Phoneutria nigriventer toxin-3 is more commonly referred to as PhTx3.
The PhTx3 neurotoxin is a broad-spectrum calcium channel blocker that inhibits glutamate release, calcium uptake and also glutamate uptake in synaptosomes.[1] Currently, it is known to naturally occur only in the venom of the spider Phoneutria nigriventer, also known as the Brazilian Wandering spider.
Studies
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Many studies have been done on this neurotoxin, including one regarding its effect on the release of 3H-acetylcholine,[2] and one comparing the effect with other toxins used by Phoneutria nigriventer.[1]
Another study made the following claims:[3]
NEUROTOXINS can help the understanding of mechanisms involved in neurotransmission. We here report that two neurotoxin isoforms, Tx3-3 and Tx3-4 obtained from the venom of the spider Phoneutria nigriventer inhibited the 45 Ca2+ influx in rat cortical synaptosomes induced by the scorpion venom tityustoxin. The IC50 for Tx3-3 and Tx3-4 were 0.32 and 7.9 nM, respectively. The neurotoxins Tx3-3 and Tx3-4 are very effective in inhibiting 45 Ca2+ influx and they should be useful in studies involving Ca2+-dependent processes.
A study done at the Universidade Federal de Minas Gerais stated this:[4]
The toxic fraction, Phoneutria nigriventer toxin-3 (PhTx3), abolished Ca2+-dependent glutamate release, but did not alter Ca2+-independent secretion of glutamate when rat brain cortical synaptosomes were depolarized with 33 mM KCl. This effect was most likely due to interference with the entry of calcium through voltage-gated calcium channels, because PhTx3 reduced by 50% the increase in intrasynaptosomal free calcium induced by membrane depolarization, and did not affect the release of glutamate evoked by a calcium ionophore (ionomycin). A polypeptide (Tx3-3) present in the PhTx3 fraction reproduced the effects of the PhTx3 fraction on transmitter release and intrasynaptosomal free calcium in the low nanomolar range. We compared the alterations produced by the Tx3-3 with the actions of toxins known to block calcium channels coupled to exocytosis: the results indicated that the Tx3-3 inhibition of glutamate release and intrasynaptosomal calcium resemble that observed with w-conotoxin MVIIC. We suggest that the Tx3-3 is a calcium-channel antagonist that blocked glutamate exocytosis.
References
edit- ^ a b Pinheiro, Ana C.N.; Gomez, Rodrigo S.; Massensini, Andre R.; Cordeiro, Marta N.; Richardson, Michael; Romano-Silva, Marco A.; Prado, Marco Antonio M.; Marco, Luiz De; Gomez, Marcus V. (October 2006). "Neuroprotective effect on brain injury by neurotoxins from the spider Phoneutria nigriventer". Neurochemistry International. 49 (5): 543–547. doi:10.1016/j.neuint.2006.04.009. PMID 16759753. S2CID 33511610. INIST 18035910.
- ^ Gomez, R.S.; Casali, T.A.A.; Romano-Silva, M.A.; Cordeiro, M.N.; Diniz, C.R.; Moraes-Santos, T.; Prado, M.A.M.; Gomez, M.V. (August 1995). "The effect of PhTx3 on the release of 3H-acetylcholine induced by tityustoxin and potassium in brain cortical slices and myenteric plexus". Neuroscience Letters. 196 (1–2): 131–133. doi:10.1016/0304-3940(95)11843-L. PMID 7501242. S2CID 12820501.
- ^ Miranda, Debora Marques; Romano-Silva, Marco Aurélio; Kalapothakis, Evanguedes; Diniz, Carlos Ribeiro; Cordeiro, Marta Nascimento; Santos, Tasso Moraes; Antonio, Marco; Prado, Máximo; Gomez, Marcus Vinicius (May 1998). "Phoneutria nigriventer toxins block tityustoxin-induced calcium influx in synaptosomes". NeuroReport. 9 (7): 1371–1373. doi:10.1097/00001756-199805110-00022. PMID 9631431. S2CID 37009866.
- ^ Prado, M A; Guatimosim, C; Gomez, M V; Diniz, C R; Cordeiro, M N; Romano-Silva, M A (15 February 1996). "A novel tool for the investigation of glutamate release from rat cerebrocortical synaptosomes: the toxin Tx3-3 from the venom of the spider Phoneutria nigriventer". Biochemical Journal. 314 (Pt 1): 145–150. doi:10.1042/bj3140145. PMC 1217017. PMID 8660275.