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Myogenic reactivity is reduced in small renal arteries isolated from relaxin-treated rats
1 Departments of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine and Magee-Womens Research Institute, Pittsburgh 15213; 3 Department of Cell Biology and Physiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213; and 2 Dep...
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Published in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2002-08, Vol.283 (2), p.349-R355 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 1 Departments of Obstetrics, Gynecology and
Reproductive Sciences, University of Pittsburgh School of Medicine and
Magee-Womens Research Institute, Pittsburgh 15213;
3 Department of Cell Biology and Physiology, University
of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213;
and 2 Department of Molecular and Integrative Physiology
and College of Medicine, University of Illinois at
Urbana-Champaign, Urbana, Illinois 61801
Administration of the ovarian hormone
relaxin to nonpregnant rats vasodilates the renal circulation
comparable to pregnancy. This vasodilation is mediated by endothelin
(ET), the ET B receptor, and nitric oxide. Furthermore,
endogenous relaxin mediates the renal vasodilation and hyperfiltration
that occur during gestation. The goal of this study was to investigate
whether myogenic reactivity of small renal and mesenteric arteries is
reduced in relaxin-treated rats comparable to the pregnant condition.
Relaxin or vehicle was administered to virgin female Long-Evans rats
for 5 days at 4 µg/h, thereby producing midgestational blood levels
of the hormone. The myogenic responses of small renal arteries
(200-300 µm in diameter) isolated from these animals were
evaluated in an isobaric arteriograph system. Myogenic reactivity was
significantly reduced in the small renal arteries from relaxin-treated
compared with vehicle-treated rats. The reduced myogenic responses were
mediated by the ET B receptor and nitric oxide since the
selective ET B receptor antagonist RES-701-1 and the
nitric oxide synthase inhibitor
N G -nitro- L -arginine methyl ester
restored myogenic reactivity to virgin levels. The influence of relaxin
was not limited to the renal circulation because myogenic reactivity
was also reduced in small mesenteric arteries isolated from
relaxin-treated rats. Thus relaxin administration to nonpregnant rats
mimics pregnancy, insofar as myogenic reactivity of small renal and
mesenteric arteries is reduced in both conditions.
nitric oxide; endothelin receptors; small mesenteric arteries; pregnancy |
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ISSN: | 0363-6119 1522-1490 |
DOI: | 10.1152/ajpregu.00635.2001 |