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Open AccessJournal ArticleDOI

Importance of Zinc in the Central Nervous System: The Zinc-Containing Neuron

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TLDR
The present review outlines the methods used to discover, define and describe zinc-containing neurons; the neuroarchitecture and synaptology of zinc- containing neural circuits; the physiology of regulated vesicular zinc release; the "life cycle" and molecular biology of vesicle zinc; the importance of synaptically released zinc in the normal and pathological processes of the cerebral cortex; and the role of specific and nonspecific stressors in the release of zinc.
Abstract
Zinc is essential to the structure and function of myriad proteins, including regulatory, structural and enzymatic. It is estimated that up to 1% of the human genome codes for zinc finger proteins. In the central nervous system, zinc has an additional role as a neurosecretory product or cofactor. In this role, zinc is highly concentrated in the synaptic vesicles of a specific contingent of neurons, called "zinc-containing" neurons. Zinc-containing neurons are a subset of glutamatergic neurons. The zinc in the vesicles probably exceeds 1 mmol/L in concentration and is only weakly coordinated with any endogenous ligand. Zinc-containing neurons are found almost exclusively in the forebrain, where in mammals they have evolved into a complex and elaborate associational network that interconnects most of the cerebral cortices and limbic structures. Indeed, one of the intriguing aspects of these neurons is that they compose somewhat of a chemospecific "private line" of the mammalian cerebral cortex. The present review outlines (1) the methods used to discover, define and describe zinc-containing neurons; (2) the neuroarchitecture and synaptology of zinc-containing neural circuits; (3) the physiology of regulated vesicular zinc release; (4) the "life cycle" and molecular biology of vesicular zinc; (5) the importance of synaptically released zinc in the normal and pathological processes of the cerebral cortex; and (6) the role of specific and nonspecific stressors in the release of zinc.

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References
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Journal ArticleDOI

Release of endogenous Zn2+ from brain tissue during activity.

TL;DR: It is demonstrated for the first time that Zn2+ is released into the extracellular space during excitation of hippocampal slices.
Book ChapterDOI

Neurobiology of zinc and zinc-containing neurons.

TL;DR: This chapter discusses separate pools of CNS zinc, which are, vesicular zinc, free zinc, and protein-bound zinc; the enzymatic zinc is, therefore, a stable pool, involved only in the specific function of the zinc-containing enzymes.
Journal ArticleDOI

The Role of Zinc in Selective Neuronal Death After Transient Global Cerebral Ischemia

TL;DR: The toxic influx of zinc may be a key mechanism underlying selective neuronal death after transient global ischemic insults and could be prevented by the intraventricular injection of a zinc chelating agent.
Journal ArticleDOI

Stimulation-induced uptake and release of zinc in hippocampal slices.

TL;DR: It is reported that the mossy-fibre neuropil and cells of origin (dentate granule cells) take up zinc preferentially, and that electrical stimulation selectively facilitates both uptake of exogenous zinc into mossY-f fibre neuro pil and release of previously incorporated 65Zn from the tissue.
Journal ArticleDOI

Zinc and brain injury

TL;DR: Manipulations aimed at reducing extracellular zinc accumulation, or cellular vulnerability to toxic zinc exposure, may provide a novel therapeutic approach toward ameliorating pathological neuronal death in these settings.
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