JPET Celsis microsomes equal better data

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by HYMAN, A. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by HYMAN, A. L.
Journal of Pharmacology And Experimental Therapeutics, Vol. 168, Issue 1, 96-105, 1969
Copyright © 1969 by American Society for Pharmacology and Experimental Therapeutics


THE DIRECT EFFECTS OF VASOACTIVE AGENTS ON PULMONARY VEINS. STUDIES OF RESPONSES TO ACETYLCHOLINE, SEROTONIN, HISTAMINE AND ISOPROTERENOL IN INTACT DOGS

ALBERT L. HYMAN 1

1 Cardiopulmonary Laboratory, Department of Surgery, Tulane University School of Medicine, New Orleans, Louisiana

In the intact dog a catheterization technique, designed to measure vascular pressures and blood volume in a hemodynamically separated lobe perfused at a constant rate of flow, was used to study the active responses of pulmonary veins to small volume infusions of vasoactive compounds. These active responses were compared to simultaneously occurring modulated responses in the other lobes which were normally perfused. These data indicate that serotonin actively constricts both the lobar arteries and veins but suggest that the more gradually active venoconstriction may modulate the more abruptly active constriction of the upstream vessels. Acetylcholine and histamine actively constrict the lobar small veins. Less direct evidence suggests that acetylcholine constricts the lobar arteries as well, but any tendency for histamine to constrict the lobar arteries is obscured by the accompanying venoconstriction. The data indicate that isoproterenol actively dilates the lobar small veins and suggest an active dilation in the lobar arteries. No active responses of larger pulmonary veins near the venoatrial junction were detected.

Submitted on December 30, 1968
Accepted on March 19, 1969




This article has been cited by other articles:


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
C. L. Ivey, B. J. Roy, and M. I. Townsley
Ablation of lung endothelial injury after pacing-induced heart failure is related to alterations in Ca2+ signaling
Am J Physiol Heart Circ Physiol, September 1, 1998; 275(3): H844 - H851.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
L. E. Fisher Jr., A. Cziraki, C. M. Steinhart, and J. D. Catravas
Unaltered pulmonary capillary surface area in the presence of changing arterial resistance
Am J Physiol Lung Cell Mol Physiol, February 1, 1998; 274(2): L264 - L269.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
S. A. Barman
Pulmonary vasoreactivity to serotonin during hypoxia is modulated by ATP-sensitive potassium channels
J Appl Physiol, August 1, 1997; 83(2): 569 - 574.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1969 by the American Society for Pharmacology and Experimental Therapeutics.