Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Patricia
Data de Publicação: 2020
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/001300000xvgb
Texto Completo: http://repositorio.ufsm.br/handle/1/24012
Resumo: Natural products are a drug discovery source for both humans and veterinary treatment. Consequently, in the last decade, essential oils have been researched as fish anesthetics and sedatives, however, there are a small number of antinociceptive drug development studies using fish as an animal model. Also, the essential oils use is limited in pisciculture maybe due to the physicochemical limitations, such as high hydrophobicity. Thus, nanotechnology can protect and facilitate these compounds dispersion in water. Therefore, through this dissertation, it is expected to improve the volatile compounds use as anesthetic and sedative agents, even as increase the antinociceptive use as well-being promoters for fish. Firstly, silver catfish (Rhamdia quelen) nociceptive method was standardized with acetic acid 15 % (3μL), formalin 1 % (10 μL) and menthol 0.5 % (1 μL) administered in the lips. Additionally, due to the Nectandra grandiflora essential oil anesthetic/sedative activity, it was suggested to evaluate the antinociceptive activity, as well as linalool. In addition, we developed a N. grandiflora essential oil nanoemulsion formulation (NEN), and evaluate the anesthetic, sedative and toxicity by immersion bath in Nile tilapia (Oreochromis niloticus) compared with the free essential oil (FEO). Chemical analyses were performed by gas chromatography coupled to mass spectrometry and flame ionization detector. Among the results, to induce the nociceptive-like behavior in silver catfish we used 15 % acetic acid (3 μL), 1 % formalin (10 μL) and 0.5 % menthol (1 μL). Nociceptive-like behavior was verified in ten locomotor parameters that were reversed with intramuscular morphine (5 mg/kg) injection, and this antinociceptive activity was antagonized by naloxone (5 mg/kg). However, only acetic acid-induced the nociceptive-like behavior at the maximum speed parameter. Given this, the volatile compounds treatment was performed only against acetic acid and the N. grandiflora essential oil (10 mg/kg) had low activity. Linalool (50 mg/kg), on the other hand, has strong antinociceptive activity by reversing all locomotors parameters, with a related mechanism to opioid receptors. Secondarily, through the spontaneous emulsification process, we developed thirteen NEN and the nanoemulsification process protected the oil chemical composition for 60 days and reduced the FEO side effects. Therefore, the NEN 100 mg/L concentration for anesthetic and 30 mg/L for sedation application are safe. Thus, FEO depressant activity was improved and also refined for tilapia. Moreover, the two fish species use covers not only nociceptive-like behavior in an unknown species but also a new O. niloticus pharmacological alternative for sedation and anesthesia. Consequently, the silver catfish new nociception experimental model proposed demonstrated specificity, since the nociceptive-like behavior was reverted by linalool and morphine, which have described analgesic activity. Briefly, this dissertation contributes to research that aims to combine volatile compound and nanotechnological knowledge into an effective and safe anesthetic drug development.
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spelling Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixesVolatile compounds as sedative, anesthetic and antinocioceptive in fishRhamdia quelenOreochromis niloticusÓleo essencialNanoemulsãoNectandra grandifloraLinalolEssential oilNanoemulsionLinaloolCNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIANatural products are a drug discovery source for both humans and veterinary treatment. Consequently, in the last decade, essential oils have been researched as fish anesthetics and sedatives, however, there are a small number of antinociceptive drug development studies using fish as an animal model. Also, the essential oils use is limited in pisciculture maybe due to the physicochemical limitations, such as high hydrophobicity. Thus, nanotechnology can protect and facilitate these compounds dispersion in water. Therefore, through this dissertation, it is expected to improve the volatile compounds use as anesthetic and sedative agents, even as increase the antinociceptive use as well-being promoters for fish. Firstly, silver catfish (Rhamdia quelen) nociceptive method was standardized with acetic acid 15 % (3μL), formalin 1 % (10 μL) and menthol 0.5 % (1 μL) administered in the lips. Additionally, due to the Nectandra grandiflora essential oil anesthetic/sedative activity, it was suggested to evaluate the antinociceptive activity, as well as linalool. In addition, we developed a N. grandiflora essential oil nanoemulsion formulation (NEN), and evaluate the anesthetic, sedative and toxicity by immersion bath in Nile tilapia (Oreochromis niloticus) compared with the free essential oil (FEO). Chemical analyses were performed by gas chromatography coupled to mass spectrometry and flame ionization detector. Among the results, to induce the nociceptive-like behavior in silver catfish we used 15 % acetic acid (3 μL), 1 % formalin (10 μL) and 0.5 % menthol (1 μL). Nociceptive-like behavior was verified in ten locomotor parameters that were reversed with intramuscular morphine (5 mg/kg) injection, and this antinociceptive activity was antagonized by naloxone (5 mg/kg). However, only acetic acid-induced the nociceptive-like behavior at the maximum speed parameter. Given this, the volatile compounds treatment was performed only against acetic acid and the N. grandiflora essential oil (10 mg/kg) had low activity. Linalool (50 mg/kg), on the other hand, has strong antinociceptive activity by reversing all locomotors parameters, with a related mechanism to opioid receptors. Secondarily, through the spontaneous emulsification process, we developed thirteen NEN and the nanoemulsification process protected the oil chemical composition for 60 days and reduced the FEO side effects. Therefore, the NEN 100 mg/L concentration for anesthetic and 30 mg/L for sedation application are safe. Thus, FEO depressant activity was improved and also refined for tilapia. Moreover, the two fish species use covers not only nociceptive-like behavior in an unknown species but also a new O. niloticus pharmacological alternative for sedation and anesthesia. Consequently, the silver catfish new nociception experimental model proposed demonstrated specificity, since the nociceptive-like behavior was reverted by linalool and morphine, which have described analgesic activity. Briefly, this dissertation contributes to research that aims to combine volatile compound and nanotechnological knowledge into an effective and safe anesthetic drug development.Produtos naturais representam uma fonte de novos medicamentos, na última década, óleos essenciais vêm sendo investigados como anestésicos e sedativos para peixes. Entretanto o desenvolvimento de antinociceptivos é pouco estudado, assim como a utilização de peixes como modelo animal. Ainda, os óleos essenciais são pouco utilizados na prática como anestésicos para peixes e isso pode estar ligado às suas limitações físico-químicas. Neste sentido, a nanotecnologia pode ser utilizada para proteger e facilitar a dispersão em água destes compostos. Logo, objetivamos aprimorar o uso de compostos voláteis como agentes anestésicos e sedativos e antinociceptivos como promotores de bem-estar em peixes. Para isso, padronizamos um método nociceptivo com o jundiá (Rhamdia quelen) com três diferentes algógenos, ácido acético 15 % (3μL), formalina 1 % (10 μL) e mentol 0,5 % (1 μL). Adicionalmente, devido a atividade anestésica/sedativa do óleo essencial de Nectandra grandiflora, foi proposta a avaliação da atividade antinociceptiva, assim como do linalol. Além disso, desenvolvemos uma formulação de nanoemulsão com este óleo essencial e avaliação da atividade anestésica e sedativa por banho de imersão, assim como sua toxicidade em tilápia do Nilo (Oreochromis niloticus). As análises químicas foram realizadas por cromatógrafo gasoso acoplado a espectrometria de massas e detector de ionização em chama. O comportamento tipo-nociceptivo do jundiá foi verificado em dez parâmetros locomotores e revertido com morfina (5 mg/kg) e antagonizado pelo pré-tratamento com naloxona (5 mg/kg). Entretanto, apenas o ácido acético induziu o comportamento tipo-nociceptivo no parâmetro de velocidade máxima. Diante disto, realizamos o tratamento dos peixes com os compostos voláteis apenas frente a ao ácido como algógeno e verificamos a fraca atividade do óleo essencial (10 mg/kg). O linalol (50 mg/kg) apresentou forte atividade antinociceptiva ao reverter todos os parâmetros de atividade locomotora, com mecanismo da atividade ligado aos receptores opioides. Em um segundo momento, através do processo de emulsificação espontânea desenvolvemos uma formulação com o óleo essencial de N. grandiflora que protegeu e diminuiu os efeitos adversos, sendo seguras a concentração de 100 mg/L como anestésico e 30 mg/L para sedação de tilápias. A utilização de duas espécies de peixes abrange não só o comportamento tipo-nocioceptivo outrora desconhecido em Rhamdia quelen, mas também uma nova alternativa farmacológica para sedação e anestesia de O. niloticus. Desta forma, o novo modelo experimental proposto para nocicepção com jundiá demonstrou especificidade, já que foi possível observar a reversão do comportamento tipo-nociceptivo para o linalol e a morfina, que possuem atividade analgésica descrita. Em suma esta dissertação colabora para pesquisas que visam aliar o conhecimento nanotecnológico com compostos voláteis no desenvolvimento de medicamentos anestésicos mais eficazes e com menores efeitos adversos.Universidade Federal de Santa MariaBrasilFarmacologiaUFSMPrograma de Pós-Graduação em FarmacologiaCentro de Ciências da SaúdeHeinzmann, Berta Mariahttp://lattes.cnpq.br/0786124562427815Baldisserotto, BernardoOurique, Aline FerreiraBarcellos, Leonardo Jose GilRodrigues, Patricia2022-04-04T14:28:20Z2022-04-04T14:28:20Z2020-02-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/24012ark:/26339/001300000xvgbporAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-04-04T14:28:20Zoai:repositorio.ufsm.br:1/24012Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2022-04-04T14:28:20Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
Volatile compounds as sedative, anesthetic and antinocioceptive in fish
title Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
spellingShingle Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
Rodrigues, Patricia
Rhamdia quelen
Oreochromis niloticus
Óleo essencial
Nanoemulsão
Nectandra grandiflora
Linalol
Essential oil
Nanoemulsion
Linalool
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
title_short Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
title_full Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
title_fullStr Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
title_full_unstemmed Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
title_sort Compostos voláteis como sedativos, anestésicos e antinociceptivos em peixes
author Rodrigues, Patricia
author_facet Rodrigues, Patricia
author_role author
dc.contributor.none.fl_str_mv Heinzmann, Berta Maria
http://lattes.cnpq.br/0786124562427815
Baldisserotto, Bernardo
Ourique, Aline Ferreira
Barcellos, Leonardo Jose Gil
dc.contributor.author.fl_str_mv Rodrigues, Patricia
dc.subject.por.fl_str_mv Rhamdia quelen
Oreochromis niloticus
Óleo essencial
Nanoemulsão
Nectandra grandiflora
Linalol
Essential oil
Nanoemulsion
Linalool
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
topic Rhamdia quelen
Oreochromis niloticus
Óleo essencial
Nanoemulsão
Nectandra grandiflora
Linalol
Essential oil
Nanoemulsion
Linalool
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
description Natural products are a drug discovery source for both humans and veterinary treatment. Consequently, in the last decade, essential oils have been researched as fish anesthetics and sedatives, however, there are a small number of antinociceptive drug development studies using fish as an animal model. Also, the essential oils use is limited in pisciculture maybe due to the physicochemical limitations, such as high hydrophobicity. Thus, nanotechnology can protect and facilitate these compounds dispersion in water. Therefore, through this dissertation, it is expected to improve the volatile compounds use as anesthetic and sedative agents, even as increase the antinociceptive use as well-being promoters for fish. Firstly, silver catfish (Rhamdia quelen) nociceptive method was standardized with acetic acid 15 % (3μL), formalin 1 % (10 μL) and menthol 0.5 % (1 μL) administered in the lips. Additionally, due to the Nectandra grandiflora essential oil anesthetic/sedative activity, it was suggested to evaluate the antinociceptive activity, as well as linalool. In addition, we developed a N. grandiflora essential oil nanoemulsion formulation (NEN), and evaluate the anesthetic, sedative and toxicity by immersion bath in Nile tilapia (Oreochromis niloticus) compared with the free essential oil (FEO). Chemical analyses were performed by gas chromatography coupled to mass spectrometry and flame ionization detector. Among the results, to induce the nociceptive-like behavior in silver catfish we used 15 % acetic acid (3 μL), 1 % formalin (10 μL) and 0.5 % menthol (1 μL). Nociceptive-like behavior was verified in ten locomotor parameters that were reversed with intramuscular morphine (5 mg/kg) injection, and this antinociceptive activity was antagonized by naloxone (5 mg/kg). However, only acetic acid-induced the nociceptive-like behavior at the maximum speed parameter. Given this, the volatile compounds treatment was performed only against acetic acid and the N. grandiflora essential oil (10 mg/kg) had low activity. Linalool (50 mg/kg), on the other hand, has strong antinociceptive activity by reversing all locomotors parameters, with a related mechanism to opioid receptors. Secondarily, through the spontaneous emulsification process, we developed thirteen NEN and the nanoemulsification process protected the oil chemical composition for 60 days and reduced the FEO side effects. Therefore, the NEN 100 mg/L concentration for anesthetic and 30 mg/L for sedation application are safe. Thus, FEO depressant activity was improved and also refined for tilapia. Moreover, the two fish species use covers not only nociceptive-like behavior in an unknown species but also a new O. niloticus pharmacological alternative for sedation and anesthesia. Consequently, the silver catfish new nociception experimental model proposed demonstrated specificity, since the nociceptive-like behavior was reverted by linalool and morphine, which have described analgesic activity. Briefly, this dissertation contributes to research that aims to combine volatile compound and nanotechnological knowledge into an effective and safe anesthetic drug development.
publishDate 2020
dc.date.none.fl_str_mv 2020-02-18
2022-04-04T14:28:20Z
2022-04-04T14:28:20Z
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 http://repositorio.ufsm.br/handle/1/24012
dc.identifier.dark.fl_str_mv ark:/26339/001300000xvgb
url http://repositorio.ufsm.br/handle/1/24012
identifier_str_mv ark:/26339/001300000xvgb
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Farmacologia
UFSM
Programa de Pós-Graduação em Farmacologia
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Farmacologia
UFSM
Programa de Pós-Graduação em Farmacologia
Centro de Ciências da Saúde
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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