Marcinko Marie C, Darrow April L, Tuia Aaron J, Shohet Ralph V
Department of Medicine, University of Hawaii John A. Burns School of Medicine, Honolulu, Hawaii.
Physiol Rep. 2019 Mar;7(6):e14036. doi: 10.14814/phy2.14036.
In this study, we created a mouse model of methamphetamine cardiomyopathy that reproduces the chronic, progressive dosing commonly encountered in addicted subjects. We gradually increased the quantity of methamphetamine given to C57Bl/6 mice from 5 to 40 mg/kg over 2 or 5 months during two study periods. At the fifth month, heart weight was increased, echocardiograms showed a dilated cardiomyopathy and survival was lower in males, with less effect in females. Interestingly, these findings correspond to previous observations in human patients, suggesting greater male susceptibility to the effects of methamphetamine on the heart. Transcriptional analysis showed changes in genes dysregulated in previous methamphetamine neurological studies as well as many that likely play a role in cardiac response to this toxic stress. We expect that a deeper understanding of the molecular biology of methamphetamine exposure in the heart will provide insights into the mechanism of cardiomyopathy in addicts and potential routes to more effective treatment.
在本研究中,我们创建了一种甲基苯丙胺心肌病小鼠模型,该模型再现了成瘾者中常见的慢性、渐进性给药情况。在两个研究阶段中,我们在2个月或5个月的时间里,将给予C57Bl/6小鼠的甲基苯丙胺剂量从5毫克/千克逐渐增加到40毫克/千克。在第五个月时,心脏重量增加,超声心动图显示扩张型心肌病,雄性小鼠的存活率较低,雌性小鼠的影响较小。有趣的是,这些发现与之前在人类患者中的观察结果一致,表明男性对甲基苯丙胺对心脏的影响更敏感。转录分析显示,在之前的甲基苯丙胺神经学研究中失调的基因发生了变化,以及许多可能在心脏对这种毒性应激的反应中起作用的基因。我们预计,对心脏中甲基苯丙胺暴露的分子生物学有更深入的了解,将为成瘾者心肌病的发病机制以及更有效治疗的潜在途径提供见解。