Jørgen Frøkiær

Oxygen tension correlates with regional blood flow in obstructed rat kidney

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperJournal articleResearchpeer-review

  • Biomedical Radio Isotope Techniques
  • The Department of Medicine and Nephrology C
  • Center of Magnetic Resonance
As renal tissue oxygen tension (P(O(2))) is determined by the balance between oxygen supply and consumption, direct tissue P(O(2)) measurements are essential when evaluating the presence of hypoxia. The present study aimed at evaluating invasively and continuously the renal medullary and cortical tissue P(O(2)) by novel fibre-optic probes in rats subjected to acute unilateral ureteral obstruction (AUUO). In parallel, regional blood flow measurements were obtained by MRI to investigate the relationship between regional blood flow and tissue oxygen tension. The abundance of transport proteins was determined by immunoblotting. In the obstructed kidney, AUUO caused a prompt decrease in medullary tissue P(O(2)) to 60% of baseline level whereas cortical tissue P(O(2)) was unchanged. By contrast, tissue P(O(2)) slightly increased in the non-obstructed kidney. These changes developed during the first 30 min after AUUO and persisted for the 3 h observation period. Medullary blood flow declined 1.5-2 h after induction of AUUO to 61% of baseline level in the obstructed kidney. By contrast, cortical blood flow increased to 108% of baseline level in the non-obstructed kidney. Finally, the abundance of phosphorylated aquaporin 2 decreased significantly in the obstructed kidney medulla, but increased in the obstructed kidney cortex. The Na(+)/K(+)-ATPase abundance increased in the obstructed kidney medulla whereas the Na(+)/K(+)/2Cl(-) co-transporter abundance remained unchanged in the obstructed kidney. In conclusion, measurements of regional blood flow reflect tissue P(O(2)) changes during AUUO suggesting that reduced regional blood flow is a predictor of local hypoxia. Furthermore, the abundance of major transport protein is independent of tissue P(O(2)).
Original languageEnglish
JournalJournal of Experimental Biology
Volume212
IssuePt 19
Pages (from-to)3156-3163
Number of pages7
ISSN0022-0949
DOIs
Publication statusPublished - 2009

    Research areas

  • rat kidney, MR

See relations at Aarhus University Citationformats

ID: 17582221