Department of Neurobiology, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
PLoS One. 2011;6(6):e20678. doi: 10.1371/journal.pone.0020678. Epub 2011 Jun 20.
Activity-induced structural remodeling of dendritic spines and glial cells was recently proposed as an important factor in neuroplasticity and suggested to accompany the induction of long-term potentiation (LTP). Although T1 and diffusion MRI have been used to study structural changes resulting from long-term training, the cellular basis of the findings obtained and their relationship to neuroplasticity are poorly understood.
METHODOLOGY/PRINCIPAL FINDING: Here we used diffusion tensor imaging (DTI) to examine the microstructural manifestations of neuroplasticity in rats that performed a spatial navigation task. We found that DTI can be used to define the selective localization of neuroplasticity induced by different tasks and that this process is age-dependent in cingulate cortex and corpus callosum and age-independent in the dentate gyrus.
CONCLUSION/SIGNIFICANCE: We relate the observed DTI changes to the structural plasticity that occurs in astrocytes and discuss the potential of MRI for probing structural neuroplasticity and hence indirectly localizing LTP.
最近提出,树突棘和神经胶质细胞的活动诱导结构重塑是神经可塑性的一个重要因素,并被认为伴随着长时程增强(LTP)的诱导。尽管 T1 和弥散 MRI 已被用于研究长期训练引起的结构变化,但对获得的发现的细胞基础及其与神经可塑性的关系知之甚少。
方法/主要发现:在这里,我们使用弥散张量成像(DTI)来研究在执行空间导航任务的大鼠中神经可塑性的微观结构表现。我们发现 DTI 可用于定义不同任务诱导的神经可塑性的选择性定位,并且该过程在扣带皮层和胼胝体中随年龄而变化,而在齿状回中与年龄无关。
结论/意义:我们将观察到的 DTI 变化与星形胶质细胞中发生的结构可塑性相关联,并讨论了 MRI 探测结构神经可塑性的潜力,从而间接地定位 LTP。