Department of Psychiatry, David Geffen School of Medicine at UCLA, Los Angeles, Calif., USA.
Dev Neurosci. 2010;32(5-6):431-41. doi: 10.1159/000320667. Epub 2010 Nov 12.
Traumatic brain injury (TBI), one of the most frequent causes of neurologic and neurobehavioral morbidity in the pediatric population, can result in lifelong challenges not only for patients, but also for their families. Survivors of a brain injury experienced during childhood - when the brain is undergoing a period of rapid development - frequently experience unique challenges as the consequences of their injuries are overlaid on normal developmental changes. Experimental studies have significantly advanced our understanding of the mechanisms and underlying molecular underpinnings of the injury response and recovery process following a TBI in the developing brain. In this paper, normal and TBI-related alterations in growth, development and metabolism are comprehensively reviewed in the postweanling/juvenile age range in the rat (postnatal days 21-60). As part of this review, TBI-related changes in gene expression are presented, with a focus on the injury-induced alterations related to cerebral growth and metabolism, and discussed in the context of existing literature related to physiological and behavioral responses to experimental TBI. Increasing evidence from the existing literature and from our own gene microarray data indicates that molecular responses related to growth, development and metabolism may play a particularly important role in the injury response and the recovery trajectory following developmental TBI. While gene expression analysis shows many of these changes occur at the level of transcription, a comprehensive review of other studies suggests that the control of metabolic substrates may preferentially be regulated through changes in transporters and enzymatic activity. The interrelation between cellular metabolism and activity-dependent neuroplasticity shows great promise as an area for future study for an optimal translation of experimental data to clinical TBI, with the ultimate goal of guiding therapeutic interventions.
创伤性脑损伤(TBI)是儿科人群中最常见的神经和神经行为发病率的原因之一,不仅会给患者,也会给他们的家庭带来终身挑战。在儿童时期经历脑损伤的幸存者——当大脑处于快速发育时期时——经常会遇到独特的挑战,因为他们的损伤后果会叠加在正常的发育变化上。实验研究极大地促进了我们对儿童时期 TBI 后损伤反应和恢复过程的机制和潜在分子基础的理解。在本文中,在大鼠(出生后第 21-60 天)的幼年期/青少年期全面综述了生长、发育和代谢的正常和与 TBI 相关的变化。作为这篇综述的一部分,介绍了与 TBI 相关的基因表达变化,重点介绍了与大脑生长和代谢相关的损伤诱导变化,并结合与实验性 TBI 的生理和行为反应相关的现有文献进行了讨论。现有文献和我们自己的基因微阵列数据的越来越多的证据表明,与生长、发育和代谢相关的分子反应可能在发育性 TBI 的损伤反应和恢复轨迹中发挥特别重要的作用。虽然基因表达分析表明许多这些变化发生在转录水平,但对其他研究的综合回顾表明,代谢底物的控制可能更优先通过转运蛋白和酶活性的变化来调节。细胞代谢和活动依赖性神经可塑性之间的相互关系显示出作为未来研究的一个很有前途的领域,以便将实验数据最佳转化为临床 TBI,最终目标是指导治疗干预。