Chronic intermittent hypoxia promotes glomerular hyperfiltration and potentiates hypoxia-evoked decreases in renal perfusion and PO 2

• Published in: Frontiers in physiology 2023, Vol.14, p.1235289
• Main Authors: Kious, Kiefer W, Savage, Kalie A, Twohey, Stephanie C E, Highum, Aubrey F, Philipose, Andrew, Díaz, Hugo S, Del Rio, Rodrigo, Lang, James A, Clayton, Sarah C, Marcus, Noah J
• Format: Article
• Language: English
• ISSN: 1664-042X; 1664-042X

Sleep apnea (SA) is highly prevalent in patients with chronic kidney disease and may contribute to the development and/or progression of this condition. Previous studies suggest that dysregulation of renal hemodynamics and oxygen flux may play a key role in this process. The present study sought to determine how chronic intermittent hypoxia (CIH) associated with SA affects regulation of renal artery blood flow (RBF), renal microcirculatory perfusion (RP), glomerular filtration rate (GFR), and cortical and medullary tissue PO as well as expression of genes that could contribute to renal injury. We hypothesized that normoxic RBF and tissue PO would be reduced after CIH, but that GFR would be increased relative to baseline, and that RBF, RP, and tissue PO would be decreased to a greater extent in CIH vs. sham during exposure to intermittent asphyxia (IA, F O 0.10/F CO 0.03). Additionally, we hypothesized that gene programs promoting oxidative stress and fibrosis would be activated by CIH in renal tissue. All physiological variables were measured at baseline (F O 0.21) and during exposure to 10 episodes of IA (excluding GFR). GFR was higher in CIH-conditioned vs. sham ( < 0.05), whereas normoxic RBF and renal tissue PO were significantly lower in CIH vs. sham ( < 0.05). Reductions in RBF, RP, and renal tissue PO during IA occurred in both groups but to a greater extent in CIH ( < 0.05). Pro-oxidative and pro-fibrotic gene programs were activated in renal tissue from CIH but not sham. CIH adversely affects renal hemodynamic regulation and oxygen flux during both normoxia and IA and results in changes in renal tissue gene expression.