| Literature DB >> 19907349 |
Li-Chun Zhao1,2, Bo Yang1, Rengang Wang1, Stuart A Lipton1, Dongxian Zhang1.
Abstract
All botulinum toxins (BoNTs, types A-G) inhibit synaptic transmitter release from motoneurons, and thus result in respiratory arrest and death. Rapid treatment with anti-BoNT antibodies can prevent progression, but recovery still requires weeks on a ventilator. Even after recovery, there is a potential for persistent fatigue in some cases of botulism even years after the insult, possibly because of motoneuron dropout for previously unknown reasons. Unique among BoNTs, the C-type (BoNT/C) cleaves two proteins involved in neurotransmitter release, syntaxin and SNAP-25, and induces apoptotic cell death in cultured cerebellar neurons. It is not clear, however, whether BoNT/C also affects neurons that encounter toxin in vivo, namely motoneurons. Here, we provide experimental evidence that BoNT/C causes a slow degeneration of motoneurons both in vitro and in vivo. This novel form of BoNT/C-induced cell death may require new treatment strategies.Entities:
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Year: 2010 PMID: 19907349 PMCID: PMC4351749 DOI: 10.1097/WNR.0b013e328330dcca
Source DB: PubMed Journal: Neuroreport ISSN: 0959-4965 Impact factor: 1.837