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DOI 10.1016/j.biopsych.2003.08.013

Медицинская библиотека · Biological psychiatry · 2004

Electroconvulsive seizures induce endothelial cell proliferation in adult rat hippocampus.

Hellsten Johan, Wennström Malin, Bengzon Johan, Mohapel Paul, Tingström Anders

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Electroconvulsive seizures, an animal model for electroconvulsive treatment, induce a strong increase in neurogenesis in the dentate gyrus of adult rats. Hippocampal neurogenesis has previously been described as occurring in an angiogenic niche. This study examines the effect of electroconvulsive seizures on proliferation of vascular cells in rat hippocampus.

METHODS

Rats were injected with bromodeoxyuridine to label proliferating cells in the dentate gyrus after single/multiple electroconvulsive seizures in a dose-response study and at various time points after single electroconvulsive seizures in a time-course study.

RESULTS

A dose-response effect on the number of bromodeoxyuridine-labeled endothelial cells located in the granule cell layer, hilus, and molecular layer was noted, as was the case with the number of neural precursors in the subgranular zone. The time-course study revealed that endothelial cell and neural precursor proliferation occurred in concert in response to a single electroconvulsive seizure.

CONCLUSIONS

Our data suggest that in response to electroconvulsive seizures, endothelial cell and neural proliferation is coregulated. The increase in endothelial cell proliferation may act to support the increased neural proliferation and neuronal activity or vice versa, possibly leading to structural changes within the hippocampus of importance for the antidepressant effect of electroconvulsive seizures.

Для цитирования: Hellsten Johan, Wennström Malin, Bengzon Johan, Mohapel Paul, Tingström Anders. Electroconvulsive seizures induce endothelial cell proliferation in adult rat hippocampus.. Biological psychiatry. 2004. DOI: 10.1016/j.biopsych.2003.08.013.

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