Institute for Ageing and Health, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne NE4 5PL, UK.
Neurobiol Aging. 2011 Feb;32(2):293-301. doi: 10.1016/j.neurobiolaging.2009.02.005. Epub 2009 Mar 9.
To investigate differences in distribution of α4β2 subtypes of nicotinic acetylcholine receptors (nAChRs) using the ligand ¹²³I-5-Iodo-3-[2(S)-2-azetidinylmethoxy] pyridine (5IA-85380) and single photon emission computed tomography (SPECT) in subjects with vascular dementia and age-matched controls. ¹²³I-5IA-85380 binding was compared to corresponding regional cerebral blood flow (rCBF) changes in the same subjects.
Thirty subjects (14 vascular dementia and 16 controls) underwent ¹²³I-5IA-85380 and rCBF ((99m)Tc-exametazime) SPECT scanning. Image analysis was performed on voxel basis using statistical parametric mapping (SPM2).
Compared to controls, reductions in relative ¹²³I-5IA-85380 uptake were identified in dorsal thalamus and right caudate in vascular dementia. Increase in scaled ¹²³I-5IA-85380 uptake in cuneus was also demonstrated in vascular dementia relative to controls. Perfusion deficits in anterior cingulate were apparent in the patient group and did not appear to be associated with ¹²³I-5IA-85380 changes.
Reduced ¹²³I-5IA-85380 uptake in vascular dementia was confined to sub-cortical regions, unlike the cortical reductions previously described in Alzheimer's disease. Elevation of normalised ¹²³I-5IA-85380 uptake in cuneus in vascular dementia could be a compensatory response to reduced cholinergic activity in dorsal thalamus.
使用配体¹²³I-5-碘-3-[2(S)-2-氮杂环丁基甲氧基]吡啶(5IA-85380)和单光子发射计算机断层扫描(SPECT)研究血管性痴呆患者与年龄匹配的对照组中α4β2 型烟碱型乙酰胆碱受体(nAChRs)的分布差异。比较了同一受试者的¹²³I-5IA-85380 结合与相应的局部脑血流(rCBF)变化。
30 名受试者(14 名血管性痴呆,16 名对照组)接受了¹²³I-5IA-85380 和 rCBF((99m)Tc-甲氧基异丁基异腈)SPECT 扫描。使用统计参数映射(SPM2)对体素基础上的图像进行分析。
与对照组相比,血管性痴呆患者的背侧丘脑和右侧尾状核的¹²³I-5IA-85380 摄取相对减少。与对照组相比,血管性痴呆患者楔前叶的¹²³I-5IA-85380 摄取增加。在前扣带皮质中存在灌注缺陷,在患者组中明显,但似乎与¹²³I-5IA-85380 的变化无关。
与以前在阿尔茨海默病中描述的皮质减少不同,血管性痴呆患者的¹²³I-5IA-85380 摄取减少仅限于皮质下区域。血管性痴呆患者楔前叶正常化¹²³I-5IA-85380 摄取的增加可能是背侧丘脑胆碱能活性降低的代偿反应。