Converting enzyme inhibitor ramipril stimulates prostacyclin synthesis by isolated rat aorta: Evidence for a kinin-dependent mechanism

Author:

Scherf H.,Pietsch R.,Landsberg G.,Kramer H. J.,Düsing R.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine

Reference16 articles.

1. Düsing R, Scherhag R, Landsberg G, Glänzer K, Kramer HJ (1983) The converting enzyme inhibitor captopril stimulates prostacyclin synthesis by isolated rat aorta. Eur J Pharmacol 91:501–504

2. Düsing R, Scherhag R, Tippelmann R, Budde U, Glänzer K, Kramer HJ (1982) Arachidonic acid metabolism in isolated rat aorta: dependence of prostacyclin biosynthesis on extracellular potassium concentration. J Biol Chem 257:1993–1996

3. Düsing R, Scherhag R, Glänzer K, Budde U, Kramer HJ (1983) Dietary linoleic acid deprivation. Effects on blood pressure and PGI2 synthesis. Am J Physiol 244:H228-H233

4. Dusting GJ, Mullins EM, Nolan RD (1981) Prostacyclin (PGI2) release accompanying angiotensin conversion in the rat mesenteric vasculature. Eur J Pharmacol 70:129–133

5. Felder K, Witter PU (1984) Effects of the new oral converting enzyme inhibitor 2-(N((S)-1-Ethoxylcarbonyl-3-phenylpropyl)-L-alanyl)-(1S,3S,5S)-2-azabicyclo (3.3.0)octane-3-carboxylic acid (Hoe 498) in essential hypertension. Drug Research 34(II):1452–1454

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