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向抑制的失衡作为衰老相关认知障碍的一种基质。

Imbalance towards inhibition as a substrate of aging-associated cognitive impairment.

作者信息

Wong Tak Pan, Marchese Giorgio, Casu Maria Antonietta, Ribeiro-da-Silva Alfredo, Cuello A Claudio, De Koninck Yves

机构信息

Department of Pharmacology and Therapeutics, McGill University, Montréal, Que., Canada H3G 1Y6.

出版信息

Neurosci Lett. 2006;397(1-2):64-8. doi: 10.1016/j.neulet.2005.11.055. Epub 2005 Dec 27.

Abstract

The number of synapses in the cerebral cortex decreases with aging. However, how this structural change translates into the cognitive impairment observed in aged animals remains unknown. Aged animals are not a homogenous group with respect to their cognitive performances; but instead, they can be separated into aged cognitively unimpaired ("normal") and aged cognitively impaired groups using a spatial memory task such as the Morris water maze. These two aged groups provide an unprecedented opportunity to isolate synaptic properties that relate to cognitive impairment from unrelated factors associated with normal aging. Using such classification, we conducted whole-cell patch-clamp recordings to measure basal spontaneous miniature excitatory (mEPSCs) and inhibitory synaptic currents (mIPSCs) bombarding layer V pyramidal neurons in the parietal cortex. We found that the frequencies of both mEPSC and mIPSC were lower in aged normal rats when compared with young rats. In contrast, aged cognitively impaired rats displayed a reduction in mEPSC frequency only. This results in an imbalance towards inhibition that may be an important substrate of the cognitive impairment in aged animals. We also found that pyramidal neurons in both aged normal and aged cognitively impaired rats exhibit similar structural attritions. Thus, cognitive impairment may be more related to an altered balance between different neurotransmitter systems than a mere reduction in synaptic structures.

摘要

大脑皮层中的突触数量会随着衰老而减少。然而,这种结构变化如何转化为在老年动物中观察到的认知障碍仍不清楚。就其认知表现而言,老年动物并非一个同质群体;相反,使用诸如莫里斯水迷宫这样的空间记忆任务,可以将它们分为老年认知未受损(“正常”)组和老年认知受损组。这两个老年组提供了一个前所未有的机会,将与认知障碍相关的突触特性与正常衰老相关的无关因素区分开来。利用这种分类方法,我们进行了全细胞膜片钳记录,以测量轰击顶叶皮层V层锥体神经元的基础自发微小兴奋性(mEPSCs)和抑制性突触电流(mIPSCs)。我们发现,与年轻大鼠相比,老年正常大鼠的mEPSC和mIPSC频率均较低。相比之下,老年认知受损大鼠仅表现出mEPSC频率降低。这导致了抑制的失衡,这可能是老年动物认知障碍的一个重要基础。我们还发现,老年正常大鼠和老年认知受损大鼠的锥体神经元都表现出类似的结构损耗。因此,认知障碍可能更多地与不同神经递质系统之间平衡的改变有关,而不仅仅是突触结构的减少。

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