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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >ENRICHED ENVIRONMENT PROMOTES SIMILAR NEURONAL AND BEHAVIORAL RECOVERY IN A YOUNG AND AGED MOUSE MODEL OF PARKINSON'S DISEASE
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ENRICHED ENVIRONMENT PROMOTES SIMILAR NEURONAL AND BEHAVIORAL RECOVERY IN A YOUNG AND AGED MOUSE MODEL OF PARKINSON'S DISEASE

机译:丰富的环境以帕金森氏病的年轻和衰老小鼠模型促进类​​似的神经元和行为恢复

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Environmental enrichment has been shown to be neuroprotective in the 1-methyl-4-phenyl-1,2,3,6-tetrahydro-pyridine (MPTP) mouse model of Parkinson's disease (PD). Because PD patients are not typically diagnosed until later neuropathological stages, the current study investigated the capacity of an enriched environment (EE) to stimulate restoration of neurons in the substantia nigra pars compacta (SNpc) and locomotor recovery after lesioning, as opposed to before. A low-dose chronic MPTP regimen was used to achieve a partial, less severe lesion of the nigrostriatal pathway not seen in acute MPTP models. Both young adult (10 weeks) and aged (12 months) C57BL/6J male mice were used to assess the effects of aging on recovery with EE intervention. After the first week of either MPTP (7 mg/kg/d in young; 5 mg/kg/d in aged) or saline injection, animals from both groups were housed in a standard environment (SE) or an EE for 3 weeks, with continued daily administration of MPTP. We are the first to report that following 3 weeks exposure to an EE, young and aged MPTP-lesioned mice showed a significant 53% and 52% restoration of tyrosine hydroxylase (TH)-labeled neurons in the SNpc, respectively. This increase in TH-labeled cells in the MPTP+EE group was correlated with recovery of free-standing rear (FSR) behavior in both age groups; however, improved locomotor control as measured by foot faults (FF) per total activity was only seen in the aged MPTP+EE group. Our data demonstrate that an EE promotes neurorestoration in TH protein expression in SNpc neurons as well as some locomotor recovery in both young and aged animals in this mouse model of PD. Published by Elsevier Ltd on behalf of IBRO.
机译:在帕金森氏病(PD)的1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)小鼠模型中,环境富集已显示出神经保护作用。由于通常直到后来的神经病理学阶段才诊断出PD患者,因此本研究调查了富集环境(EE)刺激黑质致密部(SNpc)中神经元恢复和损伤后运动恢复的能力。低剂量的慢性MPTP方案用于实现黑质纹状体途径的部分,不太严重的病变,这在急性MPTP模型中未见。使用C57BL / 6J雄性成年小鼠(10周)和成年(12个月)雄性小鼠,通过EE干预评估衰老对恢复的影响。在MPTP(年轻时为7 mg / kg / d;老年时为5 mg / kg / d)或生理盐水注射的第一周后,将两组动物都放在标准环境(SE)或EE中饲养3周,并持续每日管理MPTP。我们第一个报告称,暴露于EE的3周后,MPTP损伤的年轻和老年小鼠的SNpc中酪氨酸羟化酶(TH)标记的神经元分别显着恢复了53%和52%的恢复。 MPTP + EE组中TH标记细胞的这种增加与两个年龄组中独立式后排(FSR)行为的恢复相关。然而,仅通过老年人的MPTP + EE组,可以通过每总活动的脚部缺陷(FF)来衡量运动控制的改善。我们的数据表明,在这种PD小鼠模型中,EE促进SNpc神经元TH蛋白表达的神经修复以及幼小和成年动物的运动恢复。由Elsevier Ltd代表IBRO发布。

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