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 in | The Journal of neuroscience Vol. 33; no. 18; pp. 7905 - 7911 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Society for Neuroscience
01.05.2013
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Subjects | |
Online Access | Get full text |
ISSN | 0270-6474 1529-2401 1529-2401 |
DOI | 10.1523/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. |
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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. |
Author_xml | – sequence: 1 givenname: M. Matthew surname: Oh fullname: Oh, M. Matthew – sequence: 2 givenname: Fernando A. surname: Oliveira fullname: Oliveira, Fernando A. – sequence: 3 givenname: Jack surname: Waters fullname: Waters, Jack – sequence: 4 givenname: John F. surname: Disterhoft fullname: Disterhoft, John F. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23637181$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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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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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