Cargando…

Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure

The acute radiation syndrome is defined in large part by radiation injury in the hematopoietic and gastrointestinal (GI) systems. To identify new pathways involved in radiation-induced GI injury, this study assessed dose- and time-dependent changes in plasma metabolites in a nonhuman primate model o...

Descripción completa

Detalles Bibliográficos
Autores principales: Jun, Se-Ran, Boerma, Marjan, Udaondo, Zulema, Richardson, Sasha, Thrall, Karla D., Miousse, Isabelle R., Seng, John, Pathak, Rupak, Hauer-Jensen, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398377/
https://www.ncbi.nlm.nih.gov/pubmed/34436481
http://dx.doi.org/10.3390/metabo11080540
_version_ 1783744825053413376
author Jun, Se-Ran
Boerma, Marjan
Udaondo, Zulema
Richardson, Sasha
Thrall, Karla D.
Miousse, Isabelle R.
Seng, John
Pathak, Rupak
Hauer-Jensen, Martin
author_facet Jun, Se-Ran
Boerma, Marjan
Udaondo, Zulema
Richardson, Sasha
Thrall, Karla D.
Miousse, Isabelle R.
Seng, John
Pathak, Rupak
Hauer-Jensen, Martin
author_sort Jun, Se-Ran
collection PubMed
description The acute radiation syndrome is defined in large part by radiation injury in the hematopoietic and gastrointestinal (GI) systems. To identify new pathways involved in radiation-induced GI injury, this study assessed dose- and time-dependent changes in plasma metabolites in a nonhuman primate model of whole abdominal irradiation. Male and female adult Rhesus monkeys were exposed to 6 MV photons to the abdomen at doses ranging between 8 and 14 Gy. At time points from 1 to 60 days after irradiation, plasma samples were collected and subjected to untargeted metabolomics. With the limited sample size of females, different discovery times after irradiation between males and females were observed in metabolomics pattern. Detailed analyses are restricted to only males for the discovery power. Radiation caused an increase in fatty acid oxidation and circulating levels of corticosteroids which may be an indication of physiological stress, and amino acids, indicative of a cellular repair response. The largest changes were observed at days 9 and 10 post-irradiation, with most returning to baseline at day 30. In addition, dysregulated metabolites involved in amino acid pathways, which might indicate changes in the microbiome, were detected. In conclusion, abdominal irradiation in a nonhuman primate model caused a plasma metabolome profile indicative of GI injury. These results point to pathways that may be targeted for intervention or used as early indicators of GI radiation injury. Moreover, our results suggest that effects are sex-specific and that interventions may need to be tailored accordingly.
format Online
Article
Text
id pubmed-8398377
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-83983772021-08-29 Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure Jun, Se-Ran Boerma, Marjan Udaondo, Zulema Richardson, Sasha Thrall, Karla D. Miousse, Isabelle R. Seng, John Pathak, Rupak Hauer-Jensen, Martin Metabolites Article The acute radiation syndrome is defined in large part by radiation injury in the hematopoietic and gastrointestinal (GI) systems. To identify new pathways involved in radiation-induced GI injury, this study assessed dose- and time-dependent changes in plasma metabolites in a nonhuman primate model of whole abdominal irradiation. Male and female adult Rhesus monkeys were exposed to 6 MV photons to the abdomen at doses ranging between 8 and 14 Gy. At time points from 1 to 60 days after irradiation, plasma samples were collected and subjected to untargeted metabolomics. With the limited sample size of females, different discovery times after irradiation between males and females were observed in metabolomics pattern. Detailed analyses are restricted to only males for the discovery power. Radiation caused an increase in fatty acid oxidation and circulating levels of corticosteroids which may be an indication of physiological stress, and amino acids, indicative of a cellular repair response. The largest changes were observed at days 9 and 10 post-irradiation, with most returning to baseline at day 30. In addition, dysregulated metabolites involved in amino acid pathways, which might indicate changes in the microbiome, were detected. In conclusion, abdominal irradiation in a nonhuman primate model caused a plasma metabolome profile indicative of GI injury. These results point to pathways that may be targeted for intervention or used as early indicators of GI radiation injury. Moreover, our results suggest that effects are sex-specific and that interventions may need to be tailored accordingly. MDPI 2021-08-13 /pmc/articles/PMC8398377/ /pubmed/34436481 http://dx.doi.org/10.3390/metabo11080540 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jun, Se-Ran
Boerma, Marjan
Udaondo, Zulema
Richardson, Sasha
Thrall, Karla D.
Miousse, Isabelle R.
Seng, John
Pathak, Rupak
Hauer-Jensen, Martin
Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure
title Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure
title_full Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure
title_fullStr Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure
title_full_unstemmed Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure
title_short Plasma Metabolomics in a Nonhuman Primate Model of Abdominal Radiation Exposure
title_sort plasma metabolomics in a nonhuman primate model of abdominal radiation exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8398377/
https://www.ncbi.nlm.nih.gov/pubmed/34436481
http://dx.doi.org/10.3390/metabo11080540
work_keys_str_mv AT junseran plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT boermamarjan plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT udaondozulema plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT richardsonsasha plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT thrallkarlad plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT miousseisabeller plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT sengjohn plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT pathakrupak plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure
AT hauerjensenmartin plasmametabolomicsinanonhumanprimatemodelofabdominalradiationexposure