Aleksander S Golub, William H Nugent, Roland N Pittman, Bjorn K Song
{"title":"Rest-to-work and work-to-rest transients of interstitial PO<sub>2</sub> in spinotrapezius muscle of young and old male rats.","authors":"Aleksander S Golub, William H Nugent, Roland N Pittman, Bjorn K Song","doi":"10.14814/phy2.70260","DOIUrl":null,"url":null,"abstract":"<p><p>Muscle function declines with age. Since the primary energy source for contraction is aerobic, this study investigated age-related changes in muscle oxygenation dynamics to: characterize PO<sub>2</sub> transients during rest-work transitions, identify age-specific differences in oxygen delivery/utilization balance, and examine the relationship between interstitial and arterial oxygen tension (PO<sub>2</sub>). Interstitial PO<sub>2</sub> was measured with a high-resolution stroboscopic phosphorescence quenching technique to map intra-contractile dynamics during changes in muscle activity-rest-to-work (RtW) and work-to-rest (WtR) in rats aged three (young) and 23 (old) months. RtW (τ<sub>w</sub>) and WtR (τ<sub>r</sub>) PO<sub>2</sub> transitions had lag periods and mono-exponential time constants. In young muscles, lag was 4 s, τ<sub>w</sub> = 9.0 ± 3.7 s, and τ<sub>r</sub> = 15.4 ± 3.9 s. For old, lag was also 4 s with increases to τ<sub>w</sub> = 15.9 ± 3.5 s and τ<sub>r</sub> = 41.4 ± 8.3 s. Resting PO<sub>2</sub>'s were higher for young than for old (66.7 ± 13.7 vs. 60.2 ± 13.0 mmHg; p < 0.05). Work reduced PO<sub>2</sub> with a greater effect on old (42.5 ± 14.0 vs. 28.3 ± 16.5 mmHg; p < 0.05). Intra-contractile measurements revealed a spike in PO<sub>2</sub> (11 mmHg amplitude for >200 ms), which was absent in old. Further, sustained exercise in young showed a rising trend in PO<sub>2</sub>, while old remained at nadir. The missing PO<sub>2</sub> spike in aged muscle contributes to reduced PO<sub>2</sub> during work and may explain age-related loss of endurance.</p>","PeriodicalId":20083,"journal":{"name":"Physiological Reports","volume":"13 5","pages":"e70260"},"PeriodicalIF":2.2000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11867932/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14814/phy2.70260","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Muscle function declines with age. Since the primary energy source for contraction is aerobic, this study investigated age-related changes in muscle oxygenation dynamics to: characterize PO2 transients during rest-work transitions, identify age-specific differences in oxygen delivery/utilization balance, and examine the relationship between interstitial and arterial oxygen tension (PO2). Interstitial PO2 was measured with a high-resolution stroboscopic phosphorescence quenching technique to map intra-contractile dynamics during changes in muscle activity-rest-to-work (RtW) and work-to-rest (WtR) in rats aged three (young) and 23 (old) months. RtW (τw) and WtR (τr) PO2 transitions had lag periods and mono-exponential time constants. In young muscles, lag was 4 s, τw = 9.0 ± 3.7 s, and τr = 15.4 ± 3.9 s. For old, lag was also 4 s with increases to τw = 15.9 ± 3.5 s and τr = 41.4 ± 8.3 s. Resting PO2's were higher for young than for old (66.7 ± 13.7 vs. 60.2 ± 13.0 mmHg; p < 0.05). Work reduced PO2 with a greater effect on old (42.5 ± 14.0 vs. 28.3 ± 16.5 mmHg; p < 0.05). Intra-contractile measurements revealed a spike in PO2 (11 mmHg amplitude for >200 ms), which was absent in old. Further, sustained exercise in young showed a rising trend in PO2, while old remained at nadir. The missing PO2 spike in aged muscle contributes to reduced PO2 during work and may explain age-related loss of endurance.
期刊介绍:
Physiological Reports is an online only, open access journal that will publish peer reviewed research across all areas of basic, translational, and clinical physiology and allied disciplines. Physiological Reports is a collaboration between The Physiological Society and the American Physiological Society, and is therefore in a unique position to serve the international physiology community through quick time to publication while upholding a quality standard of sound research that constitutes a useful contribution to the field.