Selected Publication:
Stoschitzky, K; Lindner, W; Rath, M; Leitner, C; Uray, G; Zernig, G; Moshammer, T; Klein, W.
Stereoselective hemodynamic effects of (R)-and (S)-propranolol in man.
Naunyn Schmiedebergs Arch Pharmacol. 1989; 339(4):474-478
Doi: 10.1007/BF00736064
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- Leading authors Med Uni Graz
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Stoschitzky Kurt
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- Abstract:
- In a randomized, double-blind, placebo-controlled, cross-over study 24 healthy volunteers were examined before and 2 h after oral administration of 80 mg (R,S)-, 40 mg (R)- and 40 mg (S)-propranolol.HCl; 8 of them received placebo in an additional run. During exercise on a bicycle ergometer and a rest period the rate pressure product was decreased by 80 mg (R,S)-propranolol.HCl (-32.8% p less than 0.0001) and 40 mg (S)-propranolol.HCl (-32.3%; p less than 0.0001), whereas 40 mg (R)-propranolol.HCl as well as placebo showed no effect. Corresponding binding inhibition experiments using (-)-(125I)iodocyanopindolol in a sarcolemma-enriched cardiac membrane preparation yielded a eudismic ratio of 179 for (S)- over (R)-propranolol. 2 h after oral application, stereospecific HPLC analysis revealed different individual concentrations in plasma of (R)- 22.3 +/- 21.7 ng/ml) and (S)-propranolol (30.4 +/- 26.9 ng/ml) when 80 mg of (R,S)-propranolol.HCl was administered. The plasma levels were similar when 40 mg of the pure enantiomer of (R)- (22.7 +/- 20.3 ng/ml) or (S)-propranolol.HCl (28.7 +/- 22.5 ng/ml) was applied. (R)- and (S)-propranolol are two substances with different pharmacodynamic and pharmacokinetic properties. As there are methods available to produce the optically pure enantiomers, they should be used rather than the racemic mixture.
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Adult -
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Blood Pressure - drug effects
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Double-Blind Method - drug effects
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Female - drug effects
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Heart Rate - drug effects
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Hemodynamics - drug effects
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Humans - drug effects
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Iodocyanopindolol - drug effects
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Male - drug effects
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Membranes - metabolism
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Pindolol - analogs and derivatives
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Propranolol - pharmacology
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Random Allocation - pharmacology
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Sarcolemma - metabolism
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Stereoisomerism - metabolism