Artikel ; Online: Influence of age and sex on physical, cardiac electrical and functional alterations in progressive hyperoxia treatment: A time course study in a murine model.
2024 Band 191, Seite(n) 112435
Abstract: Oxygen supplementation is a widely used treatment for ICU patients. However, it can lead to hyperoxia, which in turn can result in oxidative stress, cardiac remodeling, and even mortality. This paper expands upon previous research conducted by our lab to ...
| Abstract | Oxygen supplementation is a widely used treatment for ICU patients. However, it can lead to hyperoxia, which in turn can result in oxidative stress, cardiac remodeling, and even mortality. This paper expands upon previous research conducted by our lab to establish time-dependent cardiac changes under hyperoxia. In this study, both young and aged mice (male and female) underwent 72 h of hyperoxia exposure and were monitored at 24-hour intervals for cardiac electrophysiological and functional parameters using ECG and electrocardiogram data. Our analysis showed that young male mice experienced significant weight loss as well as significant lung edema by 48 h. Although young male mice were highly susceptible to physical changes, they were resistant to early cardiac functional and electrophysiological changes compared to the other groups. Both young and aged female and aged males developed functional impairments by 24 h of hyperoxia exposure. Furthermore, sex and age differences were noted in the onset of electrophysiological changes. While some groups could resist early cardiac remodeling, our data suggests that 72 h of hyperoxia exposure is sufficient to induce significant cardiac remodeling across all age and sex groups. Our data establishes that time-dependent cardiac changes due to oxygen supplementation can have devastating consequences even with short exposure periods. These findings can aid in developing clinical practices for individuals admitted to the ICU by elucidating the impact of aging, sex, and length of stay under mechanical ventilation to limit hyperoxia-induced cardiac remodeling. |
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| Mesh-Begriff(e) | Animals ; Hyperoxia/physiopathology ; Female ; Male ; Disease Models, Animal ; Mice ; Mice, Inbred C57BL ; Sex Factors ; Electrocardiography ; Age Factors ; Aging/physiology ; Pulmonary Edema/physiopathology ; Oxygen Inhalation Therapy/methods ; Heart/physiopathology ; Heart/physiology ; Time Factors ; Ventricular Remodeling/physiology ; Oxidative Stress | |||||
| Sprache | Englisch | |||||
| Erscheinungsdatum | 2024-04-19 | |||||
| Erscheinungsland | England | |||||
| Dokumenttyp | Journal Article | |||||
| ZDB-ID | 390992-x | |||||
| ISSN | 1873-6815 ; 0531-5565 | |||||
| ISSN (online) | 1873-6815 | |||||
| ISSN | 0531-5565 | |||||
| DOI | 10.1016/j.exger.2024.112435 | |||||
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| Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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