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Updated: Jul 27, 2026

Preparation of Acute Hippocampal Slices from Rats and Transgenic Mice for the Study of Synaptic Alterations during Aging and Amyloid Pathology
Published on: March 23, 2011
Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age
D A Cottrell1, E L Blakely, M A Johnson
1Department of Neurology, The Medical School, University of Newcastle upon Tyne, NE2 4HH, Newcastle upon Tyne, UK. d.a.cottrell@ncl.ac.uk
Abstract:
The chronological accumulation of mitochondrial dysfunction has been proposed as a potential mechanism in the physiological processes of aging. Cytochrome c oxidase deficient, succinate dehydrogenase positive muscle fibers containing high copy numbers of a mitochondrial DNA mutation are a pathological hallmark of mitochondrial DNA disorders. We show that there is an age-related increase in cytochrome c oxidase-deficient cells in both hippocampal pyramidal neurons and choroid plexus epithelial cells. We suggest that these cells contribute to the cell death and dysfunction in CNS aging.

