Mersereau Erik J, Poitra Shelby L, Espinoza Ana, Crossley Dane A, Darland Tristan
University of North Dakota, Biology Department, Grand Forks, ND 58202-9019, USA.
University of Arizona, Department of Ecology and Evolutionary Biology, Tucson, AZ 85721, USA.
Comp Biochem Physiol C Toxicol Pharmacol. 2015 Jun-Jul;172-173:1-6. doi: 10.1016/j.cbpc.2015.03.007. Epub 2015 Apr 3.
Zebrafish (Danio rerio) have been used as a model organism to explore the genetic basis for responsiveness to addictive drugs like cocaine. However, very little is known about how the physiological response to cocaine is mediated in zebrafish. In the present study electrocardiograms (ECGs) were recorded from adult zebrafish treated with cocaine. Treatment with cocaine resulted in a bell-shaped dose response curve with a maximal change in heart rate seen using 5mg/L cocaine. Higher doses resulted in a higher percentage of fish showing bradycardia. The cocaine-induced tachycardia was blocked by co-treatment with propranolol, a β-adrenergic antagonist, but potentiated by co-treatment with phentolamine, an α-adrenergic antagonist. Co-treatment with atropine, a classic cholinergic antagonist, had no effect on cocaine-induced tachycardia. Cocaine treatment of adult fish changed the ECG of treated fish, inducing a dose-dependent increase in QT interval after adjusting for heart rate (QTc), while not affecting the PR or QRS intervals. The acute effects of cocaine on heart rate were examined in 5-day old embryos to see if zebrafish might serve as a suitable model organism to study possible links of embryonic physiological response to subsequent adult behavioral response to the drug. Cocaine treatment of 5-day old zebrafish embryos also resulted in a bell-shaped dose response curve, with maximal tachycardia achieved with 10mg/L. The response in embryonic fish was thus comparable to that in adults and raises the possibility that the effects of embryonic exposure to cocaine on the developing cardiovascular system can be effectively modeled in zebrafish.
斑马鱼(Danio rerio)已被用作模式生物,以探索对可卡因等成瘾性药物产生反应的遗传基础。然而,关于可卡因在斑马鱼体内的生理反应是如何介导的,人们所知甚少。在本研究中,记录了用可卡因处理的成年斑马鱼的心电图(ECG)。用可卡因处理产生了钟形剂量反应曲线,使用5mg/L可卡因时心率变化最大。更高剂量导致出现心动过缓的鱼的比例更高。可卡因诱导的心动过速被β-肾上腺素能拮抗剂普萘洛尔联合处理所阻断,但被α-肾上腺素能拮抗剂酚妥拉明联合处理所增强。与经典胆碱能拮抗剂阿托品联合处理对可卡因诱导的心动过速没有影响。可卡因处理成年鱼改变了处理后鱼的心电图,在调整心率(QTc)后,QT间期呈剂量依赖性增加,而不影响PR或QRS间期。在5天大的胚胎中研究了可卡因对心率的急性影响,以确定斑马鱼是否可能作为一个合适的模式生物,来研究胚胎生理反应与随后成年鱼对该药物行为反应之间可能的联系。用可卡因处理5天大的斑马鱼胚胎也产生了钟形剂量反应曲线,10mg/L时达到最大心动过速。因此,胚胎鱼的反应与成年鱼的反应相当,这增加了在斑马鱼中有效模拟胚胎期接触可卡因对发育中心血管系统影响的可能性。