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本文引用的文献

1
A mathematical model of the urine concentrating mechanism in the rat renal medulla. I. Formulation and base-case results.大鼠肾髓质尿液浓缩机制的数学模型。一、公式推导和基础案例结果。
Am J Physiol Renal Physiol. 2011 Feb;300(2):F356-71. doi: 10.1152/ajprenal.00203.2010. Epub 2010 Nov 10.
2
Urine concentrating mechanism in the inner medulla of the mammalian kidney: role of three-dimensional architecture.哺乳动物肾脏髓质中的尿液浓缩机制:三维结构的作用。
Acta Physiol (Oxf). 2011 Jul;202(3):361-78. doi: 10.1111/j.1748-1716.2010.02214.x. Epub 2010 Dec 7.
3
Two-compartment model of inner medullary vasculature supports dual modes of vasopressin-regulated inner medullary blood flow.双室模型的内髓血管支持血管加压素调节内髓血流的两种模式。
Am J Physiol Renal Physiol. 2010 Jul;299(1):F273-9. doi: 10.1152/ajprenal.00072.2010. Epub 2010 Apr 14.
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Architecture of inner medullary descending and ascending vasa recta: pathways for countercurrent exchange.内髓降、升直小血管的结构:逆流交换的途径。
Am J Physiol Renal Physiol. 2010 Jul;299(1):F265-72. doi: 10.1152/ajprenal.00071.2010. Epub 2010 Apr 14.
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The mammalian urine concentrating mechanism: hypotheses and uncertainties.哺乳动物尿液浓缩机制:假说与不确定性。
Physiology (Bethesda). 2009 Aug;24:250-6. doi: 10.1152/physiol.00013.2009.
6
Role of three-dimensional architecture in the urine concentrating mechanism of the rat renal inner medulla.三维结构在大鼠肾内髓质尿液浓缩机制中的作用。
Am J Physiol Renal Physiol. 2008 Nov;295(5):F1271-85. doi: 10.1152/ajprenal.90252.2008. Epub 2008 May 21.
7
Quantitative analysis of functional reconstructions reveals lateral and axial zonation in the renal inner medulla.功能重建的定量分析揭示了肾内髓质的横向和轴向分区。
Am J Physiol Renal Physiol. 2008 Jun;294(6):F1306-14. doi: 10.1152/ajprenal.00068.2008. Epub 2008 Apr 16.
8
Three-dimensional architecture of collecting ducts, loops of Henle, and blood vessels in the renal papilla.肾乳头中集合管、髓袢和血管的三维结构。
Am J Physiol Renal Physiol. 2007 Sep;293(3):F696-704. doi: 10.1152/ajprenal.00231.2007. Epub 2007 Jul 3.
9
Three-dimensional architecture of inner medullary vasa recta.髓质内直小血管的三维结构
Am J Physiol Renal Physiol. 2006 Jun;290(6):F1355-66. doi: 10.1152/ajprenal.00481.2005. Epub 2005 Dec 27.
10
A region-based mathematical model of the urine concentrating mechanism in the rat outer medulla. I. Formulation and base-case results.大鼠外髓质尿液浓缩机制的基于区域的数学模型。I. 公式推导与基础案例结果。
Am J Physiol Renal Physiol. 2005 Dec;289(6):F1346-66. doi: 10.1152/ajprenal.00346.2003. Epub 2005 May 24.

孤立的间质节段间腔可能有利于溶质和液体在大鼠肾髓质中的优先混合。

Isolated interstitial nodal spaces may facilitate preferential solute and fluid mixing in the rat renal inner medulla.

机构信息

Dept. of Mathematics, Duke University, Durham, NC 27708-0320, USA.

出版信息

Am J Physiol Renal Physiol. 2012 Apr 1;302(7):F830-9. doi: 10.1152/ajprenal.00539.2011. Epub 2011 Dec 7.

DOI:10.1152/ajprenal.00539.2011
PMID:22160770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3346697/
Abstract

Recent anatomic findings indicate that in the upper inner medulla of the rodent kidney, tubules, and vessels are organized around clusters of collecting ducts (CDs). Within CD clusters, CDs and some of the ascending vasa recta (AVR) and ascending thin limbs (ATLs), when viewed in transverse sections, form interstitial nodal spaces, which are arrayed at structured intervals throughout the inner medulla. These spaces, or microdomains, are bordered on one side by a single CD, on the opposite side by one or more ATLs, and on the other two sides by AVR. To study the interactions among these CDs, ATLs, and AVR, we have developed a mathematical compartment model, which simulates steady-state solute exchange through the microdomain at a given inner medullary level. Fluid in all compartments contains Na(+), Cl(-), urea and, in the microdomain, negative fixed charges that represent macromolecules (e.g., hyaluronan) balanced by Na(+). Fluid entry into AVR is assumed to be driven by hydraulic and oncotic pressures. Model results suggest that the isolated microdomains facilitate solute and fluid mixing among the CDs, ATLs, and AVR, promote water withdrawal from CDs, and consequently may play an important role in generating the inner medullary osmotic gradient.

摘要

最近的解剖学发现表明,在啮齿动物肾脏的内髓内层,肾小管和血管围绕着集合管(CD)簇组织。在 CD 簇内,CD 以及一些升支直小血管(AVR)和升支细段(ATL),在横切面上观察时,形成了间质节结空间,这些空间在整个内髓以有序的间隔排列。这些空间或微域,一侧由单个 CD 围成,另一侧由一个或多个 ATL 围成,另外两侧由 AVR 围成。为了研究这些 CD、ATL 和 AVR 之间的相互作用,我们开发了一个数学室模型,该模型模拟了给定内髓水平下通过微域的溶质稳态交换。所有室中的流体都含有 Na(+)、Cl(-)、尿素,并且在微域中,代表大分子(例如透明质酸)的负固定电荷由 Na(+)平衡。假定 AVR 中的流体进入是由液压和渗透压力驱动的。模型结果表明,孤立的微域促进了 CD、ATL 和 AVR 之间的溶质和流体混合,促进了 CD 中的水分提取,因此可能在内髓渗透梯度的产生中发挥重要作用。