© 2016 the American Physiological Society.Oxygen tension (PO2) of urine in the bladder could be used to monitor risk of acute kidney injury if it varies with medullary PO2. Therefore, we examined this relationship and characterized oxygen diffusion across walls of the ureter and bladder in anesthetized rabbits. A computational model was then developed to predict medullary PO2 from bladder urine PO2. Both intravenous infusion of [Phe2,Ile3,Orn8]-vasopressin and infusion of NG-nitro-L-arginine reduced urinary PO2 and medullary PO2 (8-17%), yet had opposite effects on renal blood flow and urine flow. Changes in bladder urine PO2 during these stimuli correlated strongly with changes in medullary PO2 (within-rabbit r2 = 0.87-0.90). Differences in the PO2 of saline infused into the ureter close to the kidney could be detected in the bladder, although this was diminished at lesser ureteric flow. Diffusion of oxygen across the wall of the bladder was very slow, so it was not considered in the computational model. The model predicts PO2 in the pelvic ureter (presumed to reflect medullary PO2) from known values of bladder urine PO2, urine flow, and arterial PO2. Simulations suggest that, across a physiological range of urine flow in anesthetized rabbits (0.1-0.5 ml/min for a single kidney), a change in bladder urine PO2 explains 10-50% of the change in pelvic urine/medullary PO2. Thus, it is possible to infer changes in medullary PO2 from changes in urinary PO2, so urinary PO2 may have utility as a real-time biomarker of risk of acute kidney injury.
|Journal||American Journal of Physiology - Regulatory Integrative and Comparative Physiology|
|Publication status||Published - 2016|