Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovary
Abstract Background Radiation exposure is known to cause accelerated aging and damage to the ovary, but the contribution of indirect versus direct effects is not well understood. We used the Small Animal Radiation Research Platform (SARRP) (Xstrahl) to deliver radiation to precise fields equivalent...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2018-08-01
|
Series: | Journal of Ovarian Research |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13048-018-0442-8 |
_version_ | 1797968073626484736 |
---|---|
author | Allison R. Grover Bruce F. Kimler Francesca E. Duncan |
author_facet | Allison R. Grover Bruce F. Kimler Francesca E. Duncan |
author_sort | Allison R. Grover |
collection | DOAJ |
description | Abstract Background Radiation exposure is known to cause accelerated aging and damage to the ovary, but the contribution of indirect versus direct effects is not well understood. We used the Small Animal Radiation Research Platform (SARRP) (Xstrahl) to deliver radiation to precise fields equivalent to clinical practice, allowing us to investigate systemic versus targeted damage in a structure as small as the mouse ovary. The X-ray dose was kept constant at 1 Gy, but the field varied. Mice either received total body irradiation (TBI), radiation targeted to both ovaries (T2), or radiation targeted to one ovary (left) while the contralateral ovary (right) was spared (T1). Sham mice, handled similarly to the other cohorts but not exposed to radiation, served as controls. Two weeks post-exposure, ovaries were harvested and analyzed histologically to identify and count follicles within each ovary. Results Radiation significantly reduced primordial follicles in the TBI and T2 cohorts compared to the Sham cohort. There were no significant differences between these two irradiated groups. These findings suggest that at 1 Gy, the extent of damage to the ovary caused by radiation is similar despite the different delivery methods. When investigating the T1 cohort, targeted ovaries showed a significant decrease in primordial and growing follicles compared to non-targeted contralateral ovaries. Conclusions These findings demonstrate that the SARRP is an effective strategy for delivering precise ionizing radiation to small organs such as mouse ovaries. Such tools will facilitate identifying the relative risks to ovarian function associated with different radiation fields as well as screening the efficacy of emerging fertoprotective agents. |
first_indexed | 2024-04-11T02:40:06Z |
format | Article |
id | doaj.art-7da47ddf16a04195a717e85aa65948cd |
institution | Directory Open Access Journal |
issn | 1757-2215 |
language | English |
last_indexed | 2024-04-11T02:40:06Z |
publishDate | 2018-08-01 |
publisher | BMC |
record_format | Article |
series | Journal of Ovarian Research |
spelling | doaj.art-7da47ddf16a04195a717e85aa65948cd2023-01-02T19:10:36ZengBMCJournal of Ovarian Research1757-22152018-08-0111111210.1186/s13048-018-0442-8Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovaryAllison R. Grover0Bruce F. Kimler1Francesca E. Duncan2Center for Reproductive Science, Northwestern UniversityDepartment of Radiation Oncology, Kansas University Medical CenterCenter for Reproductive Science, Northwestern UniversityAbstract Background Radiation exposure is known to cause accelerated aging and damage to the ovary, but the contribution of indirect versus direct effects is not well understood. We used the Small Animal Radiation Research Platform (SARRP) (Xstrahl) to deliver radiation to precise fields equivalent to clinical practice, allowing us to investigate systemic versus targeted damage in a structure as small as the mouse ovary. The X-ray dose was kept constant at 1 Gy, but the field varied. Mice either received total body irradiation (TBI), radiation targeted to both ovaries (T2), or radiation targeted to one ovary (left) while the contralateral ovary (right) was spared (T1). Sham mice, handled similarly to the other cohorts but not exposed to radiation, served as controls. Two weeks post-exposure, ovaries were harvested and analyzed histologically to identify and count follicles within each ovary. Results Radiation significantly reduced primordial follicles in the TBI and T2 cohorts compared to the Sham cohort. There were no significant differences between these two irradiated groups. These findings suggest that at 1 Gy, the extent of damage to the ovary caused by radiation is similar despite the different delivery methods. When investigating the T1 cohort, targeted ovaries showed a significant decrease in primordial and growing follicles compared to non-targeted contralateral ovaries. Conclusions These findings demonstrate that the SARRP is an effective strategy for delivering precise ionizing radiation to small organs such as mouse ovaries. Such tools will facilitate identifying the relative risks to ovarian function associated with different radiation fields as well as screening the efficacy of emerging fertoprotective agents.http://link.springer.com/article/10.1186/s13048-018-0442-8OvaryFollicleRadiationTotal body irradiationFertility preservationlatrogenic |
spellingShingle | Allison R. Grover Bruce F. Kimler Francesca E. Duncan Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovary Journal of Ovarian Research Ovary Follicle Radiation Total body irradiation Fertility preservation latrogenic |
title | Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovary |
title_full | Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovary |
title_fullStr | Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovary |
title_full_unstemmed | Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovary |
title_short | Use of a Small Animal Radiation Research Platform (SARRP) facilitates analysis of systemic versus targeted radiation effects in the mouse ovary |
title_sort | use of a small animal radiation research platform sarrp facilitates analysis of systemic versus targeted radiation effects in the mouse ovary |
topic | Ovary Follicle Radiation Total body irradiation Fertility preservation latrogenic |
url | http://link.springer.com/article/10.1186/s13048-018-0442-8 |
work_keys_str_mv | AT allisonrgrover useofasmallanimalradiationresearchplatformsarrpfacilitatesanalysisofsystemicversustargetedradiationeffectsinthemouseovary AT brucefkimler useofasmallanimalradiationresearchplatformsarrpfacilitatesanalysisofsystemicversustargetedradiationeffectsinthemouseovary AT francescaeduncan useofasmallanimalradiationresearchplatformsarrpfacilitatesanalysisofsystemicversustargetedradiationeffectsinthemouseovary |