脑血管完整性影响纹状体衰老相关多巴胺D1差异梯度

IF 1.7 Q3 CLINICAL NEUROLOGY
Jarkko Johansson , Nina Karalija , Alireza Salami
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引用次数: 0

摘要

现有研究表明,不同多巴胺能标记物的衰老相关损失,包括突触前多巴胺转运体和突触后DA受体。鉴于DA在神经认知功能中的核心作用,维持健康的DA系统可能是减轻与年龄相关的认知能力下降的关键。然而,衰老过程中DA损失背后的机制在很大程度上是未知的。过去的研究记录了多巴胺能完整性和脑血管健康之间的关联(通过白质病变体积)。然而,目前尚不清楚邻近病变是否会影响纹状体中与年龄相关的D1DR差异的空间模式,以及这种差异是否与记忆功能有关。本研究采用[11C]SCH23390正电子发射断层扫描评估d1受体(D1DR)可用性,FLAIR-MRI评估白质病变。研究对象为中老年健康参与者(年龄40-80岁,n = 1119,其中50%为女性)。我们发现了沿腹背轴的年龄相关差异程度变化的证据,其中尾状背轴的差异更为明显。进一步的分析显示,与病变的距离与尾状核中D1DR损失的程度之间存在关联。此外,尾状背(靠近病变)的D1DR差异与记忆表现的相关性更强。总之,目前的研究结果表明,维持脑血管健康可能是促进多巴胺能和记忆成功老化的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cerebrovascular integrity affects gradients of aging-related dopamine D1 differences in the striatum

Cerebrovascular integrity affects gradients of aging-related dopamine D1 differences in the striatum

Cerebrovascular integrity affects gradients of aging-related dopamine D1 differences in the striatum

Cerebrovascular integrity affects gradients of aging-related dopamine D1 differences in the striatum

Extant research suggest aging-related losses of different dopaminergic markers, including presynaptic dopamine transporters as well as post-synaptic DA receptors. Given the central role of DA in neurocognitive functions, maintenance of a healthy DA system may be a key to mitigate age-related cognitive decline. Mechanisms behind DA losses in aging are however largely uncharted. Past research documented an association between dopaminergic integrity and cerebrovascular health (via white matter lesion volumes). However, it remains unclear whether proximity to lesions affected the spatial patterns of age-related D1DR differences within the striatum, and whether such differences are related to mnemonic function. Here, a large cohort of middle-aged to older healthy participants (age = 40–80 years, n = 119, 50 % women) was assessed for D1-receptor (D1DR) availability with positron emission tomography using [11C]SCH23390, and for white matter lesions using FLAIR-MRI. We found evidence for variations in degree of age-related differences along the ventro-dorsal axis, with more pronounced differences in the dorsal caudate. Further analyses revealed an association between distance to lesions and extent of D1DR losses in the caudate. Furthermore, D1DR differences in dorsal caudate (proximal to lesions) was more strongly associated with memory performance. In conclusion, the present findings suggest that maintenance of cerebrovascular health may be a key factor in promoting successful dopaminergic and memory aging.

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来源期刊
Aging brain
Aging brain Neuroscience (General), Geriatrics and Gerontology
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