Pullela Ramadevi, Raber Jacob, Pfankuch Timothy, Ferriero Donna M, Claus Catherine P, Koh Seong-Eun, Yamauchi Toshihiro, Rola Radoslaw, Fike John R, Noble-Haeusslein Linda J
Department of Pediatrics, University of California, San Francisco, CA 94143-0520, USA.
Dev Neurosci. 2006;28(4-5):396-409. doi: 10.1159/000094166.
The immature brain may be particularly vulnerable to injury during critical periods of development. To address the biologic basis for this vulnerability, mice were subjected to traumatic brain injury at postnatal day 21, a time point that approximates that of the toddler-aged child. After motor and cognitive testing at either 2 weeks (juveniles) or 3 months (adults) after injury, animals were euthanized and the brains prepared for quantitative histologic assessment. Brain-injured mice exhibited hyperactivity and age-dependent anxiolysis. Cortical lesion volume and subcortical neuronal loss were greater in brain-injured adults than in juveniles. Importantly, cognitive decline was delayed in onset and coincided with loss of neurons in the hippocampus. Our findings demonstrate that trauma to the developing brain results in a prolonged period of pathogenesis in both cortical and subcortical structures. Behavioral changes are a likely consequence of regional-specific neuronal degeneration.
未成熟的大脑在发育的关键时期可能特别容易受到损伤。为了探究这种易损性的生物学基础,研究人员在出生后第21天对小鼠进行了创伤性脑损伤,这一时间点近似于学步儿童的年龄。在损伤后2周(幼年)或3个月(成年)进行运动和认知测试后,对动物实施安乐死,并对大脑进行定量组织学评估。脑损伤小鼠表现出多动和年龄依赖性的焦虑缓解。脑损伤成年小鼠的皮质损伤体积和皮质下神经元损失比幼年小鼠更大。重要的是,认知衰退的发作延迟,并与海马体中神经元的丧失同时发生。我们的研究结果表明,发育中大脑的创伤会导致皮质和皮质下结构出现长时间的发病过程。行为变化可能是区域特异性神经元变性的结果。