首页> 外文期刊>European archives of psychiatry and clinical neuroscience >Minocycline exacerbates apoptotic neurodegeneration induced by the NMDA receptor antagonist MK-801 in the early postnatal mouse brain
【24h】

Minocycline exacerbates apoptotic neurodegeneration induced by the NMDA receptor antagonist MK-801 in the early postnatal mouse brain

机译:米诺环素加重NMDA受体拮抗剂MK-801在出生后早期小鼠脑中引起的凋亡神经变性

获取原文
获取原文并翻译 | 示例
           

摘要

NMDA receptor (NMDAR) antagonists induce in perinatal rodent cortical apoptosis and protracted schizophrenia-like alterations ameliorated by antipsychotic treatment. The broad-spectrum antibiotic minocycline elicits antipsychotic and neuroprotective effects. Here we tested, if minocycline protects also against apoptosis triggered by the NMDAR antagonist MK-801 at postnatal day 7. Surprisingly, minocycline induced widespread cortical apoptosis and exacerbated MK-801-triggered cell death. In some areas such as the subiculum, the pro-apoptotic effect of minocycline was even more pronounced than that elicited by MK-801. These data reveal among antipsychotics unique pro-apoptotic properties of minocycline, raising concerns regarding consequences for brain development and the use in children.
机译:NMDA受体(NMDAR)拮抗剂诱导围产期啮齿动物皮层细胞凋亡,并通过抗精神病药物治疗缓解了长期的精神分裂症样变化。广谱抗生素米诺环素具有抗精神病和神经保护作用。在这里,我们测试了米诺环素是否还能在出生后第7天抵抗由NMDAR拮抗剂MK-801触发的凋亡。令人惊讶的是,米诺环素诱导了广泛的皮层细胞凋亡并加剧了MK-801触发的细胞死亡。在一些部位,例如下丘脑,米诺环素的促凋亡作用甚至比MK-801引起的更为明显。这些数据揭示了抗精神病药米诺环素具有独特的促凋亡特性,引起了人们对大脑发育和儿童使用后果的担忧。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号