Embryonic and juvenile snakes (Natrix maura, Linnaeus 1758) compensate for high elevation hypoxia via shifts in cardiovascular physiology and metabolism

Jérémie Souchet, Alicia Josserand, Elodie Darnet, Hugo Le Chevalier, Audrey Trochet, Romain Bertrand, Olivier Calvez, Albert Martinez-Silvestre, Olivier Guillaume, Marc Mossoll-Torres, Gilles Pottier, Hervé Philippe, Fabien Aubret, Eric J. Gangloff
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Abstract

The colonization of novel environments requires a favorable response to conditions never, or rarely, encountered in recent evolutionary history. For example, populations colonizing upslope habitats must cope with lower atmospheric pressure at elevation, and thus reduced oxygen availability. The embryo stage in oviparous organisms is particularly susceptible, given its lack of mobility and limited gas exchange via diffusion through the eggshell and membranes. Especially little is known about responses of Lepidosaurian reptiles to reduced oxygen availability. To test the role of physiological plasticity during early development in response to high elevation hypoxia, we performed a transplant experiment with the viperine snake (Natrix maura, Linnaeus 1758). We maintained gravid females originating from low elevation populations (432 m above sea level [ASL]—normoxia) at both the elevation of origin and high elevation (2877 m ASL—extreme high elevation hypoxia; approximately 72% oxygen availability relative to sea level), then incubated egg clutches at both low and high elevation. Regardless of maternal exposure to hypoxia during gestation, embryos incubated at extreme high elevation exhibited altered developmental trajectories of cardiovascular function and metabolism across the incubation period, including a reduction in late-development egg mass. This physiological response may have contributed to the maintenance of similar incubation duration, hatching success, and hatchling body size compared to embryos incubated at low elevation. Nevertheless, after being maintained in hypoxia, juveniles exhibit reduced carbon dioxide production relative to oxygen consumption, suggesting altered energy pathways compared to juveniles maintained in normoxia. These findings highlight the role of physiological plasticity in maintaining rates of survival and fitness-relevant phenotypes in novel environments.

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胚胎蛇和幼蛇(Natrix maura,Linnaeus 1758)通过心血管生理和代谢的变化来补偿高海拔缺氧。
新环境的殖民化需要对近代进化史上从未或很少遇到的条件做出有利的反应。例如,定居在上坡栖息地的种群必须应对海拔较低的大气压力,从而减少氧气供应。卵生生物的胚胎阶段特别容易受到影响,因为它缺乏移动性,通过蛋壳和膜的扩散进行的气体交换有限。尤其是对鳞翅目爬行动物对氧气供应减少的反应知之甚少。为了测试生理可塑性在高海拔缺氧早期发育过程中的作用,我们用毒蛇(Natrix maura,Linnaeus 1758)进行了移植实验。我们保留了来自低海拔人群的妊娠雌性(432 海拔高度【ASL】-正常氧含量) m ASL极端高海拔缺氧;相对于海平面大约72%的氧气可用性),然后在低海拔和高海拔下孵化卵离合器。无论母体在妊娠期间是否暴露在缺氧环境中,在极高海拔条件下孵化的胚胎在整个孵化期内都表现出心血管功能和代谢的发育轨迹发生了变化,包括后期发育卵子数量的减少。这种生理反应可能有助于维持相似的孵化持续时间、孵化成功,与在低海拔条件下孵化的胚胎相比,孵化出的幼崽的体型。然而,在保持低氧状态后,相对于氧气消耗,青少年表现出二氧化碳产生减少,这表明与保持正常氧的青少年相比,能量途径发生了改变。这些发现强调了生理可塑性在新环境中维持生存率和适应度相关表型的作用。
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来源期刊
Journal of experimental zoology. Part A, Ecological and integrative physiology
Journal of experimental zoology. Part A, Ecological and integrative physiology Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
4.90
自引率
3.60%
发文量
0
期刊介绍: The Journal of Experimental Zoology – A publishes articles at the interface between Development, Physiology, Ecology and Evolution. Contributions that help to reveal how molecular, functional and ecological variation relate to one another are particularly welcome. The Journal publishes original research in the form of rapid communications or regular research articles, as well as perspectives and reviews on topics pertaining to the scope of the Journal. Acceptable articles are limited to studies on animals.
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