Local effects induced by coral snake venoms: Evidence of myonecrosis after experimental inoculations of venoms from five species

Toxicon ◽  
1983 ◽  
Vol 21 (6) ◽  
pp. 777-783 ◽  
Author(s):  
JoséMaría Gutiérrez ◽  
Bruno Lomonte ◽  
Elsa Portilla ◽  
Luis Cerdas ◽  
Ermila Rojas
Author(s):  
Alessandra L. Cecchini ◽  
Silvana Marcussi ◽  
Lucas B. Silveira ◽  
Caroline R. Borja-Oliveira ◽  
Léa Rodrigues-Simioni ◽  
...  

1987 ◽  
Vol 29 (3) ◽  
pp. 119-126 ◽  
Author(s):  
Oswald Vital Brazil

Coral snakes, the New World Elapidae, are included in the genera Micniroides and Micrurus. The genus Mlcrurus comprises nearly all coral snake species and those which are responsible for human snake-bite accidents. The following generalizations concerning the effects induced by their venoms, and their venom-properties can be made. Coral snake venoms are neurotoxic, producing loss of muscle strenght and death by respiratory paralysis. Local edema and necrosis are not induced nor blood coagulation or hemorrhages. Proteolysis activity is absent or of very low grade. They display phospholipase A2 activity. Nephrotoxic effects are not evoked. The main toxins from elapid venoms are postsynaptic and presynaptic neurotoxins and cardiotoxins. Phospholipases A2 endowed with myonecrotic or cardiotoxin-like properties are important toxic components from some elapid venoms. The mode of action of Micrurus frontalis, M. lemniscatus, M. corallinus and M. fulvius venoms has been investigated in isolated muscle preparations and is here discussed. It is shown that while M. frontalis and M. lemniscatus venoms must contain only neurotoxins that act at the cholinergic end-plate receptor (postsynaptic neurotoxins), M. corallinus venom also inhibits evoked acetylcholine release by the motor nerve endings (presynaptic neurotoxin-like effect) and M. fulvius induces muscle fiber membrane depolarization (cardiotoxin-like effect). The effects produced by M. corallinus and M. fulvius venoms in vivo in dogs and M. frontalis venom in dogs and monkeys are also reported.


Toxicon ◽  
1970 ◽  
Vol 8 (1) ◽  
pp. 11-14 ◽  
Author(s):  
Lee J. Stevan ◽  
Edward B. Seligmann

2017 ◽  
Vol 2017 ◽  
pp. 1-52 ◽  
Author(s):  
Juliana Félix-Silva ◽  
Arnóbio Antônio Silva-Junior ◽  
Silvana Maria Zucolotto ◽  
Matheus de Freitas Fernandes-Pedrosa

Snakebites are a serious problem in public health due to their high morbimortality. Most of snake venoms produce intense local tissue damage, which could lead to temporary or permanent disability in victims. The available specific treatment is the antivenom serum therapy, whose effectiveness is reduced against these effects. Thus, the search for complementary alternatives for snakebite treatment is relevant. There are several reports of the popular use of medicinal plants against snakebites worldwide. In recent years, many studies have been published giving pharmacological evidence of benefits of several vegetal species against local effects induced by a broad range of snake venoms, including inhibitory potential against hyaluronidase, phospholipase, proteolytic, hemorrhagic, myotoxic, and edematogenic activities. In this context, this review aimed to provide an updated overview of medicinal plants used popularly as antiophidic agents and discuss the main species with pharmacological studies supporting the uses, with emphasis on plants inhibiting local effects of snake envenomation. The present review provides an updated scenario and insights into future research aiming at validation of medicinal plants as antiophidic agents and strengthens the potentiality of ethnopharmacology as a tool for design of potent inhibitors and/or development of herbal medicines against venom toxins, especially local tissue damage.


Biochimie ◽  
2017 ◽  
Vol 137 ◽  
pp. 88-98 ◽  
Author(s):  
Paola Rey-Suárez ◽  
Vitelbina Núñez ◽  
Mónica Saldarriaga-Córdoba ◽  
Bruno Lomonte

Toxicon ◽  
2008 ◽  
Vol 51 (2) ◽  
pp. 297-303 ◽  
Author(s):  
Elda E. Sánchez ◽  
Juan C. Lopez-Johnston ◽  
Alexis Rodríguez-Acosta ◽  
John C. Pérez

2016 ◽  
Vol 55 (1) ◽  
pp. 33-39 ◽  
Author(s):  
Henrique Roman Ramos ◽  
Ruth Camargo Vassão ◽  
Adolfo Rafael de Roodt ◽  
Ed Carlos Santos e Silva ◽  
Peter Mirtschin ◽  
...  

2006 ◽  
Vol 48 (3) ◽  
pp. 141-145 ◽  
Author(s):  
Fábio Bucaretchi ◽  
Stephen Hyslop ◽  
Ronan José Vieira ◽  
Adriana Safioli Toledo ◽  
Paulo Roberto Madureira ◽  
...  

Coral snakes (Micrurus spp.) are the main representatives of the Elapidae in South America. However, bites by these snakes are uncommon. We retrospectively reviewed the data from 11 individuals bitten by coral snakes over a 20-year period; four were confirmed (snake brought for identification) and seven were highly suspected (neuromuscular manifestations) cases of elapid envenoming. The cases were classified as dry-bite (n = 1, caused by M. lemniscatus; did not receive antivenom), mild (n = 2, local manifestations with no acute myasthenic syndrome; M. frontalis and Micrurus spp.), moderate (n = 5, mild myasthenia) or severe (n = 3, important myasthenia; one of them caused by M. frontalis). The main clinical features upon admission were paresthesia (local, n = 9; generalized, n = 2), local pain (n = 8), palpebral ptosis (n = 8), weakness (n = 4) and inability to stand up (n = 3). No patient developed respiratory failure. Antivenom was used in ten cases, with mild early reactions occurring in three. An anticholinesterase drug was administered in the three severe cases, with a good response in two. No deaths were observed. Despite the high toxicity of coral snake venoms, the prognosis following envenoming is good. In serious bites by M. frontalis or M. lemniscatus, the venom of which acts postsynaptically, anticholinesterases may be useful as an ancillary measure if antivenom is unavailable, if there is a delay in obtaining a sufficient amount, or in those patients given the highest recommended doses of antivenom without improvement of the paralysis or with delayed recovery.


1971 ◽  
Vol 20 (4) ◽  
pp. 646-649 ◽  
Author(s):  
Pinya Cohen ◽  
William H. Berkeley ◽  
Edward B. Seligmann
Keyword(s):  

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