Proceedings of the National Academy of Sciences · 2019 · 588 citations · 49 references
MedicineNeuroscienceRadiation OncologyMemoryRadiation BiophysicsRadiobiologyBiological Effects Of RadiationNeuroprotectionOxidative Stress In NeurotoxicityRadiation BiologyRadiation SensitivityReactive Oxygen SpeciesLong-term Neurocognitive SequelaeNeurocognitive PreservationNeurocognitive ProfileNeuroprotective MechanismsRadiation-induced Oxidative StressRadiation-related Cognitive ImpairmentTreatment-related Neurocognitive EffectsTumor Bed Irradiation
) modalities, we showed that FLASH did not cause radiation-induced deficits in learning and memory in mice. Moreover, 6 months after exposure, CONV caused permanent alterations in neurocognitive end points, whereas FLASH did not induce behaviors characteristic of anxiety and depression and did not impair extinction memory. Mechanistic investigations showed that increasing the oxygen tension in the brain through carbogen breathing reversed the neuroprotective effects of FLASH, while radiochemical studies confirmed that FLASH produced lower levels of the toxic reactive oxygen species hydrogen peroxide. In addition, FLASH did not induce neuroinflammation, a process described as oxidative stress-dependent, and was also associated with a marked preservation of neuronal morphology and dendritic spine density. The remarkable normal tissue sparing afforded by FLASH may someday provide heretofore unrealized opportunities for dose escalation to the tumor bed, capabilities that promise to hasten the translation of this groundbreaking irradiation modality into clinical practice.
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Neurotoxic reactive astrocytes are induced by activated microglia
Shane A. Liddelow, Kevin A. Guttenplan, Laura Clarke et al. · Nature · 2017 · 8K citations · Full text
Medicine, Neurobiology, Neuroscience +14
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