Mechanisms of temporal variation in single-nephron blood flow in rats

Am J Physiol. 1993 Mar;264(3 Pt 2):F427-34. doi: 10.1152/ajprenal.1993.264.3.F427.

Abstract

Modified laser-Doppler velocimetry was used to determine the number of different mechanisms regulating single-nephron blood flow. Two oscillations were identified in star vessel blood flow, one at 20-50 mHz and another at 100-200 mHz. Tubuloglomerular feedback (TGF) mediates the slower oscillation, and the faster one is probably myogenic in origin. Acute hypertension increased autospectral power in the 20-50 mHz and 100-200 mHz frequency bands to 282 +/- 50 and 248 +/- 64%, respectively, of control even though mean single-nephron blood flow was autoregulated. Mean blood flow increased 24.6 +/- 6.1% when TGF was inhibited by intratubular perfusion with furosemide, and it decreased 42.8 +/- 3.9% when TGF was saturated by tubular perfusion with artificial tubular fluid at high rates. Autospectral power in the low-frequency band decreased 50.5 +/- 9.6% during furosemide and decreased 74.9 +/- 5.9% during TGF saturation, consistent with a TGF origin of the slow oscillation. In contrast, autospectral power of the high-frequency oscillation increased 75.4 +/- 23.9% during TGF inhibition and decreased 35.8 +/- 11% when TGF was saturated, suggesting interactions between the two spontaneously oscillating components in efferent arteriole blood flow.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Arterioles / physiology
  • Blood Flow Velocity
  • Blood Pressure
  • Feedback
  • Furosemide / pharmacology
  • Homeostasis
  • Kidney Glomerulus / physiology
  • Kidney Tubules / physiology
  • Laser-Doppler Flowmetry
  • Male
  • Nephrons / blood supply*
  • Periodicity
  • Pressure
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Furosemide