dc.creatorCollaco R.C.O.
dc.creatorCogo J.C.
dc.creatorRodrigues-Simioni L.
dc.creatorRocha T.
dc.creatorOshima-Franco Y.
dc.creatorRandazzo-Moura P.
dc.date2012
dc.date2015-06-26T20:28:25Z
dc.date2015-11-26T14:24:25Z
dc.date2015-06-26T20:28:25Z
dc.date2015-11-26T14:24:25Z
dc.date.accessioned2018-03-28T21:26:36Z
dc.date.available2018-03-28T21:26:36Z
dc.identifier
dc.identifierToxicon. , v. 60, n. 4, p. 614 - 622, 2012.
dc.identifier410101
dc.identifier10.1016/j.toxicon.2012.05.014
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84863779313&partnerID=40&md5=feef52f9d651dcccaccfed15beec2d28
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/96654
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/96654
dc.identifier2-s2.0-84863779313
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1245399
dc.descriptionPhilodryas olfersii is responsible for most colubrid snakebites in Brazil. In this work, we examined the ability of an ethanolic extract from Mikania laevigata (guaco) leaves to protect against the in vitro neuromuscular activity of P. olfersii venom in mouse phrenic nerve-diaphragm (PND) and chick biventer cervicis (BC) preparations. M. laevigata extract caused moderate twitch-tension facilitation at low concentrations (107.4 ± 6.2% with 20 μl/ml and 118.9 ± 9.3% with 40 μl/ml in PND, and 120.7 ± 7.7% with 40 μl/ml and 114.5 ± 4.4% with 50 μl/ml in BC after 120 min; n = 4-6, mean ± SEM). In PND, the ethanol alone (40 μl/ml, n = 4) did not change the twitch-tension when compared with control. However, in BC, the ethanol produced a higher facilitation when compared to control. At higher concentrations (>50 μl/ml) the extract caused total and reversible blockade in both preparations. Venom (50 μg/ml) caused partial blockade in PND (58.5 ± 12%, n = 4) and almost total blockade in BC (93.5 ± 2.2%, n = 4). Pretreatment of the preparations with extract (40 μl/ml) for 30 min before incubation with venom (50 μg/ml) completely protected PND from neuromuscular blockade and delayed the blockade in BC. The extract alone caused only mild morphological alterations (12.5 ± 0.5% and 10.9 ± 2.3% fiber damage in PND and BC, respectively, compared to 2.3 ± 0.3% and 3 ± 0 in controls; n = 3), with no increase in expression of the inflammatory cytokines TNFα and IFNγ. The ethanol alone also caused slight muscle damage: 4.3 ± 2.4% in PND and 6.7 ± 3.3% in BC (both n = 3) and little or no TNFα and IFNγ expression in both preparations as observed in control. Venom (50 μg/ml) caused 53.5 ± 8.5% and 55.8 ± 4.3% fiber damage in PND and BC, respectively; (n = 3, p < 0.05 vs. controls) and enhanced expression of TNFα and IFNγ. Pretreatment of the preparations with extract protected against venom-induced muscle damage by 80.3 and 60.4 in PND and BC, respectively, and prevented TNFα and IFNγ expression. These results indicate that the M. laevigata extract protected nerve-muscle preparations against the myotoxic, neurotoxic and inflammatory effects of P. olfersii venom. © 2012 Elsevier Ltd.
dc.description60
dc.description4
dc.description614
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dc.languageen
dc.publisher
dc.relationToxicon
dc.rightsfechado
dc.sourceScopus
dc.titleProtection By Mikania Laevigata (guaco) Extract Against The Toxicity Of Philodryas Olfersii Snake Venom
dc.typeArtículos de revistas


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