Chen X, Li Y, Kline A E, Dixon C E, Zafonte R D, Wagner A K
Department of Physical Medicine and Rehabilitation, University of Pittsburgh, 3471 Fifth Avenue, Suite 201, Pittsburgh, PA 15213, USA.
Neuroscience. 2005;135(1):11-7. doi: 10.1016/j.neuroscience.2005.05.041.
Alterations in brain-derived neurotrophic factor expression have been reported in multiple brain regions acutely after traumatic brain injury, however neither injury nor post-injury environmental enrichment has been shown to affect hippocampal brain-derived neurotrophic factor gene expression in male rats chronically post-injury. Studies have demonstrated hormone-related neuroprotection for female rats after traumatic brain injury, and estrogen and exercise both influence brain-derived neurotrophic factor levels. Despite recent studies suggesting that exposure post-traumatic brain injury to environmental enrichment improves cognitive recovery in male rats, we have shown that environmental enrichment mediated improvements with spatial learning are gender specific and only positively affect males. Therefore the purpose of this study was to evaluate the effect of gender and environmental enrichment on chronic post-injury cortical and hippocampal brain-derived neurotrophic factor protein expression. Sprague-Dawley male and cycling female rats were placed into environmental enrichment or standard housing after controlled cortical impact or sham surgery. Four weeks post-surgery, hippocampal and frontal cortex brain-derived neurotrophic factor expression were examined using Western blot. Results revealed significant increases in brain-derived neurotrophic factor expression in the frontal cortex ipsilateral to injury for males (P=0.03). Environmental enrichment did not augment this effect. Neither environmental enrichment nor injury significantly affected cortical brain-derived neurotrophic factor expression for females. In the hippocampus ipsilateral to injury brain-derived neurotrophic factor expression for both males and females was half (49% and 51% respectively) of that observed in shams housed in the standard environment. For injured males, there was a trend in this region for environmental enrichment to restore brain-derived neurotrophic factor levels to sham values. However, there were robust increases in hippocampal brain-derived neurotrophic factor expression ipsilateral to the injury for injured females in environmental enrichment compared with both sham and injured females placed in standard housing (P<or=0.005). In the hippocampus contralateral to injury, there were also significant injury-related increases in brain-derived neurotrophic factor expression for females (P<or=0.05) that were not further augmented by environmental enrichment. These results show significant, region-specific gender differences in brain-derived neurotrophic factor expression with both injury and environmental enrichment that may be important for recovery. However, these data do not support a critical role for brain-derived neurotrophic factor in environmental enrichment mediated improvements with spatial learning.
据报道,创伤性脑损伤后多个脑区的脑源性神经营养因子表达会立即发生改变,然而,无论是损伤还是损伤后的环境富集,都未显示会对雄性大鼠损伤后长期的海马脑源性神经营养因子基因表达产生影响。研究表明,创伤性脑损伤后雌性大鼠存在激素相关的神经保护作用,雌激素和运动都会影响脑源性神经营养因子水平。尽管最近的研究表明,创伤性脑损伤后暴露于环境富集可改善雄性大鼠的认知恢复,但我们已经表明,环境富集介导的空间学习改善具有性别特异性,仅对雄性有积极影响。因此,本研究的目的是评估性别和环境富集对损伤后慢性期皮质和海马脑源性神经营养因子蛋白表达的影响。将Sprague-Dawley雄性大鼠和处于发情周期的雌性大鼠在控制性皮质撞击或假手术后置于环境富集或标准饲养环境中。术后四周,使用蛋白质印迹法检测海马和额叶皮质脑源性神经营养因子的表达。结果显示,雄性大鼠损伤同侧额叶皮质中的脑源性神经营养因子表达显著增加(P = 0.03)。环境富集并未增强这种作用。环境富集和损伤均未对雌性大鼠的皮质脑源性神经营养因子表达产生显著影响。在损伤同侧的海马中,雄性和雌性大鼠的脑源性神经营养因子表达均为标准环境饲养的假手术大鼠的一半(分别为49%和51%)。对于受伤的雄性大鼠,在该区域存在一种趋势,即环境富集可使脑源性神经营养因子水平恢复到假手术组的水平。然而,与置于标准饲养环境中的假手术雌性大鼠和受伤雌性大鼠相比,环境富集中受伤雌性大鼠损伤同侧海马中的脑源性神经营养因子表达有显著增加(P≤0.005)。在损伤对侧的海马中,雌性大鼠的脑源性神经营养因子表达也因损伤而显著增加(P≤0.05),环境富集并未进一步增强这种增加。这些结果表明,在脑源性神经营养因子表达方面存在显著的、区域特异性的性别差异,损伤和环境富集均可能对恢复很重要。然而,这些数据并不支持脑源性神经营养因子在环境富集介导的空间学习改善中起关键作用。