Mg transport in the deep loop of Henle was studied in 15 young rats (50-60 g) after acute systemic Mg loading (UFMg (ultrafilterable Mg) 4.77 meq/liter). Intratubular Mg was measured with a recently described fluorometric microtechnique. The mean values of the TF/P inulin and TF/UF Mg ratios were 3.32 +/- 0.13 and 4.25 +/- 0.17, respectively. The proportion of filtered Mg recovered in this part of the nephron was therefore 131.2 +/- 5.0%, indicating that an appreciable amount of Mg entered the lumen prior to the sites of puncture. A significant correlation between the TF/P inulin and TF/UF Mg ratios suggests that water reabsorption also contributes to the high concentration of Mg in the loop of Henle during systemic Mg loading. In another series of young rats (90-160 g), similarly loaded with MgCl2 (UFMg 5.81 meq/liter), Mg and inulin were measured in superficial proximal (PT) and distal tubules (DT). Punctures were paired at two sites of the same PT and DT. The Mg concentration increased progressively along the PT in such a way that 90.5% of the filtered load still remained in the late proximal loops. If superficial and deep proximal tubules behave in a similar manner, it may be concluded that the site of entry of Mg is located between the late accessible part of the PT and the bend of the loop of Henle. Only 58.0 +/- 3.0% of the filtered Mg was delivered to the DT, indicating that Mg is extensively reabsorbed in the ascending limb, despite systemic loading. The proportion of filtered Mg did not vary along the DT, indicating no net reabsorption.
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http://dx.doi.org/10.1152/ajplegacy.1975.229.6.1695 | DOI Listing |
Background: The thin descending limb (DTL) of the loop of Henle is crucial for urine concentration, as it facilitates passive water reabsorption. Despite its importance, little is known about how DTL cells form during kidney development. Single-cell RNA sequencing (scRNA-seq) studies have not definitively identified DTL cells in the developing mouse kidney.
View Article and Find Full Text PDFJ Am Soc Nephrol
January 2025
Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université Paris Cité, F-75006 Paris, France.
The renal tubule and collecting duct express a large number of proteins, all having putative immunoreactive motives. Therefore, all can be the target of pathogenic autoantibodies. However, autoimmune tubulopathies seem to be rare and we hypothesize that they are underdiagnosed.
View Article and Find Full Text PDFFront Physiol
December 2024
Department of Internal Medicine, Hypertension and Vascular Research Division, Henry ford hospital, Detroit, MI, United States.
Purpose Of Review: The thick ascending limb (TAL) of loop of Henle is essential for NaCl, calcium and magnesium homeostasis, pH balance and for urine concentration. NKCC2 is the main transporter for NaCl reabsorption in the TAL and its regulation is very complex. There have been recent advancements toward understanding how NKCC2 is regulated by protein trafficking, protein-protein interaction, and phosphorylation/dephosphorylation.
View Article and Find Full Text PDFInt J Mol Sci
December 2024
Department of Pharmacology, National Institute of Cardiology Ignacio Chávez, Juan Badiano No. 1, Col. Seccion XVI, Tlalpan, Mexico City 14080, Mexico.
Chronic hyperglycemia results in morphological and functional alterations of the kidney and microvascular damage, leading to diabetic nephropathy (DN). Since DN progresses to irreversible renal damage, it is important to elucidate a pharmacological strategy aimed for treating DN in the early stage. Here, we used the type 2 diabetic rat model to induce DN and show a nephroprotective effect following the stimulation of PPAR-α, which stabilized renal tight junction components claudin-2, claudin-5, and claudin-16.
View Article and Find Full Text PDFAm J Hypertens
December 2024
Department of Physiology & Biophysics, Cardiovascular-Renal Research Center, Cardiorenal, and Metabolic Diseases Research Center, University of Mississippi Medical Center, Jackson, MS 39216 USA.
Background: Increased circulating bilirubin attenuates angiotensin (Ang) II-induced hypertension and improves renal hemodynamics. However, the intrarenal mechanisms that mediate these effects are not known. The goal of the present study was to test the hypothesis that bilirubin generation in the renal medulla plays a protective role against Ang II-induced hypertension.
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