Wout J Claassen, Myrte Wennen, Diana Jansen, Annemijn H Jonkman, J Tim Marcus, Gustav J Strijkers, Bram F Coolen, Coen A C Ottenheijm, Leo M A Heunks
{"title":"Species-specific effects of positive end-expiratory pressure on diaphragm and chest wall geometry in mice, rats, and humans.","authors":"Wout J Claassen, Myrte Wennen, Diana Jansen, Annemijn H Jonkman, J Tim Marcus, Gustav J Strijkers, Bram F Coolen, Coen A C Ottenheijm, Leo M A Heunks","doi":"10.1152/ajpregu.00258.2025","DOIUrl":null,"url":null,"abstract":"<p><p>In critically ill mechanically ventilated patients, positive end-expiratory pressure (PEEP) is applied to limit alveolar collapse. However, PEEP will also affect diaphragm geometry and function. Various animal models are used to study the effects of mechanical ventilation on the diaphragm, but chest wall mechanics may influence diaphragm responses to PEEP. We hypothesized that interspecies differences are relevant when studying the effect of PEEP on diaphragm geometry during mechanical ventilation. Specifically, the chest wall compliance, which varies among species, may be an important determinant of the effect of PEEP on diaphragm geometry and function. This is relevant in future studies into diaphragm adaptations during PEEP and particularly in genetically engineered animal models. Using magnetic resonance imaging (MRI), we studied the effect of PEEP on diaphragm surface and thorax geometry in ventilated mice, rats, and healthy volunteers. PEEP reduced diaphragm surface in mice, rats, and humans, but the effect was smaller in mice compared with rats. This difference was not attributable to disparities in lung compliance or chest wall compliance. Compared with healthy volunteers, rats showed a larger decrease in diaphragm surface due to greater caudal displacement, whereas mice showed a similar decrease in diaphragm surface, but with more thoracic widening. These findings indicate that the effect of PEEP on diaphragm geometry is influenced by chest wall movement and varies across species. These findings are critical for interpreting diaphragm adaptations to mechanical ventilation in both animal models and patients.<b>NEW & NOTEWORTHY</b> Positive end-expiratory pressure, a parameter used to control end-expiratory lung volume in mechanical ventilation, has a smaller effect on diaphragm surface area in mice compared with rats. Compared with healthy volunteers, rats have a larger relative decrease in diaphragm surface area due to more caudal displacement, whereas mice have a similar decrease in diaphragm surface area, but have more widening of the thorax. Interspecies differences have to be taken into account in future (animal) research on the effects of mechanical ventilation on the diaphragm or interaction between lungs, chest wall, and diaphragm.</p>","PeriodicalId":7630,"journal":{"name":"American journal of physiology. Regulatory, integrative and comparative physiology","volume":" ","pages":"R571-R581"},"PeriodicalIF":2.6000,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13184903/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of physiology. Regulatory, integrative and comparative physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpregu.00258.2025","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/15 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
In critically ill mechanically ventilated patients, positive end-expiratory pressure (PEEP) is applied to limit alveolar collapse. However, PEEP will also affect diaphragm geometry and function. Various animal models are used to study the effects of mechanical ventilation on the diaphragm, but chest wall mechanics may influence diaphragm responses to PEEP. We hypothesized that interspecies differences are relevant when studying the effect of PEEP on diaphragm geometry during mechanical ventilation. Specifically, the chest wall compliance, which varies among species, may be an important determinant of the effect of PEEP on diaphragm geometry and function. This is relevant in future studies into diaphragm adaptations during PEEP and particularly in genetically engineered animal models. Using magnetic resonance imaging (MRI), we studied the effect of PEEP on diaphragm surface and thorax geometry in ventilated mice, rats, and healthy volunteers. PEEP reduced diaphragm surface in mice, rats, and humans, but the effect was smaller in mice compared with rats. This difference was not attributable to disparities in lung compliance or chest wall compliance. Compared with healthy volunteers, rats showed a larger decrease in diaphragm surface due to greater caudal displacement, whereas mice showed a similar decrease in diaphragm surface, but with more thoracic widening. These findings indicate that the effect of PEEP on diaphragm geometry is influenced by chest wall movement and varies across species. These findings are critical for interpreting diaphragm adaptations to mechanical ventilation in both animal models and patients.NEW & NOTEWORTHY Positive end-expiratory pressure, a parameter used to control end-expiratory lung volume in mechanical ventilation, has a smaller effect on diaphragm surface area in mice compared with rats. Compared with healthy volunteers, rats have a larger relative decrease in diaphragm surface area due to more caudal displacement, whereas mice have a similar decrease in diaphragm surface area, but have more widening of the thorax. Interspecies differences have to be taken into account in future (animal) research on the effects of mechanical ventilation on the diaphragm or interaction between lungs, chest wall, and diaphragm.
期刊介绍:
The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.