Abstract

In the brain, apolipoprotein E (apoE) plays an important role in lipid transport and response to environmental and age-related challenges, including neuronal repair following injury. While much has been learned from radiation studies in rodents, a gap in our knowledge is how radiation might affect the brain in primates. This is important for assessing risk to the brain following radiotherapy as part of cancer treatment or environmental radiation exposure as part of a nuclear accident, bioterrorism, or a nuclear attack. In this study, we investigated the effects of ionizing radiation on brain volumes and apoE levels in the prefrontal cortex, amygdala, and hippocampus of Rhesus macaques that were part of the Nonhuman Primate Radiation Survivor Cohort at the Wake Forest University. This unique cohort is composed of Rhesus macaques that had previously received single total body doses of 6.5–8.05 Gy of ionizing radiation. Regional apoE levels predicted regional volume in the amygdala and the prefrontal cortex. In addition, apoE levels in the amygdala, but not the hippocampus, strongly predicted relative hippocampal volume. Finally, radiation dose negatively affected relative hippocampal volume when apoE levels in the amygdala were controlled for, suggesting a protective compensatory role of regional apoE levels following radiation exposure. In a supplementary analysis, there also was a robust positive relationship between the neuroprotective protein α-klotho and apoE levels in the amygdala, further supporting the potentially protective role of apoE. Increased understanding of the effects of IR in the primate brain and the role of apoE in the irradiated brain could inform future therapies to mitigate the adverse effects of IR on the CNS.

Highlights

  • In the brain, apolipoprotein E plays an important role in lipid transport and response to environmental and age-related challenges, including neuronal repair following injury

  • We investigated whether brain apolipoprotein E (apoE) change in response to ionizing radiation (IR) in Rhesus macaques, as well as whether there is a relationship between regional apoE levels and brain volume in the hippocampus, amygdala, and prefrontal cortex (PFC)

  • Using the first session of imaging data for each macaque, we conducted an exploratory analysis of the correlations between regional apoE levels and regional relative brain volumes (Fig. 2)

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Summary

Introduction

Apolipoprotein E (apoE) plays an important role in lipid transport and response to environmental and age-related challenges, including neuronal repair following injury. We investigated the effects of ionizing radiation on brain volumes and apoE levels in the prefrontal cortex, amygdala, and hippocampus of Rhesus macaques that were part of the Nonhuman Primate Radiation Survivor Cohort at the Wake Forest University. At doses lower than those needed to induce acute radiation syndrome, multiple studies have indicated that there is a risk of developing adverse delayed effects involving inflammatory and degenerative conditions in multiple organ s­ ystems[3] This risk is relevant to the treatment of cancer, since over half of cancer patients undergo radiation therapy in some f­orm[4]. Aging rhesus macaques exhibit age-related cognitive deficits, alterations in circadian activity that are associated with cognitive impairments, immune-related measures, amyloid plaque pathology, as well as tau pathology similar in qualitative pattern and temporal sequence as ­humans[16,17,18,19,20,21]

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