Dantzler William H, Layton Anita T, Layton Harold E, Pannabecker Thomas L
Department of Physiology, College of Medicine, University of Arizona, Tucson, Arizona; and
Department of Mathematics, Duke University, Durham, North Carolina.
Clin J Am Soc Nephrol. 2014 Oct 7;9(10):1781-9. doi: 10.2215/CJN.08750812. Epub 2013 Aug 1.
The ability of mammals to produce urine hyperosmotic to plasma requires the generation of a gradient of increasing osmolality along the medulla from the corticomedullary junction to the papilla tip. Countercurrent multiplication apparently establishes this gradient in the outer medulla, where there is substantial transepithelial reabsorption of NaCl from the water-impermeable thick ascending limbs of the loops of Henle. However, this process does not establish the much steeper osmotic gradient in the inner medulla, where there are no thick ascending limbs of the loops of Henle and the water-impermeable ascending thin limbs lack active transepithelial transport of NaCl or any other solute. The mechanism generating the osmotic gradient in the inner medulla remains an unsolved mystery, although it is generally considered to involve countercurrent flows in the tubules and vessels. A possible role for the three-dimensional interactions between these inner medullary tubules and vessels in the concentrating process is suggested by creation of physiologic models that depict the three-dimensional relationships of tubules and vessels and their solute and water permeabilities in rat kidneys and by creation of mathematical models based on biologic phenomena. The current mathematical model, which incorporates experimentally determined or estimated solute and water flows through clearly defined tubular and interstitial compartments, predicts a urine osmolality in good agreement with that observed in moderately antidiuretic rats. The current model provides substantially better predictions than previous models; however, the current model still fails to predict urine osmolalities of maximally concentrating rats.
哺乳动物产生比血浆渗透压更高的尿液的能力,需要沿着髓质从皮质髓质交界处到乳头尖端建立一个渗透压逐渐升高的梯度。逆流倍增显然在外髓质中建立了这个梯度,在那里,从髓袢的水不通透的厚升支有大量的NaCl跨上皮重吸收。然而,这个过程并没有在内髓质中建立起陡峭得多的渗透梯度,在内髓质中没有髓袢的厚升支,且水不通透的细升支缺乏NaCl或任何其他溶质的主动跨上皮转运。尽管一般认为内髓质中渗透梯度的产生机制涉及肾小管和血管中的逆流,但该机制仍是一个未解之谜。通过创建描绘大鼠肾脏中肾小管和血管的三维关系及其溶质和水通透性的生理模型,以及基于生物学现象创建数学模型,提示了这些内髓质肾小管和血管之间的三维相互作用在浓缩过程中的可能作用。当前的数学模型纳入了通过实验确定或估计的溶质和水流经明确界定的肾小管和间质区室的情况,预测的尿渗透压与在中度抗利尿大鼠中观察到的情况高度一致。当前模型的预测比以前的模型有了显著改善;然而,当前模型仍然无法预测最大浓缩大鼠的尿渗透压。