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Inhibition of NOS enhances pulmonary vascular changes in stroke-prone spontaneously hypertensive rats
Departments of Pediatrics, Pharmacology, and Pathology, New York Medical College, Valhalla, New York 10595 To determine the effects of chronic nitric oxide (NO) blockade on the pulmonary vasculature, 58-day-old spontaneously hypertensive rats of the stroke-prone substrain (SHRSP) and Wistar-Kyoto ra...
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Published in: | American journal of physiology. Lung cellular and molecular physiology 2000-01, Vol.278 (1), p.81-L89 |
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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: | Departments of Pediatrics, Pharmacology, and Pathology, New York
Medical College, Valhalla, New York 10595
To determine the effects of chronic nitric oxide (NO)
blockade on the pulmonary vasculature, 58-day-old spontaneously
hypertensive rats of the stroke-prone substrain (SHRSP) and
Wistar-Kyoto rats (WKY) received
N -nitro- L -arginine
( L -NNA; 15 mg · kg 1 · day 1
orally for 8 days). Relaxation to acetylcholine (ACh) in hilar pulmonary arteries (PAs), the ratio of right ventricular (RV) to body
weight (RV/BW) to assess RV hypertrophy (RVH), and the percent medial
wall thickness (WT) of resistance PAs were examined. L -NNA
did not alter the PA relaxation, RV/BW, or WT in WKY. Although the PA
relaxation and RV/BW in control SHRSP were comparable to those in WKY,
the WT was increased (31 ± 2 vs. 19 ± 1%).
L -NNA-treated SHRSP showed two patterns: in one group, the
relaxation, RV/BW, and WT were comparable to those in the control
SHRSP; in the other, impaired relaxation (36 ± 7 vs. 88 ± 4% for
WKY) was associated with an increase in WT (37 ± 1%) and RV/BW (0.76 ± 0.05). Thus the abnormal pulmonary vasculature in SHRSP at |
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ISSN: | 1040-0605 1522-1504 |
DOI: | 10.1152/ajplung.2000.278.1.L81 |