Systemic and Regional Hemodynamic Effects of Atriopeptin II in Anesthetized Rats

The hemodynamic and renal effects of atriopeptin II were investigated in rats, using electromagnetic flowmeters and thermodilution and clearance techniques, and its direct cardiac effects were studied in isolated rat atria and ventricular muscle strips. Atriopeptin II had no effect on the rate or fo...

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Veröffentlicht in:Journal of cardiovascular pharmacology 1987-02, Vol.9 (2), p.135-141
Hauptverfasser: Criscione, Leoluca, Burdet, Richard, Hänni, Henry, Kamber, Bruno, Truog, Arnold, Hofbauer, Karl G
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container_end_page 141
container_issue 2
container_start_page 135
container_title Journal of cardiovascular pharmacology
container_volume 9
creator Criscione, Leoluca
Burdet, Richard
Hänni, Henry
Kamber, Bruno
Truog, Arnold
Hofbauer, Karl G
description The hemodynamic and renal effects of atriopeptin II were investigated in rats, using electromagnetic flowmeters and thermodilution and clearance techniques, and its direct cardiac effects were studied in isolated rat atria and ventricular muscle strips. Atriopeptin II had no effect on the rate or force of contraction of rat cardiac tissue in vitro. In anesthetized rats, i.v. injections of 1, 3, 5, and 7 mUg/kg induced only transient hemodynamic effectsblood pressure (BP) was briefly reduced, and renal blood flow (RBF) but not mesenteric blood flow (MBF) increased. Infusions over 30 min at rates of 0.3, 1, 3, and 10 mUg/kg/min caused a fall in BP, mediated by a reduction of cardiac output (CO); RBF and MBF were decreased in a dose-related manner, and systemic and regional vascular resistances rose. A reduction of RBF was also observed in clearance experiments, but glomerular filtration rate remained unchanged and the filtration fraction increased significantly. Natriuresis occurred at all rates of atriopeptin tested (0.3, I, and 3 mU-g/kg/min i.v.) These results suggest that i.v. injection of atriopeptin II induces transient hypotensive and regional vasodilatory effects. Upon i.v. infusion, BP is lowered by way of a reduction in CO, which is accompanied by systemic and regional vasoconstriction. The decrease in CO cannot be ascribed to a direct cardiodepressant action, and the effects on regional blood flows are probably due to reflex activation. The natriuretic effects of atriopeptin II are independent of renal vasodilatation and may be attributable to changes in intrarenal hemodynamics or to direct tubular effects.
doi_str_mv 10.1097/00005344-198702000-00002
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Atriopeptin II had no effect on the rate or force of contraction of rat cardiac tissue in vitro. In anesthetized rats, i.v. injections of 1, 3, 5, and 7 mUg/kg induced only transient hemodynamic effectsblood pressure (BP) was briefly reduced, and renal blood flow (RBF) but not mesenteric blood flow (MBF) increased. Infusions over 30 min at rates of 0.3, 1, 3, and 10 mUg/kg/min caused a fall in BP, mediated by a reduction of cardiac output (CO); RBF and MBF were decreased in a dose-related manner, and systemic and regional vascular resistances rose. A reduction of RBF was also observed in clearance experiments, but glomerular filtration rate remained unchanged and the filtration fraction increased significantly. Natriuresis occurred at all rates of atriopeptin tested (0.3, I, and 3 mU-g/kg/min i.v.) These results suggest that i.v. injection of atriopeptin II induces transient hypotensive and regional vasodilatory effects. Upon i.v. infusion, BP is lowered by way of a reduction in CO, which is accompanied by systemic and regional vasoconstriction. The decrease in CO cannot be ascribed to a direct cardiodepressant action, and the effects on regional blood flows are probably due to reflex activation. 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Upon i.v. infusion, BP is lowered by way of a reduction in CO, which is accompanied by systemic and regional vasoconstriction. The decrease in CO cannot be ascribed to a direct cardiodepressant action, and the effects on regional blood flows are probably due to reflex activation. 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Drug treatments</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Renal Circulation - drug effects</topic><topic>Vascular Resistance - drug effects</topic><topic>Vasodilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Criscione, Leoluca</creatorcontrib><creatorcontrib>Burdet, Richard</creatorcontrib><creatorcontrib>Hänni, Henry</creatorcontrib><creatorcontrib>Kamber, Bruno</creatorcontrib><creatorcontrib>Truog, Arnold</creatorcontrib><creatorcontrib>Hofbauer, Karl G</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cardiovascular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Criscione, Leoluca</au><au>Burdet, Richard</au><au>Hänni, Henry</au><au>Kamber, Bruno</au><au>Truog, Arnold</au><au>Hofbauer, Karl G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systemic and Regional Hemodynamic Effects of Atriopeptin II in Anesthetized Rats</atitle><jtitle>Journal of cardiovascular pharmacology</jtitle><addtitle>J Cardiovasc Pharmacol</addtitle><date>1987-02</date><risdate>1987</risdate><volume>9</volume><issue>2</issue><spage>135</spage><epage>141</epage><pages>135-141</pages><issn>0160-2446</issn><eissn>1533-4023</eissn><coden>JCPCDT</coden><abstract>The hemodynamic and renal effects of atriopeptin II were investigated in rats, using electromagnetic flowmeters and thermodilution and clearance techniques, and its direct cardiac effects were studied in isolated rat atria and ventricular muscle strips. Atriopeptin II had no effect on the rate or force of contraction of rat cardiac tissue in vitro. In anesthetized rats, i.v. injections of 1, 3, 5, and 7 mUg/kg induced only transient hemodynamic effectsblood pressure (BP) was briefly reduced, and renal blood flow (RBF) but not mesenteric blood flow (MBF) increased. Infusions over 30 min at rates of 0.3, 1, 3, and 10 mUg/kg/min caused a fall in BP, mediated by a reduction of cardiac output (CO); RBF and MBF were decreased in a dose-related manner, and systemic and regional vascular resistances rose. A reduction of RBF was also observed in clearance experiments, but glomerular filtration rate remained unchanged and the filtration fraction increased significantly. Natriuresis occurred at all rates of atriopeptin tested (0.3, I, and 3 mU-g/kg/min i.v.) These results suggest that i.v. injection of atriopeptin II induces transient hypotensive and regional vasodilatory effects. Upon i.v. infusion, BP is lowered by way of a reduction in CO, which is accompanied by systemic and regional vasoconstriction. The decrease in CO cannot be ascribed to a direct cardiodepressant action, and the effects on regional blood flows are probably due to reflex activation. The natriuretic effects of atriopeptin II are independent of renal vasodilatation and may be attributable to changes in intrarenal hemodynamics or to direct tubular effects.</abstract><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>2435989</pmid><doi>10.1097/00005344-198702000-00002</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Journals@Ovid LWW Legacy Archive; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Ovid Autoload
subjects Animals
Atrial Natriuretic Factor - pharmacology
Biological and medical sciences
Cardiovascular system
Glomerular Filtration Rate - drug effects
Heart Rate - drug effects
Hemodynamics - drug effects
In Vitro Techniques
Kidney - drug effects
Male
Medical sciences
Miscellaneous
Myocardial Contraction - drug effects
Pharmacology. Drug treatments
Rats
Rats, Inbred Strains
Renal Circulation - drug effects
Vascular Resistance - drug effects
Vasodilation
title Systemic and Regional Hemodynamic Effects of Atriopeptin II in Anesthetized Rats
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