{"refrec":{"BRefID":287932,"RR":"<b>Domínguez-Pérez, D.; Diaz-Garcia, C.; García-Delgado, N.; Sierra-Gómez, Y.; Castañeda, O.; Antunes, A.</b> (2013). Insights into the toxicological properties of a low molecular weight fraction from <i>Zoanthus sociatus</i> (Cnidaria). <i>Mar. Drugs 11(8)</i>: 2873-2881. <a href=\"https://dx.doi.org/10.3390/md11082873\" target=\"_blank\">https://dx.doi.org/10.3390/md11082873</a>","BEntID":279957,"PublicFlag":1,"CheckedFlag":1,"wosflag":1,"vabbflag":null,"RefStringPartII":". <i>Mar. Drugs 11(8)</i>: 2873-2881. <a href=\"https://dx.doi.org/10.3390/md11082873\" target=\"_blank\">https://dx.doi.org/10.3390/md11082873</a>","DocTypID":8,"DocType":"Journal article","MarineFlag":1,"FreshFlag":0,"BrackishFlag":0,"TerrestrialFlag":0,"Authorstring":"Domínguez-Pérez, D.; Diaz-Garcia, C.; García-Delgado, N.; Sierra-Gómez, Y.; Castañeda, O.; Antunes, A.","OrigTitleTranslFlag":0,"Authorstringtrunc":"Domínguez-Pérez, D. <i>et al.</i>","Englishabstract":"The phylum Cnidaria is an ancient group of venomous animals, specialized in the production and delivery of toxins. Many species belonging to the class Anthozoa have been studied and their venoms often contain a group of peptides, less than 10 kDa, that act upon ion channels. These peptides and their targets interact with high affinity producing neurotoxic and cardiotoxic effects, and even death, depending on the dose and the administration pathway. Zoanthiniaria is an order of the Subclass Hexacorallia, class Anthozoa, and unlike sea anemone (order Actiniaria), neither its diversity of toxins nor the <i>in vivo</i> effects of the venoms has been exhaustively explored. In this study we assessed some toxicological tests on mice with a low molecular weight fraction obtained by gel filtration in Sephadex G-50 from <i>Zoanthus sociatus</i> crude extract. The gel filtration chromatogram at 280 nm revealed two major peaks, the highest absorbance corresponding to the low molecular weight fraction. The toxicological effects seem to be mostly autonomic and cardiotoxic, causing death in a dose dependent manner with a LD50 of 792 μg/kg. Moreover, at a dose of 600 μg/kg the active fraction accelerated the KCl-induced lethality in mice. 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