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Multiple mild traumatic brain injury in the rat produces persistent pathological alterations in the brain

机译:大鼠中多重轻微的创伤性脑损伤会产生脑内持续的病理改变

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Abstract Multiple mild traumatic brain injury (mmTBI), in certain cases, produces persistent symptoms. However, the molecular mechanisms underlying these symptoms remain unclear. Here, we demonstrate extended pathological changes in the rat brain following mmTBI. Using the lateral fluid percussion (LFP) technique we exposed adult male Wistar rats to a mild TBI (mTBI) once a week for four weeks and compared them to surgical shams. At 90days following the last TBI or sham procedure the animals were cognitively tested in the Morris Water Maze (MWM), euthanized, and the brains removed for immunohistochemistry. At 90days following the last mTBI, NRF-2 staining was significantly decreased in the hilus of the hippocampus and cortex on the injured side, but did not significantly differ from shams on the un-injured side. CD68 positive microglia were significantly increased in the ipsilateral corpus callosum, cortex, and internal capsule of injured animals. Reactive astrocytosis, determined by increased GFAP staining, was also evident in the corpus callosum, cortex, internal capsule and thalamus on the injured side. Interestingly, the corpus callosum thickness at the midline was decreased in injured animals and had evident demyelination when compared to sham animals. Despite these findings, there were no significant differences in neurological assessments at 90days following the last injury. In MWM testing there were not significant differences in the training phase, the time spent in the thigmotaxia zone, or the target quadrant during the probe trial. However, there were significant differences between shams and injured animals in platform zone crossings during the probe trial. These results demonstrate that repetitive head trauma may produce persistent, long-term pathological alterations in brain architecture that may be difficult to detect using standard cognitive and neurological assessments. Highlights ? The lateral fluid percussion model of TBI can be effectively used for repetitive mild brain injury studies. ? Repeated mild TBI produces a long-term microglial/astrocytic activation and concurrent thinning of the corpus callosum. ? Repeated mild TBI may produce alterations in the brain that do not result in overt cognitive or neuromotor impairment.
机译:摘要在某些情况下,多种温和创伤性脑损伤(MMTBI)产生持续存在的症状。然而,这些症状的分子机制仍然不清楚。在这里,我们证明了MMTBI之后的大鼠脑中的延长病理变化。使用横向流体敲击(LFP)技术,我们将成年雄性Wistar大鼠暴露于每周一次4周并将其与外科手术进行比较。在上次TBI或假手术后90天,在莫里斯水迷宫(MWM)中,将动物在莫里斯水迷宫(MWM)中进行了安乐死,并为免疫组化除去了大脑。在上次MTBI后的90天,海马HILUS在受伤方面的HILUS和皮质皮层中的NRF-2染色显着下降,但没有显着不同于无人受伤的侧面。 IPsilidalcoralcorpus Callosum,皮质和受伤动物的内部胶囊中CD68阳性微胶质显着增加。通过增加GFAP染色而确定的活性星致织造症在胼callosum,皮质,内胶囊和丘陵上也显而易见。有趣的是,中线的胼um厚度在受伤的动物中减少,与假动物相比,损伤的脱髓鞘均显而易见。尽管有这些发现,在最后一次伤害后90天内的神经系统评估没有显着差异。在MWM测试中,训练阶段没有显着差异,在探针试验期间,ThigMotaxia区的时间或靶象限。然而,在探测试验期间平台区域交叉中的假疱疹和受伤动物之间存在显着差异。这些结果表明,重复的头部创伤可能产生脑架构的持续性,长期的病理改变,这可能难以使用标准认知和神经学评估来检测。强调 ? TBI的横向流体敲击模型可有效地用于重复轻度脑损伤研究。还重复的温和TBI产生长期的小胶质组织/星形胶质细胞活化,并同时稀疏胼callosum。还重复的温和TBI可能会产生不会导致明显认知或神经大通障碍的大脑中的改变。

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