Novel catheterization technique for the in vivo measurement of pulmonary vascular responses in rats


Hyman A. L. , Hao Q., Tower A., Kadowitz P. J. , Champion H. C. , Gumusel B., ...More

American Journal of Physiology - Heart and Circulatory Physiology, vol.43, no.4, 1998 (Peer-Reviewed Journal) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 43 Issue: 4
  • Publication Date: 1998
  • Doi Number: 10.1152/ajpheart.1998.274.4.h1218
  • Journal Name: American Journal of Physiology - Heart and Circulatory Physiology
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Keywords: pulmonary vascular bed, endothelium-derived relaxing factor-dependent vasodilation, nitric oxide, pressure-flow relationship, adrenomedullin, NITRO-L-ARGININE, CHRONICALLY HYPOXIC RATS, RELAXING FACTOR, METHYL-ESTER, RECEPTOR ANTAGONISTS, OXIDE, CIRCULATION, BRADYKININ, ACETYLCHOLINE, VASODILATION

Abstract

A novel cardiac catheterization technique was devised to investigate the pulmonary arterial pressure-blood flow relationship in intact spontaneously breathing rats (ISBR) under physiological conditions with constant left atrial pressure and controlled blood flow within the normal range. Observations using this new technique in vivo were contrasted with data derived with isolated perfused rat lungs in vitro. Unlike results in in vitro isolated perfused rat lungs, the pressure-flow curves in vivo were curvilinear, with pulmonary artery pressure increasing more rapidly at low pulmonary blood flows of 4-8 ml/min and less rapidly at higher flow rates. Pressure-flow curves were reproducible and were not altered by 1-1.5 h of arrested perfusion, cyclooxygenase blockade, or perfusion with aortic or mixed venous blood. In contrast to results in in vitro isolated perfused rat lungs, NG-nitro-L-arginine methyl ester (L-NAME) increased pulmonary arterial pressure at all but the lowest flow rates with a slight effect on the curvilinear pressure-flow relationship. L-NAME reversed pulmonary vasodilator responses to acetylcholine and bradykinin and enhanced the pulmonary vasodilator response to nitroglycerin. The present data suggest that actively induced pulmonary hypertension is under greater control by endothelium-derived relaxing factor (EDRF). Unlike previous results in in vitro perfused rat lungs, results in ISBR demonstrate that the pulmonary vasodilator response to adrenomedullin-(13-52) is not mediated by calcitonin gene-related peptide receptors, which are not coupled to the release of EDRF. These results indicate that this novel technique may provide a useful model for the study of the pulmonary circulation in the intact chest rat. Copyright © 1998 the American Physiological Society.