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Environmental enrichment (EE) is an experimental paradigm used to explore the effects of a complex and challenging environment that does not stress the animals1. EE is an animal housing technique composed of increased space, physical activity, and social interactions, which in turn increases sensory, cognitive, motor, and social stimulation2. Igloos, running wheels, saucer wheels, tube mazes, and other objects in the housing environment foster this sensory cognitive, social, and motor stimulation by promoting exploration and interaction. The layout of the objects in the enclosure changes regularly to present a novel environment, to which the mice are forced to adapt. This strategy offers mild and brief challenges that induce a beneficial, benign, and healthy adaptive response, known as eustress, as opposed to a more aversive, hostile environment or maladaptive distress3,4. By promoting eustress and limiting harmful distress, mice show a variety of favorable phenotypes.
EE is a reliable experimental model with a wide range of applications, while being devoid of elements traditionally thought of as stressful1. The effects of EE on rodents have been studied for more than half a century. In the early 1960s studies showed that cortical cholinesterase levels decreased and subcortical cholinesterase levels increased in rats that were housed in environments with increased living space, increased number of rats, and a variety of wooden toys, mazes, and platforms5,6. In addition, EE is associated with many adaptive changes in the brain, behavior, and metabolism in mice of different ages and genetic backgrounds. Therefore, EE is a useful paradigm for a broad scope of experiments studying the effects of the environment on mice. EE effects can be observed in mice as quickly as one-week exposure, and can be seen in animals as old as eighteen months7. EE is often used in neuroscience and neurobehavioral experiments to study recovery of function, learning and memory2. Moreover, EE has considerable impact on the phenotype of a variety of toxin induced and transgenic animal models of human neurological diseases including Huntington’s disease, Alzheimer’s disease, Parkinson’s disease, Epilepsy, Stroke, and more2.
However, over the years there has been inconsistency with the enrichment design making comparisons between studies from different laboratories difficult. For example, each of the studies on the EE effects relative to human neurological diseases referred to above had varying parameters to the enrichment. The study on Huntington’s disease housed 4-6 mice in large cages (44 x 28 x 12.5 cm3) containing cardboard boxes, tunnels, and sheets, as well as wooden and plastic objects that were changed every two days8,9. One of the studies done on Alzheimer’s housed 20 mice in a larger cage (1 m3) containing 2 running wheels, plastic tubes, cardboard boxes and nesting material that were changed or rearranged weekly10. Many setups of EE have similar themes such as objects to run on or hide in, yet the number of mice per EE housing, the living area, and the period of changing the environment vary much.
The inconsistent designs of EE have led to failed replication of EE effects. Our data on cancer and metabolism together suggest that the combination of stimulations provided in the following detailed EE housing protocol lead to significant anti-cancer and anti-obesity effects14,15. However, the difference of EE settings adopted by different labs might influence the outcomes of EE, as is seen in one failed attempt to reproduce EE effects on the growth of specific cancer tumors implanted in mice11. The different results could be due to a variety of reasons ranging from different growth rates of the tumor cell cultures to the type of detergent used for cleaning housing equipment11. In order to replicate the results seen in our experiments, a particular design of enrichment and animal husbandry is required. The following procedure details the EE housing that will allow other researchers to successfully replicate our efficacious enrichment model.