Neurotoxins affecting neuroexocytosis

被引:965
作者
Schiavo, G
Matteoli, M
Montecucco, C
机构
[1] Univ Padua, Dipartimento Sci Biomed, I-35100 Padua, Italy
[2] Univ Padua, Ctr Consiglio Nazl Ric Biomembrane, I-35100 Padua, Italy
[3] Univ Milan, Dipartimento Farmacol, Ctr Consiglio Nazl Ric Farmacol Mol & Cellulare, Milan, Italy
[4] Univ Milan, Dipartimento Farmacol, Ctr B Ceccarelli, Milan, Italy
[5] Imperial Canc Res Fund, London WC2A 3PX, England
关键词
D O I
10.1152/physrev.2000.80.2.717
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Neurotoxins Affecting Neuroexocytosis. Physiol. Rev. 80: 717-766, 2000. -Nerve terminals are specific sites of action of a very large number of toxins produced by many different organisms. The mechanism of action of three groups of presynaptic neurotoxins that interfere directly with the process of neurotransmitter release is reviewed, whereas presynaptic neurotoxins acting on ion channels are not dealt with here. These neurotoxins can be; grouped in three large families: 1) the clostridial neurotoxins that act inside nerves and block neurotransmitter release ria their metalloproteolytic activity directed specifically on SNARE proteins; 2) the snake presynaptic neurotoxins with phospholipase A, activity, whose site of :: action is still undefined and which induce the release of acethylcholine followed by impairment of synaptic functions; and 3) the excitatory latrotoxin-like neurotoxins that induce: a massive release of neurotransmitter at peripheral and central synapses. Their modes of binding, sites of action, and biochemical activities are discussed in relation to the symptoms of the diseases they cause. The use of these,toxins in cell biology and neuroscience is considered as well as the therapeutic utilization of the botulinum neurotoxins in human diseases characterized by hyperfunction of cholinergic terminals.
引用
收藏
页码:717 / 766
页数:50
相关论文
共 674 条
[11]   ACTION OF DIPHTHERIA-TOXIN DOES NOT DEPEND ON THE INDUCTION OF LARGE, STABLE PORES ACROSS BIOLOGICAL-MEMBRANES [J].
ALDER, GM ;
BASHFORD, CL ;
PASTERNAK, CA .
JOURNAL OF MEMBRANE BIOLOGY, 1990, 113 (01) :67-74
[12]  
ALMERS W, 1994, NATURE, V367, P682
[13]   EFFECTS OF THE POTASSIUM CHANNEL BLOCKING DENDROTOXINS ON ACETYLCHOLINE-RELEASE AND MOTOR-NERVE TERMINAL ACTIVITY [J].
ANDERSON, AJ ;
HARVEY, AL .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 93 (01) :215-221
[14]   TERMINAL SPROUTING IN MOUSE NEUROMUSCULAR-JUNCTIONS POISONED WITH BOTULINUM TYPE-A TOXIN - MORPHOLOGICAL AND ELECTROPHYSIOLOGICAL FEATURES [J].
ANGAUTPETIT, D ;
MOLGO, J ;
COMELLA, JX ;
FAILLE, L ;
TABTI, N .
NEUROSCIENCE, 1990, 37 (03) :799-808
[15]   Export of cellubrevin from the endoplasmic reticulum is controlled by BAP31 [J].
Annaert, WG ;
Becker, B ;
Kistner, U ;
Reth, M ;
Jahn, R .
JOURNAL OF CELL BIOLOGY, 1997, 139 (06) :1397-1410
[16]  
[Anonymous], 1997, VENOM PHOSPHOLIPASE
[17]  
[Anonymous], 1989, BOTULINUM NEUROTOXIN
[18]   Phospholipase A(2) - A structural review [J].
Arni, RK ;
Ward, RJ .
TOXICON, 1996, 34 (08) :827-841
[19]   INFANT BOTULISM [J].
ARNON, SS .
ANNUAL REVIEW OF MEDICINE, 1980, 31 :541-560
[20]   CHARACTERIZATION OF THE INHIBITORY-ACTION OF BOTULINUM NEUROTOXIN TYPE-A ON THE RELEASE OF SEVERAL TRANSMITTERS FROM RAT CEREBROCORTICAL SYNAPTOSOMES [J].
ASHTON, AC ;
DOLLY, JO .
JOURNAL OF NEUROCHEMISTRY, 1988, 50 (06) :1808-1816