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Mechanisms of neuronal death in brain aging and alzheimer's disease: Role of endocrine‐mediated calcium dyshomeostasis
Philip W. Landfield, Olivier Thibault, Mary L. Mazzanti, Nada M. Porter, D. Steven Kerr
Journal of Neurobiology · 1992 · ▲ 118 citations
Abstract
This paper reviews evidence that brain aging and Alzheimer's disease (AD) are somehow closely related and that the hippocampus (CA1) is highly vulnerable to cell loss under both conditions. In addition, two current lines of evidence on the mechanisms of hippocampal cell loss with aging are considered, including studies of neuronal calcium dysregulation and studies of cumulative glucocorticoid (GC) neurotoxicity. Moreover, recent electrophysiological studies have shown that excess glucocorticoid activation of hippocampal neurons increases the influx of calcium through voltage-activated calcium channels. Second messenger systems may mediate the steroid modulation of calcium channels. Therefore, it is hypothesized that excess glucocorticoid activation and neuronal calcium dysregulation may be two phases of a single process that increases the susceptibility of neurons to neurodegeneration during aging and Alzheimer's disease.
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- 10.1002/neu.480230914
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APA
Landfield, P.W., Thibault, O., Mazzanti, M.L., Porter, N.M., & Kerr, D.S. (1992). Mechanisms of neuronal death in brain aging and alzheimer's disease: Role of endocrine‐mediated calcium dyshomeostasis. <em>Journal of Neurobiology</em>. https://doi.org/10.1002/neu.480230914
Vancouver
Landfield PW, Thibault O, Mazzanti ML, Porter NM, Kerr DS. Mechanisms of neuronal death in brain aging and alzheimer's disease: Role of endocrine‐mediated calcium dyshomeostasis. Journal of Neurobiology. 1992. doi:10.1002/neu.480230914.
BibTeX
@article{philip1992Mechan,
title = {Mechanisms of neuronal death in brain aging and alzheimer's disease: Role of endocrine‐mediated calcium dyshomeostasis},
author = {Philip W. Landfield and Olivier Thibault and Mary L. Mazzanti and Nada M. Porter and D. Steven Kerr},
journal = {Journal of Neurobiology},
year = {1992},
doi = {10.1002/neu.480230914},
}
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