Pereira Frederico C, Macedo Tice R, Imam Syed Z, Ribeiro Carlos F, Ali Syed F
Neurochemistry Laboratory, Division of Neurotoxicology, HFT-132, NCTR/FDA, Jefferson, AR 72079, USA.
Neurotox Res. 2004;6(2):149-52. doi: 10.1007/BF03033217.
The most widely accepted concept of oxidative damage centers on the formation of hydroxyl radical (*OH) which has an extremely short-life and is the major damaging free radical. It was suggested that methamphetamine (METH) toxicity is mediated via production of *OH, as measured by 2,3-dihydroxybenzoic acid (2,3-DHBA). In this study we compared the effects of local caudate nucleus perfusion of METH with systemic administration of METH on *OH generation in relation to DA release. Local perfusion of METH (5 mM, 140 min) induced a higher level of dopamine (DA) release compared to the first METH injection (10 mg/kg, 3 times, i.p.). No significant correlation was found between changes in extracellular DA levels and *OH generation when perfusing METH locally; however, both increased after systemic METH administration.