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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
<10 wk of age is not accompanied by impaired relaxation in PAs or
RVH; however, impaired relaxation is associated with increased WT and RVH.
nitric oxide synthase; acetylcholine; N
-nitro-L-arginine; pulmonary
circulation; pulmonary hypertension
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