Journal of Trace Elements in Medicine and Biology · May 24, 2016

Innervation from the entorhinal cortex to the dentate gyrus and the vulnerability to Zn²

By Takeda A, Tamano H

Hippocampal Zn²⁺ homeostasis is critical for cognitive activity and hippocampus-dependent memory. Extracellular Zn²⁺ signaling is linked to extracellular glutamate signaling and leads to intracellular Zn²⁺ signaling, which is involved in cognitive activity. On the other hand, excess intracellular Zn²⁺ signaling that is induced by excess glutamate signaling is involved in cognitive decline. In the hippocampal formation, the dentate gyrus is the most vulnerable to aging and is thought to contribute to age-related cognitive decline. The layer II of the entorhinal cortex is the most vulnerable to neuronal death in Alzheimer's disease. The perforant pathway provides input from the layer II to the dentate gyrus and is one of the earliest affected pathways in Alzheimer's disease. Medial perforant pathway-dentate granule cell synapses are vulnerable to either excess intracellular Zn²⁺ or β-amyloid (Aβ)-bound zinc, which induce transient cognitive decline via attenuation of medial perforant pathway LTP. However, it is unknown whether the vulnerability to excess intracellular Zn²⁺ is involved in region-specific vulnerability to aging and Alzheimer's disease. To discover a strategy to prevent short-term cognitive decline in normal aging process and the pre-dementia stage of Alzheimer's disease, the present paper deals with vulnerability of medial perforant pathway-dentate granule cell synapses to intracellular Zn²⁺ dyshomeostasis and its possible involvement in differential vulnerability to aging and Alzheimer's disease in the hippocampal formation.

doi.org/10.1016/j.jtemb.2016.05.006PubMed 27267970Mechanisms