Volume 12 Supplement 1
P01.43. The calm mouse: an animal model of stress reduction
© Gurfein et al; licensee BioMed Central Ltd. 2012
Published: 12 June 2012
Chronic stress is associated with negative health outcomes and is linked with neuroendocrine changes, suppressed immunity, and central nervous system neuropathology. While human studies have illustrated the benefits of stress reduction, mechanistic understanding of how decreasing stress affects health and disease progression remains unclear. Furthermore, prior animal studies have focused primarily on increasing stress, and few animal models of stress reduction have been fully developed.
We have developed a “calm mouse model” with caging enhancements designed to reduce murine stress. Male BALB/c mice were divided into four groups (n=10/group): Control (Cntl), standard caging; Calm, large caging to reduce animal density, a cardboard nest box for shelter, paper nesting material to promote innate nesting behavior, and a polycarbonate tube to mimic tunneling; Control Exercise (Cntl Ex), standard caging with a running wheel, known to reduce stress; and Calm Exercise (Calm Ex), Calm caging with a running wheel.
Calm, Cntl Ex, and Calm Ex animals exhibited significantly less corticosterone production than Cntl (Day 49: Calm, M> 20.5 ng corticosterone metabolites/0.05g feces (CM), CI95 11.7 to 29.4, p< 0.0001; Cntl Ex, M> 22.5ng CM, CI95 13.4 to 31.5, p<0.0001; Calm Ex, M> 21.8 CM, CI95 11.7 to 32.0, p=0.0003). Calm animals gained greater body mass than Cntl, although they had similar weekly energy intake. We also observed changes in body composition, behavior, spleen mass, and immune function. Lastly, our in vitro studies showed that Calm Ex animals had innate and adaptive immune responses that were more sensitive to acute stress.
Our data indicate that both Calm and exercise caging generated reductions in physiologic stress measures in mice. Collectively, the Calm model represents a promising approach to studying the biological effects of stress reduction in the context of health and in conjunction with existing disease models.
This article is published under license to BioMed Central Ltd. 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.