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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
Effects of age on immunohistochemical changes in the mouse hippocampus
Toshiki Himeda1, Kumiko Mizuno, Hiroyuki Kato
1Department of Drug Metabolism and Therapeutics, Graduate School and Faculty of Pharmaceutical Sciences, The University of Tokushima, Japan.
Abstract:
We investigated the age-related changes in neuronal cell death and synaptophysin of the hippocampal CA1 sector in mice using immunohistochemistry. Microtubule-associated protein 2a, b (MAP2) and synaptophysin immunoreactivity was measured in 2-, 8-, 18-, 42- and 59-week-old mice. MAP2 immunoreactivity was unchanged in the hippocampal CA1 sector up to 42 weeks after birth. In 59-week-old mice, however, a significant decrease in MAP2 immunoreactivity was observed in the hippocampal CA1 sector. Total number of synaptophysin-positive boutons was also unchanged in the hippocampal CA1 sector up to 42 weeks of birth. In 59-week-old mice, however, a significant increase in synaptophysin-positive boutons was observed in the hippocampal CA1 sector. These results demonstrate that dendrites and axons in the hippocampal CA1 neurons are particularly susceptible to ageing processes. In contrast, a marked increase in synaptophysin-positive boutons was found in the hippocampal CA1 sector of aged mice. These findings suggest that increase in synaptophysin-positive boutons may play a role in the maintenance of the structural components in the hippocampal CA1 sector of aged mice although most postsynaptic CA1 pyramidal neurons are generated. Thus, our findings provide further valuable information on age-related neurodegeneration and deficits in hippocampus-dependent memory and synaptic plasticity.
Insights
Aging causes significant changes in the mouse hippocampus (CA1 sector), with decreased microtubule-associated protein 2a, b (MAP2) and increased synaptophysin-positive boutons in aged mice.
Area of Science:
- Neuroscience
- Aging Research
- Cell Biology
Background:
- The hippocampal CA1 sector is crucial for memory and synaptic plasticity.
- Age-related neurodegeneration can lead to cognitive decline.
Purpose of the Study:
- To investigate age-related changes in neuronal cell death and synaptophysin in the hippocampal CA1 sector of mice.
- To understand the impact of aging on neuronal structures like dendrites and axons.
Main Methods:
- Immunohistochemistry was used to measure microtubule-associated protein 2a, b (MAP2) and synaptophysin.
- Measurements were taken in mice at ages 2, 8, 18, 42, and 59 weeks.
Main Results:
- MAP2 immunoreactivity showed no significant change up to 42 weeks but decreased significantly in 59-week-old mice.
- Synaptophysin-positive boutons remained unchanged until 42 weeks, then significantly increased in 59-week-old mice.
- Dendrites and axons in the hippocampal CA1 sector appear susceptible to aging.
Conclusions:
- Aging affects neuronal structures in the hippocampal CA1 sector, with dendrites and axons being particularly vulnerable.
- Increased synaptophysin-positive boutons in aged mice may help maintain structural components.
- Findings contribute to understanding age-related neurodegeneration and hippocampus-dependent memory deficits.

