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The microvascular alterations in frontal cortex during treatment with antipsychotics: a post-mortem study
Ion Udriştoiu1, Ileana Marinescu, Mihail Cristian Pîrlog
1Department of Psychiatry, Faculty of Medicine, University of Medicine and Pharmacy of Craiova, Romania; marinescu_psy@yahoo.com.
Antipsychotics targeting D2 receptors in schizophrenia may harm frontal cortex microvessels, leading to neural loss. This suggests a link between vascular health and cognitive function in schizophrenia patients.
Area of Science:
- Neuroscience
- Psychiatry
- Vascular Biology
Background:
- Schizophrenia is a severe psychiatric disorder with biological underpinnings in the brain.
- Dopamine balance in the frontal cortex is crucial for schizophrenia outcomes.
- Alterations in frontal cortex dopamine mechanisms can impact the vascular system and cause secondary neuronal damage.
Purpose of the Study:
- To investigate alterations in neuronal architecture and microvascular integrity in the frontal cortex of schizophrenia patients treated with D2-blocking antipsychotics.
Main Methods:
- Post-mortem examination of frontal cortex sections from three schizophrenia patients treated with antipsychotics for at least 24 months.
- Classical histopathological protocols were employed for slide preparation.
Main Results:
- Significant neural loss was observed, stemming from severe microvessel damage.
- Microvascular alterations included diameter reduction, collagen and hyaline deposits, edema, pinocytosis, and vacuolization.
Conclusions:
- Potent D2-antagonist antipsychotics can compromise the neurovascular unit and small vessels in the frontal cortex.
- This compromise affects blood flow and metabolism, leading to structural microvascular changes and increased apoptosis.
- Vascular support is essential for the dopaminergic system's integrity in the frontal cortex; dysfunction exacerbates neuronal loss and clinical symptoms.
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