1998
DOI: 10.1016/s0041-0101(98)00158-5
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Pharmacotherapeutic potential of omega-conotoxin MVIIA (SNX-111), an N-type neuronal calcium channel blocker found in the venom of Conus magus

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Cited by 104 publications
(64 citation statements)
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“…A 25-amino acid Ca V 2.2 channel pore-blocking toxin, v-conotoxin MVIIA, has been isolated from the Conus magus snail and mediates potent analgesia after intrathecal delivery to rodents (Chaplan et al, 1994;Bowersox and Luther, 1998;Wang et al, 2000;Scott et al, 2002) and human patients with persistent cancer pain (Atanassoff et al, 2000;Miljanich, 2004;Staats et al, 2004;Thompson et al, 2006;Wallace et al, 2006;Ver Donck et al, 2008). This fits with the important role of Ca V 2.2 channels in neurotransmitter release from afferent terminals.…”
Section: Ca V 2 Channel Pathophysiologymentioning
confidence: 75%
“…A 25-amino acid Ca V 2.2 channel pore-blocking toxin, v-conotoxin MVIIA, has been isolated from the Conus magus snail and mediates potent analgesia after intrathecal delivery to rodents (Chaplan et al, 1994;Bowersox and Luther, 1998;Wang et al, 2000;Scott et al, 2002) and human patients with persistent cancer pain (Atanassoff et al, 2000;Miljanich, 2004;Staats et al, 2004;Thompson et al, 2006;Wallace et al, 2006;Ver Donck et al, 2008). This fits with the important role of Ca V 2.2 channels in neurotransmitter release from afferent terminals.…”
Section: Ca V 2 Channel Pathophysiologymentioning
confidence: 75%
“…28,63,65,69 Com sua seletividade com relação ao alvo molecular, o ziconotídeo bloqueia, em concentrações picomolares, o canal de cálcio do tipo N das fibras nociceptivas tipo A-δ e tipo C nas lâminas I e II da raiz dorsal do cordão nervoso de mamíferos, apresentando analgesia em vários modelos de nocicepção. 70,71 O extraordinário potencial antinociceptivo das ω-contoxinas (o ziconotídeo é mil vezes mais potente do que a morfina) emerge de duas propriedades: a particular sensibilidade das fibras tipo C a essas substâncias, como mencionado, e a ausência de tolerância ao tratamento com esses peptídeos. Em contraste com os opioides, que são agonistas de receptores acoplados à proteína G e que levam à diminuição no número de receptores após tratamento continuado e à consequente dessensibilização, o tratamento com ziconotídeo não induz tolerância após uso crônico.…”
Section: Prialt ® (Ziconotídeo ω-Conotoxina Mviia)unclassified
“…Ziconotide is a selective, reversible blocker of neuronal N-type voltage-sensitive calcium channels that produces potent antinociceptive effects by blocking neurotransmission from primary nociceptive afferents [42]. This drug and second generation non-peptide drugs are considered to be some of the best new drugs to treat chronic pain [43].…”
Section: Painmentioning
confidence: 99%