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。

IF 2.2 3区 医学 Q3 PHYSIOLOGY
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
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引用次数: 0

摘要

尽管人类精英自由潜水员在竞技自由潜水中取得了令人难以置信的成就,但还没有一项研究将精湛的潜水员(即北方象海豹)与高度适应性自由潜水员(即精英竞技自由潜水员)进行比较。在此,我们对这两种潜水模式进行了比较,并认为在海豹身上发现的血液特征反映了物种的特异性,而这两种物种共有的血液特征则是哺乳动物的基本特征。我们分析了人类精英自由潜水员(14 人)在单次最大自主呼吸暂停时的动脉血样本,以及幼年北方象海豹(3 人)在休息相关呼吸暂停时的动脉血样本。人类和象海豹的呼吸暂停持续时间(约 6.5 分钟)和呼吸暂停末期动脉血 PO2 值相当(人类:40.4±3.0mmHg;象海豹:40.4±3.0mmHg):40.4±3.0mmHg(平均值±SE),海豹:27.1±5.9mmHg;P=0.2)。尽管动脉 PCO2 有类似的增加(人类:33±5%,海豹:16.3±5%;P=0.2),但只有人类的 pH 值从基线(人类:7.45±0.01,海豹:7.39±0.02)下降到呼吸暂停结束(人类:7.37±0.01,海豹:7.38±0.02;P=0.2):与海象相比,人类的 p50 更大(分别为 29.9±1.5 和 28.7±0.6mmHg;p=0.046)。象海豹的 COHb 水平(5.9±2.6%)总体高于人类(0.8±1.2%;p50,pH 缓冲作用更大,COHb 水平更高)。血红蛋白 P50 的差异可能是由于两个物种在呼吸暂停时的生理环境不同造成的,而 pH 缓冲作用的增强和 COHb 的升高可能是象海豹被选择的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
CiteScore
5.30
自引率
3.60%
发文量
145
审稿时长
2 months
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.
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