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年老小鼠中海马依赖性皮质可塑性损伤。

Impairment of experience-dependent cortical plasticity in aged mice.

机构信息

Dept. of Molecular and Cellular Neurobiology, Nencki Institute of Experimental Biology, 3 Pasteur Street, 02-093 Warsaw, Poland.

出版信息

Neurobiol Aging. 2011 Oct;32(10):1896-905. doi: 10.1016/j.neurobiolaging.2009.11.009. Epub 2009 Dec 14.

Abstract

This study addresses the relationship between aging and experience-dependent plasticity in the mouse somatosensory cortex. Plasticity in the cortical representation of vibrissae (whiskers) was investigated in young (3 months), mature (14 months) and old (2 years) mice using [14C]2-deoxyglucose (2-DG) autoradiography. Plastic changes were evoked using two experimental paradigms. The deprivation-based protocol included unilateral deprivation of all but one row of whiskers for a week. In the conditioning protocol the animals were subjected to classical conditioning, where tactile stimulation of one row of whiskers was paired with an aversive stimulus. Both procedures evoked functional plasticity in the young group, expressed as a widening of the functional cortical representation of the spared or conditioned row. Aging had a differential effect on these two forms of plasticity. Conditioning-related plasticity was more vulnerable to aging: the plastic change was not detectable in mature animals, even though they acquired the behavioral response. Deprivation-induced plasticity also declined with age, but some effects were persistent in the oldest animals.

摘要

这项研究探讨了衰老与小鼠体感皮层经验依赖性可塑性之间的关系。通过[14C]2-脱氧葡萄糖(2-DG)放射自显影技术,研究了年轻(3 个月)、成熟(14 个月)和老年(2 岁)小鼠触须(胡须)皮层代表的可塑性。使用两种实验方案来诱发可塑性变化。基于剥夺的方案包括一周内单侧剥夺除一排以外的所有胡须。在条件化方案中,动物接受经典条件作用,即对一排胡须进行触觉刺激,并与厌恶刺激配对。这两种程序都在年轻组中引起了功能可塑性,表现为受保护或条件化的排的功能皮层代表的扩大。衰老对这两种形式的可塑性有不同的影响。与条件作用相关的可塑性更容易受到衰老的影响:即使成熟动物获得了行为反应,也无法检测到与条件作用相关的可塑性变化。剥夺诱导的可塑性也随年龄增长而下降,但在最老的动物中仍存在一些影响。

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