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Published on: December 31, 2016
Synaptophysin immunoreactivity in temporal lobe epilepsy-associated hippocampal sclerosis
M R Looney1, F C Dohan, K G Davies
1Department of Pathology, University of Tennessee, Memphis, USA.
Acta Neuropathologica
|August 12, 1999
Summary
Hippocampal sclerosis (HS) grading correlates with synaptic changes in epilepsy. Synaptophysin immunohistochemistry quantifies synaptic loss in CA1 and CA4, confirming HS severity and revealing plasticity in the dentate gyrus.
Area of Science:
- Neuroscience
- Neuropathology
- Epilepsy Research
Background:
- Hippocampal sclerosis (HS) is a common finding in temporal lobe epilepsy (TLE).
- A semiquantitative grading system for HS based on neuronal loss and gliosis exists.
- Synaptic alterations are implicated in the pathophysiology of TLE.
Purpose of the Study:
- To correlate synaptic content in hippocampal fields with an established HS grading system.
- To investigate the utility of synaptophysin immunohistochemistry in quantifying synaptic changes in TLE.
- To explore regional differences in synaptic response to HS pathology.
Main Methods:
- Synaptophysin immunohistochemistry was performed on hippocampal sections from 25 TLE patients with pre-assigned HS grades.
- Synaptic density was quantitatively assessed in specific hippocampal subfields (CA1, CA4, dentate gyrus).
- Correlations between synaptic staining intensity and HS grade were analyzed.
Main Results:
- Significant synaptic loss and increased synaptic density were observed in different hippocampal fields with increasing HS grade.
- Marked reduction in synaptic staining in CA1 and CA4 strongly correlated with HS grade.
- CA4 showed a more graded synaptic response compared to CA1's apparent 'all or nothing' response.
- The dentate gyrus molecular layer exhibited plasticity, with decreased outer and increased inner portions in high-grade HS.
Conclusions:
- Quantitative synaptophysin immunohistochemistry is a sensitive method for detecting HS and correlates well with empirical grading scales.
- CA4 demonstrates a more continuous synaptic response to TLE pathology than CA1.
- High-grade HS is associated with quantifiable synaptic plasticity in the dentate gyrus.

