Beside the therapeutic effects reviewed above, there are some other kinds of chronic pain that can be treated. In 2010, Santamato et al. reported the treatment of the neck pain that was related to nocturnal bruxism with BoNT/A. In this study, each masseter muscle was injected with a dose of about 40 units and the temporal muscle was bilaterally injected with 25 units. After three days of treatment with BoNT/A, a decrease in bruxism symptoms was noted (Santamato et al., 2010). Furthermore, Jason Abbott also used BoNT/A in women with chronic pelvic pain in 2009. They indicated

that BoNT/A (20–40 units) used in the vulva may have a continued benefit for 3–6 months after injection with limited Nutlin-3a manufacturer side effects (Abbott, 2009). The LC in the type E BoNT gives rise to a more extensively truncated SNAP-25 product that is unable to form functional complexes with its SNARE partners. Therefore, it offers a more fast acting effect compared to that of BoNT/A. Besides, it can also pseudo-irreversibly abolish release of neurotransmitters. Generally speaking, BoNT/E blocks the neurotransmission more quickly and more potently compared to BoNT/A. However, the clinical application of BoNT/A is restricted by its neuromuscular paralytic

action being transient (less than 4 weeks) in contrast to BoNT/A (more than 4 months). In the past few years, Meng J reported the construction Alectinib of a chimera of BoNT/A and/E by introducing a nucleotide sequence encoding the acceptor binding Hc domain of type A into the BoNT/E gene (Fig. 3). The recombinant EA chimeric protein can then be expressed in Escherichia coli and be purified. They found that it cleaved SNAP-25 in the trigeminal neurons and blocked CGRP release triggered by all stimuli tested, including capsaicin ( Wang et al., 2011). After that, some people proved that it was possible to show this dramatic increase in persistence of neuroparalysis ( Dolly and O’Connell, 2012). In these days, a faster and more efficient BoNT-based neurotherapeutics

becomes a possibility considering Plasmin the advances in protein engineering. BoNT/A has been under clinical trials for treatment of migraine and other chronic pain for many years. Therefore, the translation of the encouraging results from preclinical studies in animal pain models to clinical treatments of more various types of chronic pain in human sufferers can be a significant step. However, more in depth studies are necessary to reach to a point where it can be clinically applicable. None of the previous studies have established the exact mechanism responsible for analgesic effects of BoNT/A; which could provide the essential foundation of developing future therapeutic strategies. Besides, there is a lack of precise applicable doses and injecting sites to refer to. Therefore, more studies are required to determine the best and accurate method of using BoNT/A is the goal of many ongoing efforts.