Cargando…
The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice
Oxygen supplementation, although a cornerstone of emergency and cardiovascular medicine, often results in hyperoxia, a condition characterized by excessive tissue oxygen which results in adverse cardiac remodeling and subsequent injurious effects to physiological function. Cardiac remodeling is furt...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630164/ https://www.ncbi.nlm.nih.gov/pubmed/34845324 http://dx.doi.org/10.1038/s41598-021-02550-2 |
_version_ | 1784607341823393792 |
---|---|
author | Bojkovic, Katarina Rodgers, Jennifer Leigh Vichare, Riddhi Nandi, Asmita Mansour, Hussein Saleem, Faizan Abidin, Zain Ul Vanthenapalli, Sahit Cheng, Feng Panguluri, Siva Kumar |
author_facet | Bojkovic, Katarina Rodgers, Jennifer Leigh Vichare, Riddhi Nandi, Asmita Mansour, Hussein Saleem, Faizan Abidin, Zain Ul Vanthenapalli, Sahit Cheng, Feng Panguluri, Siva Kumar |
author_sort | Bojkovic, Katarina |
collection | PubMed |
description | Oxygen supplementation, although a cornerstone of emergency and cardiovascular medicine, often results in hyperoxia, a condition characterized by excessive tissue oxygen which results in adverse cardiac remodeling and subsequent injurious effects to physiological function. Cardiac remodeling is further influenced by various risk factors, including pre-existing conditions and sex. Thus, the purpose of this experiment was to investigate cardiac remodeling in Type I Diabetic (Akita) mice subjected to hyperoxic treatment. Overall, we demonstrated that Akita mice experience distinct challenges from wild type (WT) mice. Specifically, Akita males at both normoxia and hyperoxia showed significant decreases in body and heart weights, prolonged PR, QRS, and QTc intervals, and reduced %EF and %FS at normoxia compared to WT controls. Moreover, Akita males largely resemble female mice (both WT and Akita) with regards to the parameters studied. Finally, statistical analysis revealed hyperoxia to have the greatest influence on cardiac pathophysiology, followed by sex, and finally genotype. Taken together, our data suggest that Type I diabetic patients may have distinct cardiac pathophysiology under hyperoxia compared to uncomplicated patients, with males being at high risk. These findings can be used to enhance provision of care in ICU patients with Type I diabetes as a comorbid condition. |
format | Online Article Text |
id | pubmed-8630164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86301642021-12-01 The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice Bojkovic, Katarina Rodgers, Jennifer Leigh Vichare, Riddhi Nandi, Asmita Mansour, Hussein Saleem, Faizan Abidin, Zain Ul Vanthenapalli, Sahit Cheng, Feng Panguluri, Siva Kumar Sci Rep Article Oxygen supplementation, although a cornerstone of emergency and cardiovascular medicine, often results in hyperoxia, a condition characterized by excessive tissue oxygen which results in adverse cardiac remodeling and subsequent injurious effects to physiological function. Cardiac remodeling is further influenced by various risk factors, including pre-existing conditions and sex. Thus, the purpose of this experiment was to investigate cardiac remodeling in Type I Diabetic (Akita) mice subjected to hyperoxic treatment. Overall, we demonstrated that Akita mice experience distinct challenges from wild type (WT) mice. Specifically, Akita males at both normoxia and hyperoxia showed significant decreases in body and heart weights, prolonged PR, QRS, and QTc intervals, and reduced %EF and %FS at normoxia compared to WT controls. Moreover, Akita males largely resemble female mice (both WT and Akita) with regards to the parameters studied. Finally, statistical analysis revealed hyperoxia to have the greatest influence on cardiac pathophysiology, followed by sex, and finally genotype. Taken together, our data suggest that Type I diabetic patients may have distinct cardiac pathophysiology under hyperoxia compared to uncomplicated patients, with males being at high risk. These findings can be used to enhance provision of care in ICU patients with Type I diabetes as a comorbid condition. Nature Publishing Group UK 2021-11-29 /pmc/articles/PMC8630164/ /pubmed/34845324 http://dx.doi.org/10.1038/s41598-021-02550-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Bojkovic, Katarina Rodgers, Jennifer Leigh Vichare, Riddhi Nandi, Asmita Mansour, Hussein Saleem, Faizan Abidin, Zain Ul Vanthenapalli, Sahit Cheng, Feng Panguluri, Siva Kumar The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice |
title | The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice |
title_full | The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice |
title_fullStr | The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice |
title_full_unstemmed | The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice |
title_short | The implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice |
title_sort | implications of hyperoxia, type 1 diabetes and sex on cardiovascular physiology in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8630164/ https://www.ncbi.nlm.nih.gov/pubmed/34845324 http://dx.doi.org/10.1038/s41598-021-02550-2 |
work_keys_str_mv | AT bojkovickatarina theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT rodgersjenniferleigh theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT vichareriddhi theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT nandiasmita theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT mansourhussein theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT saleemfaizan theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT abidinzainul theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT vanthenapallisahit theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT chengfeng theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT pangulurisivakumar theimplicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT bojkovickatarina implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT rodgersjenniferleigh implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT vichareriddhi implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT nandiasmita implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT mansourhussein implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT saleemfaizan implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT abidinzainul implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT vanthenapallisahit implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT chengfeng implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice AT pangulurisivakumar implicationsofhyperoxiatype1diabetesandsexoncardiovascularphysiologyinmice |