Entropy generation and water conservation in the mammalian nephron.

IF 1.7 3区 生物学 Q4 PHYSIOLOGY Journal of Comparative Physiology B-Biochemical Systems and Environmental Physiology Pub Date : 2025-02-01 Epub Date: 2025-01-03 DOI:10.1007/s00360-024-01599-5
Pedro Goes Nogueira-de-Sá, José Eduardo Pereira Wilken Bicudo, José Guilherme Chaui-Berlinck
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Abstract

During the transition from fresh waters to terrestrial habitats, significant adaptive changes occurred in kidney function of vertebrates to cope with varying osmotic challenges. We investigated the mechanisms driving water conservation in the mammalian nephron, focusing on the relative contributions of active ion transport and Starling forces. We constructed a thermodynamic model to estimate the entropy generation associated with different processes within the nephron, and analyzed their relative importance in urine formation. We demonstrate that active ionic reabsorption exerts a pressure above 15,000 torr, a value more than 500 times greater than Starling forces. The entropy generation of the reabsorption process is found to be 20-fold higher than that of renal blood perfusion. These findings imply that the evolutionary history of vertebrates, particularly terrestrial mammals, has shaped the renal architecture to prioritize water conservation by means of an entropically costly process. This approach to the nephron function provides insights into the physiological adaptations of terrestrial vertebrates to conserve water and sheds light on the intricate interplay between environmental conditions and evolutionary responses in renal physiology.

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哺乳动物肾元的熵产和水分保存。
在从淡水生境向陆地生境过渡的过程中,脊椎动物的肾脏功能发生了显著的适应性变化,以应对不同的渗透挑战。我们研究了哺乳动物肾元中驱动水分保持的机制,重点研究了活性离子输运和Starling力的相对贡献。我们建立了一个热力学模型来估计与肾元内不同过程相关的熵的产生,并分析了它们在尿液形成中的相对重要性。我们证明,活性离子重吸收施加的压力超过15,000托,比斯特林力大500倍以上。重吸收过程的熵产比肾血灌注过程的熵产高20倍。这些发现表明,脊椎动物,特别是陆生哺乳动物的进化史,通过一个熵代价高昂的过程,塑造了肾脏结构,使其优先考虑水资源保护。这种研究肾元功能的方法提供了对陆生脊椎动物保存水分的生理适应的见解,并揭示了肾脏生理学中环境条件和进化反应之间复杂的相互作用。
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来源期刊
CiteScore
3.90
自引率
0.00%
发文量
51
审稿时长
3.5 months
期刊介绍: The Journal of Comparative Physiology B publishes peer-reviewed original articles and reviews on the comparative physiology of invertebrate and vertebrate animals. Special emphasis is placed on integrative studies that elucidate mechanisms at the whole-animal, organ, tissue, cellular and/or molecular levels. Review papers report on the current state of knowledge in an area of comparative physiology, and directions in which future research is needed.
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