Hypertension, Vol 19, 153-160, Copyright © 1992 by American Heart Association
K Hayashi, M Epstein and R Loutzenhiser
We recently demonstrated that the interlobular artery (ILA) constricts in
response to elevating renal arterial pressure (RAP), suggesting that the
ILA contributes to renal autoregulation. In the present study, we examined
the segmental myogenic responsiveness of the ILA in kidneys from
Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHR). The
tapered nature of the ILA allowed us to characterize the regional
responsiveness, using the basal diameter to define segments as either
proximal (greater than 60 microns), intermediate (40-60 microns), or distal
(less than 40 microns). At 80 mm Hg, segmental diameters were similar in
WKY and SHR arteries (proximal, 76.0 +/- 3.1 versus 71.6 +/- 3.5 microns;
intermediate, 48.2 +/- 1.4 versus 48.1 +/- 1.7 microns; distal, 30.7 +/-
0.9 versus 27.9 +/- 1.3 microns for WKY and SHR, respectively). In both
strains, intermediate and distal segments exhibited graded reductions in
diameter as RAP was elevated, whereas proximal segments did not.
Pressure-induced decrements in the diameters of distal ILA segments were
similar in WKY (-24 +/- 2%) and SHR (-20 +/- 2%; p greater than 0.1). The
intermediate ILA of SHR exhibited an augmented myogenic responsiveness,
constricting at lower RAP levels and exhibiting greater maximal decrements
in diameter at 180 mm Hg (i.e., - 19 +/- 2% and -12 +/- 2% for SHR and WKY,
respectively; p less than 0.05). Nifedipine (1.0 microM) reduced
pressure-induced vasoconstriction of intermediate and distal ILA segments
by 56 +/- 11% and 79 +/- 7%, respectively, in WKY.(ABSTRACT TRUNCATED AT
250 WORDS)
ARTICLES
Enhanced myogenic responsiveness of renal interlobular arteries in spontaneously hypertensive rats
Nephrology Section, Veterans Administration Medical Center, Miami, Fla 33125.
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