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Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain

The aim of this study was to develop and refine a heterologous mouse model of endometriosis-associated pain in which non-evoked responses, more relevant to the patient experience, were evaluated. Immunodeficient female mice (N = 24) were each implanted with four endometriotic human lesions (N = 12)...

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Autores principales: Tejada, Miguel A., Santos-Llamas, Ana I., Escriva, Lesley, Tarin, Juan J., Cano, Antonio, Fernández-Ramírez, Maria J., Nunez-Badinez, Paulina, De Leo, Bianca, Saunders, Philippa T. K., Vidal, Victor, Barthas, Florent, Vincent, Katy, Sweeney, Patrick J., Sillito, Rowland R., Armstrong, James Douglas, Nagel, Jens, Gomez, Raúl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962432/
https://www.ncbi.nlm.nih.gov/pubmed/35203710
http://dx.doi.org/10.3390/biomedicines10020501
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author Tejada, Miguel A.
Santos-Llamas, Ana I.
Escriva, Lesley
Tarin, Juan J.
Cano, Antonio
Fernández-Ramírez, Maria J.
Nunez-Badinez, Paulina
De Leo, Bianca
Saunders, Philippa T. K.
Vidal, Victor
Barthas, Florent
Vincent, Katy
Sweeney, Patrick J.
Sillito, Rowland R.
Armstrong, James Douglas
Nagel, Jens
Gomez, Raúl
author_facet Tejada, Miguel A.
Santos-Llamas, Ana I.
Escriva, Lesley
Tarin, Juan J.
Cano, Antonio
Fernández-Ramírez, Maria J.
Nunez-Badinez, Paulina
De Leo, Bianca
Saunders, Philippa T. K.
Vidal, Victor
Barthas, Florent
Vincent, Katy
Sweeney, Patrick J.
Sillito, Rowland R.
Armstrong, James Douglas
Nagel, Jens
Gomez, Raúl
author_sort Tejada, Miguel A.
collection PubMed
description The aim of this study was to develop and refine a heterologous mouse model of endometriosis-associated pain in which non-evoked responses, more relevant to the patient experience, were evaluated. Immunodeficient female mice (N = 24) were each implanted with four endometriotic human lesions (N = 12) or control tissue fat (N = 12) on the abdominal wall using tissue glue. Evoked pain responses were measured biweekly using von Frey filaments. Non-evoked responses were recorded weekly for 8 weeks using a home cage analysis (HCA). Endpoints were distance traveled, social proximity, time spent in the center vs. outer areas of the cage, drinking, and climbing. Significant differences between groups for von Frey response, climbing, and drinking were detected on days 14, 21, and 35 post implanting surgery, respectively, and sustained for the duration of the experiment. In conclusion, a heterologous mouse model of endometriosis-associated evoked a non-evoked pain was developed to improve the relevance of preclinical models to patient experience as a platform for drug testing.
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spelling pubmed-89624322022-03-30 Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain Tejada, Miguel A. Santos-Llamas, Ana I. Escriva, Lesley Tarin, Juan J. Cano, Antonio Fernández-Ramírez, Maria J. Nunez-Badinez, Paulina De Leo, Bianca Saunders, Philippa T. K. Vidal, Victor Barthas, Florent Vincent, Katy Sweeney, Patrick J. Sillito, Rowland R. Armstrong, James Douglas Nagel, Jens Gomez, Raúl Biomedicines Article The aim of this study was to develop and refine a heterologous mouse model of endometriosis-associated pain in which non-evoked responses, more relevant to the patient experience, were evaluated. Immunodeficient female mice (N = 24) were each implanted with four endometriotic human lesions (N = 12) or control tissue fat (N = 12) on the abdominal wall using tissue glue. Evoked pain responses were measured biweekly using von Frey filaments. Non-evoked responses were recorded weekly for 8 weeks using a home cage analysis (HCA). Endpoints were distance traveled, social proximity, time spent in the center vs. outer areas of the cage, drinking, and climbing. Significant differences between groups for von Frey response, climbing, and drinking were detected on days 14, 21, and 35 post implanting surgery, respectively, and sustained for the duration of the experiment. In conclusion, a heterologous mouse model of endometriosis-associated evoked a non-evoked pain was developed to improve the relevance of preclinical models to patient experience as a platform for drug testing. MDPI 2022-02-21 /pmc/articles/PMC8962432/ /pubmed/35203710 http://dx.doi.org/10.3390/biomedicines10020501 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tejada, Miguel A.
Santos-Llamas, Ana I.
Escriva, Lesley
Tarin, Juan J.
Cano, Antonio
Fernández-Ramírez, Maria J.
Nunez-Badinez, Paulina
De Leo, Bianca
Saunders, Philippa T. K.
Vidal, Victor
Barthas, Florent
Vincent, Katy
Sweeney, Patrick J.
Sillito, Rowland R.
Armstrong, James Douglas
Nagel, Jens
Gomez, Raúl
Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain
title Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain
title_full Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain
title_fullStr Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain
title_full_unstemmed Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain
title_short Identification of Altered Evoked and Non-Evoked Responses in a Heterologous Mouse Model of Endometriosis-Associated Pain
title_sort identification of altered evoked and non-evoked responses in a heterologous mouse model of endometriosis-associated pain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962432/
https://www.ncbi.nlm.nih.gov/pubmed/35203710
http://dx.doi.org/10.3390/biomedicines10020501
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