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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Tamoxifen abolishes estrogen's neuroprotective effect upon methamphetamine neurotoxicity of the nigrostriatal dopaminergic system.
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Tamoxifen abolishes estrogen's neuroprotective effect upon methamphetamine neurotoxicity of the nigrostriatal dopaminergic system.

机译:他莫昔芬消除了雌激素对黑质纹状体多巴胺能系统的甲基苯丙胺神经毒性的神经保护作用。

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摘要

The effects of 17beta-estradiol and the anti-estrogen, tamoxifen, on methamphetamine-induced neurotoxicity of the nigrostriatal dopaminergic system were examined in ovariectomized CD-1 mice. In Experiment 1, striatal dopamine concentrations from estrogen treated mice were significantly greater than that from non-estrogen treated mice following methamphetamine. Dopamine concentrations from estrogen+tamoxifen+methamphetamine treated mice were decreased compared to estrogen+methamphetamine treated mice and not significantly different from those of tamoxifen+methamphetamine treated mice or mice receiving methamphetamine alone. These results suggest that estrogen is functioning as a neuroprotectant of methamphetamine-induced nigrostriatal dopaminergic neurotoxicity and that this neuroprotective effect of estrogen is abolished in the presence of tamoxifen. In Experiment 2, estrogen administration after methamphetamine treatment did not produce any significant changes in dopamine concentrations compared with methamphetamine treatment alone. The data from Experiment 2 show that estrogen cannot reverse the methamphetamine-induced neurotoxicity upon the nigrostriatal dopaminergic system. Similar results were observed for the potassium-stimulated dopamine outputs from these treatment conditions as evaluated with in vitro superfusion, although a difference between the two measures for the estrogen+methamphetamine treated group was obtained in Experiment 1. These results have important implications for estrogen-tamoxifen interactions upon the nigrostriatal dopaminergic system and the gender differences which are observed in Parkinson's disease and animal models of nigrostriatal dopaminergic neurotoxicity as well as for the proposed use of tamoxifen in pre-menopausal women at risk for breast cancer.
机译:在卵巢切除的CD-1小鼠中检查了17β-雌二醇和抗雌激素他莫昔芬对甲基苯丙胺诱导的黑质纹状体多巴胺能系统神经毒性的影响。在实验1中,经甲基苯丙胺治疗后,经雌激素处理的小鼠的纹状体多巴胺浓度显着高于未经雌激素处理的小鼠。与雌激素+甲基苯丙胺治疗的小鼠相比,雌激素+他莫昔芬+甲基苯丙胺治疗的小鼠的多巴胺浓度降低,与他莫昔芬+甲基苯丙胺治疗的小鼠或仅接受甲基苯丙胺的小鼠的多巴胺浓度无显着差异。这些结果表明,雌激素起甲基苯丙胺诱导的黑纹状体多巴胺能神经毒性的神经保护作用,并且在存在他莫昔芬的情况下,雌激素的这种神经保护作用被消除。在实验2中,与仅使用甲基苯丙胺治疗相比,在甲基苯丙胺治疗后给予雌激素并未产生多巴胺浓度的任何显着变化。实验2的数据表明,雌激素不能逆转甲基苯丙胺对黑质纹状体多巴胺能系统的神经毒性。尽管在实验1中获得了两种测量雌激素+甲基苯丙胺治疗组的指标之间的差异,但通过体外灌注评估了这些治疗条件下钾刺激的多巴胺输出的相似结果。这些结果对雌激素他莫昔芬对黑质纹状体多巴胺能系统的相互作用以及在帕金森氏病和黑质纹状体多巴胺能神经毒性的动物模型中观察到的性别差异,以及建议的三苯氧胺在绝经前有乳腺癌风险的妇女中的使用。

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