Cardiovascular Disease Program, Biomedicine Discovery Institute and Department of Physiology, Monash University, Melbourne, Victoria, Australia.
Faculty of Engineering and Mathematical Sciences, The University of Western Australia, Perth, Western Australia, Australia.
Anat Rec (Hoboken). 2020 Oct;303(10):2544-2552. doi: 10.1002/ar.24260. Epub 2019 Sep 30.
Per gram of tissue, the kidneys are among our most highly perfused organs. Yet the renal cortex and, in particular, the renal medulla are susceptible to hypoxia. In turn, hypoxia is a major pathophysiological feature of both acute kidney injury and chronic kidney disease. We identify seven factors that render the kidney susceptible to hypoxia: (1) the large metabolic demand imposed by active reabsorption of sodium; (2) limitations on oxygen delivery to cortical tissue imposed by the density of peritubular capillaries; (3) the poor capacity for angiogenesis in the adult kidney; (4) the limited ability of the renal vasculature to dilate in response to hypoxia; (5) diffusive oxygen shunting between arteries and veins in the cortex and descending and ascending vasa recta in the medulla; (6) the physiological requirement for low medullary blood flow to facilitate urinary concentration; and (7) the topography of vascular-tubular arrangements in the outer medulla that limit oxygen delivery to the thick ascending limb of Henle's loop. Recent collaborative efforts between anatomists, physiologists, and mathematicians have improved our understanding of the roles of these factors in both physiological regulation of intrarenal oxygenation and development of renal hypoxia under pathophysiological conditions. We are also better able to understand these apparent maladaptations in the context of evolution. That is, they can be explained by the combined effects of historical contingency (our ancestral life in the sea) and selection pressures imposed by the multiple functions of the kidney to regulate extracellular fluid volume, retain water, and control erythrocyte production.
就每克组织而言,肾脏是我们灌注最充分的器官之一。然而,肾脏皮质,尤其是肾脏髓质,容易发生缺氧。反过来,缺氧是急性肾损伤和慢性肾脏病的主要病理生理特征。我们确定了使肾脏容易发生缺氧的七个因素:(1)主动重吸收钠所带来的巨大代谢需求;(2)肾小管周围毛细血管密度对皮质组织供氧的限制;(3)成年肾脏中血管生成能力有限;(4)肾脏血管对缺氧反应的扩张能力有限;(5)皮质中动脉和静脉之间以及髓质中降支和升支直血管之间的弥散性氧分流;(6)低髓质血流以促进尿液浓缩的生理需求;(7)外髓血管-小管排列的地形学限制了对 Henle 袢升支粗段的氧输送。解剖学家、生理学家和数学家之间的最近合作努力提高了我们对这些因素在肾内氧合的生理调节以及病理生理条件下肾脏缺氧发展中的作用的理解。我们也能够更好地理解这些在进化背景下的明显适应不良。也就是说,它们可以通过历史偶然性(我们祖先在海洋中的生活)的综合影响以及肾脏的多种功能所施加的选择压力来解释,这些功能包括调节细胞外液量、保留水分和控制红细胞生成。