Radionecrosis and cellular changes in small volume stereotactic brain radiosurgery in a porcine model.

Sci Rep

Centre for Experimental Neuroscience (CENSE), Department of Neurosurgery, Aarhus University Hospital, Palle Juul-Jensens Boulevard 165, indgang J, Plan 1, J118-125, (Krydspunkt 116), 8200, Aarhus N, Denmark.

Published: October 2020

AI Article Synopsis

  • * Researchers developed a porcine model to test the effects of high radiation doses (40-100 Gy) on small brain areas to understand how radiation affects neuronal activity.
  • * After 6 months of monitoring, they found that higher radiation doses led to damage in brain tissue: grey matter showed necrosis at 100 Gy, while white matter did so at 60 Gy, along with changes in blood vessels and brain cell structures.

Article Abstract

Stereotactic radiosurgery (SRS) has proven an effective tool for the treatment of brain tumors, arteriovenous malformation, and functional conditions. However, radiation-induced therapeutic effect in viable cells in functional SRS is also suggested. Evaluation of the proposed modulatory effect of irradiation on neuronal activity without causing cellular death requires the knowledge of radiation dose tolerance at very small tissue volume. Therefore, we aimed to establish a porcine model to study the effects of ultra-high radiosurgical doses in small volumes of the brain. Five minipigs received focal stereotactic radiosurgery with single large doses of 40-100 Gy to 5-7.5 mm fields in the left primary motor cortex and the right subcortical white matter, and one animal remained as unirradiated control. The animals were followed-up with serial MRI, PET scans, and histology 6 months post-radiation. We observed a dose-dependent relation of the histological and MRI changes at 6 months post-radiation. The necrotic lesions were seen in the grey matter at 100 Gy and in white matter at 60 Gy. Furthermore, small volume radiosurgery at different dose levels induced vascular, as well as neuronal cell changes and glial cell remodeling.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529917PMC
http://dx.doi.org/10.1038/s41598-020-72876-wDOI Listing

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