Individualized Housing Modifies the Immune-Endocrine System in CD1 Adult Male Mice.
Iván Ortega-SaezAlina Díez-SolinskaRoger GrífolsCristina MartíCarolina ZamoraMaider Muñoz-CullaOscar VegasGarikoitz AzkonaPublished in: Animals : an open access journal from MDPI (2023)
In the last years, different research groups have made considerable efforts to improve the care and use of animals in research. Mice ( Mus musculus ) are the most widely used animal species in research in the European Union and are sociable and hierarchical creatures. During experiments, researchers tend to individualize males, but no consideration is given to whether this social isolation causes them stress. The aim of this study was, therefore, to explore whether 4 weeks of social isolation could induce changes in different physiological parameters in adult Crl:CD1(ICR) (CD1) males, which may interfere with experimental results. Body weight, blood cells, and fecal corticosterone metabolites levels were the analyzed parameters. Blood and fecal samples were collected at weeks 1 and 4 of the experimental procedure. Four weeks of single housing produced a significant time-dependent decrease in monocytes and granulocytes. Fecal corticosterone metabolite levels were higher in single-housed mice after 1 week and then normalized after 4 weeks of isolation. Body weight, red blood cells, and platelets remained unchanged in both groups during this period. We can, therefore, conclude that social isolation affects some immune and endocrine parameters, and that this should be taken into account in the interpretation of research data.
Keyphrases
- body weight
- healthcare
- red blood cell
- gestational age
- mental health
- high fat diet induced
- induced apoptosis
- palliative care
- quality improvement
- mental illness
- pain management
- dendritic cells
- cell cycle arrest
- electronic health record
- randomized controlled trial
- insulin resistance
- big data
- peripheral blood
- metabolic syndrome
- young adults
- ms ms
- minimally invasive
- cell proliferation
- clinical trial
- genetic diversity