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Synapse loss in frontal cortex biopsies in Alzheimer's disease: correlation with cognitive severity
1Department of Neurology, Lexington Veterans Administration, Medical Center, KY.
Abstract:
Ultrastructural studies of biopsied cortical tissue from the right frontal lobe of 8 patients with mild to moderate Alzheimer's disease (AD) revealed that the number of synapses in lamina III of Brodmann's area 9 was significantly decreased when compared with the number in age-matched control brains (n = 9; postmortem time, less than 13 hours). Further decline in synaptic number was seen in age-matched autopsied AD specimens. In the AD brains there was significant enlargement of the mean apposition length, which correlated with degree of synapse loss; as synapse density declined, synapse size increased. The enlargement of synapses, coupled with the decrease in synaptic number, allowed the total synaptic contact area per unit volume to remain stable in the patients who underwent biopsy. In autopsied subjects who had AD, there was no further enlargement of mean synaptic contact area. There was a significant correlation between synapse counts and scores on the Mini-Mental State examination in the patients who underwent biopsy. Lower mental status scores were associated with greater loss of synapses. Choline acetyltransferase activity was significantly decreased in the biopsied group and declined further in the autopsied specimens of AD. There was no relationship between choline acetyltransferase activity and scores on the Mini-Mental State examination or synapse number. There is evidence of neural plasticity in the AD neuropil; synaptic contact size increased in patients who had biopsy and possibly compensated for the numerical loss of synapses. But by end stage of the disease, the ability of the cortex to compensate was exceeded and both synapse number and synaptic contact area declined.(ABSTRACT TRUNCATED AT 250 WORDS)
Insights
Alzheimer's disease (AD) brains show decreased synapse numbers, but increased synapse size, suggesting early neural plasticity. By end-stage AD, both synapse number and size decline, overwhelming compensatory mechanisms.
Area of Science:
- Neuroscience
- Neuropathology
- Alzheimer's Disease Research
Background:
- Alzheimer's disease (AD) is characterized by progressive neurodegeneration.
- Synaptic loss is a key feature of AD neuropathology.
- Understanding synaptic changes is crucial for developing AD therapies.
Purpose of the Study:
- To investigate ultrastructural changes in synapses in mild to moderate Alzheimer's disease (AD).
- To correlate synaptic alterations with cognitive decline and enzyme activity in AD patients.
Main Methods:
- Ultrastructural analysis of biopsied and autopsied cortical tissue from AD patients and age-matched controls.
- Quantification of synapse number, size, and synaptic contact area.
- Measurement of choline acetyltransferase activity.
Main Results:
- Significant decrease in synapse number in lamina III of Brodmann's area 9 in AD brains compared to controls.
- Enlargement of mean synaptic apposition length correlated with synapse loss; synapse size increased as density declined.
- Total synaptic contact area remained stable in biopsied AD patients due to compensatory synapse enlargement.
- Choline acetyltransferase activity was significantly decreased in AD patients.
Conclusions:
- Evidence of neural plasticity in early to moderate AD, with synaptic enlargement potentially compensating for numerical loss.
- In end-stage AD, compensatory mechanisms are exceeded, leading to a decline in both synapse number and synaptic contact area.
- Synapse loss correlates with cognitive impairment (Mini-Mental State examination scores) in AD patients.