Glucose/Fructose Delivery to the Distal Nephron Activates the Sodium-Chloride Cotransporter via the Calcium-Sensing Receptor

• Published in: Journal of the American Society of Nephrology 2023-01, Vol.34 (1), p.55-72
• Main Authors: Bahena-Lopez, Jessica Paola, Rojas-Vega, Lorena, Chávez-Canales, María, Bazua-Valenti, Silvana, Bautista-Pérez, Rocío, Lee, Ju-Hye, Madero, Magdalena, Vazquez-Manjarrez, Natalia, Alquisiras-Burgos, Ivan, Hernandez-Cruz, Arturo, Castañeda-Bueno, María, Ellison, David H, Gamba, Gerardo
• Format: Article
• Language: English
• Subjects: Acid Base and Electrolyte Disorders; Animals; Basic Research; Glucose - metabolism; Glycosuria - metabolism; HEK293 Cells; Humans; Kidney Tubules, Distal - metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Phosphorylation; Protein Serine-Threonine Kinases - metabolism; Receptors, Calcium-Sensing - metabolism; Sodium Chloride Symporters - metabolism; Solute Carrier Family 12, Member 3 - metabolism
• ISSN: 1046-6673; 1533-3450
• DOI: 10.1681/ASN.2021121544

The calcium-sensing receptor (CaSR) in the distal convoluted tubule (DCT) activates the NaCl cotransporter (NCC). Glucose acts as a positive allosteric modulator of the CaSR. Under physiologic conditions, no glucose is delivered to the DCT, and fructose delivery depends on consumption. We hypothesized that glucose/fructose delivery to the DCT modulates the CaSR in a positive allosteric way, activating the WNK4-SPAK-NCC pathway and thus increasing salt retention. We evaluated the effect of glucose/fructose arrival to the distal nephron on the CaSR-WNK4-SPAK-NCC pathway using HEK-293 cells, C57BL/6 and WNK4-knockout mice, ex vivo perfused kidneys, and healthy humans. HEK-293 cells exposed to glucose/fructose increased SPAK phosphorylation in a WNK4- and CaSR-dependent manner. C57BL/6 mice exposed to fructose or a single dose of dapagliflozin to induce transient glycosuria showed increased activity of the WNK4-SPAK-NCC pathway. The calcilytic NPS2143 ameliorated this effect, which was not observed in WNK4-KO mice. C57BL/6 mice treated with fructose or dapagliflozin showed markedly increased natriuresis after thiazide challenge. Ex vivo rat kidney perfused with glucose above the physiologic threshold levels for proximal reabsorption showed increased NCC and SPAK phosphorylation. NPS2143 prevented this effect. In healthy volunteers, cinacalcet administration, fructose intake, or a single dose of dapagliflozin increased SPAK and NCC phosphorylation in urinary extracellular vesicles. Glycosuria or fructosuria was associated with increased NCC, SPAK, and WNK4 phosphorylation in a CaSR-dependent manner.