» Articles » PMID: 23908457

Urine-concentrating Mechanism in the Inner Medulla: Function of the Thin Limbs of the Loops of Henle

Overview
Specialty Nephrology
Date 2013 Aug 3
PMID 23908457
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Segment specific loss of NFAT5 function in the kidneys is sufficient to induce a global kidney injury like phenotype.

Engel K, Kulow V, Chernyakov D, Willscher E, Fahling M, Edemir B FASEB J. 2025; 39(2):e70352.

PMID: 39874047 PMC: 11774485. DOI: 10.1096/fj.202402497R.


The SLC6A18 Transporter Is Most Likely a Na-Dependent Glycine/Urea Antiporter Responsible for Urea Secretion in the Proximal Straight Tubule: Influence of This Urea Secretion on Glomerular Filtration Rate.

Bankir L, Crambert G, Vargas-Poussou R Nephron. 2024; 148(11-12):796-822.

PMID: 38824912 PMC: 11651341. DOI: 10.1159/000539602.


Proteomic analysis of murine kidney proximal tubule sub-segment derived cell lines reveals preferences in mitochondrial pathway activity.

Ferreira R, de Almeida R, Culp C, Witzmann F, Wang M, Kher R J Proteomics. 2023; 289:104998.

PMID: 37657718 PMC: 10843797. DOI: 10.1016/j.jprot.2023.104998.


(Zebra)fishing for nephrogenesis genes.

Chambers B, Weaver N, Lara C, Nguyen T, Wingert R Tissue Barriers. 2023; 12(2):2219605.

PMID: 37254823 PMC: 11042071. DOI: 10.1080/21688370.2023.2219605.


Rate thresholds in cell signaling have functional and phenotypic consequences in non-linear time-dependent environments.

Thiemicke A, Neuert G Front Cell Dev Biol. 2023; 11:1124874.

PMID: 37025183 PMC: 10072286. DOI: 10.3389/fcell.2023.1124874.


References
1.
Jen J, Stephenson J . Externally driven countercurrent multiplication in a mathematical model of the urinary concentrating mechanism of the renal inner medulla. Bull Math Biol. 1994; 56(3):491-514. DOI: 10.1007/BF02460468. View

2.
Pannabecker T . Loop of Henle interaction with interstitial nodal spaces in the renal inner medulla. Am J Physiol Renal Physiol. 2008; 295(6):F1744-51. PMC: 2604831. DOI: 10.1152/ajprenal.90483.2008. View

3.
Pannabecker T, Dantzler W, Layton H, Layton A . Role of three-dimensional architecture in the urine concentrating mechanism of the rat renal inner medulla. Am J Physiol Renal Physiol. 2008; 295(5):F1271-85. PMC: 2584911. DOI: 10.1152/ajprenal.90252.2008. View

4.
Takahashi-Iwanaga H . The three-dimensional cytoarchitecture of the interstitial tissue in the rat kidney. Cell Tissue Res. 1991; 264(2):269-81. DOI: 10.1007/BF00313964. View

5.
Chou C, Knepper M . In vitro perfusion of chinchilla thin limb segments: segmentation and osmotic water permeability. Am J Physiol. 1992; 263(3 Pt 2):F417-26. DOI: 10.1152/ajprenal.1992.263.3.F417. View