Abstract
The naturally occurring prostacyclin (PGI2) is a highly potent vasodilator and effectively lowers blood pressure in experimental animals when applied intravenously. Prostacyclin has, however, the disadvantage that it rapidly deteriorates at physiological pH and at normal room temperature. When PGI2 is applied orally, it has no systemic effect as it is very rapidly disintegrated in the gastric juices.
Preview
Unable to display preview. Download preview PDF.
References
Casals-Stenzel J, Buse M, Losert W (1983) Comparison of the vasodepressor actions of ZK 36374, a stable prostacyclin derivative, PGI2 and PGE1 with their effect on platelet aggregation and bleeding time in rats. Prostaglandins Leukotrienes Med 10: 197–212
Casals-Stenzel J, Haberey M, Loge O, Losert W, Mannesmann G, Radiichel B, Schillinger E, Skuballa W, Town MH, Vorbriiggen H (1980) Pharmacology of a new potent and stable prostacyclin analogue, ZK 36374. Acta Therap (suppl) 614: 37
Ekerdt R, Luhm H, Topert M (1984) Blood supply can be increased in rabbit skin by a stable prostacyclin derivative without potentiation of plasma extravasation. Br J Dermatol 27:144– 146
Haberey M, Maaß B., Stürzebecher C-S (1983) Long term effects of the synthetic PGI2-mi-metic compound Iloprost (ZK 36 374) in spontaneously hypertensive rats. Naunyn-Schmiedebergs Arch Pharmacol 324 (suppl):R 62
Krug B, Küpper J, Arnold G (1985) Effects of a prostacyclin analogue (ZK 36374) on the arterial vascular system and on the integrated systemic venous bed in anesthetized dogs. In: Schrör K (ed) Prostaglandins and other eicosanoids in the cardiovascular system. Karger, Basel, pp 292–297
Schillinger E (1985) Basic pharmacological aspects of Iloprost. Proceedings symposium on Iloprost at the IXth European Congress in Cardiology, Düsseldorf, pp 11–15
Schröder G, Beckmann R, Schillinger E (1986) Studies on vasorelaxant effects and mechanisms of Iloprost in isolated preparations (this volume) pp 129–137
Schrör K, Darius H, Matzky R, Ohlendorf R (1981) The antiplatelet and cardiovascular actions of a new carbacyclin derivative (ZK 36 374) - equipotent to PGI2 in vitro. Naunyn- Schmiedebergs Arch Pharmacol 316: 252–255
Skuballa W, Vorbrüggen H (1983) Synthesis of Iloprost (ZK 36374): A chemically stable and biologically potent prostacyclin analog. Adv Prostagl Thromb and Leukotr Res 11:299– 305
Skuballa W, Vorbrüggen H (1981) A new route to 6a-carbacyclins - synthesis of a stable, biologically potent prostacyclin analogue. Angew Chem Int Ed Engl 20: 1046–1048
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1987 Springer-Verlag, Berlin Heidelberg
About this paper
Cite this paper
Haberey, M., Loge, O., Maaß, B., Ohme, G. (1987). Hemodynamic Profile of Iloprost in Rats, Rabbits and Cats. In: Gryglewski, R.J., Stock, G. (eds) Prostacyclin and Its Stable Analogue Iloprost. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71499-3_18
Download citation
DOI: https://doi.org/10.1007/978-3-642-71499-3_18
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-71501-3
Online ISBN: 978-3-642-71499-3
eBook Packages: Springer Book Archive