Cass W A, Walker D J, Manning M W
Department of Anatomy and Neurobiology, MN 224 Chandler Medical Center, University of Kentucky, Lexington, KY 40536-0298, USA.
Brain Res. 1999 May 8;827(1-2):104-12. doi: 10.1016/s0006-8993(99)01314-1.
Glial cell line-derived neurotrophic factor (GDNF) can attenuate the dopamine (DA)-depleting effects of neurotoxic doses of methamphetamine (METH) when given 1 day prior to the METH. The neurotoxic effects of METH may be due, in part, to sustained increases in extracellular levels of DA. It is therefore possible that GDNF may be altering the effects of METH by influencing extracellular levels of DA during the METH treatment. The purpose of the present study was to determine if GDNF has effects on extracellular levels of DA in the striatum by 24-h post-administration. GDNF (10 microgram in 2 microliter vehicle) or vehicle was injected into the right striatum or substantia nigra of anesthetized male rats. The next day the animals were anesthetized again and dialysis probes were positioned in both the right and left striata and perfused with artificial cerebrospinal fluid. Following the collection of baseline samples the rats were administered METH (5 mg/kg, s.c.). The METH injections dramatically increased extracellular DA levels on both sides of the brain. However, levels on the GDNF injected side were significantly greater than levels on the contralateral side. Basal levels of DA were not significantly different between the two sides, but levels of DA metabolites were elevated on the GDNF side. Post-mortem tissue levels of DA metabolites, but not DA, were also elevated in the striatum and substantia nigra. These results indicate that GDNF has significant effects on DA neuron functioning within 24 h of administration and that GDNF can augment DA overflow while inhibiting the neurotoxic effects of METH.
胶质细胞系源性神经营养因子(GDNF)在甲基苯丙胺(METH)给药前1天给予时,可减轻神经毒性剂量的METH对多巴胺(DA)的消耗作用。METH的神经毒性作用可能部分归因于细胞外DA水平的持续升高。因此,GDNF可能通过在METH治疗期间影响细胞外DA水平来改变METH的作用。本研究的目的是确定GDNF在给药后24小时是否对纹状体中DA的细胞外水平有影响。将GDNF(10微克溶于2微升载体中)或载体注射到麻醉的雄性大鼠的右纹状体或黑质中。第二天再次麻醉动物,并将透析探针置于左右纹状体中,并用人工脑脊液灌注。在收集基线样本后,给大鼠注射METH(5毫克/千克,皮下注射)。METH注射显著增加了大脑两侧的细胞外DA水平。然而,注射GDNF一侧的水平明显高于对侧。两侧的DA基础水平没有显著差异,但GDNF一侧的DA代谢产物水平升高。纹状体和黑质中DA代谢产物的死后组织水平升高,但DA水平未升高。这些结果表明,GDNF在给药后24小时内对DA神经元功能有显著影响,并且GDNF可以增加DA溢出,同时抑制METH的神经毒性作用。