Abstract

The mouse LD50 assay is routinely used for potency testing of botulinum toxins. Unfortunately, this test is associated with severe pain and distress in animals and requires large quantities of mice. Here we used cocultures of spinal cord and muscle tissue as an alternative for probing botulinum toxins. Cocultures were prepared from mouse embryonic tissue (C57/BL6J) and cultured for 24-27 days. In these cultures spontaneous muscle activity was quantified in sham- and botulinum toxin-treated cultures for up to 3 days by video microscopy. At a concentration of 58 fmol/L or higher, incobotulinumtoxin A significantly reduced the frequency of muscle contractions within 24 hours after incubation. Hence, nerve-muscle-cultures are similar sensitive as the mouse LD50 assay. The limit of detection, as observed in our study, is close to the most sensitive cell-based bioassays, capable to detect concentrations of botulinum neurotoxin A between 30 and 50 fmol/L. However, spontaneous muscle activity of individual cultures displayed considerable fluctuations when evaluated on a day-to-day basis. Generally, the authors would like to emphasize, that in its present form, this in vitro assay might be too laborious for botulinum toxin potency testing. Thus, methodical improvements to decrease data variability are the next milestone to be passed towards developing this model into an assay that can be utilized for reducing animal experimentation.

Highlights

  • Botulinum neurotoxins are zinc endopeptidases which hydrolyze synaptosomal-associated receptor (SNARE) proteins (Martens and McMahon, 2008)

  • By cleaving the plasma membrane-associated peptide SNAP-25, botulinum toxin A inhibits the release of acetylcholine at the neuromuscular junction and causes flaccid paralysis that can be fatal (Humeau et al, 2000)

  • Muscle movements were abolished by the muscle-relaxant drug succinylcholine, which targets nicotinic acetylcholine receptors, thereby interrupting neuromuscular transmission (Drexler et al, 2013). These findings confirmed that muscle contractions in nerve-muscle cultures were triggered by spinal motor neurons generating action potentials and releasing acetylcholine onto muscle fibers

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Summary

Introduction

Botulinum neurotoxins are zinc endopeptidases which hydrolyze synaptosomal-associated receptor (SNARE) proteins (Martens and McMahon, 2008). The standard procedure according to Pharm EU and USP is the classical mouse LD50 (lethal dose that kills 50% of the tested animals) assay Because this test is associated with severe distress in animals and requires large numbers of rodents, it is highly desirable to develop animal-free assays (Adler et al, 2010; Bitz, 2010; Pharm EU, 2011). Due to patent issues it is unlikely that new assays developed by manufacturers of licensed products or profit-oriented institutions will widely replace animal LD50 tests in the near future (Fernández-Salas et al, 2012) For this reason, the promotion of in vitro assays that are free to use should not be neglected

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