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

Author:

Allen Barrett D1ORCID,Alaghband Yasaman1,Kramár Eniko A2,Ru Ning1,Petit Benoit3,Grilj Veljko3,Petronek Michael S4ORCID,Pulliam Casey F4,Kim Rachel Y1,Doan Ngoc-Lien1,Baulch Janet E1,Wood Marcelo A2,Bailat Claude5,Spitz Douglas R4ORCID,Vozenin Marie-Catherine3,Limoli Charles L1

Affiliation:

1. Department of Radiation Oncology, University of California, Irvine , CA 92697-2695 , USA

2. Department of Neurobiology and Behavior, University of California, Irvine , CA 92697 , USA

3. Laboratory of Radiation Oncology, Department of Radiation Oncology, Lausanne University Hospital and University of Lausanne , Lausanne , Switzerland

4. Free Radical and Radiation Biology Program, Department of Radiation Oncology, University of Iowa , Iowa City, IA 52242 , USA

5. Institute of Radiation Physics/CHUV, Lausanne University Hospital , Lausanne , Switzerland

Abstract

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.

Funder

Spirit grant MC-V

Optical Biology Core Facility of the Developmental Biology Center

Center for Complex Biological Systems

University of California, Irvine

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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