{"title":"Effects of veno-arterial extracorporeal membrane oxygenation on skeletal muscle function and interstitial PO2 in contracting muscle of normal rats","authors":"Kazuki Hotta , Yutaka Fujii , Naoki Hitosugi , Ren Takamizawa , Tatsuro Inoue , Hajime Tamiya , Atsuhiro Tsubaki","doi":"10.1016/j.mvr.2025.104813","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>This study aimed to clarify the effects of veno-arterial extracorporeal membrane oxygenation (VA-ECMO) on skeletal muscle oxygen pressure and function in rats.</div></div><div><h3>Methods</h3><div>Male Sprague-Dawley rats (2–3 months old, <em>n</em> = 17) were randomized into control and VA-ECMO groups. All animals were anesthetized and mechanically ventilated. The VA-ECMO circuit was established by cannulating the right jugular vein and left carotid artery. Interstitial PO<sub>2</sub> in the tibialis anterior (TA) muscle was measured using a phosphorescence quenching technique during electrically induced muscle contractions. Muscle tension was analyzed to evaluate the rate of force development (RFD) and relaxation rate.</div></div><div><h3>Results</h3><div>Compared to controls, arterial oxygen pressure (PaO<sub>2</sub>) was significantly higher, while hemoglobin levels were significantly lower in the VA-ECMO group (both <em>p</em> < 0.01). Interstitial PO<sub>2</sub> was significantly reduced at rest and during contractions in the VA-ECMO group (both <em>p</em> < 0.01). Muscle relaxation was delayed, and peak tension was lower in the VA-ECMO group compared to controls (both p < 0.01).</div></div><div><h3>Conclusions</h3><div>VA-ECMO impairs skeletal muscle function and reduces interstitial PO2 in contracting muscles, effects that appear independent of hyperoxemia. These findings provide insight into the microcirculatory and functional consequences of VA-ECMO on skeletal muscle.</div></div>","PeriodicalId":18534,"journal":{"name":"Microvascular research","volume":"160 ","pages":"Article 104813"},"PeriodicalIF":2.9000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microvascular research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0026286225000329","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0
Abstract
Background
This study aimed to clarify the effects of veno-arterial extracorporeal membrane oxygenation (VA-ECMO) on skeletal muscle oxygen pressure and function in rats.
Methods
Male Sprague-Dawley rats (2–3 months old, n = 17) were randomized into control and VA-ECMO groups. All animals were anesthetized and mechanically ventilated. The VA-ECMO circuit was established by cannulating the right jugular vein and left carotid artery. Interstitial PO2 in the tibialis anterior (TA) muscle was measured using a phosphorescence quenching technique during electrically induced muscle contractions. Muscle tension was analyzed to evaluate the rate of force development (RFD) and relaxation rate.
Results
Compared to controls, arterial oxygen pressure (PaO2) was significantly higher, while hemoglobin levels were significantly lower in the VA-ECMO group (both p < 0.01). Interstitial PO2 was significantly reduced at rest and during contractions in the VA-ECMO group (both p < 0.01). Muscle relaxation was delayed, and peak tension was lower in the VA-ECMO group compared to controls (both p < 0.01).
Conclusions
VA-ECMO impairs skeletal muscle function and reduces interstitial PO2 in contracting muscles, effects that appear independent of hyperoxemia. These findings provide insight into the microcirculatory and functional consequences of VA-ECMO on skeletal muscle.
期刊介绍:
Microvascular Research is dedicated to the dissemination of fundamental information related to the microvascular field. Full-length articles presenting the results of original research and brief communications are featured.
Research Areas include:
• Angiogenesis
• Biochemistry
• Bioengineering
• Biomathematics
• Biophysics
• Cancer
• Circulatory homeostasis
• Comparative physiology
• Drug delivery
• Neuropharmacology
• Microvascular pathology
• Rheology
• Tissue Engineering.