Callahan B T, Ricaurte G A
Department of Neurology, The Johns Hopkins Medical Institutions, Baltimore, MD 21224, USA.
Neuroreport. 1998 Aug 24;9(12):2691-5. doi: 10.1097/00001756-199808240-00001.
The present study was undertaken to examine the role of temperature on the ability of 7-nitroindazole (7-NI) to prevent methamphetamine-induced dopamine (DA) neurotoxicity. Male Swiss-Webster mice received methamphetamine alone or in combination with 7-NI at either room temperature (20+/-1 degrees C) or at 28+/-1 degrees C. At 20+/-1 degrees C, 7-NI produced hypothermic effects and afforded total protection against methamphetamine-induced DA depletions in the striatum. At 28+/-1 degrees C, 7-NI produced minimal effects on body temperature and failed to prevent methamphetamine-induced DA reductions. These findings indicate that the neuroprotection afforded by 7-NI is likely related to its ability to produce hypothermia because agents that produce hypothermia and/or prevent hyperthermia are known to attenuate methamphetamine-induced neurotoxicity.
本研究旨在探讨温度对7-硝基吲唑(7-NI)预防甲基苯丙胺诱导的多巴胺(DA)神经毒性能力的影响。雄性瑞士-韦伯斯特小鼠在室温(20±1℃)或28±1℃下单独接受甲基苯丙胺或与7-NI联合给药。在20±1℃时,7-NI产生低温效应,并完全保护纹状体免受甲基苯丙胺诱导的DA耗竭。在28±1℃时,7-NI对体温影响极小,未能预防甲基苯丙胺诱导的DA减少。这些发现表明,7-NI提供的神经保护可能与其产生低温的能力有关,因为已知产生低温和/或预防体温过高的药物可减轻甲基苯丙胺诱导的神经毒性。