Slutsky · Neuron 2010 · controlled laboratory animal experiment · n=?

Enhancement of learning and memory by elevating brain magnesium.

Cited 378 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

Preclinical animal (rat) study

PubMed 20152124 · doi:10.1016/j.neuron.2009.12.026 · record verified 2026-08-26

What was done

Researchers administered a novel compound, magnesium-L-threonate (MgT), to elevate brain magnesium levels in young and aged rats. They evaluated behavioral outcomes, including learning abilities, working memory, short- and long-term memory, and pattern completion. They also analyzed underlying cellular and synaptic mechanisms, including hippocampal synaptophysin-/synaptobrevin-positive puncta density (in the dentate gyrus and CA1 subregions), presynaptic release site function and probability, NR2B-containing NMDA receptor expression, short-term synaptic facilitation, and long-term potentiation.

What was found

MgT treatment enhanced learning abilities, working memory, and short- and long-term memory in rats, as well as pattern completion in aged rats. Structurally, treated rats showed an increased density of synaptophysin-/synaptobrevin-positive puncta in DG and CA1 hippocampal regions that correlated with memory improvements. Electrophysiologically, magnesium elevated the number of functional presynaptic release sites while lowering baseline release probability, selectively boosting burst transmission. These changes, alongside upregulation of NR2B-containing NMDA receptors and downstream signaling, enhanced short-term synaptic facilitation and long-term potentiation. The abstract provides directional mechanisms and outcomes without reporting specific numerical values or effect sizes.

Why it matters

This study provides mechanistic evidence that increasing brain magnesium availability via magnesium-L-threonate can reconfigure hippocampal synapses and enhance cognitive function in rodents.

Limits

The study was conducted entirely in rats, so human efficacy, safety, and pharmacokinetics cannot be inferred directly. The abstract does not report the sample size (n), treatment duration, specific compound dosages, or exact statistical metrics.

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