Dluzen Dean E
Department of Anatomy, Northeastern Ohio Universities College of Medicine, 4209 State Route 44, PO Box 95, Rootstown, OH 44272-0095, USA.
Neurosci Lett. 2004 Apr 15;359(3):135-8. doi: 10.1016/j.neulet.2004.01.061.
The interactive effects between gender and a selective alteration in the neurotrophin, brain-derived neurotrophic factor (BDNF) upon methamphetamine (MA)-induced neurotoxicity of the nigrostriatal dopaminergic (NSDA) system were assessed. MA treatment produced a greater degree of NSDA neurotoxicity (indicated by greater reductions in corpus striatal dopamine levels) in wild type control BDNF male versus female mice. This sex difference was unaltered in heterozygous mutant BDNF (BDNF +/-) mice and in mice which overexpress BDNF (DBH:BDNF +). Both BDNF mutant conditions resulted in preservation of corpus striatal dopamine levels following MA treatment as compared with their respective MA-treated wild type controls. The relative amount of this preservation was greater in male BDNF mutants, with values being significantly greater than females in the BDNF +/- condition. These results suggest that alterations in BDNF do not alter basic gender differences in MA-induced NSDA neurotoxicity, but may produce a neuroprotection against MA which is relatively greater in males.
评估了性别与神经营养因子、脑源性神经营养因子(BDNF)的选择性改变对甲基苯丙胺(MA)诱导的黑质纹状体多巴胺能(NSDA)系统神经毒性的交互作用。与野生型对照BDNF雌性小鼠相比,MA处理使野生型对照BDNF雄性小鼠产生了更高程度的NSDA神经毒性(表现为纹状体多巴胺水平的更大幅度降低)。在杂合突变型BDNF(BDNF+/-)小鼠和过表达BDNF的小鼠(DBH:BDNF+)中,这种性别差异没有改变。与各自接受MA处理的野生型对照相比,两种BDNF突变情况均导致MA处理后纹状体多巴胺水平得以保留。这种保留的相对量在雄性BDNF突变体中更大,在BDNF+/-情况下,其值显著高于雌性。这些结果表明,BDNF的改变不会改变MA诱导的NSDA神经毒性中的基本性别差异,但可能对MA产生相对更强的神经保护作用,且这种作用在雄性中更为明显。