Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association
Autor(a) principal: | |
---|---|
Data de Publicação: | 2003 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da UFC |
Texto Completo: | http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=82 |
Resumo: | In the present work, behavioral, neurochemical (determination of monoamines and metabolites levels rat in striatum), histopatological and biochemical (lipoproteins and transaminases) alterations produced by cocaine, ethanol and the association of theses were analyzed. Females Wistar rats (180-200 g) were treated during 7 days with cocaine (Coc 10 and 20 mg/kg, i.p.), ethanol (Et 2 and 4g/kg, p.o.) and the association of theses (Coc 10 mg + Et 2g - low interaction doses; Coc 20 mg + Ethanol 4g - high interaction doses). The results demonstrated that the spontaneous locomotor activity (SLA) was increased after cocaine administration and decreased after ethanol in both doses. It was not observed alterations in the SLA in the association cocaine + ethanol. The treatment with cocaine and ethanol caused an increase in dopamine level. The association cocaine + ethanol in higher doses caused an increase of dopamine and serotonin and decrease of DOPAC levels, suggesting that those drugs would can actuate directly in those systems or, indirectly, across a process of modulation. Cocaine, ethanol and the association of theses, after subcronic administration and in both doses, caused a donwregulation of D2-like receptors, not by recurring alterations in the values of Kd. The values of Bmax and Kd of the M1 + M2-like receptors have not already suffered alterations. In the biochemical study, the administration of cocaine induced an increase the concentrations of TGO and triglycerides, and decrease of the concentrations of TGP, total cholesterol and HDL. The treatment with ethanol decreases the levels of HDL, total cholesterol and triglycerides. The association cocaine + ethanol caused in both doses decrease of triglycerides, HDL, TGP and total cholesterol. All treatments did promote histopatological alterations in cardiac and hepatic woven. Ours results suggest that the association cocaine + ethanol appears to interfere more intense in the systems of neurotransmitters and in the biochemical parameters than the use of the isolated drugs. |
id |
UFC_52711fd8ca0731cbb89199bb27c5170c |
---|---|
oai_identifier_str |
oai:www.teses.ufc.br:189 |
network_acronym_str |
UFC |
network_name_str |
Biblioteca Digital de Teses e Dissertações da UFC |
spelling |
info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisBehavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in associationAvaliaÃÃo das alteraÃÃes comportamentais, neuroquÃmicas, histopatolÃgicas e bioquÃmicas em ratos tratados com cocaÃna e etanol isoladamente ou em associaÃÃo2003-02-07Marta Maria de FranÃa Fonteles28529839315http://lattes.cnpq.br/0574180390413250Francisca ClÃa FlorenÃo de Sousa31636020372http://lattes.cnpq.br/1180465052181572LetÃcia Veras Costa-Lotufo43089810344http://lattes.cnpq.br/519314943797981884690208387http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4707397E4Iri Sandro Pampolha LimaUniversidade Federal do CearÃPrograma de PÃs-GraduaÃÃo em FarmacologiaUFCBRCocaÃna - farmacocinÃtica AnestÃsicos Locais Norepinefrina Dopamina FarmacocinÃtica Aspartato AminotransferasesCocaine - pharmacokinetics Anesthetics, Local Norepinephrine Dopamine Pharmacokinetics Aspartate AminotransferasesFARMACOLOGIAIn the present work, behavioral, neurochemical (determination of monoamines and metabolites levels rat in striatum), histopatological and biochemical (lipoproteins and transaminases) alterations produced by cocaine, ethanol and the association of theses were analyzed. Females Wistar rats (180-200 g) were treated during 7 days with cocaine (Coc 10 and 20 mg/kg, i.p.), ethanol (Et 2 and 4g/kg, p.o.) and the association of theses (Coc 10 mg + Et 2g - low interaction doses; Coc 20 mg + Ethanol 4g - high interaction doses). The results demonstrated that the spontaneous locomotor activity (SLA) was increased after cocaine administration and decreased after ethanol in both doses. It was not observed alterations in the SLA in the association cocaine + ethanol. The treatment with cocaine and ethanol caused an increase in dopamine level. The association cocaine + ethanol in higher doses caused an increase of dopamine and serotonin and decrease of DOPAC levels, suggesting that those drugs would can actuate directly in those systems or, indirectly, across a process of modulation. Cocaine, ethanol and the association of theses, after subcronic administration and in both doses, caused a donwregulation of D2-like receptors, not by recurring alterations in the values of Kd. The values of Bmax and Kd of the M1 + M2-like receptors have not already suffered alterations. In the biochemical study, the administration of cocaine induced an increase the concentrations of TGO and triglycerides, and decrease of the concentrations of TGP, total cholesterol and HDL. The treatment with ethanol decreases the levels of HDL, total cholesterol and triglycerides. The association cocaine + ethanol caused in both doses decrease of triglycerides, HDL, TGP and total cholesterol. All treatments did promote histopatological alterations in cardiac and hepatic woven. Ours results suggest that the association cocaine + ethanol appears to interfere more intense in the systems of neurotransmitters and in the biochemical parameters than the use of the isolated drugs.No presente trabalho foram estudadas as alteraÃÃes comportamentais, neuroquÃmicas (determinaÃÃes dos nÃveis de monoaminas e metabÃlitos), histopatolÃgicas e bioquÃmicas (lipoproteÃnas e transaminases) em corpo estriado de ratos tratados com cocaÃna e etanol isoladamente ou em associaÃÃo. Foram utilizadas ratas Wistar (180-200 g), que foram tratadas durante 7 dias com cocaÃna (Coc 10 e 20 mg/kg, i.p.), etanol (Et 2 e 4g/kg, v.o.) e a associaÃÃo destes (Coc 10 mg + Et 2g - interaÃÃo baixas doses; Coc 20 mg + Etanol 4g - interaÃÃo altas doses). Os resultados demonstraram que a atividade locomotora espontÃnea (ALE) foi aumentada apÃs administraÃÃo de cocaÃna em ambas as doses e diminuÃda apÃs a administraÃÃo de etanol em ambas as doses. NÃo foram observadas alteraÃÃes na ALE na associaÃÃo cocaÃna + etanol. O tratamento com cocaÃna e etanol causou um aumento de dopamina, sem alteraÃÃes nos demais neurotransmissores e metabÃlitos. A associaÃÃo cocaÃna + etanol em altas doses, promoveu aumento dos nÃveis de dopamina, diminuiÃÃo de DOPAC e aumento dos nÃveis de 5-HT, sugerindo que essas drogas poderiam atuar diretamente nesses sistemas ou, indiretamente, atravÃs de um processo de modulaÃÃo. A cocaÃna, etanol e a associaÃÃo destes, apÃs administraÃÃo sub-crÃnica e em ambas as doses, causou uma downregulation em receptores D2-sÃmile, nÃo ocorrendo alteraÃÃes nos valores de Kd. Os valores de Bmax e Kd dos receptores M1 + M2-sÃmile nÃo sofreram alteraÃÃes. No estudo bioquÃmico, a administraÃÃo de cocaÃna induziu um aumento nas concentraÃÃes de TGO e triglicerÃdeos, e diminuiÃÃo das concentraÃÃes de TGP, colesterol total e HDL. O tratamento com etanol diminuiu os nÃveis de HDL, colesterol total e triglicerÃdeos. A associaÃÃo cocaÃna + etanol promoveu em ambas as doses diminuiÃÃo de trigicerÃdeos, HDL, TGP e colesterol total. Todos os tratamentos promoveram alteraÃÃes histopatolÃgicas em tecido cardÃaco e hepÃtico. Nossos resultados sugerem que a associaÃÃo cocaÃna + etanol parece interferir de maneira mais intensa nos sistemas de neurotransmissÃo e nos parÃmetros bioquÃmicos do que o uso das drogas isoladas. Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgicohttp://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=82application/pdfinfo:eu-repo/semantics/openAccessporreponame:Biblioteca Digital de Teses e Dissertações da UFCinstname:Universidade Federal do Cearáinstacron:UFC2019-01-21T11:13:10Zmail@mail.com - |
dc.title.mk.fl_str_mv |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association |
dc.title.alternative.pt.fl_str_mv |
AvaliaÃÃo das alteraÃÃes comportamentais, neuroquÃmicas, histopatolÃgicas e bioquÃmicas em ratos tratados com cocaÃna e etanol isoladamente ou em associaÃÃo |
title |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association |
spellingShingle |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association Iri Sandro Pampolha Lima CocaÃna - farmacocinÃtica AnestÃsicos Locais Norepinefrina Dopamina FarmacocinÃtica Aspartato Aminotransferases Cocaine - pharmacokinetics Anesthetics, Local Norepinephrine Dopamine Pharmacokinetics Aspartate Aminotransferases FARMACOLOGIA |
title_short |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association |
title_full |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association |
title_fullStr |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association |
title_full_unstemmed |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association |
title_sort |
Behavioral, neurochemical, histopatological and biochemical alterations in rats treated with cocaine and ethanol singly or in association |
author |
Iri Sandro Pampolha Lima |
author_facet |
Iri Sandro Pampolha Lima |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Marta Maria de FranÃa Fonteles |
dc.contributor.advisor1ID.fl_str_mv |
28529839315 |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/0574180390413250 |
dc.contributor.referee1.fl_str_mv |
Francisca ClÃa FlorenÃo de Sousa |
dc.contributor.referee1ID.fl_str_mv |
31636020372 |
dc.contributor.referee1Lattes.fl_str_mv |
http://lattes.cnpq.br/1180465052181572 |
dc.contributor.referee2.fl_str_mv |
LetÃcia Veras Costa-Lotufo |
dc.contributor.referee2ID.fl_str_mv |
43089810344 |
dc.contributor.referee2Lattes.fl_str_mv |
http://lattes.cnpq.br/5193149437979818 |
dc.contributor.authorID.fl_str_mv |
84690208387 |
dc.contributor.authorLattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.jsp?id=K4707397E4 |
dc.contributor.author.fl_str_mv |
Iri Sandro Pampolha Lima |
contributor_str_mv |
Marta Maria de FranÃa Fonteles Francisca ClÃa FlorenÃo de Sousa LetÃcia Veras Costa-Lotufo |
dc.subject.por.fl_str_mv |
CocaÃna - farmacocinÃtica AnestÃsicos Locais Norepinefrina Dopamina FarmacocinÃtica Aspartato Aminotransferases |
topic |
CocaÃna - farmacocinÃtica AnestÃsicos Locais Norepinefrina Dopamina FarmacocinÃtica Aspartato Aminotransferases Cocaine - pharmacokinetics Anesthetics, Local Norepinephrine Dopamine Pharmacokinetics Aspartate Aminotransferases FARMACOLOGIA |
dc.subject.eng.fl_str_mv |
Cocaine - pharmacokinetics Anesthetics, Local Norepinephrine Dopamine Pharmacokinetics Aspartate Aminotransferases |
dc.subject.cnpq.fl_str_mv |
FARMACOLOGIA |
dc.description.sponsorship.fl_txt_mv |
Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico |
dc.description.abstract.por.fl_txt_mv |
In the present work, behavioral, neurochemical (determination of monoamines and metabolites levels rat in striatum), histopatological and biochemical (lipoproteins and transaminases) alterations produced by cocaine, ethanol and the association of theses were analyzed. Females Wistar rats (180-200 g) were treated during 7 days with cocaine (Coc 10 and 20 mg/kg, i.p.), ethanol (Et 2 and 4g/kg, p.o.) and the association of theses (Coc 10 mg + Et 2g - low interaction doses; Coc 20 mg + Ethanol 4g - high interaction doses). The results demonstrated that the spontaneous locomotor activity (SLA) was increased after cocaine administration and decreased after ethanol in both doses. It was not observed alterations in the SLA in the association cocaine + ethanol. The treatment with cocaine and ethanol caused an increase in dopamine level. The association cocaine + ethanol in higher doses caused an increase of dopamine and serotonin and decrease of DOPAC levels, suggesting that those drugs would can actuate directly in those systems or, indirectly, across a process of modulation. Cocaine, ethanol and the association of theses, after subcronic administration and in both doses, caused a donwregulation of D2-like receptors, not by recurring alterations in the values of Kd. The values of Bmax and Kd of the M1 + M2-like receptors have not already suffered alterations. In the biochemical study, the administration of cocaine induced an increase the concentrations of TGO and triglycerides, and decrease of the concentrations of TGP, total cholesterol and HDL. The treatment with ethanol decreases the levels of HDL, total cholesterol and triglycerides. The association cocaine + ethanol caused in both doses decrease of triglycerides, HDL, TGP and total cholesterol. All treatments did promote histopatological alterations in cardiac and hepatic woven. Ours results suggest that the association cocaine + ethanol appears to interfere more intense in the systems of neurotransmitters and in the biochemical parameters than the use of the isolated drugs. No presente trabalho foram estudadas as alteraÃÃes comportamentais, neuroquÃmicas (determinaÃÃes dos nÃveis de monoaminas e metabÃlitos), histopatolÃgicas e bioquÃmicas (lipoproteÃnas e transaminases) em corpo estriado de ratos tratados com cocaÃna e etanol isoladamente ou em associaÃÃo. Foram utilizadas ratas Wistar (180-200 g), que foram tratadas durante 7 dias com cocaÃna (Coc 10 e 20 mg/kg, i.p.), etanol (Et 2 e 4g/kg, v.o.) e a associaÃÃo destes (Coc 10 mg + Et 2g - interaÃÃo baixas doses; Coc 20 mg + Etanol 4g - interaÃÃo altas doses). Os resultados demonstraram que a atividade locomotora espontÃnea (ALE) foi aumentada apÃs administraÃÃo de cocaÃna em ambas as doses e diminuÃda apÃs a administraÃÃo de etanol em ambas as doses. NÃo foram observadas alteraÃÃes na ALE na associaÃÃo cocaÃna + etanol. O tratamento com cocaÃna e etanol causou um aumento de dopamina, sem alteraÃÃes nos demais neurotransmissores e metabÃlitos. A associaÃÃo cocaÃna + etanol em altas doses, promoveu aumento dos nÃveis de dopamina, diminuiÃÃo de DOPAC e aumento dos nÃveis de 5-HT, sugerindo que essas drogas poderiam atuar diretamente nesses sistemas ou, indiretamente, atravÃs de um processo de modulaÃÃo. A cocaÃna, etanol e a associaÃÃo destes, apÃs administraÃÃo sub-crÃnica e em ambas as doses, causou uma downregulation em receptores D2-sÃmile, nÃo ocorrendo alteraÃÃes nos valores de Kd. Os valores de Bmax e Kd dos receptores M1 + M2-sÃmile nÃo sofreram alteraÃÃes. No estudo bioquÃmico, a administraÃÃo de cocaÃna induziu um aumento nas concentraÃÃes de TGO e triglicerÃdeos, e diminuiÃÃo das concentraÃÃes de TGP, colesterol total e HDL. O tratamento com etanol diminuiu os nÃveis de HDL, colesterol total e triglicerÃdeos. A associaÃÃo cocaÃna + etanol promoveu em ambas as doses diminuiÃÃo de trigicerÃdeos, HDL, TGP e colesterol total. Todos os tratamentos promoveram alteraÃÃes histopatolÃgicas em tecido cardÃaco e hepÃtico. Nossos resultados sugerem que a associaÃÃo cocaÃna + etanol parece interferir de maneira mais intensa nos sistemas de neurotransmissÃo e nos parÃmetros bioquÃmicos do que o uso das drogas isoladas. |
description |
In the present work, behavioral, neurochemical (determination of monoamines and metabolites levels rat in striatum), histopatological and biochemical (lipoproteins and transaminases) alterations produced by cocaine, ethanol and the association of theses were analyzed. Females Wistar rats (180-200 g) were treated during 7 days with cocaine (Coc 10 and 20 mg/kg, i.p.), ethanol (Et 2 and 4g/kg, p.o.) and the association of theses (Coc 10 mg + Et 2g - low interaction doses; Coc 20 mg + Ethanol 4g - high interaction doses). The results demonstrated that the spontaneous locomotor activity (SLA) was increased after cocaine administration and decreased after ethanol in both doses. It was not observed alterations in the SLA in the association cocaine + ethanol. The treatment with cocaine and ethanol caused an increase in dopamine level. The association cocaine + ethanol in higher doses caused an increase of dopamine and serotonin and decrease of DOPAC levels, suggesting that those drugs would can actuate directly in those systems or, indirectly, across a process of modulation. Cocaine, ethanol and the association of theses, after subcronic administration and in both doses, caused a donwregulation of D2-like receptors, not by recurring alterations in the values of Kd. The values of Bmax and Kd of the M1 + M2-like receptors have not already suffered alterations. In the biochemical study, the administration of cocaine induced an increase the concentrations of TGO and triglycerides, and decrease of the concentrations of TGP, total cholesterol and HDL. The treatment with ethanol decreases the levels of HDL, total cholesterol and triglycerides. The association cocaine + ethanol caused in both doses decrease of triglycerides, HDL, TGP and total cholesterol. All treatments did promote histopatological alterations in cardiac and hepatic woven. Ours results suggest that the association cocaine + ethanol appears to interfere more intense in the systems of neurotransmitters and in the biochemical parameters than the use of the isolated drugs. |
publishDate |
2003 |
dc.date.issued.fl_str_mv |
2003-02-07 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
status_str |
publishedVersion |
format |
masterThesis |
dc.identifier.uri.fl_str_mv |
http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=82 |
url |
http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=82 |
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 |
dc.publisher.none.fl_str_mv |
Universidade Federal do Cearà |
dc.publisher.program.fl_str_mv |
Programa de PÃs-GraduaÃÃo em Farmacologia |
dc.publisher.initials.fl_str_mv |
UFC |
dc.publisher.country.fl_str_mv |
BR |
publisher.none.fl_str_mv |
Universidade Federal do Cearà |
dc.source.none.fl_str_mv |
reponame:Biblioteca Digital de Teses e Dissertações da UFC instname:Universidade Federal do Ceará instacron:UFC |
reponame_str |
Biblioteca Digital de Teses e Dissertações da UFC |
collection |
Biblioteca Digital de Teses e Dissertações da UFC |
instname_str |
Universidade Federal do Ceará |
instacron_str |
UFC |
institution |
UFC |
repository.name.fl_str_mv |
-
|
repository.mail.fl_str_mv |
mail@mail.com |
_version_ |
1643295113266331648 |