Toxicology and pharmacology of botulinum and tetanus neurotoxins: an update

被引:45
作者
Pirazzini, Marco [1 ,2 ]
Montecucco, Cesare [1 ,3 ]
Rossetto, Ornella [1 ,2 ,3 ]
机构
[1] Univ Padua, Dept Biomed Sci, Via Ugo Bassi 58 B, I-35131 Padua, Italy
[2] Univ Padua, Ctr Interdipartimentale Ric Miol, CIR Myo, Via Bassi 58 B, I-35131 Padua, Italy
[3] CNR, Inst Neurosci, Via Ugo Bassi 58 B, I-35131 Padua, Italy
关键词
Tetanus; Botulism; Neurotoxins; Toxicity; Cholinergic; Therapy; TOXIN TYPE-A; INTERCHAIN DISULFIDE BOND; MAJOR DEPRESSIVE DISORDER; SMALL-MOLECULE INHIBITORS; DOUBLE-BLIND; NEUROTRANSMITTER RELEASE; THIOREDOXIN REDUCTASE; CLOSTRIDIUM-BOTULINUM; SYNAPTIC VESICLES; CERVICAL DYSTONIA;
D O I
10.1007/s00204-022-03271-9
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Tetanus and botulinum neurotoxins cause the neuroparalytic syndromes of tetanus and botulism, respectively, by delivering inside different types of neurons, metalloproteases specifically cleaving the SNARE proteins that are essential for the release of neurotransmitters. Research on their mechanism of action is intensively carried out in order to devise improved therapies based on antibodies and chemical drugs. Recently, major results have been obtained with human monoclonal antibodies and with single chain antibodies that have allowed one to neutralize the metalloprotease activity of botulinum neurotoxin type A1 inside neurons. In addition, a method has been devised to induce a rapid molecular evolution of the metalloprotease domain of botulinum neurotoxin followed by selection driven to re-target the metalloprotease activity versus novel targets with respect to the SNARE proteins. At the same time, an intense and wide spectrum clinical research on novel therapeutics based on botulinum neurotoxins is carried out, which are also reviewed here.
引用
收藏
页码:1521 / 1539
页数:19
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