Effects of Proton and Combined Proton and 56Fe Radiation on the Hippocampus

The space radiation environment contains protons and 56Fe, which could pose a significant hazard to space flight crews during and after missions. The space environment involves complex radiation exposures, thus, the effects of a dose of protons might be modulated by a dose of heavy-ion radiation. The brain, and particularly the hippocampus, may be susceptible to space radiation-induced changes. In this study, we first determined the dose-response effect of proton radiation (150 MeV) on hippocampus-dependent cognition 1 and 3 months after exposure. Based on those results, we subsequently exposed mice to protons alone (150 MeV, 0.1 Gy), 56Fe alone (600 MeV/n, 0.5 Gy) or combined proton and 56Fe radiations (protons first) with the two exposures separated by 24 h. At one month postirradiation, all animal groups showed novel object recognition. However, at three months postirradiation, mice exposed to either protons or combined proton and 56Fe radiations showed impaired novel object recognition, which was not observed in mice irradiated with 56Fe alone. The mechanisms in these impairments might involve inflammation. In mice irradiated with protons alone or 56Fe alone three months earlier, there was a negative correlation between a measure of novel object recognition and the number of newly born activated microglia in the dentate gyrus. Next, cytokine and chemokine levels were assessed in the hippocampus. At one month after exposure the levels of IL-12 were higher in mice exposed to combined radiations compared with sham-irradiated mice, while the levels of IFN-γ were lower in mice exposed to 56Fe radiation alone or combined radiations. In addition, IL-4 levels were lower in 56Fe-irradiated mice compared with proton-irradiated mice and TNF-α levels were lower in proton-irradiated mice than in mice receiving combined radiations. At three months after exposure, macrophage-derived chemokine (MDC) and eotaxin levels were lower in mice receiving combined radiations. The levels of MDC and eotaxin correlated and the levels of MDC, but not eotaxin, correlated with the percentage of newly born activated microglia in the blades of the dentate gyrus. Finally, hippocampal IL-6 levels were higher in mice receiving combined radiations compared with mice receiving 56Fe radiation alone. These data demonstrate the sensitivity of novel object recognition for detecting cognitive injury three months after exposure to proton radiation alone, and combined exposure to proton and 56Fe radiations, and that newly-born activated microglia and inflammation might be involved in this injury.

[1]  M. Drew,et al.  Arrest of adult hippocampal neurogenesis in mice impairs single- but not multiple-trial contextual fear conditioning. , 2010, Behavioral neuroscience.

[2]  J. Fike,et al.  Effects of whole body 56Fe radiation on contextual freezing and Arc-positive cells in the dentate gyrus , 2013, Behavioural Brain Research.

[3]  Andre Obenaus,et al.  Trauma‐induced alterations in cognition and Arc expression are reduced by previous exposure to 56Fe irradiation , 2012, Hippocampus.

[4]  J. Walsh,et al.  Hypoxia/Reoxygenation Impairs Memory Formation via Adenosine-Dependent Activation of Caspase 1 , 2012, The Journal of Neuroscience.

[5]  Jacob Raber,et al.  Effects of 56Fe-Particle Cranial Radiation on Hippocampus-Dependent Cognition Depend on the Salience of the Environmental Stimuli , 2011, Radiation research.

[6]  K. Manda,et al.  Memory impairment, oxidative damage and apoptosis induced by space radiation: Ameliorative potential of α-lipoic acid , 2008, Behavioural Brain Research.

[7]  R. Vlkolinský,et al.  The effects of low doses of proton, iron or silicon radiation on spatial learning in a mouse model of Alzheimer's disease , 2014, Journal of Radiation Research.

[8]  J. Raber,et al.  28Silicon Irradiation Impairs Contextual Fear Memory in B6D2F1 Mice , 2015, Radiation research.

[9]  D. Amaral,et al.  Entorhinal Cortex Lesions Disrupt the Relational Organization of Memory in Monkeys , 2004, The Journal of Neuroscience.

[10]  R. Vlkolinský,et al.  Effects of proton radiation on evoked and spontaneous neuronal activity in the hippocampus of APP/PSEN1 transgenic mice , 2014, Journal of Radiation Research.

[11]  Jacob Raber,et al.  Early Effects of Whole-Body 56Fe Irradiation on Hippocampal Function in C57BL/6J Mice , 2013, Radiation research.

[12]  K. Manda,et al.  Radiation-induced cognitive dysfunction and cerebellar oxidative stress in mice: Protective effect of α-lipoic acid , 2007, Behavioural Brain Research.

[13]  J. Fike,et al.  High-LET Radiation Induces Inflammation and Persistent Changes in Markers of Hippocampal Neurogenesis , 2005, Radiation research.

[14]  Larry R Squire,et al.  Spatial memory, recognition memory, and the hippocampus. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[15]  G. Nelson,et al.  Effects of Protons and HZE Particles on Glutamate Transport in Astrocytes, Neurons and Mixed Cultures , 2010, Radiation research.

[16]  Jacob Raber,et al.  Sex‐dependent effects of 56Fe irradiation on contextual fear conditioning in C57BL/6J mice , 2009, Hippocampus.

[17]  C. Barnes,et al.  Neuroinflammation Alters the Hippocampal Pattern of Behaviorally Induced Arc Expression , 2005, The Journal of Neuroscience.

[18]  K. Jin,et al.  Defective adult neurogenesis in CB1 cannabinoid receptor knockout mice. , 2004, Molecular pharmacology.

[19]  Robert E. Clark,et al.  Impaired Recognition Memory in Rats after Damage to the Hippocampus , 2000, The Journal of Neuroscience.

[20]  S. Impey,et al.  Transgenic miR132 Alters Neuronal Spine Density and Impairs Novel Object Recognition Memory , 2010, PloS one.

[21]  N. Ron-Harel,et al.  Dysregulation of kisspeptin and neurogenesis at adolescence link inborn immune deficits to the late onset of abnormal sensorimotor gating in congenital psychological disorders , 2010, Molecular Psychiatry.

[22]  B. Shukitt-Hale,et al.  Spatial Learning and Memory Deficits Induced by Exposure to Iron-56-Particle Radiation , 2000, Radiation research.

[23]  R. Miller,et al.  Chemokines regulate hippocampal neuronal signaling and gp120 neurotoxicity. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[24]  E. Hauben,et al.  Low‐dose γ‐irradiation promotes survival of injured neurons in the central nervous system via homeostasis‐driven proliferation of T cells , 2004, The European journal of neuroscience.

[25]  Francis A. Cucinotta,et al.  Space Radiation Cancer Risk Projections and Uncertainties - 2010 , 2011 .

[26]  Andre Obenaus,et al.  Hippocampal Neurogenesis and Neuroinflammation after Cranial Irradiation with 56Fe Particles , 2008, Radiation research.

[27]  M. O’Banion,et al.  Central Nervous System Effects of Whole-Body Proton Irradiation , 2014, Radiation research.

[28]  Richard A Britten,et al.  Low (20 cGy) Doses of 1 GeV/u 56Fe-Particle Radiation Lead to a Persistent Reduction in the Spatial Learning Ability of Rats , 2012, Radiation research.

[29]  R. Roesler,et al.  Reversal of age-related deficits in object recognition memory in rats with l-deprenyl , 2005, Experimental Gerontology.

[30]  Wan Huang,et al.  Interleukin-12 inhibits eotaxin secretion of cultured primary lung cells and alleviates airway inflammation in vivo. , 2002, Cytokine.

[31]  J. Aggleton,et al.  Spontaneous object recognition and object location memory in rats: the effects of lesions in the cingulate cortices, the medial prefrontal cortex, the cingulum bundle and the fornix , 1997, Experimental Brain Research.

[32]  J. Kaye,et al.  The ageing systemic milieu negatively regulates neurogenesis and cognitive function , 2011 .

[33]  C. Barnes,et al.  Memantine protects against LPS-induced neuroinflammation, restores behaviorally-induced gene expression and spatial learning in the rat , 2006, Neuroscience.

[34]  Carol A Barnes,et al.  Imaging neural activity with temporal and cellular resolution using FISH , 2001, Current Opinion in Neurobiology.

[35]  J. Fike,et al.  28Silicon Radiation-Induced Enhancement of Synaptic Plasticity in the Hippocampus of Naïve and Cognitively Tested Mice , 2014, Radiation research.

[36]  C. Sandi,et al.  Effects of chronic stress on contextual fear conditioning and the hippocampal expression of the neural cell adhesion molecule, its polysialylation, and L1 , 2001, Neuroscience.

[37]  Bruce L. McNaughton,et al.  Environment-specific expression of the immediate-early gene Arc in hippocampal neuronal ensembles , 1999, Nature Neuroscience.

[38]  M. Montenarh,et al.  Regulation of CAK kinase activity by p53 , 1998, Oncogene.

[39]  D. Mumby,et al.  Retrograde and anterograde object recognition in rats with hippocampal lesions , 2003, Hippocampus.

[40]  C. Heldin,et al.  Interleukin-6 and Neural Stem Cells: More than Gliogenesis to Further Clarify the Specific Role of Il-6 and Its Specific Il-6r on Nscs' Phenotype Change and Differentiation, We , 2008 .

[41]  J. Fike,et al.  Effects of 56Fe radiation on hippocampal function in mice deficient in chemokine receptor 2 (CCR2) , 2013, Behavioural Brain Research.

[42]  M. Monje,et al.  Irradiation induces neural precursor-cell dysfunction , 2002, Nature Medicine.

[43]  M. Pecaut,et al.  Behavioral consequences of radiation exposure to simulated space radiation in the C57BL/6 mouse: Open field, rotorod, and acoustic startle , 2002, Cognitive, affective & behavioral neuroscience.

[44]  Carol A Barnes,et al.  Spatial Exploration-Induced Arc mRNA and Protein Expression: Evidence for Selective, Network-Specific Reactivation , 2005, The Journal of Neuroscience.

[45]  S. Vandenberg,et al.  Radiation-induced impairment of hippocampal neurogenesis is associated with cognitive deficits in young mice , 2004, Experimental Neurology.

[46]  Hiroki Toda,et al.  Inflammatory Blockade Restores Adult Hippocampal Neurogenesis , 2003, Science.

[47]  B Shukitt-Hale,et al.  The effects of proton exposure on neurochemistry and behavior. , 2004, Advances in space research : the official journal of the Committee on Space Research.

[48]  T. Bliss,et al.  Arc/Arg3.1 Is Essential for the Consolidation of Synaptic Plasticity and Memories , 2006, Neuron.

[49]  I. Spigelman,et al.  Radiation-Induced Alterations in Synaptic Neurotransmission of Dentate Granule Cells Depend on the Dose and Species of Charged Particles , 2014, Radiation research.