Yang L-Y, Chu Y-H, Tweedie D, Yu Q-S, Pick C G, Hoffer B J, Greig N H, Wang J-Y
Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Drug Design & Development Section, Translational Gerontology Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, USA.
Exp Neurol. 2015 Jul;269:56-66. doi: 10.1016/j.expneurol.2015.03.015. Epub 2015 Mar 24.
Traumatic brain injury (TBI) is a major cause of death and disability worldwide. Programmed death of neuronal cells plays a crucial role in acute and chronic neurodegeneration following TBI. The tumor suppressor protein p53, a transcription factor, has been recognized as an important regulator of apoptotic neuronal death. The p53 inactivator pifithrin-α (PFT-α) has been shown to be neuroprotective against stroke. A previous cellular study indicated that PFT-α oxygen analog (PFT-α (O)) is more stable and active than PFT-α. We aimed to investigate whether inhibition of p53 using PFT-α or PFT-α (O) would be a potential neuroprotective strategy for TBI. To evaluate whether these drugs protect against excitotoxicity in vitro, primary rat cortical cultures were challenged with glutamate (50mM) in the presence or absence of various concentrations of the p53 inhibitors PFT-α or PFT-α (O). Cell viability was estimated by LDH assay. In vivo, adult Sprague Dawley rats were subjected to controlled cortical impact (CCI, with 4m/s velocity, 2mm deformation). Five hours after injury, PFT-α or PFT-α (O) (2mg/kg, i.v.) was administered to animals. Sensory and motor functions were evaluated by behavioral tests at 24h after TBI. The p53-positive neurons were identified by double staining with cell-specific markers. Levels of mRNA encoding for p53-regulated genes (BAX, PUMA, Bcl-2 and p21) were measured by reverse transcription followed by real time-PCR from TBI animals without or with PFT-α/PFT-α (O) treatment. We found that PFT-α(O) (10 μM) enhanced neuronal survival against glutamate-induced cytotoxicity in vitro more effectively than PFT-α (10 μM). In vivo PFT-α (O) treatment enhanced functional recovery and decreased contusion volume at 24h post-injury. Neuroprotection by PFT-α (O) treatment also reduced p53-positive neurons in the cortical contusion region. In addition, p53-regulated PUMA mRNA levels at 8h were significantly reduced by PFT-α (O) administration after TBI. PFT-α (O) treatment also decreased phospho-p53 positive neurons in the cortical contusion region. Our data suggest that PFT-α (O) provided a significant reduction of cortical cell death and protected neurons from glutamate-induced excitotoxicity in vitro, as well as improved neurological functional outcome and reduced brain injury in vivo via anti-apoptotic mechanisms. The inhibition of p53-induced apoptosis by PFT-α (O) provides a useful tool to evaluate reversible apoptotic mechanisms and may develop into a novel therapeutic strategy for TBI.
创伤性脑损伤(TBI)是全球范围内死亡和残疾的主要原因。神经元细胞的程序性死亡在TBI后的急性和慢性神经退行性变中起关键作用。肿瘤抑制蛋白p53作为一种转录因子,已被公认为凋亡性神经元死亡的重要调节因子。p53灭活剂pifithrin-α(PFT-α)已被证明对中风具有神经保护作用。先前的细胞研究表明,PFT-α氧类似物(PFT-α(O))比PFT-α更稳定且活性更高。我们旨在研究使用PFT-α或PFT-α(O)抑制p53是否会成为TBI的一种潜在神经保护策略。为了评估这些药物在体外是否能预防兴奋性毒性,在存在或不存在不同浓度的p53抑制剂PFT-α或PFT-α(O)的情况下,用谷氨酸(50mM)刺激原代大鼠皮质培养物。通过乳酸脱氢酶(LDH)测定评估细胞活力。在体内,成年Sprague Dawley大鼠接受控制性皮质撞击(CCI,速度为4m/s,变形2mm)。损伤后5小时,给动物静脉注射PFT-α或PFT-α(O)(2mg/kg)。在TBI后24小时通过行为测试评估感觉和运动功能。通过与细胞特异性标记物双重染色鉴定p53阳性神经元。通过逆转录随后对未接受或接受PFT-α/PFT-α(O)治疗的TBI动物进行实时PCR,测量p53调节基因(BAX、PUMA、Bcl-2和p21)的mRNA水平。我们发现,在体外,PFT-α(O)(10μM)比PFT-α(10μM)更有效地提高神经元对谷氨酸诱导的细胞毒性的存活率。在体内,PFT-α(O)治疗可增强损伤后24小时的功能恢复并减小挫伤体积。PFT-α(O)治疗的神经保护作用还减少了皮质挫伤区域的p53阳性神经元。此外,TBI后给予PFT-α(O)可使8小时时p53调节的PUMA mRNA水平显著降低。PFT-α(O)治疗还减少了皮质挫伤区域磷酸化p53阳性神经元。我们的数据表明,PFT-α(O)可显著减少皮质细胞死亡,并在体外保护神经元免受谷氨酸诱导的兴奋性毒性,以及通过抗凋亡机制在体内改善神经功能结局并减轻脑损伤。PFT-α(O)对p53诱导的凋亡的抑制作用为评估可逆性凋亡机制提供了一种有用的工具,并可能发展成为TBI的一种新型治疗策略。