Jayanthi Subramaniam, Ladenheim Bruce, Cadet Jean Lud
Molecular Neuropsychiatry Section, Division of Intramural Research (DIR), National Institute of Drug Abuse (NIDA), National Institutes of Health (NIH), P.O. Box 5180, Baltimore, Maryland 21224, USA.
Ann N Y Acad Sci. 1998 May;844(1):92-102. doi: 10.1111/j.1749-6632.1998.tb08224.x.
The present study was conducted to investigate the effects of methamphetamine (METH)-induced toxicity on brain cortical and striatal antioxidant defense systems. Because METH-induced toxicity is attenuated in copper/zinc-superoxide dismutase transgenic (Cu/Zn-SOD-Tg) mice, we sought to determine if METH had differential effect on antioxidant enzymes on these mice in comparison to non-Tg mice. METH (4 × 10 mg/kg) induced a significant decrease in Cu/Zn-SOD activity in the cortical region without altering striatal enzymatic activity in non-Tg mice; whereas homozygous SOD-Tg mice showed a significant increase in the striatum. In addition, METH caused decrease in catalase (CAT) activity in the striatum of non-Tg mice and significant increase in the cortex of homozygous SOD-Tg mice. METH also induced decreases in glutathione peroxidase (GSH-Px) in both cortical and striatal regions of non-Tg mice and in the striatum of heterozygous SOD-Tg mice. Lipid peroxidation was increased in both cortices and striata of non-Tg and heterozygous SOD-Tg mice, whereas the homozygous SOD-Tg mice were not affected. These results are discussed in terms of their substantiation of a role for oxygen-based radicals in METH-induced toxicity in rodents.
本研究旨在调查甲基苯丙胺(METH)诱导的毒性对大脑皮质和纹状体抗氧化防御系统的影响。由于METH诱导的毒性在铜/锌超氧化物歧化酶转基因(Cu/Zn-SOD-Tg)小鼠中减弱,我们试图确定与非转基因小鼠相比,METH对这些小鼠的抗氧化酶是否有不同的影响。METH(4×10mg/kg)使非转基因小鼠皮质区域的Cu/Zn-SOD活性显著降低,而纹状体酶活性未改变;而纯合子SOD-Tg小鼠纹状体中的活性显著增加。此外,METH导致非转基因小鼠纹状体中过氧化氢酶(CAT)活性降低,而纯合子SOD-Tg小鼠皮质中的活性显著增加。METH还使非转基因小鼠的皮质和纹状体区域以及杂合子SOD-Tg小鼠的纹状体中的谷胱甘肽过氧化物酶(GSH-Px)降低。非转基因和杂合子SOD-Tg小鼠的皮质和纹状体中的脂质过氧化均增加,而纯合子SOD-Tg小鼠未受影响。根据这些结果对基于氧的自由基在啮齿动物METH诱导的毒性中的作用进行了讨论。