Wan F J, Lin H C, Lin Y S, Tseng C J
Institute of Undersea and Hyperbaric Medicine, National Defense Medical Center, Taipei, Taiwan, ROC.
Neuropharmacology. 2000 Jan 28;39(3):419-26. doi: 10.1016/s0028-3908(99)00143-4.
Recent evidence suggests that free radicals can be produced in the brain following systemic administration of repeated or high doses of D-amphetamine (AMPH). However, it has been proposed that the toxic effects of AMPH are mostly secondary to AMPH-induced hyperthermia, and agents that protect against AMPH neurotoxicity do so by blocking AMPH-induced hyperthermia or causing hypothermia. In this study, we examined the effects of AMPH on the formation of hydroxyl radicals (*OH) following its infusion into the rat striatum via a microdialysis probe. We found that intra-striatal perfusion of AMPH (10 microM) caused an increased formation of hydroxyl radicals but did not raise the core temperatures of the rats. Pretreatment with the NMDA antagonist MK-801 (0.5 mg/kg) attenuated hydroxyl radical production elicited by AMPH infusion, although core body temperatures in AMPH-treated rats were not significantly altered. Additionally, infusion of AMPH in the striatum increased extracellular dopamine concentration and this effect was potentiated by MK-801 pretreatment. Thus, these results demonstrate that direct infusion of AMPH in the striatum induces hydroxyl radical production without causing hyperthermia, and also imply that activation of glutamate NMDA receptors mediates, at least in part, AMPH-induced hydroxyl radical formation in the rat striatum.
最近的证据表明,在全身重复给药或高剂量给予D-苯丙胺(AMPH)后,大脑中会产生自由基。然而,有人提出,AMPH的毒性作用主要继发于AMPH诱导的体温过高,而预防AMPH神经毒性的药物是通过阻断AMPH诱导的体温过高或导致体温过低来实现的。在本研究中,我们通过微透析探针将AMPH注入大鼠纹状体后,检测了其对羟自由基(*OH)形成的影响。我们发现,纹状体内灌注AMPH(10 microM)会导致羟自由基形成增加,但不会提高大鼠的核心体温。用NMDA拮抗剂MK-801(0.5 mg/kg)预处理可减弱AMPH灌注引起的羟自由基产生,尽管AMPH处理的大鼠的核心体温没有明显改变。此外,在纹状体中注入AMPH会增加细胞外多巴胺浓度,而这种作用会被MK-801预处理增强。因此,这些结果表明,在纹状体中直接注入AMPH会诱导羟自由基产生而不引起体温过高,并且还意味着谷氨酸NMDA受体的激活至少部分介导了大鼠纹状体中AMPH诱导的羟自由基形成。