The impact of environmental enrichment in laboratory rats--behavioural and neurochemical aspects |
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Authors: | Simpson Joy Kelly John P |
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Affiliation: | Department of Pharmacology and Therapeutics, National University of Ireland, Galway, Ireland |
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Abstract: | The provision of environmental enrichment (EE) for laboratory rats is recommended in European guidelines governing laboratory animal welfare. It is believed the EE implementation can improve animals’ well-being and EE has been used to demonstrate learning and plasticity of the brain in response to the environment. This review suggests that the definition and duration of EE varies considerably across laboratories. Notwithstanding this, some EE protocols have revealed profound effects on brain neurochemistry and resulting behaviour, suggesting that EE can have the potential to significantly modify these parameters in rats. For this review, a literature search was conducted using PubMed and the search terms “Environmental Enrichment” and “rats”. From the results of this search the most important variables for consideration in the implementation of EE are identified and summarised, and include cage size and housing density; rat age, sex and strain; duration of EE; the EE protocol and enrichment items employed; and the use of appropriate controls. The effects of EE in a number of behavioural tests and its effects on neurotransmitters, neurotrophic factors, stress hormones and neurogenesis and proliferation are outlined. The findings summarised in the present review show the range of EE protocols employed and their effects in tests of activity, learning and affect, as well neurochemical effects which mediate enhanced plasticity in the brain. EE, as is provided in many laboratories, may be of benefit to the animals, however it is important that future work aims to provide a better understanding of EE effects on research outcomes. |
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Keywords: | EE, Environmental enrichment OFT, Open field test EPM, Elevated plus maze FST, Forced swim test MWM, Morris water maze NOR, Novel object recognition RAM, Radial arm maze WM, Working memory CNS, Central nervous system PND, Post-natal day EtOH, Ethanol IC, Isolated condition SC, Standard (group) condition AMP, Amphetamine SD, Sprague Dawley WIS, Wistar SHR, Spontaneously hypertensive LE, Long-Evans NO, Novel object ADHD, Attention deficit/hyperactivity disorder CPP, Conditioned place preference WKY, Wistar Kyoto NH, Neonatal handling RHA, Roman high avoidance RLA, Roman low avoidance LIS, Lister-hooded BPM, Behavioural pattern monitor FH, Fawn-hooded CORT, Corticosterone COC, Cocaine HPA axis, Hypothalamic-pituitary-adrenal axis ACTH, Adrenocorticotrophic hormone BDNF, Brain-derived neurotrophic factor NGF, Nerve growth factor 5HT, Serotonin DA, Dopamine NA, Noradrenalin ACh, Acetylcholine GABA, gamma-aminobutyric acid PFC, Prefrontal cortex DAT, Dopamine Transporter 5HIAA, 5-Hydroxyindoleacetic acid AMPA, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid NMDA, N-methyl- smallcaps" >d-aspartic acid EAAC, Excitatory Amino Acid Carrier LTP, Long term potentiation NT-3, Neurotrophin 3 TBI, Traumatic brain injury SCI, Spinal cord injury APS, Airpuff stressor |
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