Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer's disease

Nat Commun. 2021 May 10;12(1):2603. doi: 10.1038/s41467-021-22742-8.

Abstract

Synaptic disturbances in excitatory to inhibitory (E/I) balance in forebrain circuits are thought to contribute to the progression of Alzheimer's disease (AD) and dementia, although direct evidence for such imbalance in humans is lacking. We assessed anatomical and electrophysiological synaptic E/I ratios in post-mortem parietal cortex samples from middle-aged individuals with AD (early-onset) or Down syndrome (DS) by fluorescence deconvolution tomography and microtransplantation of synaptic membranes. Both approaches revealed significantly elevated E/I ratios for AD, but not DS, versus controls. Gene expression studies in an independent AD cohort also demonstrated elevated E/I ratios in individuals with AD as compared to controls. These findings provide evidence of a marked pro-excitatory perturbation of synaptic E/I balance in AD parietal cortex, a region within the default mode network that is overly active in the disorder, and support the hypothesis that E/I imbalances disrupt cognition-related shifts in cortical activity which contribute to the intellectual decline in AD.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / physiopathology*
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Anura
  • Autopsy
  • Cognitive Dysfunction / metabolism
  • Cognitive Dysfunction / physiopathology*
  • Disks Large Homolog 4 Protein / metabolism
  • Down Syndrome / metabolism
  • Down Syndrome / physiopathology*
  • Female
  • GABA Plasma Membrane Transport Proteins / genetics
  • GABA Plasma Membrane Transport Proteins / metabolism
  • Gene Expression Regulation / genetics
  • Gene Expression Regulation / physiology
  • Humans
  • Male
  • Membrane Proteins / metabolism
  • Middle Aged
  • Nerve Net / physiopathology
  • Oocytes / physiology
  • Parietal Lobe / anatomy & histology*
  • Parietal Lobe / metabolism*
  • Parietal Lobe / physiopathology
  • Synapses / metabolism*
  • Synapses / pathology
  • Synaptic Membranes / metabolism
  • Synaptic Membranes / physiology*
  • Synaptosomes / metabolism
  • Synaptosomes / pathology
  • Tomography, Optical
  • Transcriptome / genetics

Substances

  • Amyloid beta-Peptides
  • DLG4 protein, human
  • Disks Large Homolog 4 Protein
  • GABA Plasma Membrane Transport Proteins
  • Membrane Proteins
  • SLC6A1 protein, human
  • gephyrin