Document Detail


Osmotically released vasopressin augments cardiopulmonary reflex inhibition of the circulation.
MedLine Citation:
PMID:  3364609     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Exogenous arginine vasopressin (AVP) has been shown to augment the inhibitory influence of arterial and cardiopulmonary baroreflexes. This study examined the influence of osmotically released AVP on the inhibitory responses to activation of cardiopulmonary receptors by administration of veratrum alkaloids. Three groups of conscious dogs, with carotid sinus intact, with prior sinoaortic denervation (SAD), and with prior lesion of the area postrema (AP), were instrumented for monitoring arterial pressure and heart rate and with left circumflex coronary artery or left atrial catheters for administration of veratrum alkaloids. Conscious dogs were administered veratridine (0.5-1.0 microgram.kg-1.min-1) under control conditions, after infusion of hypertonic saline (HS, 6% NaCl), and after HS in the presence of the AVP vascular (V1) receptor antagonist. In carotid sinus-intact dogs, veratridine reduced arterial pressure (-10 +/- 0.4 mmHg). After HS infusion, the depressor response to veratridine was significantly greater (-18 +/- 0.8 mmHg). The enhanced depressor response during HS infusion was prevented by administration of the AVP antagonist (-8 +/- 0.6 mmHg). Responses to veratrum alkaloids in SAD dogs were similar. In AP-lesioned animals, the depressor effects of veratridine (-9 +/- 0.5 mmHg) were similar to intact animals. However, the response to veratridine during HS was not altered (-9 +/- 0.8 mmHg) in AP-lesioned dogs. Results suggest that osmotically stimulated AVP augments the inhibitory effects of cardiopulmonary reflexes and that this effect is mediated through the area postrema via the V1 receptor.
Authors:
E M Hasser; S E DiCarlo; R J Applegate; V S Bishop
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The American journal of physiology     Volume:  254     ISSN:  0002-9513     ISO Abbreviation:  Am. J. Physiol.     Publication Date:  1988 May 
Date Detail:
Created Date:  1988-06-09     Completed Date:  1988-06-09     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  0370511     Medline TA:  Am J Physiol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  R815-20     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, University of Texas Health Science Center, San Antonio 78284-7764.
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MeSH Terms
Descriptor/Qualifier:
Animals
Arginine Vasopressin / blood*
Cardiovascular Physiological Phenomena*
Carotid Sinus / physiology
Denervation
Dogs
Heart / drug effects,  physiology*
Lung / physiology*
Medulla Oblongata / physiology
Pressoreceptors / physiology
Protoveratrines / pharmacology
Reference Values
Reflex / physiology*
Saline Solution, Hypertonic / pharmacology
Sinoatrial Node / physiology
Veratridine / pharmacology
Grant Support
ID/Acronym/Agency:
HL-12415/HL/NHLBI NIH HHS; HL-36080/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Protoveratrines; 0/Saline Solution, Hypertonic; 113-79-1/Arginine Vasopressin; 71-62-5/Veratridine

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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