Warren Matthew W, Kobeissy Firas H, Liu Ming Cheng, Hayes Ronald L, Gold Mark S, Wang Kevin K W
College of Medicine, University of Florida, Gainsville, FL 32610, USA.
J Addict Dis. 2006;25(4):115-23. doi: 10.1300/J069v25n04_11.
Ecstasy use is a growing problem in the United States. Techniques to demonstrate and characterize the toxicity associated with its use have been limited and employed infrequently. In this study, we compare the deleterious effects of ecstasy use in rats with that of methamphetamine and traumatic brain injury. Specifically, we investigate the degradation of structural proteins alphaII-spectrin and tau by the pro-necrotic calpain and pro-apoptotic caspase systems. Ecstasy-induced neurotoxicity is shown after 24 hours, although to a much lesser extent than that of methamphetamine or traumatic brain injury. Neurotoxicity is still evident after 72 hours. Furthermore, apoptosis of the liver is seen 72 hours after ecstasy use. Use of protease inhibitors may be useful in preventing ecstasy-induced toxicity.
摇头丸的使用在美国是一个日益严重的问题。用于证明和表征与其使用相关毒性的技术一直有限且很少使用。在本研究中,我们将大鼠使用摇头丸的有害影响与甲基苯丙胺和创伤性脑损伤的有害影响进行比较。具体而言,我们研究坏死前钙蛋白酶和促凋亡半胱天冬酶系统对结构蛋白αII-血影蛋白和tau的降解作用。虽然摇头丸诱导的神经毒性在24小时后出现,但其程度远低于甲基苯丙胺或创伤性脑损伤。72小时后神经毒性仍然明显。此外,使用摇头丸72小时后可见肝脏细胞凋亡。使用蛋白酶抑制剂可能有助于预防摇头丸诱导的毒性。