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  1. Article ; Online: Vesicular Glutamate Transporter Changes in the Cortical Default Mode Network During the Clinical and Pathological Progression of Alzheimer's Disease.

    Mi, Zhiping / Abrahamson, Eric E / Ryu, Angela Y / Malek-Ahmadi, Michael / Kofler, Julia K / Fish, Kenneth N / Sweet, Robert A / Villemagne, Victor L / Schneider, Julie A / Mufson, Elliott J / Ikonomovic, Milos D

    Journal of Alzheimer's disease : JAD

    2023  Volume 94, Issue 1, Page(s) 227–246

    Abstract: Background: Altered glutamatergic neurotransmission may contribute to impaired default mode network (DMN) function in Alzheimer's disease (AD). Among the DMN hub regions, frontal cortex (FC) was suggested to undergo a glutamatergic plasticity response ... ...

    Abstract Background: Altered glutamatergic neurotransmission may contribute to impaired default mode network (DMN) function in Alzheimer's disease (AD). Among the DMN hub regions, frontal cortex (FC) was suggested to undergo a glutamatergic plasticity response in prodromal AD, while the status of glutamatergic synapses in the precuneus (PreC) during clinical-neuropathological AD progression is not known.
    Objective: To quantify vesicular glutamate transporter VGluT1- and VGluT2-containing synaptic terminals in PreC and FC across clinical stages of AD.
    Methods: Unbiased sampling and quantitative confocal immunofluorescence of cortical VGluT1- and VGluT2-immunoreactive profiles and spinophilin-labeled dendritic spines were performed in cases with no cognitive impairment (NCI), mild cognitive impairment (MCI), mild-moderate AD (mAD), or moderate-severe AD (sAD).
    Results: In both regions, loss of VGluT1-positive profile density was seen in sAD compared to NCI, MCI, and mAD. VGluT1-positive profile intensity in PreC did not differ across groups, while in FC it was greater in MCI, mAD, and sAD compared to NCI. VGluT2 measures were stable in PreC while FC had greater VGluT2-positive profile density in MCI compared to sAD, but not NCI or mAD. Spinophilin measures in PreC were lower in mAD and sAD compared to NCI, while in FC they were stable across groups. Lower VGluT1 and spinophilin measures in PreC, but not FC, correlated with greater neuropathology.
    Conclusion: Frank loss of VGluT1 in advanced AD relative to NCI occurs in both DMN regions. In FC, an upregulation of VGluT1 protein content in remaining glutamatergic terminals may contribute to this region's plasticity response in AD.
    MeSH term(s) Humans ; Alzheimer Disease/pathology ; Vesicular Glutamate Transport Proteins/metabolism ; Default Mode Network ; Vesicular Glutamate Transport Protein 2/metabolism ; Presynaptic Terminals/metabolism ; Vesicular Glutamate Transport Protein 1/metabolism
    Chemical Substances Vesicular Glutamate Transport Proteins ; Vesicular Glutamate Transport Protein 2 ; Vesicular Glutamate Transport Protein 1
    Language English
    Publishing date 2023-05-19
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1440127-7
    ISSN 1875-8908 ; 1387-2877
    ISSN (online) 1875-8908
    ISSN 1387-2877
    DOI 10.3233/JAD-221063
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Loss of precuneus dendritic spines immunopositive for spinophilin is related to cognitive impairment in early Alzheimer's disease.

    Mi, Zhiping / Abrahamson, Eric E / Ryu, Angela Y / Fish, Kenneth N / Sweet, Robert A / Mufson, Elliott J / Ikonomovic, Milos D

    Neurobiology of aging

    2017  Volume 55, Page(s) 159–166

    Abstract: 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 ...

    Abstract 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 (Aβ) 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 Aβ pathology and may contribute to cognitive symptoms early in the disease.
    MeSH term(s) Aged, 80 and over ; Alzheimer Disease/complications ; Alzheimer Disease/genetics ; Alzheimer Disease/pathology ; Amyloid beta-Peptides/metabolism ; Aniline Compounds ; Biomarkers/metabolism ; Cognitive Dysfunction/diagnosis ; Cognitive Dysfunction/etiology ; Dendritic Spines/metabolism ; Dendritic Spines/pathology ; Female ; Humans ; Male ; Microfilament Proteins/metabolism ; Nerve Tissue Proteins/metabolism ; Parietal Lobe/metabolism ; Parietal Lobe/pathology ; Plaque, Amyloid/diagnosis ; Plaque, Amyloid/metabolism ; Thiazoles
    Chemical Substances 2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole ; Amyloid beta-Peptides ; Aniline Compounds ; Biomarkers ; Microfilament Proteins ; Nerve Tissue Proteins ; Thiazoles ; neurabin
    Language English
    Publishing date 2017-02-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 604505-4
    ISSN 1558-1497 ; 0197-4580
    ISSN (online) 1558-1497
    ISSN 0197-4580
    DOI 10.1016/j.neurobiolaging.2017.01.022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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