP随时间呈上升趋势。同样,在健康志愿者中,肌钙蛋白血清水平未观察到变化,而N末端脑利钠肽前体(NT proBNP)的变化与在大鼠中观察到的变化相当。
总之,利钠肽可能是慢性可卡因滥用者心脏功能障碍易感性的早期指标。