Charith Horadagoda, Christopher Lambeth, Kristina Kairaitis, Terence Amis
{"title":"胸骨舌骨肌功能的肺体积调节:麻醉大鼠模型。","authors":"Charith Horadagoda, Christopher Lambeth, Kristina Kairaitis, Terence Amis","doi":"10.1152/japplphysiol.00280.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Lung volume change modifies pharyngeal airway patency by altering breathing-related passive force transmission between lower and upper airways (via tracheal and other connections). We hypothesise that such force transmission may also impact active upper airway dilator muscle function by altering resting muscle length. The aim of this study was to determine the relationship between end expiratory lung volume (EELV) and ability of sternohyoid muscle (SH) contraction to alter pharyngeal airway patency. Eleven supine, anesthetized, spontaneously breathing Wistar rats with sealed snout mask to monitor airflow (<i>̇</i>) and mask pressure (P<sub>M</sub>) were positioned in head-out plethysmograph (P<sub>BOX</sub>). Graded changes in P<sub>BOX</sub> (±8cmH<sub>2</sub>O) were applied, tracheal pressure (P<sub>tr</sub>), SH length (SHL) and tension (SHT<sub>P</sub>) were monitored. Change in EELV (ΔEELV) and upper-airway resistance (R<sub>UA</sub>-Passive) (%baseline) were calculated. Electrical stimulation of SH at each P<sub>BOX</sub> was performed, and changes in SH tension (SHT<sub>A</sub>) and R<sub>UA</sub> (ΔR<sub>UA</sub>= R<sub>UA</sub>-Passive - R<sub>UA</sub>-Active) calculated. Data were analysed using mixed-effects models. Increasing EELV increased SHL by 0.062 mm/ml (0.037 - 0.086) [mean(95%CI)], increased SHT<sub>P</sub> by 5.42 mN/ml (3.96 - 6.87), and decreased R<sub>UA</sub>-Passive by 4%/ml (1.1 - 7.4), while decreasing EELV decreased SHL by 0.31 mm/ml (0.14 - 0.49), SHT<sub>P</sub> by 17.8 mN/ml (11.7 - 23.9), and increased R<sub>UA</sub>-Passive by 132%/ml (95.6 - 168.3). Increasing EELV decreased SHT<sub>A</sub> by 19.7%/ml (10.6 - 28.8) and ΔR<sub>UA</sub> by 60.1%/ml (27.1 - 93.1), while decreasing EELV also decreased both SHT<sub>A</sub>, by 57.5%/ml (31.4 - 84.2) and ΔR<sub>UA</sub> by 139.0%/ml (46.8 - 231.2), (all p<0.05). Maximal SHT<sub>A</sub> and ΔR<sub>UA</sub> occurred at baseline EELV. We conclude that while shifts in EELV impact passive upper airway function, they also negatively impact active SH pharyngeal dilator function, potentially via generation of a sub-optimal resting SHL.</p>","PeriodicalId":15160,"journal":{"name":"Journal of applied physiology","volume":" ","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lung Volume Modulation of Sternohyoid Muscle Function: An Anesthetised Rat Model.\",\"authors\":\"Charith Horadagoda, Christopher Lambeth, Kristina Kairaitis, Terence Amis\",\"doi\":\"10.1152/japplphysiol.00280.2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Lung volume change modifies pharyngeal airway patency by altering breathing-related passive force transmission between lower and upper airways (via tracheal and other connections). We hypothesise that such force transmission may also impact active upper airway dilator muscle function by altering resting muscle length. The aim of this study was to determine the relationship between end expiratory lung volume (EELV) and ability of sternohyoid muscle (SH) contraction to alter pharyngeal airway patency. Eleven supine, anesthetized, spontaneously breathing Wistar rats with sealed snout mask to monitor airflow (<i>̇</i>) and mask pressure (P<sub>M</sub>) were positioned in head-out plethysmograph (P<sub>BOX</sub>). Graded changes in P<sub>BOX</sub> (±8cmH<sub>2</sub>O) were applied, tracheal pressure (P<sub>tr</sub>), SH length (SHL) and tension (SHT<sub>P</sub>) were monitored. Change in EELV (ΔEELV) and upper-airway resistance (R<sub>UA</sub>-Passive) (%baseline) were calculated. Electrical stimulation of SH at each P<sub>BOX</sub> was performed, and changes in SH tension (SHT<sub>A</sub>) and R<sub>UA</sub> (ΔR<sub>UA</sub>= R<sub>UA</sub>-Passive - R<sub>UA</sub>-Active) calculated. Data were analysed using mixed-effects models. Increasing EELV increased SHL by 0.062 mm/ml (0.037 - 0.086) [mean(95%CI)], increased SHT<sub>P</sub> by 5.42 mN/ml (3.96 - 6.87), and decreased R<sub>UA</sub>-Passive by 4%/ml (1.1 - 7.4), while decreasing EELV decreased SHL by 0.31 mm/ml (0.14 - 0.49), SHT<sub>P</sub> by 17.8 mN/ml (11.7 - 23.9), and increased R<sub>UA</sub>-Passive by 132%/ml (95.6 - 168.3). Increasing EELV decreased SHT<sub>A</sub> by 19.7%/ml (10.6 - 28.8) and ΔR<sub>UA</sub> by 60.1%/ml (27.1 - 93.1), while decreasing EELV also decreased both SHT<sub>A</sub>, by 57.5%/ml (31.4 - 84.2) and ΔR<sub>UA</sub> by 139.0%/ml (46.8 - 231.2), (all p<0.05). Maximal SHT<sub>A</sub> and ΔR<sub>UA</sub> occurred at baseline EELV. We conclude that while shifts in EELV impact passive upper airway function, they also negatively impact active SH pharyngeal dilator function, potentially via generation of a sub-optimal resting SHL.</p>\",\"PeriodicalId\":15160,\"journal\":{\"name\":\"Journal of applied physiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of applied physiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1152/japplphysiol.00280.2025\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHYSIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of applied physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/japplphysiol.00280.2025","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
Lung Volume Modulation of Sternohyoid Muscle Function: An Anesthetised Rat Model.
Lung volume change modifies pharyngeal airway patency by altering breathing-related passive force transmission between lower and upper airways (via tracheal and other connections). We hypothesise that such force transmission may also impact active upper airway dilator muscle function by altering resting muscle length. The aim of this study was to determine the relationship between end expiratory lung volume (EELV) and ability of sternohyoid muscle (SH) contraction to alter pharyngeal airway patency. Eleven supine, anesthetized, spontaneously breathing Wistar rats with sealed snout mask to monitor airflow (̇) and mask pressure (PM) were positioned in head-out plethysmograph (PBOX). Graded changes in PBOX (±8cmH2O) were applied, tracheal pressure (Ptr), SH length (SHL) and tension (SHTP) were monitored. Change in EELV (ΔEELV) and upper-airway resistance (RUA-Passive) (%baseline) were calculated. Electrical stimulation of SH at each PBOX was performed, and changes in SH tension (SHTA) and RUA (ΔRUA= RUA-Passive - RUA-Active) calculated. Data were analysed using mixed-effects models. Increasing EELV increased SHL by 0.062 mm/ml (0.037 - 0.086) [mean(95%CI)], increased SHTP by 5.42 mN/ml (3.96 - 6.87), and decreased RUA-Passive by 4%/ml (1.1 - 7.4), while decreasing EELV decreased SHL by 0.31 mm/ml (0.14 - 0.49), SHTP by 17.8 mN/ml (11.7 - 23.9), and increased RUA-Passive by 132%/ml (95.6 - 168.3). Increasing EELV decreased SHTA by 19.7%/ml (10.6 - 28.8) and ΔRUA by 60.1%/ml (27.1 - 93.1), while decreasing EELV also decreased both SHTA, by 57.5%/ml (31.4 - 84.2) and ΔRUA by 139.0%/ml (46.8 - 231.2), (all p<0.05). Maximal SHTA and ΔRUA occurred at baseline EELV. We conclude that while shifts in EELV impact passive upper airway function, they also negatively impact active SH pharyngeal dilator function, potentially via generation of a sub-optimal resting SHL.
期刊介绍:
The Journal of Applied Physiology publishes the highest quality original research and reviews that examine novel adaptive and integrative physiological mechanisms in humans and animals that advance the field. The journal encourages the submission of manuscripts that examine the acute and adaptive responses of various organs, tissues, cells and/or molecular pathways to environmental, physiological and/or pathophysiological stressors. As an applied physiology journal, topics of interest are not limited to a particular organ system. The journal, therefore, considers a wide array of integrative and translational research topics examining the mechanisms involved in disease processes and mitigation strategies, as well as the promotion of health and well-being throughout the lifespan. Priority is given to manuscripts that provide mechanistic insight deemed to exert an impact on the field.