Journal
NEUROSCIENCE
Volume 164, Issue 4, Pages 1557-1564Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2009.09.051
Keywords
stereology; frontal cortex; hippocampus; antidepressant; transcranial magnetic stimulation
Categories
Funding
- NIMH [MH60884, MH60877, MH64168, MH62185, MH40210]
- Stanley Medical Research Institute
- National Alliance for Research on Schizophrenia and Depression
- Copenhagen Hospital Corporation Research Council
- Neuronetics
- Brainsway
- Cyberonics
- NIH
- AFAR
- NARSAD
- Stanley Medical Research Foundation
- DARPA
- Advanced Neuromodulation Systemsl St. Jude
- NYSTAR
- North Star
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Anatomical evidence of brain damage from electroconvulsive therapy (ECT) is lacking; but there are no modern stereological studies in primates documenting its safety. Magnetic seizure therapy (MST) is under development as a less invasive form of convulsive therapy, and there is only one prior report on its anatomical effects. We discerned no histological lesions in the brains of higher mammals subjected to electroconvulsive shock (ECS) or MST, under conditions that model closely those used in humans. We sought to extend these findings by determining whether these interventions affected the number of neurons or glia in the frontal cortex or hippocampus. Twenty-four animals received 6 weeks of ECS, MST, or anesthesia alone, 4 days per week. After perfusion fixation, numbers of neurons and glia in frontal cortex and hippocampus were determined by unbiased stereological methods. We found no effect of either intervention on volumes or total number or numerical density of neurons or glia in hippocampus, frontal cortex, or subregions of these structures. Induction of seizures in a rigorous model of human ECT and MST therapy does not cause a change in the number of neurons or glia in potentially vulnerable regions of brain. This study, while limited to young, healthy, adult subjects, provides further evidence that ECT and MST, when appropriately applied, do not cause structural damage to the brain. (C) 2009 IBRO. Published by Elsevier Ltd. All rights reserved.
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