Elucidating the neurological mechanism of the FLASH effect in juvenile mice exposed to hypofractionated radiotherapy

Barrett D. Allen(University of California, Irvine), Yasaman Alaghband(University of California, Irvine), Enikö A. Kramár(University of California, Irvine), Ning Ru(University of California, Irvine), Benoît Petit(University of Lausanne), Veljko Grilj(University of Lausanne), Michael S. Petronek(University of Iowa), Casey Pulliam(University of Iowa), Rachel Y Kim(University of California, Irvine), Ngoc-Lien Doan(University of California, Irvine), Janet E. Baulch(University of California, Irvine), Marcelo A. Wood(University of California, Irvine), Claude Bailat(Institute of Radiation Physics), Douglas R. Spitz(University of Iowa), Marie‐Catherine Vozenin(University of Lausanne), Charles L. Limoli(University of California, Irvine)
Neuro-Oncology
November 5, 2022
Cited by 62Open Access
Full Text

Abstract

BACKGROUND: Ultrahigh dose-rate radiotherapy (FLASH-RT) affords improvements in the therapeutic index by minimizing normal tissue toxicities without compromising antitumor efficacy compared to conventional dose-rate radiotherapy (CONV-RT). To investigate the translational potential of FLASH-RT to a human pediatric medulloblastoma brain tumor, we used a radiosensitive juvenile mouse model to assess adverse long-term neurological outcomes. METHODS: Cohorts of 3-week-old male and female C57Bl/6 mice exposed to hypofractionated (2 × 10 Gy, FLASH-RT or CONV-RT) whole brain irradiation and unirradiated controls underwent behavioral testing to ascertain cognitive status four months posttreatment. Animals were sacrificed 6 months post-irradiation and tissues were analyzed for neurological and cerebrovascular decrements. RESULTS: The neurological impact of FLASH-RT was analyzed over a 6-month follow-up. FLASH-RT ameliorated neurocognitive decrements induced by CONV-RT and preserved synaptic plasticity and integrity at the electrophysiological (long-term potentiation), molecular (synaptophysin), and structural (Bassoon/Homer-1 bouton) levels in multiple brain regions. The benefits of FLASH-RT were also linked to reduced neuroinflammation (activated microglia) and the preservation of the cerebrovascular structure, by maintaining aquaporin-4 levels and minimizing microglia colocalized to vessels. CONCLUSIONS: Hypofractionated FLASH-RT affords significant and long-term normal tissue protection in the radiosensitive juvenile mouse brain when compared to CONV-RT. The capability of FLASH-RT to preserve critical cognitive outcomes and electrophysiological properties over 6-months is noteworthy and highlights its potential for resolving long-standing complications faced by pediatric brain tumor survivors. While care must be exercised before clinical translation is realized, present findings document the marked benefits of FLASH-RT that extend from synapse to cognition and the microvasculature.


Related Papers

No related papers found

Powered by citation graph analysis