TY - JOUR
T1 - Inhibitory effect of local anaesthetics on reactive oxygen species production by human neutrophils
AU - Mikawa, K.
AU - Akamatsu, H.
AU - Nishina, K.
AU - Shiga, M.
AU - Maekawa, N.
AU - Obara, H.
AU - Niwa, Y.
PY - 1997
Y1 - 1997
N2 - Background: Reactive oxygen species (ROS) generated from neutrophils accumulated in various major organs are thought to play a pivotal role in the pathogenesis of host auto-injury. Lidocaine has been shown to reduce the injury. We investigated the effect of local anaesthetics (lidocaine, mepivacaine and bupivacaine) on ROS production by neutrophils using an in vitro system. Methods: We measured the production of superoxide (ferricytochrome c method), hydrogen peroxide (H2O2: scopoletin fluorescence technique), and hydroxyl radical (OH·: ethylene gas method) by neutrophils isolated from human adult volunteers in the absence and presence of lidocaine (2-200 μg/mL), mepivacaine (3-300 μg/mL), and bupivacaine (3-300 μg/mL). We also measured the ROS generation in a cell-free (xanthine-xanthine oxidase) system. Results: Lidocaine and mepivacaine at higher levels significantly decreased the production of ROS by neutrophils. However, these local anaesthetics at clinically relevant blood concentrations had no effect on the levels of ROS. Furthermore, lidocaine and mepivacaine failed to reduce ROS generated by the cell-free system. Bupivacaine did not decrease ROS generation by either generating system. Conclusion: In conclusion, in the present in vitro system, only concentrations of lidocaine and mepivacaine 100-fold higher than clinically feasible ones reduced ROS production by human neutrophils. However, the local anaesthetics at clinically relevant blood concentrations had no suppressive effect. Further studies using in vivo systems are required to elucidate the inhibitory effects of local anaesthetics on ROS generation in clinical settings.
AB - Background: Reactive oxygen species (ROS) generated from neutrophils accumulated in various major organs are thought to play a pivotal role in the pathogenesis of host auto-injury. Lidocaine has been shown to reduce the injury. We investigated the effect of local anaesthetics (lidocaine, mepivacaine and bupivacaine) on ROS production by neutrophils using an in vitro system. Methods: We measured the production of superoxide (ferricytochrome c method), hydrogen peroxide (H2O2: scopoletin fluorescence technique), and hydroxyl radical (OH·: ethylene gas method) by neutrophils isolated from human adult volunteers in the absence and presence of lidocaine (2-200 μg/mL), mepivacaine (3-300 μg/mL), and bupivacaine (3-300 μg/mL). We also measured the ROS generation in a cell-free (xanthine-xanthine oxidase) system. Results: Lidocaine and mepivacaine at higher levels significantly decreased the production of ROS by neutrophils. However, these local anaesthetics at clinically relevant blood concentrations had no effect on the levels of ROS. Furthermore, lidocaine and mepivacaine failed to reduce ROS generated by the cell-free system. Bupivacaine did not decrease ROS generation by either generating system. Conclusion: In conclusion, in the present in vitro system, only concentrations of lidocaine and mepivacaine 100-fold higher than clinically feasible ones reduced ROS production by human neutrophils. However, the local anaesthetics at clinically relevant blood concentrations had no suppressive effect. Further studies using in vivo systems are required to elucidate the inhibitory effects of local anaesthetics on ROS generation in clinical settings.
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U2 - 10.1111/j.1399-6576.1997.tb04735.x
DO - 10.1111/j.1399-6576.1997.tb04735.x
M3 - Article
C2 - 9150783
AN - SCOPUS:0030937667
SN - 0001-5172
VL - 41
SP - 524
EP - 528
JO - Acta Anaesthesiologica Scandinavica
JF - Acta Anaesthesiologica Scandinavica
IS - 4
ER -