Lidocaine-induced cell death in a human model of neuronal apoptosis

P. Friederich, T. P. Schmitz

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

Background and objective: Clinical studies suggest that lidocaine may induce irreversible neurological damage after spinal application in human beings. The mechanisms underlying the possible cytotoxic action of lidocaine have only been suggested from animal studies. This study aimed to investigate if lidocaine exhibited cytotoxic action in a human model widely used for the study of neuronal apoptosis. This is important to know as it may help one to judge on possible neurotoxic risks imposed by the spinal application of lidocaine. Methods: The concentration- and time-dependent effects of lidocaine on retinoic acid-differentiated human neuroblastoma SH-SY5Y cells were quantified by trypan blue staining, the release of lactate dehydrogenase, immunocytochemistry and flow cytometry. Results: The local anaesthetic caused a significant increase in the number of cells staining positive for trypan blue, a significant increase of LDH release into the incubation medium, and a significant increase of 7AAD and annexin V binding. Lidocaine induced apoptosis already at 3 mm. At a concentration of 10 mmol 47% of the cells and at 30 mmol 98% of the cell population was necrotic. Both necrosis and apoptosis were time-dependent. Conclusions: The results demonstrate that lidocaine exhibited neurotoxic effects in a human model established for the study of drug-induced neuronal apoptosis. The results were consistent with the neurotoxic clinical effects of lidocaine. These effects may be produced by more than a single mechanism.

Original languageEnglish
Pages (from-to)564-570
Number of pages7
JournalEuropean Journal of Anaesthesiology
Volume19
Issue number8
DOIs
StatePublished - 2002
Externally publishedYes

Keywords

  • Anaesthesia conduction, anaesthesia local
  • Anaesthetics, local, lidocaine
  • Cell death, apoptosis
  • Cell death, necrosis
  • Neurotoxins

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