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A toxin from the spider Phoneutria nigriventer that blocks calcium channels coupled to exocytosis
Author(s) -
Guatimosim C.,
RomanoSilva M. A.,
Cruz J. S.,
Beirão P. S. L.,
Kalapothakis E.,
MoraesSantos T.,
Cordeiro M. N.,
Diniz C. R.,
Gomez M. V.,
Prado M. A. M.
Publication year - 1997
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0701381
Subject(s) - exocytosis , synaptic vesicle , calcium , voltage dependent calcium channel , spider toxin , chemistry , neurotransmission , depolarization , t type calcium channel , stx1a , biophysics , population , neuroscience , biology , biochemistry , vesicle , glutamate receptor , membrane , receptor , medicine , environmental health , organic chemistry
1 The aim of the present experiments was to investigate the pharmacological action of a toxin from the spider Phoneutria nigriventer , Tx3‐3, on the function of calcium channels that control exocytosis of synaptic vesicles. 2 Tx3‐3, in confirmation of previous work, diminished the intracellular calcium increase induced by membrane depolarization with KCl (25 m M ) in rat cerebrocortical synaptosomes. The toxin was very potent (IC 50 0.9 n M ) at inhibiting calcium channels that regulate calcium entry in synaptosomes. In addition, Tx3‐3 blocked the exocytosis of synaptic vesicles, as measured with the fluorescent dye FM1‐43. 3 Using ω‐toxins that interact selectively with distinct neuronal calcium channels, we investigated whether the target of Tx3‐3 overlaps with known channels that mediate exocytosis. The results indicate that the main population of voltage‐sensitive calcium channels altered by Tx3‐3 can also be inhibited by ω‐agatoxin IVA, an antagonist of P/Q calcium channels. ω‐conotoxin GVIA, which inhibits N type calcium channels did not decrease significantly the entry of calcium or exocytosis of synaptic vesicles in depolarized synaptosomes. 4 It is concluded that Tx3‐3 potently inhibits ω‐agatoxin IVA‐sensitive calcium channels, which are involved in controlling exocytosis in rat brain cortical synaptosomes.British Journal of Pharmacology (1997) 122 , 591–597; doi: 10.1038/sj.bjp.0701381