Cargando…
Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy
Although an effective treatment for pediatric brain tumors, cranial radiation therapy (CRT) damages surrounding healthy tissue, thereby disrupting brain development. Animal models of pediatric CRT have primarily relied on visual tasks to assess cognitive impairment. Moreover, there has been a lack o...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6084003/ https://www.ncbi.nlm.nih.gov/pubmed/30116180 http://dx.doi.org/10.3389/fnbeh.2018.00158 |
_version_ | 1783346085631098880 |
---|---|
author | Perez, Emma C. Rodgers, Shaefali P. Inoue, Taeko Pedersen, Steen E. Leasure, J. Leigh Gaber, M. Waleed |
author_facet | Perez, Emma C. Rodgers, Shaefali P. Inoue, Taeko Pedersen, Steen E. Leasure, J. Leigh Gaber, M. Waleed |
author_sort | Perez, Emma C. |
collection | PubMed |
description | Although an effective treatment for pediatric brain tumors, cranial radiation therapy (CRT) damages surrounding healthy tissue, thereby disrupting brain development. Animal models of pediatric CRT have primarily relied on visual tasks to assess cognitive impairment. Moreover, there has been a lack of sex comparisons as most research on the cognitive effects of pediatric CRT does not include females. Therefore, we utilized olfaction, an ethologically relevant sensory modality, to assess cognitive impairment in an animal model of CRT that included both male and female mice. Specifically, we used the novel odor recognition (NOdorR) task with social odors to test recognition memory, a cognitive parameter that has been associated with olfactory neurogenesis, a form of cellular plasticity damaged by CRT. In addition to odor recognition memory, olfactory ability or discrimination of non-social and social odors were assessed both acutely and 3 months after CRT. Magnetic resonance imaging (MRI) and histology were performed after behavioral testing to assess long-term damage by CRT. Long-term but not acute radiation-induced impairment in odor recognition memory was observed, consistent with delayed onset of cognitive impairment in human patients. Males showed greater exploration of social odors than females, but general exploration was not affected by irradiation. However, irradiated males had impaired odor recognition memory in adulthood, compared to non-irradiated males (or simply male controls). Female olfactory recognition memory, in contrast, was dependent on estrus stage. CRT damage was demonstrated by (1) histological evaluation of olfactory neurogenesis, which suggested a reduction in CRT versus control, and (2) imaging analyses which showed that the majority of brain regions were reduced in volume by CRT. Specifically, two regions involved in social odor processing (amygdala and piriform cortex) were damaged by cranial irradiation in males but not females, paralleling olfactory recognition findings. |
format | Online Article Text |
id | pubmed-6084003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60840032018-08-16 Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy Perez, Emma C. Rodgers, Shaefali P. Inoue, Taeko Pedersen, Steen E. Leasure, J. Leigh Gaber, M. Waleed Front Behav Neurosci Neuroscience Although an effective treatment for pediatric brain tumors, cranial radiation therapy (CRT) damages surrounding healthy tissue, thereby disrupting brain development. Animal models of pediatric CRT have primarily relied on visual tasks to assess cognitive impairment. Moreover, there has been a lack of sex comparisons as most research on the cognitive effects of pediatric CRT does not include females. Therefore, we utilized olfaction, an ethologically relevant sensory modality, to assess cognitive impairment in an animal model of CRT that included both male and female mice. Specifically, we used the novel odor recognition (NOdorR) task with social odors to test recognition memory, a cognitive parameter that has been associated with olfactory neurogenesis, a form of cellular plasticity damaged by CRT. In addition to odor recognition memory, olfactory ability or discrimination of non-social and social odors were assessed both acutely and 3 months after CRT. Magnetic resonance imaging (MRI) and histology were performed after behavioral testing to assess long-term damage by CRT. Long-term but not acute radiation-induced impairment in odor recognition memory was observed, consistent with delayed onset of cognitive impairment in human patients. Males showed greater exploration of social odors than females, but general exploration was not affected by irradiation. However, irradiated males had impaired odor recognition memory in adulthood, compared to non-irradiated males (or simply male controls). Female olfactory recognition memory, in contrast, was dependent on estrus stage. CRT damage was demonstrated by (1) histological evaluation of olfactory neurogenesis, which suggested a reduction in CRT versus control, and (2) imaging analyses which showed that the majority of brain regions were reduced in volume by CRT. Specifically, two regions involved in social odor processing (amygdala and piriform cortex) were damaged by cranial irradiation in males but not females, paralleling olfactory recognition findings. Frontiers Media S.A. 2018-08-02 /pmc/articles/PMC6084003/ /pubmed/30116180 http://dx.doi.org/10.3389/fnbeh.2018.00158 Text en Copyright © 2018 Perez, Rodgers, Inoue, Pedersen, Leasure and Gaber. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Perez, Emma C. Rodgers, Shaefali P. Inoue, Taeko Pedersen, Steen E. Leasure, J. Leigh Gaber, M. Waleed Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy |
title | Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy |
title_full | Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy |
title_fullStr | Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy |
title_full_unstemmed | Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy |
title_short | Olfactory Memory Impairment Differs by Sex in a Rodent Model of Pediatric Radiotherapy |
title_sort | olfactory memory impairment differs by sex in a rodent model of pediatric radiotherapy |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6084003/ https://www.ncbi.nlm.nih.gov/pubmed/30116180 http://dx.doi.org/10.3389/fnbeh.2018.00158 |
work_keys_str_mv | AT perezemmac olfactorymemoryimpairmentdiffersbysexinarodentmodelofpediatricradiotherapy AT rodgersshaefalip olfactorymemoryimpairmentdiffersbysexinarodentmodelofpediatricradiotherapy AT inouetaeko olfactorymemoryimpairmentdiffersbysexinarodentmodelofpediatricradiotherapy AT pedersensteene olfactorymemoryimpairmentdiffersbysexinarodentmodelofpediatricradiotherapy AT leasurejleigh olfactorymemoryimpairmentdiffersbysexinarodentmodelofpediatricradiotherapy AT gabermwaleed olfactorymemoryimpairmentdiffersbysexinarodentmodelofpediatricradiotherapy |