Abstract
Cognitive impairments can be a significant problem after a traumatic brain injury (TBI), which affects millions worldwide each year. There is a need for establish reproducible cognitive assays in rodents to better understand disease mechanisms and to develop therapeutic interventions towards treating TBI-induced impairments. Our goal was to validate and standardize the radial arm water maze (RAWM) test as an assay to screen for cognitive impairments caused by TBI. RAWM is a visuo-spatial learning test, originally designed for use with rats, and later adapted for mice. The present study investigates whether test procedures, such us the presence of extra-maze cues influences learning and memory performance. C57BL/6 mice were tested in an 8-arm RAWM using a four-day protocol. We demonstrated that two days of training, exposing the mice to extra-maze cues and a visible platform, influenced learning and memory performance. Mice that did not receive training performed poorer compared to mice trained. To further validate our RAWM protocol, we used scopolamine. We, also, demonstrated that a single mild closed head injury (CHI) caused deficits in this task at two weeks post-CHI. Our data supported the use of 7 trials per day and a spaced training protocol as key factor to unmask memory impairment following CHI. Here, we provide a detailed standard operating procedure for RAWM test, which can be applied to a variety of mouse models including neurodegenerative diseases and pathology, as well as when pharmacological approaches are used.
Highlights
Traumatic brain injury (TBI) is a major public health problem worldwide and leads to temporary or permanent physical and cognitive impairments
We evaluated if the use of extra-maze cues and a visible escape platform is essential for the mice to learn the task and has a positive influence on radial arm water maze (RAWM) output, or if the mice were using other extra maze cues or non-visuo-spatial search strategies
Our results indicate that using a weaker training protocol, like reducing the number of trials, is more sensitive to identify differences in cognition related to a single mild closed head injury (CHI) at 2-week postinjury
Summary
Traumatic brain injury (TBI) is a major public health problem worldwide and leads to temporary or permanent physical and cognitive impairments. People with a history of TBI have an increase risk to develop dementia and neurodegenerative disease [1, 2]. Radial-arm water maze in a mouse model of TBI
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