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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
Glycogenosomes in the aging rat brain: their occurrence in the visual pathways
1The Department of Clinical Neurosciences, Institute of Psychiatry, and Guy's, King's and St Thomas' School of Medicine, De Crespigny Park, London, UK. jbc@chestnut.u-net.com
Glycogen bodies, or glycogenosomes, accumulate in the visual pathways of aging rats, particularly in the superior colliculi and retinal photoreceptor cells. Their exact role remains unclear, but age-related accumulation is documented.
Area of Science:
- Neuroscience
- Cell Biology
- Aging Research
Background:
- Glycogen bodies (glycogenosomes) are known in peripheral neurites of aging rats.
- Their presence and significance in central nervous system tissue are poorly understood.
Purpose of the Study:
- To document the occurrence, localization, and age-related density changes of glycogen bodies in the visual pathways of aging rats.
- To investigate potential mechanisms for glycogen body accumulation.
Main Methods:
- Light microscopy and periodic acid-Schiff (PAS) staining on brain sections from aging rats.
- Diastase digestion to confirm glycogen content.
- Observation of retinal photoreceptor cells.
Main Results:
- Glycogen bodies increased in number in the superior colliculi from 5 months of age, becoming more numerous in older rats (1-2+ years).
- They were also found in the optic tract, optic chiasm, optic nerves, and retinal photoreceptor cells, with age-related accumulation.
- Glycogen bodies were small (rarely >4 microm) and their presence in nerve fibers is not attributed to physical trauma or polyglucosan bodies.
Conclusions:
- Glycogen bodies accumulate with age in specific regions of the rat visual system, including the superior colliculi and retina.
- While light damage and oxidative stress are suggested for retinal accumulation, the cause in retino-tectal nerve fibers is uncertain.
- The findings highlight an age-related change in neural tissue with unknown functional significance.
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