Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Manancial - Repositório Digital da UFSM |
dARK ID: | ark:/26339/0013000004sqt |
Texto Completo: | http://repositorio.ufsm.br/handle/1/11246 |
Resumo: | Mercury is a metal without any biological function. The exposure to mercury in any of different chemical forms can induce toxic effects on living organisms. This toxicity is commonly attributed to the high affinity that this metal has for sulfhydryl groups (SH) and oxidative stress induction. Zinc is an essential metal important in many biochemical and cellular functions, and stands out among the compounds studied for preventing the damage caused by toxic metals such as mercury. Recently we verify the effectiveness of pre-treatment with zinc against the effects caused by mercury in rats sacrificed 24 hours after administration of the toxic metal. However, despite the zinc to prevent some alterations, many questions remain. Thus, we sought to evaluate the toxic effects of mercury in rats analyzed 12 and 48 hours after exposure, and the possible preventive effect of zinc. For this, Wistar rats were injected (s.c.) with 0.9% NaCl (saline) or ZnCl2 (27 mg/kg) and 24 hours later, saline or HgCl2 (5 mg/kg). The animals were sacrificed 12 or 48 hours after administration of mercury. We evaluated the activity of enzymes δ- aminolevulinic acid dehydratase and alanine aminotransferase, and levels of total and nonprotein thiols, ascorbic acid, urea and creatinine, besides analyze metal content in liver, kidney and blood. Body and organs weight were also evaluated. In animals sacrificed 12 hours after treatment with mercury was verified: decrease of ascorbic acid levels and increase of kidney weight, as well as accumulation of mercury and zinc in the kidneys and liver. The zinc pretreatment prevented completely the mercury effect on renal weight of these animals. In 48 hours after mercury exposure, these effects were observed: decrease of weight gain and increase of renal weight, increase of urea and creatinine levels, and reduction of the δ-ALA-D activity and kidney total thiols levels. Furthermore, the treatment with mercury increased levels of this metal in the kidneys and liver. Zinc partially prevented the changes in gain weight and creatinine levels. In conclusion, these results show that mercury caused different modifications in both periods studied and the zinc pretreatment prevented some of the parameters altered by mercury exposure. |
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Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zincoHgCl2 toxicity in female Wistar rats analyzed 12 and 48 hours after exposure: possible zinc preventive effectδ-aminolevulinato desidrataseMercúrioZincoFêmeasNefrotoxicidadeδ-aminolevulinate dehydrataseMercuryZincFemalesNephrotoxicityCNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICAMercury is a metal without any biological function. The exposure to mercury in any of different chemical forms can induce toxic effects on living organisms. This toxicity is commonly attributed to the high affinity that this metal has for sulfhydryl groups (SH) and oxidative stress induction. Zinc is an essential metal important in many biochemical and cellular functions, and stands out among the compounds studied for preventing the damage caused by toxic metals such as mercury. Recently we verify the effectiveness of pre-treatment with zinc against the effects caused by mercury in rats sacrificed 24 hours after administration of the toxic metal. However, despite the zinc to prevent some alterations, many questions remain. Thus, we sought to evaluate the toxic effects of mercury in rats analyzed 12 and 48 hours after exposure, and the possible preventive effect of zinc. For this, Wistar rats were injected (s.c.) with 0.9% NaCl (saline) or ZnCl2 (27 mg/kg) and 24 hours later, saline or HgCl2 (5 mg/kg). The animals were sacrificed 12 or 48 hours after administration of mercury. We evaluated the activity of enzymes δ- aminolevulinic acid dehydratase and alanine aminotransferase, and levels of total and nonprotein thiols, ascorbic acid, urea and creatinine, besides analyze metal content in liver, kidney and blood. Body and organs weight were also evaluated. In animals sacrificed 12 hours after treatment with mercury was verified: decrease of ascorbic acid levels and increase of kidney weight, as well as accumulation of mercury and zinc in the kidneys and liver. The zinc pretreatment prevented completely the mercury effect on renal weight of these animals. In 48 hours after mercury exposure, these effects were observed: decrease of weight gain and increase of renal weight, increase of urea and creatinine levels, and reduction of the δ-ALA-D activity and kidney total thiols levels. Furthermore, the treatment with mercury increased levels of this metal in the kidneys and liver. Zinc partially prevented the changes in gain weight and creatinine levels. In conclusion, these results show that mercury caused different modifications in both periods studied and the zinc pretreatment prevented some of the parameters altered by mercury exposure.Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorO mercúrio é um metal sem qualquer função biológica. A exposição ao mercúrio em qualquer uma de suas diferentes formas químicas pode induzir efeitos tóxicos aos organismos vivos. Esta toxicidade é comumente atribuída à alta afinidade que esse metal possui por grupamentos sulfidrílicos (-SH) e a indução de estresse oxidativo. O zinco é um metal essencial importante em muitas funções bioquímicas e celulares, e destaca-se dentre os compostos estudados, pela prevenção dos danos causados por metais tóxicos como o mercúrio. Recentemente verificamos a eficácia do pré-tratamento com zinco contra os efeitos causados pelo mercúrio em ratas sacrificadas 24 horas após a administração do metal tóxico. Contudo, apesar do zinco prevenir algumas alterações, muitas questões permanecem. Assim, buscamos avaliar os efeitos tóxicos do mercúrio em ratas analisados 12 e 48 horas após a exposição, e o possível efeito preventivo do zinco. Para isso, ratas Wistar foram injetadas (s.c.) com NaCl 0,9% (salina) ou ZnCl2 (27 mg/kg) e 24 horas mais tarde, com salina ou HgCl2 (5 mg/kg). Os animais foram mortos 12 ou 48 horas após a administração de mercúrio. Avaliamos a atividade das enzimas δ-aminolevulinato desidratase e alanina aminotransferase, assim como níveis de tióis totais e não proteicos, níveis de ácido ascórbico, ureia e creatinina, além de analisarmos o conteúdo de metal em fígado, rins e sangue. O peso corporal e de órgãos também foram avaliados. Nos animais mortos 12 horas após o tratamento com mercúrio verificou-se: diminuição dos níveis de ácido ascórbico e aumento do peso renal, assim como acúmulo dos metais mercúrio e zinco em rins e fígado. O pré-tratamento com zinco preveniu totalmente o efeito do mercúrio sobre o peso renal. Em 48 horas após a exposição ao mercúrio, os efeitos observados foram: diminuição do ganho de peso e aumento do peso renal, aumento nos níveis de ureia e creatinina, e diminuição da atividade da δ-ALA-D e dos níveis de tióis totais renal. Ainda, o tratamento com mercúrio aumentou os níveis desse metal em rins e fígado. O zinco preveniu parcialmente as alterações no ganho de peso e nos níveis de creatinina. Em conclusão, estes resultados mostram que o mercúrio provocou diferentes modificações nos dois períodos estudados e que o pré-tratamento com zinco preveniu alguns dos parâmetros alterados pela exposição ao mercúrio.Universidade Federal de Santa MariaBRBioquímicaUFSMPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica ToxicológicaPereira, Maria Esterhttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4728086Y2Souza, Diego dehttp://lattes.cnpq.br/3561369550388349Braga, Marcos Martinshttp://lattes.cnpq.br/8487219314125458Fonseca, Mariana Mesquita2016-07-212016-07-212016-02-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfFONSECA, Mariana Mesquita. HgCl2 TOXICITY IN FEMALE WISTAR RATS ANALYZED 12 AND 48 HOURS AFTER EXPOSURE: POSSIBLE ZINC PREVENTIVE EFFECT. 2016. 52 f. Dissertação (Mestrado em Ciências Biológicas) - Universidade Federal de Santa Maria, Santa Maria, 2016.http://repositorio.ufsm.br/handle/1/11246ark:/26339/0013000004sqtporinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2017-07-30T04:03:49Zoai:repositorio.ufsm.br:1/11246Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2017-07-30T04:03:49Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false |
dc.title.none.fl_str_mv |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco HgCl2 toxicity in female Wistar rats analyzed 12 and 48 hours after exposure: possible zinc preventive effect |
title |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco |
spellingShingle |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco Fonseca, Mariana Mesquita δ-aminolevulinato desidratase Mercúrio Zinco Fêmeas Nefrotoxicidade δ-aminolevulinate dehydratase Mercury Zinc Females Nephrotoxicity CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA |
title_short |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco |
title_full |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco |
title_fullStr |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco |
title_full_unstemmed |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco |
title_sort |
Toxicidade do HgCl2 em ratas Wistar analisadas 12 e 48 horas após a exposição: possível efeito preventivo do zinco |
author |
Fonseca, Mariana Mesquita |
author_facet |
Fonseca, Mariana Mesquita |
author_role |
author |
dc.contributor.none.fl_str_mv |
Pereira, Maria Ester http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4728086Y2 Souza, Diego de http://lattes.cnpq.br/3561369550388349 Braga, Marcos Martins http://lattes.cnpq.br/8487219314125458 |
dc.contributor.author.fl_str_mv |
Fonseca, Mariana Mesquita |
dc.subject.por.fl_str_mv |
δ-aminolevulinato desidratase Mercúrio Zinco Fêmeas Nefrotoxicidade δ-aminolevulinate dehydratase Mercury Zinc Females Nephrotoxicity CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA |
topic |
δ-aminolevulinato desidratase Mercúrio Zinco Fêmeas Nefrotoxicidade δ-aminolevulinate dehydratase Mercury Zinc Females Nephrotoxicity CNPQ::CIENCIAS BIOLOGICAS::BIOQUIMICA |
description |
Mercury is a metal without any biological function. The exposure to mercury in any of different chemical forms can induce toxic effects on living organisms. This toxicity is commonly attributed to the high affinity that this metal has for sulfhydryl groups (SH) and oxidative stress induction. Zinc is an essential metal important in many biochemical and cellular functions, and stands out among the compounds studied for preventing the damage caused by toxic metals such as mercury. Recently we verify the effectiveness of pre-treatment with zinc against the effects caused by mercury in rats sacrificed 24 hours after administration of the toxic metal. However, despite the zinc to prevent some alterations, many questions remain. Thus, we sought to evaluate the toxic effects of mercury in rats analyzed 12 and 48 hours after exposure, and the possible preventive effect of zinc. For this, Wistar rats were injected (s.c.) with 0.9% NaCl (saline) or ZnCl2 (27 mg/kg) and 24 hours later, saline or HgCl2 (5 mg/kg). The animals were sacrificed 12 or 48 hours after administration of mercury. We evaluated the activity of enzymes δ- aminolevulinic acid dehydratase and alanine aminotransferase, and levels of total and nonprotein thiols, ascorbic acid, urea and creatinine, besides analyze metal content in liver, kidney and blood. Body and organs weight were also evaluated. In animals sacrificed 12 hours after treatment with mercury was verified: decrease of ascorbic acid levels and increase of kidney weight, as well as accumulation of mercury and zinc in the kidneys and liver. The zinc pretreatment prevented completely the mercury effect on renal weight of these animals. In 48 hours after mercury exposure, these effects were observed: decrease of weight gain and increase of renal weight, increase of urea and creatinine levels, and reduction of the δ-ALA-D activity and kidney total thiols levels. Furthermore, the treatment with mercury increased levels of this metal in the kidneys and liver. Zinc partially prevented the changes in gain weight and creatinine levels. In conclusion, these results show that mercury caused different modifications in both periods studied and the zinc pretreatment prevented some of the parameters altered by mercury exposure. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-07-21 2016-07-21 2016-02-10 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
FONSECA, Mariana Mesquita. HgCl2 TOXICITY IN FEMALE WISTAR RATS ANALYZED 12 AND 48 HOURS AFTER EXPOSURE: POSSIBLE ZINC PREVENTIVE EFFECT. 2016. 52 f. Dissertação (Mestrado em Ciências Biológicas) - Universidade Federal de Santa Maria, Santa Maria, 2016. http://repositorio.ufsm.br/handle/1/11246 |
dc.identifier.dark.fl_str_mv |
ark:/26339/0013000004sqt |
identifier_str_mv |
FONSECA, Mariana Mesquita. HgCl2 TOXICITY IN FEMALE WISTAR RATS ANALYZED 12 AND 48 HOURS AFTER EXPOSURE: POSSIBLE ZINC PREVENTIVE EFFECT. 2016. 52 f. Dissertação (Mestrado em Ciências Biológicas) - Universidade Federal de Santa Maria, Santa Maria, 2016. ark:/26339/0013000004sqt |
url |
http://repositorio.ufsm.br/handle/1/11246 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Santa Maria BR Bioquímica UFSM Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica |
publisher.none.fl_str_mv |
Universidade Federal de Santa Maria BR Bioquímica UFSM Programa de Pós-Graduação em Ciências Biológicas: Bioquímica Toxicológica |
dc.source.none.fl_str_mv |
reponame:Manancial - Repositório Digital da UFSM instname:Universidade Federal de Santa Maria (UFSM) instacron:UFSM |
instname_str |
Universidade Federal de Santa Maria (UFSM) |
instacron_str |
UFSM |
institution |
UFSM |
reponame_str |
Manancial - Repositório Digital da UFSM |
collection |
Manancial - Repositório Digital da UFSM |
repository.name.fl_str_mv |
Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM) |
repository.mail.fl_str_mv |
atendimento.sib@ufsm.br||tedebc@gmail.com |
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1815172283352743936 |