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dc.contributor.authorKritsada Pruksaphonen_US
dc.contributor.authorKae Yi Taniden_US
dc.contributor.authorChoo Hock Tanen_US
dc.contributor.authorPavinee Simsiriwongen_US
dc.contributor.authorJosé María Gutiérreziden_US
dc.contributor.authorKavi Ratanabanangkooniden_US
dc.date.accessioned2020-10-14T08:41:37Z-
dc.date.available2020-10-14T08:41:37Z-
dc.date.issued2020-08-01en_US
dc.identifier.issn19352735en_US
dc.identifier.issn19352727en_US
dc.identifier.other2-s2.0-85090523813en_US
dc.identifier.other10.1371/journal.pntd.0008581en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85090523813&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70798-
dc.description.abstract© 2020 Pruksaphon et al. The aim of this study was to develop an in vitro assay for use in place of in vivo assays of snake venom lethality and antivenom neutralizing potency. A novel in vitro assay has been developed based on the binding of post-synaptically acting α-neurotoxins to nicotinic acetyl-choline receptor (nAChR), and the ability of antivenoms to prevent this binding. The assay gave high correlation in previous studies with the in vivo murine lethality tests (Median Lethal Dose, LD50), and the neutralization of lethality assays (Median Effective Dose, ED50) by antisera against Naja kaouthia, Naja naja and Bungarus candidus venoms. Here we show that, for the neurotoxic venoms of 20 elapid snake species from eight genera and four conti-nents, the in vitro median inhibitory concentrations (IC50s) for α-neurotoxin binding to purified nAChR correlated well with the in vivo LD50s of the venoms (R2 = 0.8526, p<0.001). Furthermore, using this assay, the in vitro ED50s of a horse pan-specific antiserum against these venoms correlated significantly with the corresponding in vivo murine ED50s, with R2 = 0.6896 (p < 0.01). In the case of four elapid venoms devoid or having a very low con-centration of α-neurotoxins, no inhibition of nAChR binding was observed. Within the philosophy of 3Rs (Replacement, Reduction and Refinement) in animal testing, the in vitro α-neurotoxin-nAChR binding assay can effectively substitute the mouse lethality test for toxicity and antivenom potency evaluation for neurotoxic venoms in which α-neurotoxins pre-dominate. This will greatly reduce the number of mice used in toxicological research and antivenom production laboratories. The simpler, faster, cheaper and less variable in vitro assay should also expedite the development of pan-specific antivenoms against various medically important snakes in many parts of the world.en_US
dc.subjectMedicineen_US
dc.titleAn in vitro α-neurotoxin—nachr binding assay correlates with lethality and in vivo neutralization of a large number of elapid neurotoxic snake venoms from four continentsen_US
dc.typeJournalen_US
article.title.sourcetitlePLoS Neglected Tropical Diseasesen_US
article.volume14en_US
article.stream.affiliationsUniversidad de Costa Ricaen_US
article.stream.affiliationsUniversity of Malayaen_US
article.stream.affiliationsChulabhorn Research Instituteen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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