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Biometric Data Comparison Between Lewis and Sprague Dawley Rats

Introduction: Pressure mapping systems are often used for indirect assessment of kinematic gait parameter differences after repair of critical peripheral nerve defects in small animal models. However, there does not appear to be any literature that studies the differences in normal gait pattern of S...

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Autores principales: Steiner, Richard, Dhar, Madhu, Stephenson, Stacy M., Newby, Steven, Bow, Austin, Pedersen, Alisha, Anderson, David E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932974/
https://www.ncbi.nlm.nih.gov/pubmed/31921924
http://dx.doi.org/10.3389/fvets.2019.00469
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author Steiner, Richard
Dhar, Madhu
Stephenson, Stacy M.
Newby, Steven
Bow, Austin
Pedersen, Alisha
Anderson, David E.
author_facet Steiner, Richard
Dhar, Madhu
Stephenson, Stacy M.
Newby, Steven
Bow, Austin
Pedersen, Alisha
Anderson, David E.
author_sort Steiner, Richard
collection PubMed
description Introduction: Pressure mapping systems are often used for indirect assessment of kinematic gait parameter differences after repair of critical peripheral nerve defects in small animal models. However, there does not appear to be any literature that studies the differences in normal gait pattern of Sprague Dawley rats compared to Lewis rats using a Tekscan VH4 pressure mat system. The purpose of this study is to assess the gait profile of Lewis and Sprague Dawley rats generated by Tekscan's VH4 system to detect similarities and/or differences in gait parameters involving both force and temporal variables. Materials and Methods: The gait profile of 14 Lewis and 14 Sprague Dawley rats was recorded using a Tekscan VH4 pressure map system with two successful walks per animal and gait parameter data was normalized for mean variance between the two rodent strains. Results: The results showed that temporal and normalized force parameters were not significantly different between the two types of rats. Maximum force, contact area, stride length, and adjusted pressure variables were significantly different between the two strains, likely attributed to the body size and weight differential between the strains. Variation in some of these parameters were considered due to differences in overall body size between the two strains, variations in gait kinematics between individual rodent subjects, and the limitations of the current experimental design. Conclusion: For future in vivo models, either Sprague Dawley or Lewis rat strains would be acceptable animal models when comparing base-line gait profiles using the Tekscan VH4 pressure map system when assessing critical defect repairs of peripheral nerves.
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spelling pubmed-69329742020-01-09 Biometric Data Comparison Between Lewis and Sprague Dawley Rats Steiner, Richard Dhar, Madhu Stephenson, Stacy M. Newby, Steven Bow, Austin Pedersen, Alisha Anderson, David E. Front Vet Sci Veterinary Science Introduction: Pressure mapping systems are often used for indirect assessment of kinematic gait parameter differences after repair of critical peripheral nerve defects in small animal models. However, there does not appear to be any literature that studies the differences in normal gait pattern of Sprague Dawley rats compared to Lewis rats using a Tekscan VH4 pressure mat system. The purpose of this study is to assess the gait profile of Lewis and Sprague Dawley rats generated by Tekscan's VH4 system to detect similarities and/or differences in gait parameters involving both force and temporal variables. Materials and Methods: The gait profile of 14 Lewis and 14 Sprague Dawley rats was recorded using a Tekscan VH4 pressure map system with two successful walks per animal and gait parameter data was normalized for mean variance between the two rodent strains. Results: The results showed that temporal and normalized force parameters were not significantly different between the two types of rats. Maximum force, contact area, stride length, and adjusted pressure variables were significantly different between the two strains, likely attributed to the body size and weight differential between the strains. Variation in some of these parameters were considered due to differences in overall body size between the two strains, variations in gait kinematics between individual rodent subjects, and the limitations of the current experimental design. Conclusion: For future in vivo models, either Sprague Dawley or Lewis rat strains would be acceptable animal models when comparing base-line gait profiles using the Tekscan VH4 pressure map system when assessing critical defect repairs of peripheral nerves. Frontiers Media S.A. 2019-12-20 /pmc/articles/PMC6932974/ /pubmed/31921924 http://dx.doi.org/10.3389/fvets.2019.00469 Text en Copyright © 2019 Steiner, Dhar, Stephenson, Newby, Bow, Pedersen and Anderson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Steiner, Richard
Dhar, Madhu
Stephenson, Stacy M.
Newby, Steven
Bow, Austin
Pedersen, Alisha
Anderson, David E.
Biometric Data Comparison Between Lewis and Sprague Dawley Rats
title Biometric Data Comparison Between Lewis and Sprague Dawley Rats
title_full Biometric Data Comparison Between Lewis and Sprague Dawley Rats
title_fullStr Biometric Data Comparison Between Lewis and Sprague Dawley Rats
title_full_unstemmed Biometric Data Comparison Between Lewis and Sprague Dawley Rats
title_short Biometric Data Comparison Between Lewis and Sprague Dawley Rats
title_sort biometric data comparison between lewis and sprague dawley rats
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932974/
https://www.ncbi.nlm.nih.gov/pubmed/31921924
http://dx.doi.org/10.3389/fvets.2019.00469
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