Elevation of brain magnesium prevents and reverses cognitive deficits and synaptic loss in Alzheimer's disease mouse model

J Neurosci. 2013 May 8;33(19):8423-41. doi: 10.1523/JNEUROSCI.4610-12.2013.

Abstract

Profound synapse loss is one of the major pathological hallmarks associated with Alzheimer's disease (AD) and might underlie memory impairment. Our previous work demonstrated that the magnesium ion is a critical factor in controlling synapse density/plasticity. Here, we investigated whether elevation of brain magnesium by the use of a recently developed compound, magnesium-l-threonate (MgT), can ameliorate the AD-like pathologies and cognitive deficits in the APPswe/PS1dE9 mice, a transgenic (Tg) mouse model of AD. MgT treatment reduced Aβ plaque and prevented synapse loss and memory decline in the Tg mice. Strikingly, MgT treatment was effective even when given to the mice at the end stage of their AD-like pathological progression. To explore how elevation of brain magnesium ameliorates the AD-like pathologies in the brains of Tg mice, we studied molecules critical for APP metabolism and signaling pathways implicated in synaptic plasticity/density. In the Tg mice, the NMDAR/CREB/BDNF signaling was downregulated, whereas calpain/calcineurin/Cdk5 neurodegenerative signaling and β-secretase (BACE1) expression were upregulated. MgT treatment prevented the impairment of these signaling pathways, stabilized BACE1 expression, and reduced soluble APPβ and β-C-terminal fragments in the Tg mice. At the molecular level, elevation of extracellular magnesium prevented the high-Aβ-induced reductions in synaptic NMDARs by preventing calcineurin overactivation in hippocampal slices. Correlation studies suggested that the protection of NMDAR signaling might underlie the stabilization of BACE1 expression. Our results suggest that elevation of brain magnesium exerts substantial synaptoprotective effects in a mouse model of AD and may have therapeutic potential for treating AD in humans.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Alzheimer Disease / complications*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / pathology*
  • Amyloid beta-Peptides / cerebrospinal fluid
  • Amyloid beta-Protein Precursor / genetics
  • Analysis of Variance
  • Animals
  • Body Weight / drug effects
  • Brain / drug effects
  • Brain / metabolism*
  • Brain / pathology
  • Butyrates / pharmacology
  • Butyrates / therapeutic use
  • Cognition Disorders / etiology*
  • Cognition Disorders / prevention & control
  • Disease Models, Animal
  • Exploratory Behavior / drug effects
  • Glutamate Decarboxylase / metabolism
  • Humans
  • Magnesium / metabolism*
  • Magnesium / therapeutic use
  • Male
  • Maze Learning / drug effects
  • Mice
  • Mice, Transgenic
  • Microscopy, Electron, Transmission
  • Mutation / genetics
  • Neurons / drug effects
  • Neurons / physiology
  • Neuroprotective Agents / therapeutic use*
  • Patch-Clamp Techniques
  • Peptide Fragments / cerebrospinal fluid
  • Presenilin-1 / genetics
  • Presynaptic Terminals / pathology
  • Presynaptic Terminals / ultrastructure
  • Reaction Time / drug effects
  • Synapses / drug effects
  • Synapses / pathology*
  • Synapses / ultrastructure
  • Tissue Distribution
  • Vesicular Acetylcholine Transport Proteins / metabolism

Substances

  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Butyrates
  • Neuroprotective Agents
  • PSEN1 protein, human
  • Peptide Fragments
  • Presenilin-1
  • Slc18a3 protein, mouse
  • Vesicular Acetylcholine Transport Proteins
  • amyloid beta-protein (1-40)
  • amyloid beta-protein (1-42)
  • Glutamate Decarboxylase
  • glutamate decarboxylase 2
  • Magnesium
  • threonic acid