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Pupillary Response as Assessment of Effective Seizure Induction by Electroconvulsive Therapy
Published on: April 11, 2019
Differential plastic changes in synthesis and binding in the mouse somatostatin system after electroconvulsive
Mikkel Vestergaard Olesen1, Casper René Gøtzsche1, Søren Hofman Christiansen1
11Laboratory of Neural Plasticity,Center for Neuroscience,University of Copenhagen,Copenhagen,Denmark.
Electroconvulsive stimulation (ECS) alters somatostatin (SST) and its receptor (SSTR) levels in the mouse brain, suggesting a role in ECT
Area of Science:
- Neuroscience
- Neuropharmacology
- Molecular Psychiatry
Background:
- Electroconvulsive therapy (ECT) effectively treats major depression, but its mechanisms are unclear.
- Somatostatin (SST) and its receptors (SSTRs) are implicated in ECT's effects due to SST's anticonvulsant properties and regulation by ECS.
- The impact of ECS on the SST receptor system remains largely unexplored.
Purpose of the Study:
- To investigate the effects of single and repeated electroconvulsive stimulation (ECS) on somatostatin (SST) and SST receptor (SSTR1-4) expression and binding.
- To examine these changes in specific mouse brain regions, including the hippocampus and cortex.
Main Methods:
- Mice were subjected to single or repeated electroconvulsive stimulation (ECS).
- Quantitative analysis of SST and SSTR (SSTR1-4) mRNA and protein expression was performed.
- Somatostatin receptor binding was assessed using radioligand binding assays ([125I]LTT-SST28).
- Analyses focused on hippocampal subregions (dentate gyrus, CA1, CA3) and parietal/piriform cortices.
Main Results:
- Repeated ECS increased SST and SSTR1 expression in the dentate gyrus, while single ECS downregulated SSTR2.
- ECS modulated SST binding and SSTR expression across different brain regions and time points.
- Elevated SST mRNA and binding were observed in the hippocampus and cortex following ECS treatments.
Conclusions:
- ECS induces complex neuroplastic changes in the somatostatin system.
- These alterations in SST and SSTR expression and binding may contribute to the anticonvulsant and therapeutic effects of ECT.
- The somatostatin system is a potential mediator of ECT's beneficial actions in depression.
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