• Medientyp: E-Artikel
  • Titel: In VitroNegative Inotropic Effect of Low Concentrations of Bupivacaine Relates to Diminished Ca2+ Sensitivity but Not to Ca2+ Handling or β-Adrenoceptor Signaling
  • Beteiligte: Flenner, Frederik; Arlt, Nicole; Nasib, Mahtab; Schobesberger, Sophie; Koch, Thea; Ravens, Ursula; Friedrich, Felix; Nikolaev, Viacheslav; Christ, Torsten; Stehr, Sebastian N.
  • Erschienen: Ovid Technologies (Wolters Kluwer Health), 2018
  • Erschienen in: Anesthesiology
  • Sprache: Englisch
  • DOI: 10.1097/aln.0000000000002180
  • ISSN: 0003-3022
  • Schlagwörter: Anesthesiology and Pain Medicine
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Systemic toxicity of local anesthetics is predominantly complicated by their myocardial toxicity. Especially long-acting local anesthetics exert a negative inotropic effect that has been described at lower concentrations than defined for blockade of myocardial ion channels. We evaluated the negative inotropic effect of bupivacaine at a concentration described for clinical toxicity testing the hypothesis that negative inotropy is a result of reduced Ca2+ sensitivity rather than blockade of ion channels.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We simultaneously measured force development and action potentials in guinea pig right papillary muscles (n = 5 to 7). L-type Ca2+ currents (n = 8 to 16) and Ca2+ transients (n = 10 to 11) were measured in isolated cardiomyocytes. Sensitivity of myofilaments to Ca2+ was assessed in skinned fibers (n = 10). Potential effects of bupivacaine on 3′,5′-cyclic adenosine monophosphate concentrations were measured using Förster Resonance Energy Transfer (n = 12 to 14) microscopy.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Bupivacaine reduced force in a concentration-dependent manner from 173 ± 119 µN at baseline to 28 ± 13 µN at 300 µM (mean ± SD). At concentrations giving half-maximum negative inotropic effects (5 µM), the maximum upstroke velocity of action potentials, as a surrogate of sodium channel activity, was unaffected. Maximum positive inotropic effects of isoprenaline were also reduced to 50%. Neither basal nor isoprenaline-induced 3′,5′-cyclic adenosine monophosphate accumulation, L-type Ca2+ currents, or Ca2+ transients were affected by 5 µM bupivacaine, but this concentration significantly decreased Ca2+ sensitivity of myofilaments, changing the negative logarithm of the half-maximum effective Ca2+ concentrations from 5.66 to 5.56 –log[M].</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>We provide evidence that the negative inotropic effect of bupivacaine may be caused mainly by a reduction in myofilament sensitivity to Ca2+.</jats:p></jats:sec>
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