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多巴胺转运体 PET 成像在正常衰老中的研究:多巴胺转运体的下降及其在运动功能保护中的可能作用。

Dopamine transporter PET in normal aging: dopamine transporter decline and its possible role in preservation of motor function.

机构信息

Pacific Parkinson's Research Centre, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Synapse. 2010 Feb;64(2):146-51. doi: 10.1002/syn.20708.

Abstract

OBJECTIVES

To determine the impact of age-related decline in dopamine transporter (DAT) expression on motor function in the elderly.

METHODS

About 33 normal individuals of a wide age range were scanned with PET employing d-threo-[(11)C]-methylphenidate (MP, a marker of DAT) and [(11)C]-dihydrotetrabenazine (DTBZ, that binds to the vesicular monoamine transporter Type 2). Motor function was assessed using the Purdue Pegboard Test (PPB). We analyzed the relationship between [(11)C]-MP and motor performance.

RESULTS

Age ranged from 27- to 77-year old (mean +/- SD, 54.75 +/- 14.14). There was no age-related decline in binding potentials (BP) for [(11)C]-DTBZ. In contrast, [(11)C]-MP BP was inversely related to age in all striatal regions analyzed (caudate: reduction of 11.2% per decade, P < 0.0001, r = -0.86; putamen: reduction of 10.5% per decade, P < 0.0001, r = -0.80). A differential effect of [(11)C]-MP on PPB could be observed according to age group. There was a positive relation between the PPB and [(11)C]-MP in young individuals (coefficient = 13.56), whereas in individuals greater than 57 years this relationship was negative (coefficient = -19.53, P = 0.031).

CONCLUSIONS

Our findings confirm prior observations of age-related DAT decline and suggest that this phenomenon is independent of changes in VMAT2. After the fifth decade of life, this reduction in DAT binding is associated with a motor performance comparable to mid-adult life. These findings imply that biochemical processes associated with healthy aging may offset the naturaldecline in motor function observed in the elderly.

摘要

目的

确定多巴胺转运体(DAT)表达随年龄增长而下降对老年人运动功能的影响。

方法

使用 PET 扫描了年龄范围很广的约 33 名正常个体,采用 d-threo-[(11)C]-甲基苯丙胺(MP,DAT 的标志物)和 [(11)C]-二氢四苯并嗪(DTBZ,与囊泡单胺转运体 2 结合)。使用 Purdue 钉板测试(PPB)评估运动功能。我们分析了 [(11)C]-MP 与运动表现之间的关系。

结果

年龄范围为 27-77 岁(平均值 +/- SD,54.75 +/- 14.14)。[(11)C]-DTBZ 的结合潜能(BP)与年龄无关。相比之下,[(11)C]-MP BP 与分析的所有纹状体区域的年龄呈负相关(尾状核:每十年减少 11.2%,P < 0.0001,r = -0.86;壳核:每十年减少 10.5%,P < 0.0001,r = -0.80)。根据年龄组,可以观察到 [(11)C]-MP 对 PPB 的不同影响。在年轻个体中,PPB 与 [(11)C]-MP 之间存在正相关(系数= 13.56),而在大于 57 岁的个体中,这种关系为负(系数=-19.53,P = 0.031)。

结论

我们的研究结果证实了先前关于年龄相关 DAT 下降的观察结果,并表明这种现象与 VMAT2 的变化无关。50 岁以后,DAT 结合的这种减少与中年生活相当的运动表现相关。这些发现意味着与健康衰老相关的生化过程可能会抵消老年人观察到的运动功能自然下降。

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