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成年大鼠弥漫性颅脑损伤后,神经发生和神经胶质增生受到刺激。

Neurogenesis and glial proliferation are stimulated following diffuse traumatic brain injury in adult rats.

机构信息

National Trauma Research Institute, The Alfred Hospital, Melbourne, Victoria, Australia.

出版信息

J Neurosci Res. 2011 Jul;89(7):986-1000. doi: 10.1002/jnr.22635. Epub 2011 Apr 12.

DOI:10.1002/jnr.22635
PMID:21488090
Abstract

Although increased neurogenesis has been described in rodent models of focal traumatic brain injury (TBI), the neurogenic response occurring after diffuse TBI uncomplicated by focal injury has not been examined to date, despite the pervasiveness of this distinct type of brain injury in the TBI patient population. Here we characterize multiple stages of neurogenesis following a traumatic axonal injury (TAI) model of diffuse TBI as well as the proliferative response of glial cells. TAI was induced in adult rats using an impact-acceleration model, and 5-bromo-2'-deoxyuridine (BrdU) was administered on days 1-4 posttrauma or sham operation to label mitotic cells. Using immunohistochemistry for BrdU combined with phenotype-specific markers, we found that proliferation was increased following TAI in the subventricular zone of the lateral ventricles and in the hippocampal subgranular zone, although the ultimate production of new dentate granule neurons at 8 weeks was not significantly enhanced. Also, abundant proliferating and reactive astrocytes, microglia, and polydendrocytes were detected throughout the brain following TAI, indicating that a robust glial response occurs in this model, although very few new cells in the nonneurogenic brain regions became mature neurons. We conclude that diffuse brain injury stimulates early stages of a neurogenic response similar to that described for models of focal TBI.

摘要

虽然在局灶性创伤性脑损伤(TBI)的啮齿动物模型中已经描述了神经发生增加,但迄今为止,尚未检查弥漫性 TBI 后发生的神经发生反应,尽管这种明显类型的脑损伤在 TBI 患者人群中普遍存在。在这里,我们描述了弥漫性 TBI 的创伤性轴索损伤(TAI)模型后多个阶段的神经发生以及神经胶质细胞的增殖反应。使用冲击加速模型在成年大鼠中诱导 TAI,并在创伤或假手术后的第 1-4 天给予 5-溴-2'-脱氧尿苷(BrdU)以标记有丝分裂细胞。通过 BrdU 与表型特异性标志物的免疫组织化学联合使用,我们发现 TAI 后侧脑室室下区和海马颗粒下区的增殖增加,尽管 8 周时新齿状颗粒神经元的最终产生没有明显增强。此外,在 TAI 后整个大脑中都检测到大量增殖和反应性星形胶质细胞、小胶质细胞和多形性室管膜细胞,表明该模型中发生了强烈的神经胶质反应,尽管非神经发生脑区中的很少新细胞成为成熟神经元。我们得出结论,弥漫性脑损伤刺激类似于局灶性 TBI 模型描述的神经发生的早期阶段。

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