The venom of the Eastern coral snake Micrurus fulvius can cause respiratory paralysis in the bitten patient, which is attributable to -neurotoxins (-NTx). The aim of this work was to study the biodistribution and lymphatic tracking by molecular imaging of the main -NTx of M. fulvius venom. -NTx was bioconjugated with the chelator diethylenetriaminepenta-acetic acid (DTPA) and radiolabeled with the radionuclide Gallium-67. Radiolabeling efficiency was 60%-78%; radiochemical purity 92%; and stability at 48 h 85%. The median lethal dose (LD50) and PLA(2) activity of bioconjugated -NTx decreased 3 and 2.5 times, respectively, in comparison with native -NTx. The immune recognition by polyclonal antibodies decreased 10 times. Biodistribution of -NTx-DTPA-Ga-67 in rats showed increased uptake in popliteal, lumbar nodes and kidneys that was not observed with Ga-67-free. Accumulation in organs at 24 h was less than 1%, except for kidneys, where the average was 3.7%. The inoculation site works as a depot, since 10% of the initial dose of -NTx-DTPA-Ga-67 remains there for up to 48 h. This work clearly demonstrates the lymphatic system participation in the biodistribution of -NTx-DTPA-Ga-67. Our approach could be applied to analyze the role of the lymphatic system in snakebite for a better understanding of envenoming.

Made available in DSpace on 2016-08-10T10:53:39Z (GMT). No. of bitstreams: 1 ANITA DE MOURA PESSOA.pdf: 1926127 bytes, checksum: 0390ad20d8a270313d55fe8cd8841043 (MD5) Previous issue date: 2012-05-22 / Venomous animals accidents are of great importance in any Country especially due to the significant number of people involved and the relevance of these accidents. There is an annual average of 24,000 snakebite accidents in Brasil and from these 1% are related to the genus Micrurus, which represents the true coralsnakes. In this study I evaluated the biological aspects of the accidents caused by coralsnakes in Brasil, including aspects related to municipality, sex and age of the patients, time between the accident and the first medical evaluation and biological and toxinological diversity. I analyzed 787 reports available in the SINAN electronic system, from 2007 to 2010. According to the data, 691 patients were discharged as totally healed, three died, and 93 were reported as no data available. The majority of the accidents were reported from the northeast region (52%). The time between 0 and 3 hours for the first medical evaluation is a general rule for the whole Country which contributes for a satisfactory result of the treatment. The clinical cases available in the literature show that the coralsnake envenomation may or may not present symptoms, however the administration of the anti-coralsnake serum is recommended in all cases as all are considered as grave. From the 27 described species of coralsnakes for Brasil 20 occur in the northern region and, among them, nothing is known about the venom composition of at least 13 species. In a long term this might become a problem as the immunization pool for antivenin production is based only in three species. The study of biology and natural history of this group is important to facilitate the maintenance of these animals in captivity. It is also necessary to evaluate the antigenic pool and verify the efficacy of the antivenin against all species. / Os acidentes por animais peçonhentos têm grande importância médico sanitária no país. No Brasil ocorre uma média anual de 24.000 acidentes com serpentes peçonhentas, desses, 1% com o gênero Micrurus, representado pelas cobras corais verdadeiras. Neste trabalho foram avaliados os aspectos biológicos dos acidentes causados por cobras corais no Brasil, incluindo aspectos relacionados com o município e região brasileira, sexo e faixa etária dos acidentados, tempo decorrido entre o acidente e o atendimento, diversidade biológica e toxinológica. Foram analisadas as informações de 787 notificações disponíveis no sistema eletrônico do SINAN, no período de 2007 a 2010. De acordo com os dados, 691 pacientes foram liberados totalmente curados, três vieram a óbito, e 93 não há informação. A maioria dos acidentes foram registrados na região Nordeste do país (52%). O intervalo de zero a três horas entre acidente e atendimento, prevalece em alta para todas as regiões, o que contribui para um resultado satisfatório do tratamento. Os casos clínicos disponíveis na literatura mostram que o envenenamento elapídico pode apresentar sintomatologia ou não, porém a administração do soro antielapídico é recomendada em todos os casos, pois todos são considerados graves. Das 27 espécies de cobras corais descritas para o Brasil, 20 ocorrem na região norte, dentre elas, não se conhece o veneno de 13 espécies. A longo prazo esse pode ser um problema diante do pool de imunização para a produção de soro, que é composto por somente três espécies. O estudo da biologia e história natural desse grupo é importante para facilitar a manutenção desses animais em cativeiro. É necessário também, a avaliação do pool antigênico para verificar a eficácia do antiveneno para todas as espécies.

Due to shared coevolutionary history of snakes and primates with snakes acting as their main predators, snakes elicit fear in most of the primates, humans included. Humans are able to notice a stimulus that elicits fear, e.g., a snake, much faster. Such ability might have surely positively affected their survival in the past. In the nature, aposematic coloration acts as a warning of a dangerous prey to its predators not to devour it. The highly poisonous American coral snakes have this coloration pattern. The harmless king snakes of the Central and North Americas gain an anti-predatory advantage by becoming the coral snakes 'Batesian mimics, copying their bright pattern. Such pattern elicits an innate fear reaction in various species of wild birds who avoid a mere contact with patterned plastic dummies. The question arises whether other taxa, including primates and humans, generally recognize such pattern as dangerous. The aim of this study was to find whether humans fear coral snakes, although they have not long coevolutionary history with them. Further it was analyze, which visual factors of the snakes affect this fear reaction (i.e., a warning coloration, pattern or shape of snake). The atractiveness of these snakes was tested. Another question was whether humans are able to intuitively recognize...

De uma biblioteca de cDNA da glândula de veneno da cobra coral brasileira Micrurus corallinus foi isolada uma seqüência denominada NXH8. Esta seqüência de cDNA apresenta similaridade estrutural com a família de toxinas de serpentes em 'três dígitos' ricas em pontes dissulfeto. A subclasse melhor conhecida nesta família, são as alfa neurotoxinas. Uma outra seqüência distinta, denominada NXH1 e suas isoformas NXH3 e NXH7, foram isoladas anteriormente. Pertencem à mesma família de toxinas e estão presentes na mesma biblioteca. Alguns resultados da caracterização de NXH1, são utilizados neste estudo, em comparação com NXH8. Algumas características estruturais tornam a seqüência NXH8 diferente da classe usual das alfa neurotoxinas, vindo a constituir possivelmente uma nova subclasse da família. A proteína NXH8 foi expressa em diversos vetores de expressão em Escherichia coli. A proteína recombinante, expressa pelo vetor pRSET C - NXH8 foi utilizada para imunizar camundongos. O soro contra NXH8, assim como o soro anti - elapídico do Instituto Butantan, reconhece a toxina recombinante em ELISA e Western blot. O soro anti - NXH8 detecta apenas uma banda do veneno de M. corallinus em Western blot, mas apresenta reatividade cruzada com componentes do veneno de alguns elapídeos neotropicais e do velho mundo. Em contraste, dados anteriores demonstraram que o soro anti - NXH1 é específico para um componente único do veneno de M. corallinus. O veneno de M. corallinus tem alfa neurotoxinas que bloqueiam o receptor pós - sináptico nicotínico de acetilcolina nas membranas do músculo esquelético de ratos. O soro anti - NXH8 é capaz de impedir a ligação de componentes do veneno bruto a esses receptores. Já o soro contra NXH1 não apresenta a mesma capacidade inibitória. Isto indica que NXH8 tem afinidade pelo receptor nicotínico muscular de acetilcolina, ou que NXH8 compartilha de um epítopo neutralizante presente também nas alfa neurotoxinas do veneno da cobra coral M. corallinus. / A cDNA sequence encoding a putative new toxin, NXH8, was isolated from the cDNA library constructed from the venom gland of the Brazilian coral snake, Micrurus corallinus. This sequence shows a structural similarity with the snake toxin family known as 'three-fingered' toxins, a family of toxins with approximately 60 to 70 amino acids and usually 4 to 5 disulfide bonds. Irrespective of whether these proteins are functionally different, their amino acid sequences can be readily aligned, using 8 half-cystines as conserved elements, suggesting the presence of common structural features. The best known subclass of three-finger-type toxins are the curaremimetic toxins, also called alpha-neurotoxins, found in most venoms from Elapid and Sea snakes. Another toxin with a distinct sequence, known as NXH1 and its isoforms NXH3 and NXH7 had been previously isolated. They belong to the same family of toxins and were characterized from the same cDNA library. In the present study, a comparative biochemical, pharmacological and structural analyses of NXH1 and NXH8 were described. Few structural characteristics of NXH8 seem to indicate that it differs from the usual class of alpha – neurotoxins, belonging, possibly, to a new subclass of 'three-finger' toxins. The NXH8 protein was expressed in various E. coli expression vectors and the resulted recombinant toxin from pRSETC-NXH8 plasmid was used as a "toxoid" for mice immunization. The anti - NXH8 sera, as well as the anti – elapid sera from the Butantan Institute, recognized the recombinant toxin by both ELISA and Western blot assays. In contrast to the claim that anti - NXH1 sera is specific to one component of M. corallinus’s venom, the anti – NXH8 sera show cross reactivity to venom of some Neotropical and Old World elapids. The M. corallinus's venom contains alpha – toxins, which inhibit post-synaptic nicotinic acetylcholine receptor of neonatal rat skeletal muscle membrane. The anti - NXH8 serum was capable of blocking the binding of the components of the crude venom to these receptors. In contrast, the anti – NXH1 serum did not show this inhibitory effect. This indicates that either NXH8 presents affinity for muscular nicotinic acetylcholine receptor or it shares a neutralizing epitope also present in M. corallinus’s alpha – neurotoxins.

De uma biblioteca de cDNA da glândula de veneno da cobra coral brasileira Micrurus corallinus foi isolada uma seqüência denominada NXH8. Esta seqüência de cDNA apresenta similaridade estrutural com a família de toxinas de serpentes em 'três dígitos' ricas em pontes dissulfeto. A subclasse melhor conhecida nesta família, são as alfa neurotoxinas. Uma outra seqüência distinta, denominada NXH1 e suas isoformas NXH3 e NXH7, foram isoladas anteriormente. Pertencem à mesma família de toxinas e estão presentes na mesma biblioteca. Alguns resultados da caracterização de NXH1, são utilizados neste estudo, em comparação com NXH8. Algumas características estruturais tornam a seqüência NXH8 diferente da classe usual das alfa neurotoxinas, vindo a constituir possivelmente uma nova subclasse da família. A proteína NXH8 foi expressa em diversos vetores de expressão em Escherichia coli. A proteína recombinante, expressa pelo vetor pRSET C - NXH8 foi utilizada para imunizar camundongos. O soro contra NXH8, assim como o soro anti - elapídico do Instituto Butantan, reconhece a toxina recombinante em ELISA e Western blot. O soro anti - NXH8 detecta apenas uma banda do veneno de M. corallinus em Western blot, mas apresenta reatividade cruzada com componentes do veneno de alguns elapídeos neotropicais e do velho mundo. Em contraste, dados anteriores demonstraram que o soro anti - NXH1 é específico para um componente único do veneno de M. corallinus. O veneno de M. corallinus tem alfa neurotoxinas que bloqueiam o receptor pós - sináptico nicotínico de acetilcolina nas membranas do músculo esquelético de ratos. O soro anti - NXH8 é capaz de impedir a ligação de componentes do veneno bruto a esses receptores. Já o soro contra NXH1 não apresenta a mesma capacidade inibitória. Isto indica que NXH8 tem afinidade pelo receptor nicotínico muscular de acetilcolina, ou que NXH8 compartilha de um epítopo neutralizante presente também nas alfa neurotoxinas do veneno da cobra coral M. corallinus. / A cDNA sequence encoding a putative new toxin, NXH8, was isolated from the cDNA library constructed from the venom gland of the Brazilian coral snake, Micrurus corallinus. This sequence shows a structural similarity with the snake toxin family known as 'three-fingered' toxins, a family of toxins with approximately 60 to 70 amino acids and usually 4 to 5 disulfide bonds. Irrespective of whether these proteins are functionally different, their amino acid sequences can be readily aligned, using 8 half-cystines as conserved elements, suggesting the presence of common structural features. The best known subclass of three-finger-type toxins are the curaremimetic toxins, also called alpha-neurotoxins, found in most venoms from Elapid and Sea snakes. Another toxin with a distinct sequence, known as NXH1 and its isoforms NXH3 and NXH7 had been previously isolated. They belong to the same family of toxins and were characterized from the same cDNA library. In the present study, a comparative biochemical, pharmacological and structural analyses of NXH1 and NXH8 were described. Few structural characteristics of NXH8 seem to indicate that it differs from the usual class of alpha – neurotoxins, belonging, possibly, to a new subclass of 'three-finger' toxins. The NXH8 protein was expressed in various E. coli expression vectors and the resulted recombinant toxin from pRSETC-NXH8 plasmid was used as a "toxoid" for mice immunization. The anti - NXH8 sera, as well as the anti – elapid sera from the Butantan Institute, recognized the recombinant toxin by both ELISA and Western blot assays. In contrast to the claim that anti - NXH1 sera is specific to one component of M. corallinus’s venom, the anti – NXH8 sera show cross reactivity to venom of some Neotropical and Old World elapids. The M. corallinus's venom contains alpha – toxins, which inhibit post-synaptic nicotinic acetylcholine receptor of neonatal rat skeletal muscle membrane. The anti - NXH8 serum was capable of blocking the binding of the components of the crude venom to these receptors. In contrast, the anti – NXH1 serum did not show this inhibitory effect. This indicates that either NXH8 presents affinity for muscular nicotinic acetylcholine receptor or it shares a neutralizing epitope also present in M. corallinus’s alpha – neurotoxins.