The chronic constriction injury (CCI) of sciatic nerve was used as a model of neuropathic pain. This model was originally proposed by Bennett and Xie (1988) and can be adapted for both rats and mice. The study conducted by Marinelli et al., in 2010 (Marinelli et al., 2010) mainly investigated the effects of BoNT/A on neuropathic pain. They demonstrated that the BoNT/A counteracted the neuropathic pain induced by chronic constriction injury (CCI) to the sciatic nerve both in mice and in rats. They suggest that this effect

was already present after a single intraplantar (i.pl.) or intrathecal (i.t.) neurotoxin administration. This significantly reduced the sciatic nerve ligation-induced mechanical allodynia in mice and rats along with the thermal hyperalgesia in rats. This effect on the CCI model indicated Selleckchem LBH589 the BoNT/A interfering function mediated by blocking neuroexoctosis through the cleavage

of synaptosome-associated protein of SNAP-25. Meanwhile, according to the previous reports, the inhibitory effects on GABA (Verderio et al., 2004), glutamate (Cui et al., 2004), CGRP (Lucioni et al., 2008) and SP (Ishikawa et al., 2000) are also involved in CCI model. Therefore, the mechanism should be similar to that of the inflammation pain. Furthermore, Marinelli et al. reported that a single injection of BoNT/A was sufficient not only to reduce the mechanical allodynia and cold hyperalgesia selleck chemicals llc but also to improve the functional recovery of injured paw and to enhance the regeneration processes in the injured nerve (Marinelli et al., 2010). Protein Tyrosine Kinase inhibitor It is

extremely important that BoNT/A exerts analgesic effects and simultaneously is able to accelerate the process of nerve regeneration (Marinelli et al., 2010), which opens promising prospects on the development of new pharmacotherapeutic approach against neuropathic pain. The model of diabetic neuropathic pain is another frequently-used neuropathic pain. Rats were induced to become diabetic by a single intraperitoneal injection of streptozotocin (80 mg/kg). In 2010, Bach-Rojecky et al. (Bach-Rojecky et al., 2010) reported that the diabetic animals with at least 25% lower pain thresholds compared to that of the non-diabetic group were considered neuropathic and were injected with BoNT/A either subcutaneously (3, 5 and 7 U/kg) or intrathecally (1 U/kg). The results presented as pain reduction after BoNT/A injection in the animals with diabetic neuropathy. They also shared their hypothesis on the mechanism of this effect based on their results. Basically, they believed that the bilateral pain reduction after unilateral toxin application and the effectiveness of lower dose with the faster onset after the intrathecal injection was suggestive of the involvement of the central nervous system in the antinociceptive action of BoNT/A in painful diabetic neuropathy.