期刊论文详细信息
NEUROBIOLOGY OF AGING 卷:55
Loss of precuneus dendritic spines immunopositive for spinophilin is related to cognitive impairment in early Alzheimer's disease
Article
Mi, Zhiping1,2  Abrahamson, Eric E.1,2  Ryu, Angela Y.1  Fish, Kenneth N.3  Sweet, Robert A.1,3,4  Mufson, Elliott J.5  Ikonomovic, Milos D.1,2,3 
[1] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[2] VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA USA
[3] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA
[4] VA Pittsburgh Healthcare Syst, Mental Illness Res Educ & Clin Ctr, Pittsburgh, PA USA
[5] Barrow Neurol Inst, Dept Neurobiol, Phoenix, AZ 85013 USA
关键词: Amyloid;    Default mode network;    Episodic memory;    Mild cognitive impairment;    Synapse;   
DOI  :  10.1016/j.neurobiolaging.2017.01.022
来源: Elsevier
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【 摘 要 】

Precuneus (PreC) cortex is affected with amyloid plaques early in Alzheimer's disease (AD), and this pathology may be associated with alterations in PreC synapses and cognitive impairment. We quantified the spinophilin-immunoreactive (ir) dendritic spine density and the intensity of spinophilin immunofluorescence, the latter as a measure of relative protein levels of spinophilin, in PreC lamina III from 33 subjects with clinical diagnoses of no cognitive impairment (NCI), mild cognitive impairment (MCI), mild-moderate AD (mAD), or severe AD (sAD). Both measures of spinophilin were lower in mAD and sAD compared with NCI. The MCI group had higher protein levels of spinophilin compared with mAD and sAD, and higher spinophilin-ir dendritic spine density compared with sAD. Lower spinophilin-ir dendritic spine density and relative protein levels of spinophilin were associated with greater amyloid beta (A beta) plaque burden, detected with a derivative of Pittsburgh compound-B (6-CN-PiB), and worse cognitive performance. Clinical onset of AD is marked by the loss of PreC spinophilin-ir dendritic spines that is related to A beta pathology and may contribute to cognitive symptoms early in the disease. Published by Elsevier Inc.

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