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A stereological study of the numbers of neurons and glia in the primary visual cortex across the lifespan of male and female rhesus monkeys

机译:对雄性和雌性恒河猴生命期初级视皮层神经元和神经胶质细胞数量的立体研究

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摘要

Mild age-related declines in visual function occur in humans and monkeys, independent of ocular pathology, suggesting involvement of central visual pathways (Spear [1993] Vision Res 33:2589-2609). Although many factors might account for this decline, a loss of neurons in primary visual cortex (V1) could be a contributing factor. Previous studies of neuron numbers in V1 reported stability across age, but were limited in the ages and genders studied and sampled only limited parts of V1 or limited cell types, allowing for the possibility of a subtle loss of neurons. We pursued this question in 26 behaviorally tested adult male and female rhesus monkeys ranging from 7.4 to 31.0 years of age by using design-based stereology to estimate numbers of NeuN-labeled neurons and thionin-stained glia within three laminar zones, supragranular (layers II-IVB), granular (IVC), and infragranular (V-VI), across the entirety of V1. There were no significant differences between males and females on any measures, except for total brain weight (P = 0.0038). There was an average of 416,000,000 neurons in V1, but no effect of age on this total or numbers within any laminar zone. Similarly, there was an average of 184,000,000 glia in V1 (44% of the number of neurons), but no effect of age on this total. However, there was a significant age-related increase in numbers of glia in the infragranular zone, perhaps reflecting a glial response to pathology in myelinated projection fibers. This study provides further evidence that in normal aging neurons are not lost and hence cannot account for age-related dysfunction.
机译:与人的年龄有关的视觉功能的轻度衰落在人和猴子中发生,独立于眼部病理,提示中央视觉通路的参与(Spear [1993] Vision Res 33:2589-2609)。尽管许多因素可能是造成这种下降的原因,但初级视觉皮层(V1)中神经元的丢失可能是一个促成因素。先前对V1中神经元数量的研究报告了整个年龄的稳定性,但是受研究的年龄和性别的限制,仅对V1的有限部分或有限的细胞类型进行了采样,从而有可能造成神经元的细微损失。我们在26个行为测试的成年雄性和雌性恒河猴(年龄从7.4至31.0岁)中追踪了这个问题,方法是使用基于设计的立体学来估计三个上层(片上层)区域中被NeuN标记的神经元和被硫蛋白染色的神经胶质的数量-IVB),颗粒状(IVC)和颗粒下(V-VI),涵盖整个V1。除总脑重外,其他任何方面的男女之间均无显着差异(P = 0.0038)。 V1中平均有416,000,000个神经元,但在任何层流区内,年龄对此总数或数量均无影响。同样,V1中平均有184,000,000胶质细胞(占神经元数量的44%),但年龄对此总数没有影响。但是,与年龄相关的神经胶质细胞的数目明显增加,这可能反映了神经胶质对投射髓鞘纤维的病理反应。这项研究提供了进一步的证据,表明在正常衰老中神经元不会丢失,因此不能解释与年龄有关的功能障碍。

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