Whiting Mark D, Hamm Robert J
Department of Psychology, Virginia Commonwealth University, Richmond, Virginia 23284-2018, USA.
J Neurotrauma. 2006 Oct;23(10):1529-34. doi: 10.1089/neu.2006.23.1529.
Memory impairment following traumatic brain injury (TBI) is common in both humans and animals. A noteworthy feature of memory dysfunction in human TBI is impaired memory performance that is dependent on the delay between initial learning and recall of information. However, previous studies of TBI-induced memory impairment in animals have failed to control for the initial amount of learning between sham and injured animals. The present study demonstrates that experimental TBI in rats produces delay-dependent memory impairment, even when the initial degree of learning is controlled for. Animals were injured at a moderate level of lateral fluid percussion (LFP) injury (n = 10) or received a sham injury (n = 9), and then trained in a water T-maze version of the delayed-non-matching-to-place (DNMP) task beginning 10 days post-injury. Acquisition training consisted of 15 trials per day on post-injury days 11-15 using a minimal (7-sec) delay between the sample and choice phases of the task. Following acquisition, the delay between the sample and choice phases of the task was progressively increased to 15, 30, and 120 sec. Injured animals acquired the task at the same rate as sham animals and performed equally well at the 15-sec delay (p > 0.05). However, as the delay increased to 30 and 120 sec, the performance of the injured animals deteriorated (p < 0.05). These results indicate that LFP injury produces delay-dependent memory impairments in rats. This is therefore a valid model of an important feature of memory impairment in human TBI, and should be a useful addition to the available methods for assessing memory impairment and the effect of therapeutic interventions after TBI.
创伤性脑损伤(TBI)后的记忆障碍在人类和动物中都很常见。人类TBI记忆功能障碍的一个值得注意的特征是记忆表现受损,这取决于最初学习和信息回忆之间的延迟。然而,先前关于TBI诱导的动物记忆障碍的研究未能控制假手术组和受伤动物之间的初始学习量。本研究表明,即使控制了初始学习程度,大鼠实验性TBI仍会产生延迟依赖性记忆障碍。动物接受中度水平的侧脑室液压冲击伤(LFP)(n = 10)或假手术(n = 9),然后在受伤后10天开始在水T迷宫中进行延迟非匹配位置(DNMP)任务训练。习得训练包括在受伤后第11 - 15天每天进行15次试验,任务的样本阶段和选择阶段之间的延迟最短为7秒。习得训练后,任务的样本阶段和选择阶段之间的延迟逐渐增加到15、30和120秒。受伤动物与假手术动物以相同的速度习得任务,并且在15秒延迟时表现同样良好(p > 0.05)。然而,随着延迟增加到30秒和120秒,受伤动物的表现变差(p < 0.05)。这些结果表明,LFP损伤会在大鼠中产生延迟依赖性记忆障碍。因此,这是人类TBI记忆障碍一个重要特征的有效模型,应该是评估TBI后记忆障碍和治疗干预效果的现有方法的有益补充。