How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces?
- Autores
- Scioscia, Nathalia Paula; Pensel, Patricia Eugenia; Albani, Clara Maria; Fabbri, Julia; Denegri, Guillermo Maria; Elissondo, María Celina
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Portal vein injection is a technique used for the development of different murine models of pathologies and parasitic diseases in the liver. These procedures require laparotomy and must be performed under anesthesia and analgesia to prevent discomfort, pain and /or distress. In order to optimize the survival rate of animals, the purpose of this study was to evaluate an injectable anesthesia protocol for the development of a murine model of hepatic cystic echinococcosis in female CF-1 mice. Animal procedures and management protocols were approved by the Institutional Animal Care and Use Committee of the Faculty of Exact and Natural Sciences, National University of Mar del Plata (RDs 468/17 and 211/2018). Forty three mice (Mus musculus; 6-7 weeks of age, body weight 26 ± 2 g) were allocated into six groups: 1) ketamine/xylazine 100/10 mg/kg; 2) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg; 3) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg + yohimbine; 4) ketamine/xylazine 80/8 mg/kg; 5) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg; and 6) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine. Atropine sulfate (0.4 mg/kg, subcutaneously) and tramadol hydrochloride [2 mg/kg, via intraperitoneal (IP)] were administered as pre-anesthetic drugs. The anesthetic cocktail (ketamine/xylazine) was applied IP and after confirming the loss of reflexes of mice, portal vein infection with Echinococcus granulosus protoscoleces was carried out. Yohimbine (a reverser of xylazine, 0.5 mg/kg) was injected IP immediately at the end of the suture. All groups achieve a deep surgical anesthetic plane and profound analgesia, except mice treated only with ketamine/xylazine at the doses of 80/8 mg/kg. Pre-anesthetic drugs application significantly reduced time induction of animals compared with those that received only the anesthetic cocktail (P < 0.05). The mice that underwent laparotomy and received yohimbine after surgery had a survival rate of 100 %. Moreover, treatment with yohimbine significantly reduced the recovery time of mice treated with pre-anesthetic drugs and ketamine/xylazine 80/8 mg/kg. In addition, we found differences between the response to the doses of ketamine/xylazine in animals treated with pre-anesthetic drugs and yohimbine. The recovery time of mice treated with ketamine/xylazine 80/8 mg/kg was significantly faster than that observed under doses of 100/10 mg/kg, respectively (P < 0.01). Therefore, the duration of action was significantly shorter when the applied doses of ketamine/xylazine were 80 and 8 mg/kg. We recommend the protocol that applied pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine as safe and reliable for the portal vein infection of mice with protoscoleces of E. granulosus.
Fil: Scioscia, Nathalia Paula. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina
Fil: Pensel, Patricia Eugenia. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina
Fil: Albani, Clara Maria. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina
Fil: Fabbri, Julia. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina
Fil: Denegri, Guillermo Maria. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina
Fil: Elissondo, María Celina. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina
II Reunión Científica Internacional, VII Reunión Científica Regional y VI Congreso Nacional de Ciencia y Tecnología de Animales de Laboratorio
Argentina
Asociación Argentina de Ciencia y Tecnología de Animales de Laboratorio - Materia
-
Echinococcus granulosus
Portal vein - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/156208
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How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces?Scioscia, Nathalia PaulaPensel, Patricia EugeniaAlbani, Clara MariaFabbri, JuliaDenegri, Guillermo MariaElissondo, María CelinaEchinococcus granulosusPortal veinhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Portal vein injection is a technique used for the development of different murine models of pathologies and parasitic diseases in the liver. These procedures require laparotomy and must be performed under anesthesia and analgesia to prevent discomfort, pain and /or distress. In order to optimize the survival rate of animals, the purpose of this study was to evaluate an injectable anesthesia protocol for the development of a murine model of hepatic cystic echinococcosis in female CF-1 mice. Animal procedures and management protocols were approved by the Institutional Animal Care and Use Committee of the Faculty of Exact and Natural Sciences, National University of Mar del Plata (RDs 468/17 and 211/2018). Forty three mice (Mus musculus; 6-7 weeks of age, body weight 26 ± 2 g) were allocated into six groups: 1) ketamine/xylazine 100/10 mg/kg; 2) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg; 3) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg + yohimbine; 4) ketamine/xylazine 80/8 mg/kg; 5) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg; and 6) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine. Atropine sulfate (0.4 mg/kg, subcutaneously) and tramadol hydrochloride [2 mg/kg, via intraperitoneal (IP)] were administered as pre-anesthetic drugs. The anesthetic cocktail (ketamine/xylazine) was applied IP and after confirming the loss of reflexes of mice, portal vein infection with Echinococcus granulosus protoscoleces was carried out. Yohimbine (a reverser of xylazine, 0.5 mg/kg) was injected IP immediately at the end of the suture. All groups achieve a deep surgical anesthetic plane and profound analgesia, except mice treated only with ketamine/xylazine at the doses of 80/8 mg/kg. Pre-anesthetic drugs application significantly reduced time induction of animals compared with those that received only the anesthetic cocktail (P < 0.05). The mice that underwent laparotomy and received yohimbine after surgery had a survival rate of 100 %. Moreover, treatment with yohimbine significantly reduced the recovery time of mice treated with pre-anesthetic drugs and ketamine/xylazine 80/8 mg/kg. In addition, we found differences between the response to the doses of ketamine/xylazine in animals treated with pre-anesthetic drugs and yohimbine. The recovery time of mice treated with ketamine/xylazine 80/8 mg/kg was significantly faster than that observed under doses of 100/10 mg/kg, respectively (P < 0.01). Therefore, the duration of action was significantly shorter when the applied doses of ketamine/xylazine were 80 and 8 mg/kg. We recommend the protocol that applied pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine as safe and reliable for the portal vein infection of mice with protoscoleces of E. granulosus.Fil: Scioscia, Nathalia Paula. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; ArgentinaFil: Pensel, Patricia Eugenia. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; ArgentinaFil: Albani, Clara Maria. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; ArgentinaFil: Fabbri, Julia. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; ArgentinaFil: Denegri, Guillermo Maria. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; ArgentinaFil: Elissondo, María Celina. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; ArgentinaII Reunión Científica Internacional, VII Reunión Científica Regional y VI Congreso Nacional de Ciencia y Tecnología de Animales de LaboratorioArgentinaAsociación Argentina de Ciencia y Tecnología de Animales de LaboratorioAsociación Argentina de Ciencia y Tecnología de Animales de Laboratorio2021info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/156208How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces?; II Reunión Científica Internacional, VII Reunión Científica Regional y VI Congreso Nacional de Ciencia y Tecnología de Animales de Laboratorio; Argentina; 2021; 66-67978-987-47524-0-6CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://aacytal.com.ar/wp-content/uploads/CongresoAACyTAL2021_Actas-del-Congreso.pdfInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T15:11:28Zoai:ri.conicet.gov.ar:11336/156208instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 15:11:29.05CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? |
title |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? |
spellingShingle |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? Scioscia, Nathalia Paula Echinococcus granulosus Portal vein |
title_short |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? |
title_full |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? |
title_fullStr |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? |
title_full_unstemmed |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? |
title_sort |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces? |
dc.creator.none.fl_str_mv |
Scioscia, Nathalia Paula Pensel, Patricia Eugenia Albani, Clara Maria Fabbri, Julia Denegri, Guillermo Maria Elissondo, María Celina |
author |
Scioscia, Nathalia Paula |
author_facet |
Scioscia, Nathalia Paula Pensel, Patricia Eugenia Albani, Clara Maria Fabbri, Julia Denegri, Guillermo Maria Elissondo, María Celina |
author_role |
author |
author2 |
Pensel, Patricia Eugenia Albani, Clara Maria Fabbri, Julia Denegri, Guillermo Maria Elissondo, María Celina |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Echinococcus granulosus Portal vein |
topic |
Echinococcus granulosus Portal vein |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Portal vein injection is a technique used for the development of different murine models of pathologies and parasitic diseases in the liver. These procedures require laparotomy and must be performed under anesthesia and analgesia to prevent discomfort, pain and /or distress. In order to optimize the survival rate of animals, the purpose of this study was to evaluate an injectable anesthesia protocol for the development of a murine model of hepatic cystic echinococcosis in female CF-1 mice. Animal procedures and management protocols were approved by the Institutional Animal Care and Use Committee of the Faculty of Exact and Natural Sciences, National University of Mar del Plata (RDs 468/17 and 211/2018). Forty three mice (Mus musculus; 6-7 weeks of age, body weight 26 ± 2 g) were allocated into six groups: 1) ketamine/xylazine 100/10 mg/kg; 2) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg; 3) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg + yohimbine; 4) ketamine/xylazine 80/8 mg/kg; 5) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg; and 6) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine. Atropine sulfate (0.4 mg/kg, subcutaneously) and tramadol hydrochloride [2 mg/kg, via intraperitoneal (IP)] were administered as pre-anesthetic drugs. The anesthetic cocktail (ketamine/xylazine) was applied IP and after confirming the loss of reflexes of mice, portal vein infection with Echinococcus granulosus protoscoleces was carried out. Yohimbine (a reverser of xylazine, 0.5 mg/kg) was injected IP immediately at the end of the suture. All groups achieve a deep surgical anesthetic plane and profound analgesia, except mice treated only with ketamine/xylazine at the doses of 80/8 mg/kg. Pre-anesthetic drugs application significantly reduced time induction of animals compared with those that received only the anesthetic cocktail (P < 0.05). The mice that underwent laparotomy and received yohimbine after surgery had a survival rate of 100 %. Moreover, treatment with yohimbine significantly reduced the recovery time of mice treated with pre-anesthetic drugs and ketamine/xylazine 80/8 mg/kg. In addition, we found differences between the response to the doses of ketamine/xylazine in animals treated with pre-anesthetic drugs and yohimbine. The recovery time of mice treated with ketamine/xylazine 80/8 mg/kg was significantly faster than that observed under doses of 100/10 mg/kg, respectively (P < 0.01). Therefore, the duration of action was significantly shorter when the applied doses of ketamine/xylazine were 80 and 8 mg/kg. We recommend the protocol that applied pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine as safe and reliable for the portal vein infection of mice with protoscoleces of E. granulosus. Fil: Scioscia, Nathalia Paula. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina Fil: Pensel, Patricia Eugenia. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina Fil: Albani, Clara Maria. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina Fil: Fabbri, Julia. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina Fil: Denegri, Guillermo Maria. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina Fil: Elissondo, María Celina. Universidad Nacional de Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Mar del Plata. Instituto de Investigaciones En Produccion, Sanidad y Ambiente.; Argentina II Reunión Científica Internacional, VII Reunión Científica Regional y VI Congreso Nacional de Ciencia y Tecnología de Animales de Laboratorio Argentina Asociación Argentina de Ciencia y Tecnología de Animales de Laboratorio |
description |
Portal vein injection is a technique used for the development of different murine models of pathologies and parasitic diseases in the liver. These procedures require laparotomy and must be performed under anesthesia and analgesia to prevent discomfort, pain and /or distress. In order to optimize the survival rate of animals, the purpose of this study was to evaluate an injectable anesthesia protocol for the development of a murine model of hepatic cystic echinococcosis in female CF-1 mice. Animal procedures and management protocols were approved by the Institutional Animal Care and Use Committee of the Faculty of Exact and Natural Sciences, National University of Mar del Plata (RDs 468/17 and 211/2018). Forty three mice (Mus musculus; 6-7 weeks of age, body weight 26 ± 2 g) were allocated into six groups: 1) ketamine/xylazine 100/10 mg/kg; 2) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg; 3) pre-anesthetic drugs + ketamine/xylazine 100/10 mg/kg + yohimbine; 4) ketamine/xylazine 80/8 mg/kg; 5) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg; and 6) pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine. Atropine sulfate (0.4 mg/kg, subcutaneously) and tramadol hydrochloride [2 mg/kg, via intraperitoneal (IP)] were administered as pre-anesthetic drugs. The anesthetic cocktail (ketamine/xylazine) was applied IP and after confirming the loss of reflexes of mice, portal vein infection with Echinococcus granulosus protoscoleces was carried out. Yohimbine (a reverser of xylazine, 0.5 mg/kg) was injected IP immediately at the end of the suture. All groups achieve a deep surgical anesthetic plane and profound analgesia, except mice treated only with ketamine/xylazine at the doses of 80/8 mg/kg. Pre-anesthetic drugs application significantly reduced time induction of animals compared with those that received only the anesthetic cocktail (P < 0.05). The mice that underwent laparotomy and received yohimbine after surgery had a survival rate of 100 %. Moreover, treatment with yohimbine significantly reduced the recovery time of mice treated with pre-anesthetic drugs and ketamine/xylazine 80/8 mg/kg. In addition, we found differences between the response to the doses of ketamine/xylazine in animals treated with pre-anesthetic drugs and yohimbine. The recovery time of mice treated with ketamine/xylazine 80/8 mg/kg was significantly faster than that observed under doses of 100/10 mg/kg, respectively (P < 0.01). Therefore, the duration of action was significantly shorter when the applied doses of ketamine/xylazine were 80 and 8 mg/kg. We recommend the protocol that applied pre-anesthetic drugs + ketamine/xylazine 80/8 mg/kg + yohimbine as safe and reliable for the portal vein infection of mice with protoscoleces of E. granulosus. |
publishDate |
2021 |
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2021 |
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http://hdl.handle.net/11336/156208 How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces?; II Reunión Científica Internacional, VII Reunión Científica Regional y VI Congreso Nacional de Ciencia y Tecnología de Animales de Laboratorio; Argentina; 2021; 66-67 978-987-47524-0-6 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/156208 |
identifier_str_mv |
How to improve the survival of female cf-1 mice during the infection via the portal vein with Echinococcus granulosus protoscoleces?; II Reunión Científica Internacional, VII Reunión Científica Regional y VI Congreso Nacional de Ciencia y Tecnología de Animales de Laboratorio; Argentina; 2021; 66-67 978-987-47524-0-6 CONICET Digital CONICET |
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eng |
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Asociación Argentina de Ciencia y Tecnología de Animales de Laboratorio |
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Asociación Argentina de Ciencia y Tecnología de Animales de Laboratorio |
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