Figure 1From: Development of an in vitro model to measure bioactivity of botulinum neurotoxin A in rat bladder muscle strips Schematic representation of the in vitro model. The organ bath was continuously perfused with Krebs’ solution. Chemical stimulation was performed by perfusion the bath with 80 mM KCl or 1 μM CCh and flushing the bath with Krebs’ solution in between. During BoNT-A incubation, the bath was continuously perfused by the same concentration of BoNT-A (0.03, 0.2, 0.3 nM).Back to article page