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Ropivacaine and lidocaine inhibit proliferation of non-transformed cultured adult human fibroblasts, endothelial cells and keratinocytes

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Abstract

Local anaesthetics are known to affect a variety of cell functions, many of which are involved in the inflammatory response. Local anaesthetics have also been shown to influence cell proliferation. The aim of this study was to examine the effect of two local anaesthetics (ropivacaine and lidocaine) on cell proliferation of cultured human fibroblasts, vascular endothelial cells and epithelial cells, i.e. keratinocytes, as earlier studies have not included primary human cell types. Significant inhibition of fibroblast proliferation was observed with concentrations of 50 μM ropivacaine or 100 μM lidocaine in 1% newborn calf serum and 500 μM ropivacaine or lidocaine in 10% newborn calf serum. The proliferation of endothelial cells was significantly inhibited by 1 mM ropivacaine in 5% human serum and 500 μM ropivacaine or 100 μM lidocaine in 40% human serum. Significant inhibition was not obtained with lidocaine when these cells were cultured in 5% HS. Significant inhibition of keratinocytes was obtained with 100 μM ropivacaine and 500 μM lidocaine. The effective concentrations are within the range of therapeutical concentrationsin vivo and there seems to be a general correlation between the local anaesthetic potency and the inhibiting effect on cell proliferation. This suggest a mechanism by which local anaesthetics may exhibit anti-hyperproliferative effects in clinical situations.

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Authors and Affiliations

  1. Astra Pain Control, Preclinical Research & Development, S-151 85, Södertälje, Sweden

    Titti Martinsson & Carl-Johan Dalsgaard

  2. Department of Anatomy, Karolinska Institute, S-10401, Stockholm, Sweden

    Anders Haegerstrand

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  1. Titti Martinsson
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  2. Anders Haegerstrand
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  3. Carl-Johan Dalsgaard
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Martinsson, T., Haegerstrand, A. & Dalsgaard, CJ. Ropivacaine and lidocaine inhibit proliferation of non-transformed cultured adult human fibroblasts, endothelial cells and keratinocytes. Agents and Actions 40, 78–85 (1993). https://doi.org/10.1007/BF01976755

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