Cognitive Evaluation Using Morris Water Maze in Neurotrauma
The Morris water maze (MWM) task is one of the most widely used and versatile tools in behavioral neuroscience for evaluating spatial learning and memory. With regard to detecting cognitive deficits following central nervous system (CNS) injuries, MWM has been commonly utilized in various animal models of neurotrauma, such as fluid percussion injury (FPI), cortical controlled impact (CCI) injury, weight-drop impact injury, and penetrating ballistic-like brain injury (PBBI). More importantly, it serves as a therapeutic index for assessing the efficacy of treatment interventions on cognitive performance following neurotrauma. Thus, it is critical to design an MWM testing paradigm that is sensitive yet discriminating for the purpose of evaluating potential therapeutic interventions. In this chapter, we discuss how multiple test manipulations, including the size of platform, numbers of trials per day, the frequency of retesting intervals, and the texture of platform surface, impact MWM’s ability to detect cognitive deficits using a rat model of PBBI.
This is a preview of subscription content, log in via an institution to check access.
Access this chapter
Subscribe and save
Springer+ Basic
€32.70 /Month
- Get 10 units per month
- Download Article/Chapter or eBook
- 1 Unit = 1 Article or 1 Chapter
- Cancel anytime
Buy Now
Price includes VAT (France)
eBook EUR 93.08 Price includes VAT (France)
Softcover Book EUR 116.04 Price includes VAT (France)
Hardcover Book EUR 158.24 Price includes VAT (France)
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
Severity-Dependent Long-Term Spatial Learning-Memory Impairment in a Mouse Model of Traumatic Brain Injury
Article 18 August 2016
Reduced long-term memory in a rat model of 8 minutes ventricular fibrillation cardiac arrest: a pilot trial
Article Open access 13 June 2016
Head Rotational Acceleration Characteristics Influence Behavioral and Diffusion Tensor Imaging Outcomes Following Concussion
Article 25 October 2014
References
- Morris R (1984) Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods 11:47–60 ArticleCASPubMedGoogle Scholar
- McNamara RK, Skelton RW (1993) The neuropharmacological and neurochemical basis of place learning in the Morris water maze. Brain Res Brain Res Rev 18:33–49 ArticleCASPubMedGoogle Scholar
- D’Hooge R, De Deyn PP (2001) Applications of the Morris water maze in the study of learning and memory. Brain Res Brain Res Rev 36:60–90 ArticlePubMedGoogle Scholar
- Hellawell DJ, Taylor RT, Pentland B (1999) Cognitive and psychosocial outcome following moderate or severe traumatic brain injury. Brain Inj 13:489–504 ArticleCASPubMedGoogle Scholar
- Shear DA, Galani R, Hoffman SW, Stein DG (2002) Progesterone protects against necrotic damage and behavioral abnormalities caused by traumatic brain injury. Exp Neurol 178:59–67 ArticleCASPubMedGoogle Scholar
- Shear DA, Tate MC, Archer DR, Hoffman SW, Hulce VD, Laplaca MC, Stein DG (2004) Neural progenitor cell transplants promote long-term functional recovery after traumatic brain injury. Brain Res 1026:11–22 ArticleCASPubMedGoogle Scholar
- Morris RG, Garrud P, Rawlins JN, O’Keefe J (1982) Place navigation impaired in rats with hippocampal lesions. Nature 297:681–683 ArticleCASPubMedGoogle Scholar
- Smith DH, Okiyama K, Thomas MJ, Claussen B, McIntosh TK (1991) Evaluation of memory dysfunction following experimental brain injury using the Morris water maze. J Neurotrauma 8:259–269 ArticleCASPubMedGoogle Scholar
- Cain DP, Boon F, Corcoran ME (2006) Thalamic and hippocampal mechanisms in spatial navigation: a dissociation between brain mechanisms for learning how versus learning where to navigate. Behav Brain Res 170:241–256 ArticlePubMedGoogle Scholar
- Packard MG (2009) Anxiety, cognition, and habit: a multiple memory systems perspective. Brain Res 1293:121–128 ArticleCASPubMedGoogle Scholar
- Devan BD, McDonald RJ, White NM (1999) Effects of medial and lateral caudate-putamen lesions on place- and cue-guided behaviors in the water maze: relation to thigmotaxis. Behav Brain Res 100:5–14 ArticleCASPubMedGoogle Scholar
- Shear DA, Lu XC, Bombard MC, Pedersen R, Chen Z, Davis A, Tortella FC (2010) Longitudinal characterization of motor and cognitive deficits in a model of penetrating ballistic-like brain injury. J Neurotrauma 27:1911–1923 ArticlePubMedGoogle Scholar
- Hoffman SW, Fulop Z, Stein DG (1994) Bilateral frontal cortical contusion in rats: behavioral and anatomic consequences. J Neurotrauma 11:417–431 ArticleCASPubMedGoogle Scholar
- DiMattia BD, Kesner RP (1988) Spatial cognitive maps: differential role of parietal cortex and hippocampal formation. Behav Neurosci 102:471–480 ArticleCASPubMedGoogle Scholar
- Hamm RJ, Dixon CE, Gbadebo DM, Singha AK, Jenkins LW, Lyeth BG, Hayes RL (1992) Cognitive deficits following traumatic brain injury produced by controlled cortical impact. J Neurotrauma 9:11–20 ArticleCASPubMedGoogle Scholar
- Bramlett HM, Green EJ, Dietrich WD (1997) Hippocampally dependent and independent chronic spatial navigational deficits following parasagittal fluid percussion brain injury in the rat. Brain Res 762:195–202 ArticleCASPubMedGoogle Scholar
- Beaumont A, Marmarou A, Czigner A, Yamamoto M, Demetriadou K, Shirotani T, Marmarou C, Dunbar J (1999) The impact-acceleration model of head injury: injury severity predicts motor and cognitive performance after trauma. Neurol Res 21:742–754 ArticleCASPubMedGoogle Scholar
- Fox GB, Faden AI (1998) Traumatic brain injury causes delayed motor and cognitive impairment in a mutant mouse strain known to exhibit delayed Wallerian degeneration. J Neurosci Res 53:718–727 ArticleCASPubMedGoogle Scholar
- Hamm RJ, Temple MD, Pike BR, O’Dell DM, Buck DL, Lyeth BG (1996) Working memory deficits following traumatic brain injury in the rat. J Neurotrauma 13:317–323 ArticleCASPubMedGoogle Scholar
- Williams AJ, Hartings JA, Lu XC, Rolli ML, Dave JR, Tortella FC (2005) Characterization of a new rat model of penetrating ballistic brain injury. J Neurotrauma 22:313–331 ArticlePubMedGoogle Scholar
- Williams AJ, Hartings JA, Lu XC, Rolli ML, Tortella FC (2006) Penetrating ballistic-like brain injury in the rat: differential time courses of hemorrhage, cell death, inflammation, and remote degeneration. J Neurotrauma 23:1828–1846 ArticlePubMedGoogle Scholar
- Williams AJ, Ling GS, Tortella FC (2006) Severity level and injury track determine outcome following a penetrating ballistic-like brain injury in the rat. Neurosci Lett 408:183–188 ArticleCASPubMedGoogle Scholar
- Chen Z, Tortella FC, Dave JR, Marshall VS, Clarke DL, Sing G, Du F, Lu XC (2009) Human amnion-derived multipotent progenitor cell treatment alleviates traumatic brain injury-induced axonal degeneration. J Neurotrauma 26:1987–1997 ArticlePubMedGoogle Scholar
Disclaimers
The views of the authors do not purport or reflect the position of the Department of the Army or the Department of Defense (para 4-3, AR 360-5). The authors declare that there are no conflicts of interest in this protocol. This research is funded by Combat Casualty Care Research Program.
Author information
Authors and Affiliations
- Brain Trauma Neuroprotection and Neurorestoration Branch, Center for Military Psychiatry and Neuroscience, Walter Reed Army Institute of Research, Silver Spring, MD, USA Ying Deng-Bryant Ph.D., Lai Yee Leung, Krista Caudle, Frank Tortella & Deborah Shear
- Ying Deng-Bryant Ph.D.