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Studies on Vasorelaxant Effects and Mechanisms of Iloprost in Isolated Preparations

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Prostacyclin and Its Stable Analogue Iloprost

Abstract

PGI2, the main cyclo-oxygenase product generated by blood vessels [14], is known to possess powerful vasodilatory properties in different vascular beds [10, 22]. Iloprost is slightly more active than PGI2 in relaxing isolated strips from bovine coronary arteries and rabbit arteries which are commonly used as bioassay systems for PGI2-mimetic vasorelaxing properties [2, 3, 5]. The PGI2-induced alterations in vascular tone seem to be mediated by specific vascular receptor sites. Iloprost binds specifically and reversibly to prostacyclin-like receptors in various preparations including vascular smooth muscle [19, 23]. Whether the interaction of PGI2 with the vascular PGI2 receptor is followed by an activation of adenylate cyclase and an increase in cAMP is still controversial [4, 12, 15, 18, 20].

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© 1987 Springer-Verlag, Berlin Heidelberg

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Schröder, G., Beckmann, R., Schillinger, E. (1987). Studies on Vasorelaxant Effects and Mechanisms of Iloprost in Isolated Preparations. 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_15

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  • DOI: https://doi.org/10.1007/978-3-642-71499-3_15

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-71501-3

  • Online ISBN: 978-3-642-71499-3

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