Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais

Detalhes bibliográficos
Autor(a) principal: Prieto, Carla Soares de Lima
Data de Publicação: 2013
Tipo de documento: Tese
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UERJ
Texto Completo: http://www.bdtd.uerj.br/handle/1/16140
Resumo: Organophosphate pesticides are widely used and its use consist on a severe public health problem. The classic effect of these compounds involve irreversible inhibition of the enzyme acetylcholinesterase, causing an accumulation of acetylcholine at cholinergic synapses and, consequently, cholinergic hyperstimulation. However, when the doses of exposure are low, other the mechanisms of action may play a role and other neurotransmitter systems may be affected. Considering that children are particularly vulnerable to effects of these compounds, in this study we investigated the effects of methamidophos and chlorpyrifos organophosphate exposure during development on cholinergic and serotonergic systems and behavior. For this purpose, Swiss mice received subcutaneous injections of methamidophos or chlorpyrifos, or vehicle from the third to the nineth postnatal day (PN3 - PN9). Initially, a dose-response study was performed and the doses of 1mg/kg methamidophos and 3mg/kg chlorphrifos, which promoted 20% inhibition of acetylcholinesterase activity in brain were chosen to be used in the next set of experiments. At PN10, one day after exposure, a group of animals was sacrificed and the brainstem and cortex collected and stored to further analysis of cholinergic and serotonergic systems. From PN60 to PN63 the animals were submitted to behavioral tests in order to evaluate: anxiety, locomotor activity, decision making, depressive-like behavior and learning/memory. After the last test, the animals were sacrificed and the brainstem and cortex collected and stored to further analysis of cholinergic and serotonergic systems. At PN10, methamidophos and chlorpyrifos promoted alterations that suggest an increase of cholinergic activity respectively on the brainstem and cortex of females. As for the serotonergic system: only chlorpyrifos elicited alterations: There were increases in 5HT1A receptor and 5HT transporter binding in females and a decrease in 5HT2 receptor binding. At PN63, the activity of acetylcholinesterase had returned to control levels. Despite that, methamidophos elicited a decrease in the activity of choline acetyltransferase in the cortex and in choline transporter binding in the brainstem. As for the serotonergic system, methamidophos and chlorpyrifos promoted decreased 5HT1A receptor binding respectively in the brainstem and cortex of females and chlorpyrifos increased its binding in males. Methamidophos exposure elicited increased 5HT2 binding whereas chlorpyrifos exposure decreased female 5HT transporter binding. Methamidophos elicited behavioral alterations suggestive of increased depressive-like behavior while chlorpyrifos exposure was associated to increased anxiety levels and memory/learning deficits. Our results indicate that metamidophos and chlorpyrifos exposure during development distinctively affect the cholinergic and serotonergic systems even at toxicologically equivalent doses. There were immediate and late-emergent neurochemical effects that may play a role on the behavioral outcomes. Finally, the present study reinforces the epidemiologic association between pesticides exposure and mood disorders and suggest that organophosphate exposure during early development programs for late effects.
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spelling Villaça, Yael de Abreuhttp://lattes.cnpq.br/2110538573461886Castro, Newton Gonçalves dehttp://lattes.cnpq.br/0585051132094289Calaza, Karin da Costahttp://lattes.cnpq.br/5859948736421528Almeida, Olga Maria Martins Silva dehttp://lattes.cnpq.br/2438645505018032http://lattes.cnpq.br/4526004572649712Prieto, Carla Soares de Lima2021-04-26T01:10:50Z2013-08-212013-05-29PRIETO, Carla Soares de Lima. Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais. 2013. 105 f. Tese (Doutorado em Biociências Nucleares; Ecologia) - Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2013.http://www.bdtd.uerj.br/handle/1/16140Organophosphate pesticides are widely used and its use consist on a severe public health problem. The classic effect of these compounds involve irreversible inhibition of the enzyme acetylcholinesterase, causing an accumulation of acetylcholine at cholinergic synapses and, consequently, cholinergic hyperstimulation. However, when the doses of exposure are low, other the mechanisms of action may play a role and other neurotransmitter systems may be affected. Considering that children are particularly vulnerable to effects of these compounds, in this study we investigated the effects of methamidophos and chlorpyrifos organophosphate exposure during development on cholinergic and serotonergic systems and behavior. For this purpose, Swiss mice received subcutaneous injections of methamidophos or chlorpyrifos, or vehicle from the third to the nineth postnatal day (PN3 - PN9). Initially, a dose-response study was performed and the doses of 1mg/kg methamidophos and 3mg/kg chlorphrifos, which promoted 20% inhibition of acetylcholinesterase activity in brain were chosen to be used in the next set of experiments. At PN10, one day after exposure, a group of animals was sacrificed and the brainstem and cortex collected and stored to further analysis of cholinergic and serotonergic systems. From PN60 to PN63 the animals were submitted to behavioral tests in order to evaluate: anxiety, locomotor activity, decision making, depressive-like behavior and learning/memory. After the last test, the animals were sacrificed and the brainstem and cortex collected and stored to further analysis of cholinergic and serotonergic systems. At PN10, methamidophos and chlorpyrifos promoted alterations that suggest an increase of cholinergic activity respectively on the brainstem and cortex of females. As for the serotonergic system: only chlorpyrifos elicited alterations: There were increases in 5HT1A receptor and 5HT transporter binding in females and a decrease in 5HT2 receptor binding. At PN63, the activity of acetylcholinesterase had returned to control levels. Despite that, methamidophos elicited a decrease in the activity of choline acetyltransferase in the cortex and in choline transporter binding in the brainstem. As for the serotonergic system, methamidophos and chlorpyrifos promoted decreased 5HT1A receptor binding respectively in the brainstem and cortex of females and chlorpyrifos increased its binding in males. Methamidophos exposure elicited increased 5HT2 binding whereas chlorpyrifos exposure decreased female 5HT transporter binding. Methamidophos elicited behavioral alterations suggestive of increased depressive-like behavior while chlorpyrifos exposure was associated to increased anxiety levels and memory/learning deficits. Our results indicate that metamidophos and chlorpyrifos exposure during development distinctively affect the cholinergic and serotonergic systems even at toxicologically equivalent doses. There were immediate and late-emergent neurochemical effects that may play a role on the behavioral outcomes. Finally, the present study reinforces the epidemiologic association between pesticides exposure and mood disorders and suggest that organophosphate exposure during early development programs for late effects.Pesticidas organofosforados são amplamente usados e seu uso constitui um grave problema de saúde pública. A ação clássica destes compostos é a inibição irreversível da acetilcolinesterase, promovendo acúmulo de acetilcolina nas sinapses e hiperestimulação colinérgica. No entanto, as consequências da exposição a baixas doses podem se estender a outros mecanismos de ação e sistemas neurotransmissores. Considerando que crianças constituem um grupo particularmente vulnerável aos efeitos de pesticidas, neste trabalho investigamos os efeitos da exposição aos organofosforados metamidofós (MET) e clorpirifós (CPF) durante o desenvolvimento sobre os sistemas colinérgico e serotoninérgico e sobre o comportamento de camundongos. Para isso, camundongos suíços foram expostos a injeções subcutâneas de MET, clorpirifós ou veículo do terceiro (PN3) ao nono (PN9) dias de vida pós-natal. As doses de exposição foram previamente escolhidas através da construção de uma curva dose-resposta que identificou como mais adequadas para este estudo as doses de 1mg/kg de MET e 3mg/kg de CPF, as quais promoveram em torno de 20% de inibição da acetilcolinesterase. Em PN10, parte dos animais foi sacrificada e foram avaliados os sistemas colinérgico e serotoninérgico no tronco encefálico e córtex cerebral. De PN60 a PN63, os animais foram submetidos a uma bateria de testes comportamentais. Em seguida, estes animais também foram sacrificados tendo sido avaliados os sistemas colinérgico e serotoninérgico. Em PN10, MET e CPF causaram alterações que sugerem aumento da atividade colinérgica respectivamente no tronco e córtex em fêmeas. No sistema serotoninérgico, apenas CPF promoveu alterações, aumentando a ligação ao receptor 5HT1A e transportador 5HT em fêmeas e diminuindo na ligação ao 5HT2. Em PN63, a atividade da acetilcolinesterase foi reestabelecida em todos os grupos. Ainda assim, MET diminuiu a atividade da colina acetiltransferase no córtex e a ligação ao transportador colinérgico no tronco. Quanto aos efeitos do CPF, no tronco, houve redução da atividade da colina acetiltransferase em fêmeas e aumento em machos. Sobre o sistema serotoninérgico, MET e CPF promoveram diminuições no 5HT1A respectivamente no tronco e córtex das fêmeas e CPF aumentou a ligação no córtex de machos. A ligação ao 5HT2 foi aumentada após o tratamento com MET e ao transportador 5HT foi diminuída em fêmeas após o tratamento com clorpirifós. Sobre o comportamento, identificamos comportamento associado à depressão em animais expostos a MET e aumento dos níveis de ansiedade, além de prejuízo de aprendizado/memória após exposição à CPF. Desta forma, nossos resultados indicam que a exposição à metamidofós e clorpirifós durante o desenvolvimento é capaz de alterar, de diferentes formas, a atividade colinérgica e serotoninérgica, mesmo que as doses de exposição sejam toxicologicamente equivalentes. Foram verificados efeitos nas vias neuroquímicas logo após a exposição e após um longo período de interrupção do tratamento, indicando efeitos tardios em sistemas importantes que podem estar associados às alterações comportamentais. Finalmente, o presente estudo reforça a associação epidemiológica entre pesticidas e alterações psiquiátricas e a capacidade da programação de alterações a longo-prazo quando a exposição se dá durante o desenvolvimento.Submitted by Boris INFORMAT (boris@uerj.br) on 2021-04-26T01:10:50Z No. of bitstreams: 1 TESE_ARQUIVO_UNICO_CARLA FINAL PDF.pdf: 6876975 bytes, checksum: 8265e33704cea8ebb53969ddc9f6c6ea (MD5)Made available in DSpace on 2021-04-26T01:10:50Z (GMT). No. of bitstreams: 1 TESE_ARQUIVO_UNICO_CARLA FINAL PDF.pdf: 6876975 bytes, checksum: 8265e33704cea8ebb53969ddc9f6c6ea (MD5) Previous issue date: 2013-05-29application/pdfporUniversidade do Estado do Rio de JaneiroPrograma de Pós-Graduação em BiociênciasUERJBRCentro Biomédico::Instituto de Biologia Roberto Alcantara GomesOrganophosphateDevelopmentCholinergic systemSerotoninergic systemBehaviorOrganofosforadosDesenvolvimentoSistema colinérgicoSistema serotoninérgicoComportamentoPesticidas ToxicologiaPesticidas Efeito fisiológicoManifestações neurocomportamentaisDesenvolvimento infantil Efeito de drogasInseticidas organofosforados Efeitos adversosCNPQ::CIENCIAS BIOLOGICAS::FISIOLOGIA::FISIOLOGIA DE ORGAOS E SISTEMASNeurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentaisNeurotoxicity of organophosphate pesticides during development: biochemical and behavioral alterationsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UERJinstname:Universidade do Estado do Rio de Janeiro (UERJ)instacron:UERJORIGINALTESE_ARQUIVO_UNICO_CARLA FINAL PDF.pdfapplication/pdf6876975http://www.bdtd.uerj.br/bitstream/1/16140/1/TESE_ARQUIVO_UNICO_CARLA+FINAL+PDF.pdf8265e33704cea8ebb53969ddc9f6c6eaMD511/161402024-02-26 11:24:58.062oai:www.bdtd.uerj.br:1/16140Biblioteca Digital de Teses e Dissertaçõeshttp://www.bdtd.uerj.br/PUBhttps://www.bdtd.uerj.br:8443/oai/requestbdtd.suporte@uerj.bropendoar:29032024-02-26T14:24:58Biblioteca Digital de Teses e Dissertações da UERJ - Universidade do Estado do Rio de Janeiro (UERJ)false
dc.title.por.fl_str_mv Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
dc.title.alternative.eng.fl_str_mv Neurotoxicity of organophosphate pesticides during development: biochemical and behavioral alterations
title Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
spellingShingle Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
Prieto, Carla Soares de Lima
Organophosphate
Development
Cholinergic system
Serotoninergic system
Behavior
Organofosforados
Desenvolvimento
Sistema colinérgico
Sistema serotoninérgico
Comportamento
Pesticidas Toxicologia
Pesticidas Efeito fisiológico
Manifestações neurocomportamentais
Desenvolvimento infantil Efeito de drogas
Inseticidas organofosforados Efeitos adversos
CNPQ::CIENCIAS BIOLOGICAS::FISIOLOGIA::FISIOLOGIA DE ORGAOS E SISTEMAS
title_short Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
title_full Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
title_fullStr Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
title_full_unstemmed Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
title_sort Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais
author Prieto, Carla Soares de Lima
author_facet Prieto, Carla Soares de Lima
author_role author
dc.contributor.advisor1.fl_str_mv Villaça, Yael de Abreu
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/2110538573461886
dc.contributor.referee1.fl_str_mv Castro, Newton Gonçalves de
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/0585051132094289
dc.contributor.referee2.fl_str_mv Calaza, Karin da Costa
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/5859948736421528
dc.contributor.referee3.fl_str_mv Almeida, Olga Maria Martins Silva de
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/2438645505018032
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/4526004572649712
dc.contributor.author.fl_str_mv Prieto, Carla Soares de Lima
contributor_str_mv Villaça, Yael de Abreu
Castro, Newton Gonçalves de
Calaza, Karin da Costa
Almeida, Olga Maria Martins Silva de
dc.subject.eng.fl_str_mv Organophosphate
Development
Cholinergic system
Serotoninergic system
Behavior
topic Organophosphate
Development
Cholinergic system
Serotoninergic system
Behavior
Organofosforados
Desenvolvimento
Sistema colinérgico
Sistema serotoninérgico
Comportamento
Pesticidas Toxicologia
Pesticidas Efeito fisiológico
Manifestações neurocomportamentais
Desenvolvimento infantil Efeito de drogas
Inseticidas organofosforados Efeitos adversos
CNPQ::CIENCIAS BIOLOGICAS::FISIOLOGIA::FISIOLOGIA DE ORGAOS E SISTEMAS
dc.subject.por.fl_str_mv Organofosforados
Desenvolvimento
Sistema colinérgico
Sistema serotoninérgico
Comportamento
Pesticidas Toxicologia
Pesticidas Efeito fisiológico
Manifestações neurocomportamentais
Desenvolvimento infantil Efeito de drogas
Inseticidas organofosforados Efeitos adversos
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS BIOLOGICAS::FISIOLOGIA::FISIOLOGIA DE ORGAOS E SISTEMAS
description Organophosphate pesticides are widely used and its use consist on a severe public health problem. The classic effect of these compounds involve irreversible inhibition of the enzyme acetylcholinesterase, causing an accumulation of acetylcholine at cholinergic synapses and, consequently, cholinergic hyperstimulation. However, when the doses of exposure are low, other the mechanisms of action may play a role and other neurotransmitter systems may be affected. Considering that children are particularly vulnerable to effects of these compounds, in this study we investigated the effects of methamidophos and chlorpyrifos organophosphate exposure during development on cholinergic and serotonergic systems and behavior. For this purpose, Swiss mice received subcutaneous injections of methamidophos or chlorpyrifos, or vehicle from the third to the nineth postnatal day (PN3 - PN9). Initially, a dose-response study was performed and the doses of 1mg/kg methamidophos and 3mg/kg chlorphrifos, which promoted 20% inhibition of acetylcholinesterase activity in brain were chosen to be used in the next set of experiments. At PN10, one day after exposure, a group of animals was sacrificed and the brainstem and cortex collected and stored to further analysis of cholinergic and serotonergic systems. From PN60 to PN63 the animals were submitted to behavioral tests in order to evaluate: anxiety, locomotor activity, decision making, depressive-like behavior and learning/memory. After the last test, the animals were sacrificed and the brainstem and cortex collected and stored to further analysis of cholinergic and serotonergic systems. At PN10, methamidophos and chlorpyrifos promoted alterations that suggest an increase of cholinergic activity respectively on the brainstem and cortex of females. As for the serotonergic system: only chlorpyrifos elicited alterations: There were increases in 5HT1A receptor and 5HT transporter binding in females and a decrease in 5HT2 receptor binding. At PN63, the activity of acetylcholinesterase had returned to control levels. Despite that, methamidophos elicited a decrease in the activity of choline acetyltransferase in the cortex and in choline transporter binding in the brainstem. As for the serotonergic system, methamidophos and chlorpyrifos promoted decreased 5HT1A receptor binding respectively in the brainstem and cortex of females and chlorpyrifos increased its binding in males. Methamidophos exposure elicited increased 5HT2 binding whereas chlorpyrifos exposure decreased female 5HT transporter binding. Methamidophos elicited behavioral alterations suggestive of increased depressive-like behavior while chlorpyrifos exposure was associated to increased anxiety levels and memory/learning deficits. Our results indicate that metamidophos and chlorpyrifos exposure during development distinctively affect the cholinergic and serotonergic systems even at toxicologically equivalent doses. There were immediate and late-emergent neurochemical effects that may play a role on the behavioral outcomes. Finally, the present study reinforces the epidemiologic association between pesticides exposure and mood disorders and suggest that organophosphate exposure during early development programs for late effects.
publishDate 2013
dc.date.available.fl_str_mv 2013-08-21
dc.date.issued.fl_str_mv 2013-05-29
dc.date.accessioned.fl_str_mv 2021-04-26T01:10:50Z
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dc.identifier.citation.fl_str_mv PRIETO, Carla Soares de Lima. Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais. 2013. 105 f. Tese (Doutorado em Biociências Nucleares; Ecologia) - Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2013.
dc.identifier.uri.fl_str_mv http://www.bdtd.uerj.br/handle/1/16140
identifier_str_mv PRIETO, Carla Soares de Lima. Neurotoxicidade de pesticidas organofosforados durante o desenvolvimento: alterações bioquímicas e comportamentais. 2013. 105 f. Tese (Doutorado em Biociências Nucleares; Ecologia) - Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2013.
url http://www.bdtd.uerj.br/handle/1/16140
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dc.publisher.department.fl_str_mv Centro Biomédico::Instituto de Biologia Roberto Alcantara Gomes
publisher.none.fl_str_mv Universidade do Estado do Rio de Janeiro
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