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Am J Physiol Lung Cell Mol Physiol 278: L81-L89, 2000;
1040-0605/00 $5.00
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Vol. 278, Issue 1, L81-L89, January 2000

Inhibition of NOS enhances pulmonary vascular changes in stroke-prone spontaneously hypertensive rats

Rajamma Mathew, Newton Y.-T. Fan, Ning Yuan, Praveen N. Chander, Michael H. Gewitz, and Charles T. Stier Jr.

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 Nomega -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; Nomega -nitro-L-arginine; pulmonary circulation; pulmonary hypertension





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