2011
DOI: 10.1002/jat.1728
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Palytoxin causes nonoxidative necrotic damage to PC12 cells in culture

Abstract: Palytoxin (PTX) is a potent marine toxin that causies serious damage to various tissues and organs. It has been reported to affect the transport of cations across the plasma membranes, which is commonly recognized as being the principal mechanism of its highly toxic action on mammals, including humans. However, although some marine toxins have been shown to cause toxic effects on the nervous system by interfering with the transmission of nerve impulses, the effect of PTX on neuronal cells has not yet been full… Show more

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Cited by 9 publications
(3 citation statements)
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“…PTX was shown to induce ion currents (channels permeable to Na + and K + and slightly permeable to Ca 2+ , choline and tetramethylammonium) in mouse neuroblastoma cells [144]. As a matter of fact, the activity on cation transport is commonly recognized to be PTX’s main toxic mechanism [145]. …”
Section: Cytotoxicity Of Cnidarian Extracts On Cultured Cellsmentioning
confidence: 99%
See 1 more Smart Citation
“…PTX was shown to induce ion currents (channels permeable to Na + and K + and slightly permeable to Ca 2+ , choline and tetramethylammonium) in mouse neuroblastoma cells [144]. As a matter of fact, the activity on cation transport is commonly recognized to be PTX’s main toxic mechanism [145]. …”
Section: Cytotoxicity Of Cnidarian Extracts On Cultured Cellsmentioning
confidence: 99%
“…PTX seems to cause cell membrane damage through a non-oxidative necrotic process. The exposure to PTX was seen to cause release of lactate dehydrogenase into the culture medium [145]. In Caco-2 cells, PTX at a concentration of 8.9 ± 3.7 × 10 −12 M reduced the mitochondrial activity by 50% and induced cytotoxicity when tested with Sulforhodamine B assay (EC 50 = 2.0 ± 0.6 × 10 −11 M) as well as with LDH release (EC 50 = 4.5 ± 1.4 × 10 −9 M) [151].…”
Section: Cytotoxicity Of Cnidarian Extracts On Cultured Cellsmentioning
confidence: 99%
“…Other findings in the field of PaP toxin research may open new possibilities to define endpoints for development of functional assays, e.g., the role of oxidative stress in exposure of keratinocytes to Pltx (Pelin et al, 2013b) or non-oxidative necrosis induced by Pltx in PC12 cells (Sagara et al, 2013).…”
Section: )mentioning
confidence: 99%