Methods and findings in experimental and clinical pharmacology | Vol.19, Issue.1 | | Pages 27-33
Effects of bupivacaine and its isomers on guinea pig tracheal smooth muscle.
The effects of racemic bupivacaine and its (-)-(S)- and (+)-(R)-isomers on guinea pig tracheal smooth muscle tension were studied in vitro. Racemic bupivacaine had a dual action with contraction at low concentrations (6.9-55 x 10(-6) M) and relaxation at high concentrations (1.1-18 x 10(-4) M), (-)-(S)-Bupivacaine had dual action comparable to that of racemic bupivacaine, while (+)-(R)-bupivacaine had only weak contractile effects with more marked relaxant effects. The contractile effects of bupivacaine were abolished in Ca(2+)-free medium and by verapamil, while the relaxant effects were not influenced by verapamil or Ca(2+)-free medium. The (-)-(S)-isomer is responsible for the contractile effects of racemic bupivacaine, whereas both (-)-(S)- and (+)-(R)-isomers contribute to its relaxant effects. In preparations denuded of epithelium, the (maximal) responses were attenuated to 86% of maximum contraction and 48% of maximum relaxation, suggesting that the epithelium plays a larger role in relaxant than in contractile responses to bupivacaine. It is concluded that bupivacaine has a dual action on guinea pig tracheal smooth muscle with epithelium-independent. Ca(2+)-dependent contraction at low concentrations and epithelium-dependent, Ca(2+)-independent relaxation at higher concentrations.
Original Text (This is the original text for your reference.)
Effects of bupivacaine and its isomers on guinea pig tracheal smooth muscle.
The effects of racemic bupivacaine and its (-)-(S)- and (+)-(R)-isomers on guinea pig tracheal smooth muscle tension were studied in vitro. Racemic bupivacaine had a dual action with contraction at low concentrations (6.9-55 x 10(-6) M) and relaxation at high concentrations (1.1-18 x 10(-4) M), (-)-(S)-Bupivacaine had dual action comparable to that of racemic bupivacaine, while (+)-(R)-bupivacaine had only weak contractile effects with more marked relaxant effects. The contractile effects of bupivacaine were abolished in Ca(2+)-free medium and by verapamil, while the relaxant effects were not influenced by verapamil or Ca(2+)-free medium. The (-)-(S)-isomer is responsible for the contractile effects of racemic bupivacaine, whereas both (-)-(S)- and (+)-(R)-isomers contribute to its relaxant effects. In preparations denuded of epithelium, the (maximal) responses were attenuated to 86% of maximum contraction and 48% of maximum relaxation, suggesting that the epithelium plays a larger role in relaxant than in contractile responses to bupivacaine. It is concluded that bupivacaine has a dual action on guinea pig tracheal smooth muscle with epithelium-independent. Ca(2+)-dependent contraction at low concentrations and epithelium-dependent, Ca(2+)-independent relaxation at higher concentrations.
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