Altered Calcium Metabolism in Aging CA1 Hippocampal Pyramidal Neurons

Altered neuronal calcium homeostasis is widely hypothesized to underlie cognitive deficits in normal aging subjects, but the mechanisms that underlie this change are unknown, possibly due to a paucity of direct measurements from aging neurons. Using CCD and two-photon calcium imaging techniques on C...

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Published inThe Journal of neuroscience Vol. 33; no. 18; pp. 7905 - 7911
Main Authors Oh, M. Matthew, Oliveira, Fernando A., Waters, Jack, Disterhoft, John F.
Format Journal Article
LanguageEnglish
Published United States Society for Neuroscience 01.05.2013
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Online AccessGet full text
ISSN0270-6474
1529-2401
1529-2401
DOI10.1523/JNEUROSCI.5457-12.2013

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Abstract Altered neuronal calcium homeostasis is widely hypothesized to underlie cognitive deficits in normal aging subjects, but the mechanisms that underlie this change are unknown, possibly due to a paucity of direct measurements from aging neurons. Using CCD and two-photon calcium imaging techniques on CA1 pyramidal neurons from young and aged rats, we show that calcium influx across the plasma membrane increases with aging, and that this change is countered by increased intracellular calcium buffering. The additional buffer in aging neurons balances the increased calcium influx following a small number (<3) action potentials, but is overwhelmed during sustained or theta-like activity which leads to a greater rise in intracellular calcium concentration in aging than that in young neurons. Our results demonstrate that calcium overload occurs regularly in aging CA1 pyramidal neurons under physiological conditions. This overload may be a critical factor in age-related decline in hippocampus-dependent cognitive function.
AbstractList Altered neuronal calcium homeostasis is widely hypothesized to underlie cognitive deficits in normal aging subjects, but the mechanisms that underlie this change are unknown, possibly due to a paucity of direct measurements from aging neurons. Using CCD and two-photon calcium imaging techniques on CA1 pyramidal neurons from young and aged rats, we show that calcium influx across the plasma membrane increases with aging, and that this change is countered by increased intracellular calcium buffering. The additional buffer in aging neurons balances the increased calcium influx following a small number (<3) action potentials, but is overwhelmed during sustained or theta-like activity which leads to a greater rise in intracellular calcium concentration in aging than that in young neurons. Our results demonstrate that calcium overload occurs regularly in aging CA1 pyramidal neurons under physiological conditions. This overload may be a critical factor in age-related decline in hippocampus-dependent cognitive function.Altered neuronal calcium homeostasis is widely hypothesized to underlie cognitive deficits in normal aging subjects, but the mechanisms that underlie this change are unknown, possibly due to a paucity of direct measurements from aging neurons. Using CCD and two-photon calcium imaging techniques on CA1 pyramidal neurons from young and aged rats, we show that calcium influx across the plasma membrane increases with aging, and that this change is countered by increased intracellular calcium buffering. The additional buffer in aging neurons balances the increased calcium influx following a small number (<3) action potentials, but is overwhelmed during sustained or theta-like activity which leads to a greater rise in intracellular calcium concentration in aging than that in young neurons. Our results demonstrate that calcium overload occurs regularly in aging CA1 pyramidal neurons under physiological conditions. This overload may be a critical factor in age-related decline in hippocampus-dependent cognitive function.
Altered neuronal calcium homeostasis is widely hypothesized to underlie cognitive deficits in normal aging subjects, but the mechanisms that underlie this change are unknown, possibly due to a paucity of direct measurements from aging neurons. Using CCD and two-photon calcium imaging techniques on CA1 pyramidal neurons from young and aged rats, we show that calcium influx across the plasma membrane increases with aging, and that this change is countered by increased intracellular calcium buffering. The additional buffer in aging neurons balances the increased calcium influx following a small number (<3) action potentials, but is overwhelmed during sustained or theta-like activity which leads to a greater rise in intracellular calcium concentration in aging than that in young neurons. Our results demonstrate that calcium overload occurs regularly in aging CA1 pyramidal neurons under physiological conditions. This overload may be a critical factor in age-related decline in hippocampus-dependent cognitive function.
Author Waters, Jack
Oh, M. Matthew
Disterhoft, John F.
Oliveira, Fernando A.
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J.W. and J.F.D. contributed equally as second authors.
M.M.O. and F.A.O. contributed equally as first authors.
F.A. Oliveira's present address: Departamento de Ciências Biológicas, Setor de Fisiologia e Farmacologia, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil.
Author contributions: M.M.O., F.A.O., J.W., and J.D. designed research; M.M.O. and F.A.O. performed research; M.M.O., F.A.O., J.W., and J.D. analyzed data; M.M.O., F.A.O., J.W., and J.D. wrote the paper.
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Snippet Altered neuronal calcium homeostasis is widely hypothesized to underlie cognitive deficits in normal aging subjects, but the mechanisms that underlie this...
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StartPage 7905
SubjectTerms Age Factors
Aging - physiology
Analysis of Variance
Animals
Biophysics
CA1 Region, Hippocampal - cytology
Calcium - metabolism
Chelating Agents - pharmacokinetics
Egtazic Acid - analogs & derivatives
Egtazic Acid - pharmacokinetics
Electric Stimulation
Fluorescent Dyes - metabolism
In Vitro Techniques
Male
Membrane Potentials - drug effects
Membrane Potentials - physiology
Microscopy, Confocal
Patch-Clamp Techniques
Pyramidal Cells - drug effects
Pyramidal Cells - physiology
Rats
Rats, Inbred F344
Time Factors
Title Altered Calcium Metabolism in Aging CA1 Hippocampal Pyramidal Neurons
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https://www.proquest.com/docview/1551627598
https://pubmed.ncbi.nlm.nih.gov/PMC3679661
https://www.jneurosci.org/content/jneuro/33/18/7905.full.pdf
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