Characteristic time courses of cortical and medullary sodium signals measured by noninvasive (23) Na-MRI in rat kidney induced by furosemide

J Magn Reson Imaging. 2015 Jun;41(6):1622-8. doi: 10.1002/jmri.24732. Epub 2014 Aug 28.

Abstract

Background: To characterize regional kidney sodium response by MRI following NKCC2 inhibition.

Methods: Regional renal sodium signals were monitored noninvasively using (23) Na-MRI at 9.4T with a temporal resolution of 1.5 min in anesthetized rats (N = 14). A mild NKCC2 inhibition was induced using a slow intravenous furosemide infusion. Time course of sodium signal was modeled as an exponential transient with a single characteristic time constant.

Results: Under normal physiological conditions, the renal sodium signals in medullary and cortical regions were stable and found to respond differently to furosemide challenge. Furosemide infusion at 1.2 mg/kg/h (N = 7) increased sodium signal in the cortex by 40 ± 6% (P < 7 × 10(-5) ) whereas decreased in the medulla by 29 ± 2% (P < 3 × 10(-6) ) with different temporal kinetics. The characteristic time constants of the change were determined to be: 8 ± 2 and 70 ± 10 min for medulla and cortex. Also, the medullary change occurred 9(±3) times faster than cortical independent of furosemide infusion rate up to 35 mg/kg/h.

Conclusion: The pharmacological effects in terms of regional kidney sodium signal changes induced by NKCC2 inhibition are region-specific and highly predictable. Using noninvasive sodium MRI, we obtained regional renal sodium kinetics data sets in response to a low dose furosemide infusion in normal rats.

Keywords: diuretics; kidney; regional kidney sodium; sodium MRI.

MeSH terms

  • Animals
  • Diuretics / pharmacology*
  • Furosemide / pharmacology*
  • Kidney Cortex / drug effects*
  • Kidney Medulla / drug effects*
  • Magnetic Resonance Imaging / methods*
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Sodium / metabolism*

Substances

  • Diuretics
  • Furosemide
  • Sodium