Differential stereoselective effects of levobupivacaine, bupivacaine and dexbupivacaine on the heart in isolated rat hearts

  • Urashima Kazuya
    Department of Clinical Pharmacy and Clinical Pharmacokinetics, Osaka University of Pharmaceutical Sciences
  • Sohma Yoshiro
    Department of Physiology, Osaka Medical College
  • Ijiri Yoshio
    Department of Pharmacy, Osaka Medical College Hospital
  • Terai Shiori
    Department of Hygienic Chemistry, Osaka University of Pharmaceutical Sciences
  • Umeda Takashi
    Department of Clinical Acupuncture, Kansai College of Oriental Medicine
  • Kawakami Yuka
    Department of Clinical Pharmacy and Clinical Pharmacokinetics, Osaka University of Pharmaceutical Sciences
  • Nishihori Takako
    Department of Clinical Pharmacy and Clinical Pharmacokinetics, Osaka University of Pharmaceutical Sciences
  • Hirotani Yoshihiko
    Department of Clinical Pharmacy and Clinical Pharmacokinetics, Osaka University of Pharmaceutical Sciences
  • Tanaka Kazuhiko
    Department of Clinical Pharmacy and Clinical Pharmacokinetics, Osaka University of Pharmaceutical Sciences

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抄録

Bupivacaine(BUP) has an advantage over other local anesthetics because of its long-acting sensory anesthesia, but because of its high affinity for the myocardial Na+ channel it can be cardiotoxic. Levobupivacaine(LBUP) is an S(-)-isomer of the racemate BUP, and dexbupivacaine(DBUP) is an R(+)-isomer. LBUP has less neuronal and cardiac toxicity than BUP and DBUP, but DBUP induces more negative chronotropism and arrhythmogenic effects than either LBUP or BUP.<BR>

収録刊行物

  • 循環制御

    循環制御 26 (2), 140-147, 2005

    日本循環制御医学会

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