Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Acta Pharmaceutica Sinica ; (12): 758-762, 2002.
Article in Chinese | WPRIM | ID: wpr-312055

ABSTRACT

<p><b>AIM</b>To study the effects of rhBNP on the cardiac hemodynamics and renal function in dogs with heart failure.</p><p><b>METHODS</b>Congestive heart failure in dogs was induced by either rapid ventricular pacing (RVP), 250 beats.min-1 for 7-14 days or by thoracic inferior vena cava constriction (TIVCC) to 1/2 its original diameter. When remarkable hemodynamic changes appeared rhBNP was infused intravenously at the dosage of 10, 30 and 100 ng.kg-1.min-1, each dose lasting 30 min.</p><p><b>RESULTS</b>In dogs (n = 7) with RVP heart failure, intravenous infusion of rhBNP at 10-100 ng.kg-1.min-1, caused decreases in mean arterial pressure (MAP), left ventricular systolic pressure (LVSP), LVdP/dtmax, pulmonary arterial pressure (PAP), left ventricular end diastolic pressure (LVEDP), total peripheral vascular resistance (TPR) and renal vascular resistance (RVR) dose-dependently, without significant changes in cardiac output (CO), LVdp/dt/P, left ventricular work (LVW), renal blood flow (RBF) and heart rate (HR). This suggested that rhBNP reduced the pre-load and after-load of the dogs with congestive heart failure but showed no distinct effect on the contractility of the heart. In dogs (n = 7) with TIVCC heart failure, there were remarkable decreases in MAP and LVEDP following the rhBNP infusion, without further reduction of CO, but no marked change in HR, LVSP, LVdP/dtmax, RAP and TPR. In both animal models of heart failure, there were significant increases in urine volume and sodium excretion which were more significant in TIVCC dogs than in RVP dogs.</p><p><b>CONCLUSION</b>rhBNP reduced the pre-load and after-load in dogs with heart failure and showed remarkable diuretic effect, but did not affect the contractility of the heart.</p>


Subject(s)
Animals , Dogs , Female , Male , Blood Pressure , Diuretics , Pharmacology , Therapeutic Uses , Heart Failure , Drug Therapy , Urine , Hemodynamics , Kidney , Kidney Function Tests , Natriuretic Peptide, Brain , Pharmacology , Therapeutic Uses , Recombinant Proteins , Pharmacology , Therapeutic Uses , Sodium , Urine , Vascular Resistance , Vasodilator Agents , Pharmacology
2.
Acta Pharmaceutica Sinica ; (12): 506-509, 2002.
Article in Chinese | WPRIM | ID: wpr-251112

ABSTRACT

<p><b>AIM</b>To study the effects of rhBNP and milrinone on the cardiac hemodynamics and renal function in anesthetized dogs.</p><p><b>METHODS</b>The actions of rhBNP given cumulatively i.v. 10, 30 and 100 ng.kg-1 for 30 min and milrinone of single dose (100 micrograms.kg-1, i.v.) on cardiac hemodynamics and renal function were studied in anesthetized open-chest dogs.</p><p><b>RESULTS</b>In anesthetized dogs (n = 7) intravenous infusion of rhBNP at 10-100 ng.kg-1, caused decreases in mean arterial pressure (MAP), left ventricular systolic pressure (LVSP), LVdp/dtmax, pulmonary arterial pressure (PAP), left ventricular end diastolic pressure (LVEDP), total peripheral resistance (TPR) and renal vascular resistance (RVR) dose-dependently, without significant changes in cardiac output (CO), LV(dp/dt)/P, renal blood flow (RBF) and heart rate (HR), increases in urinary volume and sodium excretion. In anesthetized dogs (n = 6), there were remarkable decreases in MAP, LVEDP, PAP, TPR, RBF, RVR and urinary volume following the MIL (100 micrograms.kg-1, i.v.), with significant increases of LVSP, +/- LVdp/dtmax, HR and CO, but no marked changes in urinary volume and sodium excretion.</p><p><b>CONCLUSION</b>rhBNP reduces the pre-load and after-load in the anaesthetized dogs but showed no distinct effect on the contractility of the heart. Positive inotropic and chronotropic actions have been demonstrated after intravenous injection of milrinone 100 micrograms.kg-1 in anesthetized dogs.</p>


Subject(s)
Animals , Dogs , Female , Male , Anesthesia , Cardiotonic Agents , Pharmacology , Drug Interactions , Heart , Physiology , Hemodynamics , Kidney , Physiology , Milrinone , Pharmacology , Natriuretic Peptide, Brain , Pharmacology , Recombinant Proteins , Pharmacology , Sodium , Blood , Urine , Urine
SELECTION OF CITATIONS
SEARCH DETAIL