Reduced cognitive deficits after FLASH irradiation of whole mouse brain are associated with less hippocampal dendritic spine loss and neuroinflammation

dc.contributor.authorSimmons, Danielle A.
dc.contributor.authorLartey, Frederick M.
dc.contributor.authorSchüler, Emil
dc.contributor.authorRafat, Marjan
dc.contributor.authorKing, Gregory
dc.contributor.authorKim, Anna
dc.contributor.authorKo, Ryan
dc.contributor.authorSemaan, Sarah
dc.contributor.authorGonzalez, Selena
dc.contributor.authorJenkins, Melissa
dc.contributor.authorPradhan, Pooja
dc.contributor.authorShih, Zion
dc.contributor.authorWang, Jinghui
dc.contributor.authorEyben, Rievon
dc.contributor.authorGraves, Edward E.
dc.contributor.authorMaxim, Peter G.
dc.contributor.authorLongo, Frank M.
dc.contributor.authorLoo, Billy W., Jr.
dc.contributor.departmentRadiation Oncology, School of Medicineen_US
dc.date.accessioned2020-08-20T16:40:40Z
dc.date.available2020-08-20T16:40:40Z
dc.date.issued2019-10
dc.description.abstractAim To evaluate the impact of ultra-rapid FLASH mouse whole brain irradiation on hippocampal dendritic spines and neuroinflammation, factors associated with cognitive impairment after brain irradiation. Methods We administered 30 Gy whole brain irradiation to C57BL6/J mice in sub-second (FLASH) vs. 240 s conventional delivery time keeping all other parameters constant, using a custom configured clinical linac. Ten weeks post-irradiation, we evaluated spatial and non-spatial object recognition using novel object location and object recognition testing. We measured dendritic spine density by tracing Golgi-stained hippocampal neurons and evaluated neuroinflammation by CD68 immunostaining, a marker of activated microglia, and expression of 10 pro-inflammatory cytokines using a multiplex immunoassay. Results At ten weeks post-irradiation, compared to unirradiated controls, conventional delivery time irradiation significantly impaired novel object location and recognition tasks whereas the same dose given in FLASH delivery did not. Conventional delivery time, but not FLASH, was associated with significant loss of dendritic spine density in hippocampal apical dendrites, with a similar non-significant trend in basal dendrites. Conventional delivery time was associated with significantly increased CD68-positive microglia compared to controls whereas FLASH was not. Conventional delivery time was associated with significant increases in 5 of 10 pro-inflammatory cytokines in the hippocampus (and non-significant increases in another 3), whereas FLASH was associated with smaller increases in only 3. Conclusion Reduced cognitive impairment and associated neurodegeneration were observed with FLASH compared to conventional delivery time irradiation, potentially through decreased induction of neuroinflammation, suggesting a promising approach to increasing therapeutic index in radiation therapy of brain tumors.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationSimmons, D. A., Lartey, F. M., Schüler, E., Rafat, M., King, G., Kim, A., Ko, R., Semaan, S., Gonzalez, S., Jenkins, M., Pradhan, P., Shih, Z., Wang, J., von Eyben, R., Graves, E. E., Maxim, P. G., Longo, F. M., & Loo, B. W. (2019). Reduced cognitive deficits after FLASH irradiation of whole mouse brain are associated with less hippocampal dendritic spine loss and neuroinflammation. Radiotherapy and Oncology, 139, 4–10. https://doi.org/10.1016/j.radonc.2019.06.006en_US
dc.identifier.urihttps://hdl.handle.net/1805/23656
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.radonc.2019.06.006en_US
dc.relation.journalRadiotherapy and Oncologyen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectwhole brain radiationen_US
dc.subjectradiation-induced cognitive impairmenten_US
dc.subjectFLASHen_US
dc.titleReduced cognitive deficits after FLASH irradiation of whole mouse brain are associated with less hippocampal dendritic spine loss and neuroinflammationen_US
dc.typeArticleen_US
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