Courtney V Brown, J Chris McKnight, Anthony R Bain, Joshua C Tremblay, Alexander Patrician, Birgitte I McDonald, Cassondra L Williams, Allyson G Hindle, Logan J Pallin, Daniel P Costa, Zeljko Dujic, David B Macleod, Terrie M Williams, Paul J Ponganis, Philip N Ainslie
{"title":"人类自由潜水精英和北方象海豹(Mirounga angustirostris)对呼吸暂停的特定和共同血液学反应。","authors":"Courtney V Brown, J Chris McKnight, Anthony R Bain, Joshua C Tremblay, Alexander Patrician, Birgitte I McDonald, Cassondra L Williams, Allyson G Hindle, Logan J Pallin, Daniel P Costa, Zeljko Dujic, David B Macleod, Terrie M Williams, Paul J Ponganis, Philip N Ainslie","doi":"10.1152/ajpregu.00286.2023","DOIUrl":null,"url":null,"abstract":"<p><p>Despite elite human free divers achieving incredible feats in competitive free diving, there has yet to be a study that compares consummate divers, (i.e. northern elephant seals) to highly conditioned free divers (i.e., elite competitive free-diving humans). Herein, we compare these two diving models and suggest that hematological traits detected in seals reflect species-specific specializations, while hematological traits shared between the two species are fundamental mammalian characteristics. Arterial blood samples were analyzed in elite human free divers (<i>n</i> = 14) during a single, maximal volitional apnea and in juvenile northern elephant seals (<i>n</i> = 3) during rest-associated apnea. Humans and elephant seals had comparable apnea durations (∼6.5 min) and end-apneic arterial Po<sub>2</sub> [humans: 40.4 ± 3.0 mmHg (means ± SE); seals: 27.1 ± 5.9 mmHg; <i>P</i> = 0.2]. Despite similar increases in arterial Pco<sub>2</sub> (humans: 33 ± 5%; seals: 16.3 ± 5%; <i>P</i> = 0.2), only humans experienced reductions in pH from baseline (humans: 7.45 ± 0.01; seals: 7.39 ± 0.02) to end apnea (humans: 7.37 ± 0.01; seals: 7.38 ± 0.02; <i>P</i> < 0.0001). Hemoglobin P<sub>50</sub> was greater in humans compared to elephant seals (29.9 ± 1.5 and 28.7 ± 0.6 mmHg, respectively; <i>P</i> = 0.046). Elephant seals overall had higher carboxyhemoglobin (COHb) levels (5.9 ± 2.6%) compared to humans (0.8 ± 1.2%; <i>P</i> < 0.0001); however, following apnea, COHb was reduced in seals (baseline: 6.1 ± 0.3%; end apnea: 5.6 ± 0.3%) and was slightly elevated in humans (baseline: 0.7 ± 0.1%; end apnea: 0.9 ± 0.1%; <i>P</i> < 0.0002, both comparisons). Our data indicate that during static apnea, seals have reduced hemoglobin P<sub>50</sub>, greater pH buffering, and increased COHb levels. The differences in hemoglobin P<sub>50</sub> are likely due to the differences in the physiological environment between the two species during apnea, whereas enhanced pH buffering and higher COHb may represent traits selected for in elephant seals.<b>NEW & NOTEWORTHY</b> This study uses similar methods and protocols in elite human free divers and northern elephant seals. Using highly conditioned divers (elite free-diving humans) and highly adapted divers (northern elephant seals), we explored which hematological traits are fundamentally mammalian and which may have been selected for. We found differences in P<sub>50</sub>, which may be due to different physiological environments between species, while elevated pH buffering and carbon monoxide levels might have been selected for in seals.</p>","PeriodicalId":7630,"journal":{"name":"American journal of physiology. Regulatory, integrative and comparative physiology","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Selected and shared hematological responses to apnea in elite human free divers and northern elephant seals (<i>Mirounga angustirostris</i>).\",\"authors\":\"Courtney V Brown, J Chris McKnight, Anthony R Bain, Joshua C Tremblay, Alexander Patrician, Birgitte I McDonald, Cassondra L Williams, Allyson G Hindle, Logan J Pallin, Daniel P Costa, Zeljko Dujic, David B Macleod, Terrie M Williams, Paul J Ponganis, Philip N Ainslie\",\"doi\":\"10.1152/ajpregu.00286.2023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Despite elite human free divers achieving incredible feats in competitive free diving, there has yet to be a study that compares consummate divers, (i.e. northern elephant seals) to highly conditioned free divers (i.e., elite competitive free-diving humans). Herein, we compare these two diving models and suggest that hematological traits detected in seals reflect species-specific specializations, while hematological traits shared between the two species are fundamental mammalian characteristics. Arterial blood samples were analyzed in elite human free divers (<i>n</i> = 14) during a single, maximal volitional apnea and in juvenile northern elephant seals (<i>n</i> = 3) during rest-associated apnea. Humans and elephant seals had comparable apnea durations (∼6.5 min) and end-apneic arterial Po<sub>2</sub> [humans: 40.4 ± 3.0 mmHg (means ± SE); seals: 27.1 ± 5.9 mmHg; <i>P</i> = 0.2]. Despite similar increases in arterial Pco<sub>2</sub> (humans: 33 ± 5%; seals: 16.3 ± 5%; <i>P</i> = 0.2), only humans experienced reductions in pH from baseline (humans: 7.45 ± 0.01; seals: 7.39 ± 0.02) to end apnea (humans: 7.37 ± 0.01; seals: 7.38 ± 0.02; <i>P</i> < 0.0001). Hemoglobin P<sub>50</sub> was greater in humans compared to elephant seals (29.9 ± 1.5 and 28.7 ± 0.6 mmHg, respectively; <i>P</i> = 0.046). Elephant seals overall had higher carboxyhemoglobin (COHb) levels (5.9 ± 2.6%) compared to humans (0.8 ± 1.2%; <i>P</i> < 0.0001); however, following apnea, COHb was reduced in seals (baseline: 6.1 ± 0.3%; end apnea: 5.6 ± 0.3%) and was slightly elevated in humans (baseline: 0.7 ± 0.1%; end apnea: 0.9 ± 0.1%; <i>P</i> < 0.0002, both comparisons). Our data indicate that during static apnea, seals have reduced hemoglobin P<sub>50</sub>, greater pH buffering, and increased COHb levels. The differences in hemoglobin P<sub>50</sub> are likely due to the differences in the physiological environment between the two species during apnea, whereas enhanced pH buffering and higher COHb may represent traits selected for in elephant seals.<b>NEW & NOTEWORTHY</b> This study uses similar methods and protocols in elite human free divers and northern elephant seals. Using highly conditioned divers (elite free-diving humans) and highly adapted divers (northern elephant seals), we explored which hematological traits are fundamentally mammalian and which may have been selected for. We found differences in P<sub>50</sub>, which may be due to different physiological environments between species, while elevated pH buffering and carbon monoxide levels might have been selected for in seals.</p>\",\"PeriodicalId\":7630,\"journal\":{\"name\":\"American journal of physiology. 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Regulatory, integrative and comparative physiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/ajpregu.00286.2023","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/5/20 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
Selected and shared hematological responses to apnea in elite human free divers and northern elephant seals (Mirounga angustirostris).
Despite elite human free divers achieving incredible feats in competitive free diving, there has yet to be a study that compares consummate divers, (i.e. northern elephant seals) to highly conditioned free divers (i.e., elite competitive free-diving humans). Herein, we compare these two diving models and suggest that hematological traits detected in seals reflect species-specific specializations, while hematological traits shared between the two species are fundamental mammalian characteristics. Arterial blood samples were analyzed in elite human free divers (n = 14) during a single, maximal volitional apnea and in juvenile northern elephant seals (n = 3) during rest-associated apnea. Humans and elephant seals had comparable apnea durations (∼6.5 min) and end-apneic arterial Po2 [humans: 40.4 ± 3.0 mmHg (means ± SE); seals: 27.1 ± 5.9 mmHg; P = 0.2]. Despite similar increases in arterial Pco2 (humans: 33 ± 5%; seals: 16.3 ± 5%; P = 0.2), only humans experienced reductions in pH from baseline (humans: 7.45 ± 0.01; seals: 7.39 ± 0.02) to end apnea (humans: 7.37 ± 0.01; seals: 7.38 ± 0.02; P < 0.0001). Hemoglobin P50 was greater in humans compared to elephant seals (29.9 ± 1.5 and 28.7 ± 0.6 mmHg, respectively; P = 0.046). Elephant seals overall had higher carboxyhemoglobin (COHb) levels (5.9 ± 2.6%) compared to humans (0.8 ± 1.2%; P < 0.0001); however, following apnea, COHb was reduced in seals (baseline: 6.1 ± 0.3%; end apnea: 5.6 ± 0.3%) and was slightly elevated in humans (baseline: 0.7 ± 0.1%; end apnea: 0.9 ± 0.1%; P < 0.0002, both comparisons). Our data indicate that during static apnea, seals have reduced hemoglobin P50, greater pH buffering, and increased COHb levels. The differences in hemoglobin P50 are likely due to the differences in the physiological environment between the two species during apnea, whereas enhanced pH buffering and higher COHb may represent traits selected for in elephant seals.NEW & NOTEWORTHY This study uses similar methods and protocols in elite human free divers and northern elephant seals. Using highly conditioned divers (elite free-diving humans) and highly adapted divers (northern elephant seals), we explored which hematological traits are fundamentally mammalian and which may have been selected for. We found differences in P50, which may be due to different physiological environments between species, while elevated pH buffering and carbon monoxide levels might have been selected for in seals.
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.