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衰老对腹侧和背侧纹状体突触可塑性的差异影响。

Differential effect of aging on synaptic plasticity in the ventral and dorsal striatum.

作者信息

Wang Yanyan

机构信息

Department of Pharmacology, Beckman Institute for Advanced Science and Technology, MC-251, University of Illinois at Urbana-Champaign, 405 N. Mathews Avenue, Urbana, IL 61801, USA.

出版信息

Neurobiol Learn Mem. 2008 Jan;89(1):70-5. doi: 10.1016/j.nlm.2007.08.015. Epub 2007 Oct 17.

Abstract

Both the ventral and dorsal striatum are involved in various forms of motor, motivational and learning behaviors. Previously, we demonstrated that several striatum-dependent motor and learning behaviors were reduced in mice with increased age. In this study, we investigated the effects of aging on synaptic plasticity in brain slices containing the nucleus accumbens (NAc) or caudate-putamen (CPu), using electrophysiological recordings. We showed that long-term depression (LTD) was reduced or absent in the NAc of aged C57BL/6 mice, whereas the amount of LTD in the CPu of young and aged mice was similar. The LTD induced by 10-Hz stimulation is NMDAR-dependent in the NAc, but NMDAR-independent in the CPu. Our results suggest that NAc LTD may be more sensitive than CPu LTD to the effects of normal aging with a possibility that NMDAR-dependent LTD may be more susceptible to the aging process than non-NMDAR LTD. We also showed that paired-pulse facilitation was diminished in the NAc and CPu in aged mice, suggesting that aging is accompanied by significant decline in presynaptic function in both the ventral and dorsal striata. The age-related reduction in synaptic plasticity may be a cellular mechanism underlying the age-related impairments in striatum-dependent motor and cognitive functions.

摘要

腹侧纹状体和背侧纹状体均参与多种形式的运动、动机和学习行为。此前,我们证明随着小鼠年龄增长,几种依赖纹状体的运动和学习行为会减少。在本研究中,我们使用电生理记录方法,研究了衰老对包含伏隔核(NAc)或尾状核 - 壳核(CPu)的脑片突触可塑性的影响。我们发现,老年C57BL / 6小鼠的NAc中长时程抑制(LTD)减少或缺失,而年轻和老年小鼠CPu中的LTD量相似。10 Hz刺激诱导的LTD在NAc中依赖N - 甲基 - D - 天冬氨酸受体(NMDAR),但在CPu中不依赖NMDAR。我们的结果表明,NAc的LTD可能比CPu的LTD对正常衰老的影响更敏感,并且依赖NMDAR的LTD可能比非NMDAR的LTD更容易受到衰老过程的影响。我们还发现老年小鼠的NAc和CPu中配对脉冲易化减弱,这表明衰老伴随着腹侧和背侧纹状体突触前功能的显著下降。与年龄相关的突触可塑性降低可能是与年龄相关的纹状体依赖性运动和认知功能损害的细胞机制。

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