Pharmacodynamic effects of iomeprol for injection in experimental animals

Iomeprol for injection is a new nonionic triiodinated contrast medium for diagnostic radiology, which combines low osmolality with low viscosity. The effects of iomeprol for injection on the cardiovascular system, blood parameters, renal function and the central nervous system were studied after int...

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Veröffentlicht in:European journal of radiology 1994-05, Vol.18 (SUPPL 1), p.S32-S42
Hauptverfasser: Cipolla, Piervitto, Tirone, Piero, Luzzani, Franco, de Haën, Christoph
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container_end_page S42
container_issue SUPPL 1
container_start_page S32
container_title European journal of radiology
container_volume 18
creator Cipolla, Piervitto
Tirone, Piero
Luzzani, Franco
de Haën, Christoph
description Iomeprol for injection is a new nonionic triiodinated contrast medium for diagnostic radiology, which combines low osmolality with low viscosity. The effects of iomeprol for injection on the cardiovascular system, blood parameters, renal function and the central nervous system were studied after intravascular administration to several animal species of doses at least as high as the highest presumed clinical doses. The following observations were made with respect to the central circulatory system: moderate and short-lasting increases of left ventricular end-diastolic pressure and cardiac output, no significant effects on heart rate either in vitro or in vivo, some episodes of arrhythmia and ventricular fibrillations only at doses far higher than the highest presumed clinical ones, no significant increases in diastolic and systolic coronary flow. The following observations were made with respect to peripheral circulation: no significant changes on blood pressure, moderate and short-lasting increases in renal and pulmonary arterial flow, together with a decrease in peripheral vascular resistance, no crossing of the blood-brain barrier in healthy animals. Cardiovascular and haemodynamic changes were all significantly milder than those induced by ionic contrast media (CM) and were similar to effects caused by some other nonionic contrast media. When injected into the femoral artery of rats, iomeprol was shown to be less algogenic than iopamidol and iohexol. In comparison with the same reference CM, iomeprol affected to a lesser extent the filterability of red blood cells in vitro and showed a less marked effect on their deformability. When administered intravenously at very high dosages, iomeprol had no effect on the glomerular filtration rate, but increased both renal blood flow and diuresis. Proteinuria and enzymuria were also increased, albeit more transiently. The neurotolerance of iomeprol for injection after intravenous administration was higher than or at worst equal to that of iopamidol and iohexol. Iomeprol is therefore a promising new contrast agent particularly suitable for intravascular use in humans.
doi_str_mv 10.1016/0720-048X(94)90092-2
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The effects of iomeprol for injection on the cardiovascular system, blood parameters, renal function and the central nervous system were studied after intravascular administration to several animal species of doses at least as high as the highest presumed clinical doses. The following observations were made with respect to the central circulatory system: moderate and short-lasting increases of left ventricular end-diastolic pressure and cardiac output, no significant effects on heart rate either in vitro or in vivo, some episodes of arrhythmia and ventricular fibrillations only at doses far higher than the highest presumed clinical ones, no significant increases in diastolic and systolic coronary flow. The following observations were made with respect to peripheral circulation: no significant changes on blood pressure, moderate and short-lasting increases in renal and pulmonary arterial flow, together with a decrease in peripheral vascular resistance, no crossing of the blood-brain barrier in healthy animals. Cardiovascular and haemodynamic changes were all significantly milder than those induced by ionic contrast media (CM) and were similar to effects caused by some other nonionic contrast media. When injected into the femoral artery of rats, iomeprol was shown to be less algogenic than iopamidol and iohexol. In comparison with the same reference CM, iomeprol affected to a lesser extent the filterability of red blood cells in vitro and showed a less marked effect on their deformability. When administered intravenously at very high dosages, iomeprol had no effect on the glomerular filtration rate, but increased both renal blood flow and diuresis. 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The effects of iomeprol for injection on the cardiovascular system, blood parameters, renal function and the central nervous system were studied after intravascular administration to several animal species of doses at least as high as the highest presumed clinical doses. The following observations were made with respect to the central circulatory system: moderate and short-lasting increases of left ventricular end-diastolic pressure and cardiac output, no significant effects on heart rate either in vitro or in vivo, some episodes of arrhythmia and ventricular fibrillations only at doses far higher than the highest presumed clinical ones, no significant increases in diastolic and systolic coronary flow. 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Proteinuria and enzymuria were also increased, albeit more transiently. The neurotolerance of iomeprol for injection after intravenous administration was higher than or at worst equal to that of iopamidol and iohexol. Iomeprol is therefore a promising new contrast agent particularly suitable for intravascular use in humans.</description><subject>Animals</subject><subject>Blood Circulation - drug effects</subject><subject>Blood Coagulation - drug effects</subject><subject>Blood Pressure - drug effects</subject><subject>Blood-Brain Barrier - drug effects</subject><subject>Brain - drug effects</subject><subject>Cardiac Output - drug effects</subject><subject>Contrast Media - administration &amp; dosage</subject><subject>Contrast Media - pharmacology</subject><subject>Contrast media, effects on blood</subject><subject>Contrast media, effects on cardiovascular system</subject><subject>Contrast media, effects on CNS</subject><subject>Contrast media, effects on kidney</subject><subject>Contrast media, experimental study</subject><subject>Contrast media, safety</subject><subject>Coronary Circulation - drug effects</subject><subject>Dogs</subject><subject>Erythrocyte Deformability - drug effects</subject><subject>Glomerular Filtration Rate - drug effects</subject><subject>Heart Rate - drug effects</subject><subject>Injections, Intra-Arterial - adverse effects</subject><subject>Injections, Intravenous</subject><subject>Iopamidol - administration &amp; 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The effects of iomeprol for injection on the cardiovascular system, blood parameters, renal function and the central nervous system were studied after intravascular administration to several animal species of doses at least as high as the highest presumed clinical doses. The following observations were made with respect to the central circulatory system: moderate and short-lasting increases of left ventricular end-diastolic pressure and cardiac output, no significant effects on heart rate either in vitro or in vivo, some episodes of arrhythmia and ventricular fibrillations only at doses far higher than the highest presumed clinical ones, no significant increases in diastolic and systolic coronary flow. The following observations were made with respect to peripheral circulation: no significant changes on blood pressure, moderate and short-lasting increases in renal and pulmonary arterial flow, together with a decrease in peripheral vascular resistance, no crossing of the blood-brain barrier in healthy animals. Cardiovascular and haemodynamic changes were all significantly milder than those induced by ionic contrast media (CM) and were similar to effects caused by some other nonionic contrast media. When injected into the femoral artery of rats, iomeprol was shown to be less algogenic than iopamidol and iohexol. In comparison with the same reference CM, iomeprol affected to a lesser extent the filterability of red blood cells in vitro and showed a less marked effect on their deformability. When administered intravenously at very high dosages, iomeprol had no effect on the glomerular filtration rate, but increased both renal blood flow and diuresis. Proteinuria and enzymuria were also increased, albeit more transiently. The neurotolerance of iomeprol for injection after intravenous administration was higher than or at worst equal to that of iopamidol and iohexol. Iomeprol is therefore a promising new contrast agent particularly suitable for intravascular use in humans.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>8020517</pmid><doi>10.1016/0720-048X(94)90092-2</doi></addata></record>
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subjects Animals
Blood Circulation - drug effects
Blood Coagulation - drug effects
Blood Pressure - drug effects
Blood-Brain Barrier - drug effects
Brain - drug effects
Cardiac Output - drug effects
Contrast Media - administration & dosage
Contrast Media - pharmacology
Contrast media, effects on blood
Contrast media, effects on cardiovascular system
Contrast media, effects on CNS
Contrast media, effects on kidney
Contrast media, experimental study
Contrast media, safety
Coronary Circulation - drug effects
Dogs
Erythrocyte Deformability - drug effects
Glomerular Filtration Rate - drug effects
Heart Rate - drug effects
Injections, Intra-Arterial - adverse effects
Injections, Intravenous
Iopamidol - administration & dosage
Iopamidol - analogs & derivatives
Iopamidol - pharmacology
Male
Mice
Myocardial Contraction - drug effects
Pain - etiology
Platelet Aggregation - drug effects
Proteinuria - chemically induced
Rabbits
Rats
Rats, Sprague-Dawley
Swine
Vascular Resistance - drug effects
Ventricular Fibrillation - chemically induced
title Pharmacodynamic effects of iomeprol for injection in experimental animals
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