Maegele Marc, Lippert-Gruener Marcela, Ester-Bode Thorsten, Garbe Janika, Bouillon Bertil, Neugebauer Edmund, Klug Norfrid, Lefering Rolf, Neiss Wolfram F, Angelov Doychin N
Biochemical and Experimental Division, Faculty of Medicine, University of Cologne, Germany.
Eur J Neurosci. 2005 May;21(9):2406-18. doi: 10.1111/j.1460-9568.2005.04070.x.
This study was designed to determine whether exposure to multimodal early onset stimulation (MEOS) combined with environmental enrichment (EE) after traumatic brain injury (TBI) would improve neurological recovery and to elucidate its morphological correlates. Male Sprague-Dawley rats were subjected to lateral fluid percussion (LFP) brain injury or to sham operation. After LFP, one-third of the animals (injured and sham) were placed under conditions of standard housing (SH), one-third were kept in EE only, and one-third received EE + MEOS. Assessment of neuromotor function 24 h post-injury using a standardized composite neuroscore test revealed an identical pattern of neurological impairment in all animals subjected to LFP. Neuromotor dysfunction in SH animals remained on a similar level throughout the experiment, while improvements were noted in both other groups 7 days post-injury (dpi). On 15 dpi, reversal of neuromotor dysfunction was significantly better in EE + MEOS animals vs. SH- and EE-only groups. In parallel, the comparison of lesion volume in EE + MEOS- vs. EE-only vs. SH rats revealed that animals exposed to EE + MEOS had consistently the lowest values (mm3, mean +/- SD; n = 6 rats in each group) as measured in serial brain sections immunostained for neuron-specific enolase (5.2 +/- 3.4 < or = 5.5 +/- 4.1 < 9.5 +/- 1.9), caspase 3-active/C3A (5.9 +/- 4.0 < or = 6.4 +/- 3.9 < 10.3 +/- 1.8) and glial fibrillary acidic protein (6.0 +/- 3.4 < or = 6.5 +/- 4.3 < 10.7 +/- 1.2). This first report on the effect of EE + MEOS treatment strongly indicates that the combined exposure reduces CNS scar formation and reverses neuromotor deficits after TBI in rats.
本研究旨在确定创伤性脑损伤(TBI)后暴露于多模式早期刺激(MEOS)联合环境富集(EE)是否能改善神经功能恢复,并阐明其形态学相关性。雄性Sprague-Dawley大鼠接受侧方流体冲击(LFP)脑损伤或假手术。LFP后,三分之一的动物(损伤组和假手术组)置于标准饲养条件(SH)下,三分之一仅饲养在EE环境中,三分之一接受EE + MEOS。损伤后24小时使用标准化综合神经评分测试评估神经运动功能,结果显示所有接受LFP的动物神经功能损伤模式相同。SH组动物的神经运动功能障碍在整个实验过程中保持在相似水平,而其他两组在损伤后7天(dpi)均有改善。在15 dpi时,EE + MEOS组动物的神经运动功能障碍逆转明显优于SH组和仅EE组。同时,对EE + MEOS组、仅EE组和SH组大鼠的损伤体积进行比较,结果显示,在对神经元特异性烯醇化酶进行免疫染色的连续脑切片中(每组n = 6只大鼠),接受EE + MEOS的动物损伤体积始终最低(mm³,平均值±标准差;5.2±3.4≤5.5±4.1<9.5±1.9),半胱天冬酶3活性/C3A(5.9±4.0≤6.4±3.9<10.3±1.8)和胶质纤维酸性蛋白(6.0±3.4≤6.5±4.3<10.7±1.2)。这篇关于EE + MEOS治疗效果的首次报告有力地表明,联合暴露可减少大鼠TBI后中枢神经系统瘢痕形成并逆转神经运动缺陷。