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Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect

BACKGROUND: Rabbits are widely used in biomedical research and especially as animal models in atherosclerosis studies. Blood biochemistry is used to monitor progression of disease, before final evaluation including pathology of arteries and organs. The aim of the present study was to assess the cons...

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Autores principales: Dontas, Ismene A, Marinou, Katerina A, Iliopoulos, Dimitrios, Tsantila, Nektaria, Agrogiannis, George, Papalois, Apostolos, Karatzas, Theodore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163193/
https://www.ncbi.nlm.nih.gov/pubmed/21838924
http://dx.doi.org/10.1186/1476-511X-10-139
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author Dontas, Ismene A
Marinou, Katerina A
Iliopoulos, Dimitrios
Tsantila, Nektaria
Agrogiannis, George
Papalois, Apostolos
Karatzas, Theodore
author_facet Dontas, Ismene A
Marinou, Katerina A
Iliopoulos, Dimitrios
Tsantila, Nektaria
Agrogiannis, George
Papalois, Apostolos
Karatzas, Theodore
author_sort Dontas, Ismene A
collection PubMed
description BACKGROUND: Rabbits are widely used in biomedical research and especially as animal models in atherosclerosis studies. Blood biochemistry is used to monitor progression of disease, before final evaluation including pathology of arteries and organs. The aim of the present study was to assess the consistency of the biochemical profile of New Zealand White rabbits on standard diet from 3 to 6 months of age, during which they are often used experimentally. METHODS AND RESULTS: Eight conventional male 3-month-old New Zealand White rabbits were used. Blood samples were taken at baseline, 1, 2 and 3 months later. Plasma glucose, total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triacylglycerol concentrations, and alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma glutamyl transferase activities and malondialdehyde were measured. Statistically significant time-related changes were observed in glucose, total cholesterol and triacylglycerol, which were not correlated with aortic lesions at 6 months of age. Similarly, hepatic enzyme activity had significant time-related changes, without a corresponding liver pathology. CONCLUSIONS: Age progression and stress due to single housing may be the underlying reasons for these biochemistry changes. These early changes, indicative of metabolic alterations, should be taken into account even in short-term lipid/atherosclerosis studies, where age and standard diet are not expected to have an effect on the control group of a study.
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spelling pubmed-31631932011-08-29 Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect Dontas, Ismene A Marinou, Katerina A Iliopoulos, Dimitrios Tsantila, Nektaria Agrogiannis, George Papalois, Apostolos Karatzas, Theodore Lipids Health Dis Research BACKGROUND: Rabbits are widely used in biomedical research and especially as animal models in atherosclerosis studies. Blood biochemistry is used to monitor progression of disease, before final evaluation including pathology of arteries and organs. The aim of the present study was to assess the consistency of the biochemical profile of New Zealand White rabbits on standard diet from 3 to 6 months of age, during which they are often used experimentally. METHODS AND RESULTS: Eight conventional male 3-month-old New Zealand White rabbits were used. Blood samples were taken at baseline, 1, 2 and 3 months later. Plasma glucose, total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, triacylglycerol concentrations, and alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma glutamyl transferase activities and malondialdehyde were measured. Statistically significant time-related changes were observed in glucose, total cholesterol and triacylglycerol, which were not correlated with aortic lesions at 6 months of age. Similarly, hepatic enzyme activity had significant time-related changes, without a corresponding liver pathology. CONCLUSIONS: Age progression and stress due to single housing may be the underlying reasons for these biochemistry changes. These early changes, indicative of metabolic alterations, should be taken into account even in short-term lipid/atherosclerosis studies, where age and standard diet are not expected to have an effect on the control group of a study. BioMed Central 2011-08-14 /pmc/articles/PMC3163193/ /pubmed/21838924 http://dx.doi.org/10.1186/1476-511X-10-139 Text en Copyright ©2011 Dontas et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Dontas, Ismene A
Marinou, Katerina A
Iliopoulos, Dimitrios
Tsantila, Nektaria
Agrogiannis, George
Papalois, Apostolos
Karatzas, Theodore
Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect
title Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect
title_full Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect
title_fullStr Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect
title_full_unstemmed Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect
title_short Changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect
title_sort changes of blood biochemistry in the rabbit animal model in atherosclerosis research; a time- or stress-effect
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163193/
https://www.ncbi.nlm.nih.gov/pubmed/21838924
http://dx.doi.org/10.1186/1476-511X-10-139
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