Premium
Compared peripheral vascular responses to intravenous and intra‐arterial administrations of positive inotropic agents in conscious dogs
Author(s) -
Gosgnach M.,
Gérard JL,
Berdeaux A.,
Giudicelli JF
Publication year - 1991
Publication title -
fundamental and clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.655
H-Index - 73
eISSN - 1472-8206
pISSN - 0767-3981
DOI - 10.1111/j.1472-8206.1991.tb00759.x
Subject(s) - medicine , dobutamine , milrinone , inotrope , anesthesia , cardiac output , hemodynamics , contractility , cardiology , vasodilation
Summary— In addition to their direct effects on cardiac contractility, a number of positive inotropic agents also induce, through direct peripheral vasodilation, a reduction in afterload which is of major importance in their beneficial effects in the treatment of congestive heart failure. However, the induced increase in cardiac output can indirectly improve perfusion of peripheral vessels through a flow‐mediated mechanism. Thus, the goal of the present study was to compare the direct peripheral vasomotor effects assessed in the iliac vascular bed of four positive inotropic agents: DPI 201–106, ouabain, milrinone and dobutamine, in the presence and absence of simultaneous changes in cardiac function. These drugs were administered either through intravenous or intra‐arterial (aorto‐iliac catheter) routes in 6 conscious dogs, chronically instrumented for the measurement of heart rate, arterial pressure, left ventricular d P /d t , iliac artery blood flow and iliac artery diameter (sonomicrometry). Intravenous doses were selected as those inducing equipotent positive inotropic responses whereas intra‐arterial doses were below those required to induce any significant change in systemic hemodynamics. Ouabain decreased and milrinone increased both iliac blood flow and diameter after either intravenous or intra‐arterial administrations. In contrast, iliac blood flow did not change after intraarterial administration of DPI 201–106 and dobutamine whereas iliac diameter was not modified by DPI 201–106 and even decreased with dobutamine. After intravenous administration, DPI 201–106 but not dobutamine, increased both iliac blood flow and diameter. Thus, this experimental preparation can differentiate inotropic agents with direct vasodilating (milrinone) or constricting (ouabain) properties and those (DPI 201–106 and dobutamine) with indirect vasodilating effects most likely mediated by the improvement in cardiac function.