Ojo Joseph O, Greenberg M Banks, Leary Paige, Mouzon Benoit, Bachmeier Corbin, Mullan Michael, Diamond David M, Crawford Fiona
Roskamp Institute Sarasota, FL, USA.
Roskamp Institute Sarasota, FL, USA ; Research and Development Service, James A. Haley Veterans' Hospital Tampa, FL, USA ; Department of Life sciences, The Open University Milton Keynes, UK.
Front Behav Neurosci. 2014 Jun 23;8:213. doi: 10.3389/fnbeh.2014.00213. eCollection 2014.
Co-morbid mild traumatic brain injury (mTBI) and post-traumatic stress disorder (PTSD) has become the signature disorder for returning combat veterans. The clinical heterogeneity and overlapping symptomatology of mTBI and PTSD underscore the need to develop a preclinical model that will enable the characterization of unique and overlapping features and allow discrimination between both disorders. This study details the development and implementation of a novel experimental paradigm for PTSD and combined PTSD-mTBI. The PTSD paradigm involved exposure to a danger-related predator odor under repeated restraint over a 21 day period and a physical trauma (inescapable footshock). We administered this paradigm alone, or in combination with a previously established mTBI model. We report outcomes of behavioral, pathological and biochemical profiles at an acute timepoint. PTSD animals demonstrated recall of traumatic memories, anxiety and an impaired social behavior. In both mTBI and combination groups there was a pattern of disinhibitory like behavior. mTBI abrogated both contextual fear and impairments in social behavior seen in PTSD animals. No major impairment in spatial memory was observed in any group. Examination of neuroendocrine and neuroimmune responses in plasma revealed a trend toward increase in corticosterone in PTSD and combination groups, and an apparent increase in Th1 and Th17 proinflammatory cytokine(s) in the PTSD only and mTBI only groups respectively. In the brain there were no gross neuropathological changes in any groups. We observed that mTBI on a background of repeated trauma exposure resulted in an augmentation of axonal injury and inflammatory markers, neurofilament L and ICAM-1 respectively. Our observations thus far suggest that this novel stress-trauma-related paradigm may be a useful model for investigating further the overlapping and distinct spatio-temporal and behavioral/biochemical relationship between mTBI and PTSD experienced by combat veterans.
合并存在的轻度创伤性脑损伤(mTBI)和创伤后应激障碍(PTSD)已成为退伍军人回国后的典型病症。mTBI和PTSD的临床异质性和症状重叠凸显了开发一种临床前模型的必要性,该模型将能够表征独特和重叠的特征,并区分这两种病症。本研究详细介绍了一种针对PTSD以及合并PTSD-mTBI的新型实验范式的开发和实施。PTSD范式包括在21天内反复约束下暴露于与危险相关的捕食者气味以及一次身体创伤(不可逃避的足部电击)。我们单独应用此范式,或与先前建立的mTBI模型联合应用。我们报告了急性时间点的行为、病理和生化特征结果。PTSD动物表现出创伤性记忆的回忆、焦虑和社交行为受损。在mTBI组和联合组中均存在一种去抑制样行为模式。mTBI消除了PTSD动物中出现的情境性恐惧和社交行为障碍。在任何组中均未观察到空间记忆的重大损害。对血浆中神经内分泌和神经免疫反应的检查显示,PTSD组和联合组中皮质酮有升高趋势,仅PTSD组和仅mTBI组中Th1和Th17促炎细胞因子分别有明显升高。在大脑中,任何组均未出现明显的神经病理变化。我们观察到,在反复创伤暴露背景下的mTBI导致轴突损伤和炎症标志物(分别为神经丝L和细胞间黏附分子-1)增加。我们目前的观察结果表明,这种新型的应激-创伤相关范式可能是进一步研究退伍军人所经历的mTBI和PTSD之间重叠且独特的时空及行为/生化关系的有用模型。