模拟极端深海潜水员鹅喙鲸(Ziphius cavirostris)的不同代谢率和心输出量对估计组织和血液中O2和CO2水平的影响。

IF 2.8 4区 医学 Q2 PHYSIOLOGY
Andreas Fahlman, Gregory S Schorr, David A Sweeney, Brenda K Rone, Shannon N Coates, Austin S Allen, Lucia M Martín López, Susan M Jarvis, Erin A Falcone
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引用次数: 0

摘要

高分辨率的运动数据来自居维叶喙鲸或鹅喙鲸(Ziphius cavirostris,以下简称Ziphius, n = 8)标签部署(4.1-19.2天),用于估计血液和组织中的O2和CO2水平。利用加速度和磁力计数据,根据活动与氧气消耗率的关系估算运动成本(LC)。我们估计,潜水代谢率(DMR)随着潜水时间的增加而下降,在极短潜水(2分钟-1公斤-1)时为6.18 mL O2 min-1公斤-1,在中等潜水(17.5和≤33.3分钟)和长潜水(>33.3分钟)时分别为2.06 mL O2 min-1公斤-1。计算的有氧潜水极限(cADL)、平均行为ADL (bADL)和动态ADL (dADL)分别为62.4、61.3(44.3 ~ 75.4)和41.7 (2.0 ~ 102.5)min。尽管该模型假设了生理和代谢的调整,但在这些动物表现出的许多典型的长时间深潜中,肌肉中的氧气都耗尽了。基于模型结果,我们推测Ziphius的大部分觅食潜水是由其他代谢途径提供燃料的,例如磷酸肌酸或糖酵解。在觅食过程中,依靠这些替代的代谢途径可能需要很长的恢复期,包括主要的有氧潜水。扰乱这种正常的潜水模式可能会破坏这种正常的潜水模式,导致可能造成创伤的行为和生理变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modelling the effect of varying metabolic rate and cardiac output on estimated tissue and blood O2 and CO2 levels in an extreme deep-diver, the goose-beaked whale (Ziphius cavirostris).

High-resolution movement data from Cuvier's beaked, or goose-beaked whale (Ziphius cavirostris, hereafter Ziphius, n = 8) tag deployments (4.1-19.2 days) were used to estimate blood and tissue O2 and CO2 levels. Acceleration and magnetometry data were used to estimate the locomotion cost (LC) from the relationship between activity and the O2 consumption rate. We estimated that the diving metabolic rate (DMR) decreased with increasing dive duration, ranging from 6.18 mL O2 min-1 kg-1 for very short dives (<1.0 min) to 1.65 mL O2 min-1 kg-1 and 2.06 mL O2 min-1 kg-1 for intermediate (>17.5 and ≤33.3 min) and long dives (>33.3 min), respectively. The calculated aerobic dive limit (cADL), average behavioural ADL (bADL) and dynamic ADL (dADL) were 62.4, 61.3 (44.3-75.4) and 41.7 (2.0-102.5) min, respectively. Despite the physiological and metabolic adjustments assumed by the model, the muscle O2 ran out for many of the stereotypical long, deep dives exhibited by these animals. Based on the model results, we speculate that a large portion of the foraging dives in Ziphius are fuelled by alternative metabolic pathways, for example, phosphocreatine or glycolysis. A reliance on these alternative metabolic pathways during foraging may require long recovery periods, including primarily aerobic dives. Disturbing this normal dive pattern may disrupt this normal dive pattern, leading to behavioural and physiological changes that could cause trauma.

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来源期刊
Experimental Physiology
Experimental Physiology 医学-生理学
CiteScore
5.10
自引率
3.70%
发文量
262
审稿时长
1 months
期刊介绍: Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged. Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.
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