Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp

Detalhes bibliográficos
Ano de defesa: 2022
Autor(a) principal: SOUZA, Juliana Kelly Urtigas de lattes
Orientador(a): LIMA FILHO, José Vitor Moreira
Banca de defesa: DORVIGNY, Betty Mancebo, RAMOS, Márcio Viana, SOARES, Anísio Francisco, SILVA JUNIOR, Valdemiro Amaro da
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal Rural de Pernambuco
Programa de Pós-Graduação: Programa de Pós-Graduação em Biociência Animal
Departamento: Departamento de Morfologia e Fisiologia Animal
País: Brasil
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/9651
Resumo: Proteases isolated from the latex of the medicinal plant of Calotropis procera have been investigated in different models of inflammation. Considering previous studies that indicated anti-inflammatory properties of a mixture of proteases called LPp2, in this work, a mixture of proteases called LPp3 was investigated in an experimental salmonellosis model. Thus, macrophage cultures were exposed to different concentrations of LPp3 and infected with Salmonella enterica Sor. Typhimurium. In another infection model, Swiss mice were infected intraperitoneally with S. Typhimurium and then treated (intravenously) with LPp3. The results showed that LPp3 has no direct antibacterial action against Salmonella in vitro and was unable to increase the cell viability of infected macrophages. In the in vivo assays, after 6 h of infection, animals treated with LPp3 (10 mg/kg) had a higher bacterial load in the spleen and liver compared to untreated control (PBS) or Dexamethasone-administered groups. Treatments with LPp3 (1, 5 and 10 mg/kg) inhibited the recruitment of leukocytes to the infectious site after Salmonella inoculum in the peritoneal cavity. However, gene expression levels of inflammatory cytokines measured in the spleen, such as TNF-alpha and IL1-beta, were significantly increased in animals treated with 10 mg/kg relative to infected/untreated animals. It was concludedthat LPp3, as already demonstrated for LPp2, is rich in enzymes with strong anti-inflammatory action, which could explain the lower elimination of bacteria at higher doses.
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spelling LIMA FILHO, José Vitor MoreiraDORVIGNY, Betty ManceboRAMOS, Márcio VianaSOARES, Anísio FranciscoSILVA JUNIOR, Valdemiro Amaro dahttp://lattes.cnpq.br/4267884826232996SOUZA, Juliana Kelly Urtigas de2024-07-09T19:26:06Z2022-11-16SOUZA, Juliana Kelly Urtigas de. Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp. 2022. 54 f. Dissertação (Programa de Pós-Graduação em Biociência Animal) - Universidade Federal Rural de Pernambuco, Recife.http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/9651Proteases isolated from the latex of the medicinal plant of Calotropis procera have been investigated in different models of inflammation. Considering previous studies that indicated anti-inflammatory properties of a mixture of proteases called LPp2, in this work, a mixture of proteases called LPp3 was investigated in an experimental salmonellosis model. Thus, macrophage cultures were exposed to different concentrations of LPp3 and infected with Salmonella enterica Sor. Typhimurium. In another infection model, Swiss mice were infected intraperitoneally with S. Typhimurium and then treated (intravenously) with LPp3. The results showed that LPp3 has no direct antibacterial action against Salmonella in vitro and was unable to increase the cell viability of infected macrophages. In the in vivo assays, after 6 h of infection, animals treated with LPp3 (10 mg/kg) had a higher bacterial load in the spleen and liver compared to untreated control (PBS) or Dexamethasone-administered groups. Treatments with LPp3 (1, 5 and 10 mg/kg) inhibited the recruitment of leukocytes to the infectious site after Salmonella inoculum in the peritoneal cavity. However, gene expression levels of inflammatory cytokines measured in the spleen, such as TNF-alpha and IL1-beta, were significantly increased in animals treated with 10 mg/kg relative to infected/untreated animals. It was concludedthat LPp3, as already demonstrated for LPp2, is rich in enzymes with strong anti-inflammatory action, which could explain the lower elimination of bacteria at higher doses.Proteases isoladas do látex da planta medicinal de Calotropis procera têm sido investigadas em diferentes modelos de inflamação. Considerando estudos anteriores que indicaram propriedades anti-inflamatórias de uma mistura de proteases chamada LPp2, neste trabalho, uma mistura de proteases denominada LPp3, ainda pouco estudada, foi investigada em um modelo de salmonelose experimental. Em um dos modelos utilizados de infecção, culturas de macrófagos foram expostas a diferentes concentrações de LPp3 e infectadas com Salmonella enterica Sor. Typhimurium. No modelo de infecção in vivo, camundongos Swiss foram infectados, via intraperitoneal, com S. Typhimurium e, a seguir, tratados (via endovenosa) com LPp3. Os resultados mostraram que LPp3 não possui ação antibacteriana direta contra Salmonella in vitro e foi incapaz de aumentar a viabilidade celular de macrófagos infectados. Nos ensaios in vivo, após 6 h de infecção, os animais tratados com LPp3 (10 mg/kg) tiveram uma maior carga bacteriana no baço e fígado em relação aos grupos controles não tratados (PBS) ou administrados com Dexametasona. Os tratamentos com LPp3 (1,5 e 10 mg/kg) inibiram o recrutamento de leucócitos para o sítio infeccioso após o inóculo de Salmonella, na cavidade peritoneal. Contudo, os níveis de expressão gênica de citocinas inflamatórias medidos no baço, tais como, TNF-alfa e IL1-beta estavam significativamente aumentados nos animais tratados com 10 mg/kg em relação aos animais infectados e não tratados. Concluiu-se que LPp3, assim como já demonstrado para LPp2, rica em enzimas proteolíticas, exibe forte ação anti-inflamatória, o que poderia explicar a menor eliminação de bactérias em dosagens mais elevadas.Submitted by (ana.araujo@ufrpe.br) on 2024-07-09T19:26:06Z No. of bitstreams: 1 Juliana Kelly Urtigas de Souza.pdf: 1681224 bytes, checksum: 6104e56af9e23774e0f0809c8a0273be (MD5)Made available in DSpace on 2024-07-09T19:26:06Z (GMT). No. of bitstreams: 1 Juliana Kelly Urtigas de Souza.pdf: 1681224 bytes, checksum: 6104e56af9e23774e0f0809c8a0273be (MD5) Previous issue date: 2022-11-16Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal Rural de PernambucoPrograma de Pós-Graduação em Biociência AnimalUFRPEBrasilDepartamento de Morfologia e Fisiologia AnimalCalotropis proceraLátexEnzimas proteolíticasAção anti-inflamatóriaSalmonella typhimuriumCIENCIAS AGRARIAS::MEDICINA VETERINARIAPotencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella sspinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis-1510757014399315592600600600600-89223641879873962044536702642350173192075167498588264571info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFRPEinstname:Universidade Federal Rural de Pernambuco (UFRPE)instacron:UFRPEORIGINALJuliana Kelly Urtigas de Souza.pdfJuliana Kelly Urtigas de Souza.pdfapplication/pdf1681224http://www.tede2.ufrpe.br:8080/tede2/bitstream/tede2/9651/2/Juliana+Kelly+Urtigas+de+Souza.pdf6104e56af9e23774e0f0809c8a0273beMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82165http://www.tede2.ufrpe.br:8080/tede2/bitstream/tede2/9651/1/license.txtbd3efa91386c1718a7f26a329fdcb468MD51tede2/96512024-07-09 16:26:06.535oai:tede2: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Biblioteca Digital de Teses e Dissertaçõeshttp://www.tede2.ufrpe.br:8080/tede/PUBhttp://www.tede2.ufrpe.br:8080/oai/requestbdtd@ufrpe.br ||bdtd@ufrpe.bropendoar:2024-07-09T19:26:06Biblioteca Digital de Teses e Dissertações da UFRPE - Universidade Federal Rural de Pernambuco (UFRPE)false
dc.title.por.fl_str_mv Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
title Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
spellingShingle Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
SOUZA, Juliana Kelly Urtigas de
Calotropis procera
Látex
Enzimas proteolíticas
Ação anti-inflamatória
Salmonella typhimurium
CIENCIAS AGRARIAS::MEDICINA VETERINARIA
title_short Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
title_full Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
title_fullStr Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
title_full_unstemmed Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
title_sort Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp
author SOUZA, Juliana Kelly Urtigas de
author_facet SOUZA, Juliana Kelly Urtigas de
author_role author
dc.contributor.advisor1.fl_str_mv LIMA FILHO, José Vitor Moreira
dc.contributor.referee1.fl_str_mv DORVIGNY, Betty Mancebo
dc.contributor.referee2.fl_str_mv RAMOS, Márcio Viana
dc.contributor.referee3.fl_str_mv SOARES, Anísio Francisco
dc.contributor.referee4.fl_str_mv SILVA JUNIOR, Valdemiro Amaro da
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/4267884826232996
dc.contributor.author.fl_str_mv SOUZA, Juliana Kelly Urtigas de
contributor_str_mv LIMA FILHO, José Vitor Moreira
DORVIGNY, Betty Mancebo
RAMOS, Márcio Viana
SOARES, Anísio Francisco
SILVA JUNIOR, Valdemiro Amaro da
dc.subject.por.fl_str_mv Calotropis procera
Látex
Enzimas proteolíticas
Ação anti-inflamatória
Salmonella typhimurium
topic Calotropis procera
Látex
Enzimas proteolíticas
Ação anti-inflamatória
Salmonella typhimurium
CIENCIAS AGRARIAS::MEDICINA VETERINARIA
dc.subject.cnpq.fl_str_mv CIENCIAS AGRARIAS::MEDICINA VETERINARIA
description Proteases isolated from the latex of the medicinal plant of Calotropis procera have been investigated in different models of inflammation. Considering previous studies that indicated anti-inflammatory properties of a mixture of proteases called LPp2, in this work, a mixture of proteases called LPp3 was investigated in an experimental salmonellosis model. Thus, macrophage cultures were exposed to different concentrations of LPp3 and infected with Salmonella enterica Sor. Typhimurium. In another infection model, Swiss mice were infected intraperitoneally with S. Typhimurium and then treated (intravenously) with LPp3. The results showed that LPp3 has no direct antibacterial action against Salmonella in vitro and was unable to increase the cell viability of infected macrophages. In the in vivo assays, after 6 h of infection, animals treated with LPp3 (10 mg/kg) had a higher bacterial load in the spleen and liver compared to untreated control (PBS) or Dexamethasone-administered groups. Treatments with LPp3 (1, 5 and 10 mg/kg) inhibited the recruitment of leukocytes to the infectious site after Salmonella inoculum in the peritoneal cavity. However, gene expression levels of inflammatory cytokines measured in the spleen, such as TNF-alpha and IL1-beta, were significantly increased in animals treated with 10 mg/kg relative to infected/untreated animals. It was concludedthat LPp3, as already demonstrated for LPp2, is rich in enzymes with strong anti-inflammatory action, which could explain the lower elimination of bacteria at higher doses.
publishDate 2022
dc.date.issued.fl_str_mv 2022-11-16
dc.date.accessioned.fl_str_mv 2024-07-09T19:26:06Z
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dc.identifier.citation.fl_str_mv SOUZA, Juliana Kelly Urtigas de. Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp. 2022. 54 f. Dissertação (Programa de Pós-Graduação em Biociência Animal) - Universidade Federal Rural de Pernambuco, Recife.
dc.identifier.uri.fl_str_mv http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/9651
identifier_str_mv SOUZA, Juliana Kelly Urtigas de. Potencial de peptidases extraídas do látex da Calotropis procera como agente imunoterápico contra Salmonella ssp. 2022. 54 f. Dissertação (Programa de Pós-Graduação em Biociência Animal) - Universidade Federal Rural de Pernambuco, Recife.
url http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/9651
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dc.publisher.department.fl_str_mv Departamento de Morfologia e Fisiologia Animal
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