Spatial memory performance and hippocampal neuron number in osteoporotic SAMP6 mice

• Published in: Experimental neurology 2006-10, Vol.201 (2), p.452-460
• Main Authors: Liu, Cun-Zhi, Yu, Jian-Chun, Cheng, Hai-Yan, Jiang, Zhi-Guo, Li, Tan, Zhang, Xue-Zhu, Zhang, Lin-Lin, Han, Jing-Xian
• Format: Article
• Language: English
• Subjects: Age Factors; Aging; Analysis of Variance; Animals; Behavior, Animal - physiology; Biological and medical sciences; Cell Count; Cognition Disorders - etiology; Cognition Disorders - physiopathology; Development. Senescence. Regeneration. Transplantation; Disease Models, Animal; Fundamental and applied biological sciences. Psychology; Hippocampus; Hippocampus - pathology; Hippocampus - physiopathology; Isolated neuron and nerve. Neuroglia; Male; Maze Learning - physiology; Memory - physiology; Mice; Mice, Inbred Strains; Morris water maze; Neurons; Neurons - pathology; Osteoporosis - complications; Osteoporosis - physiopathology; Psychomotor Performance - physiology; Reference memory; SAMP6; Senescence-accelerated mouse; Spatial Behavior - physiology; Spatial memory; Specific Pathogen-Free Organisms; Swimming; Vertebrates: nervous system and sense organs; Working memory
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1016/j.expneurol.2006.04.025

The senescence-accelerated mouse strain P6 (SAMP6) is an inbred mouse that represents a clinically relevant model of senile osteoporosis. However, whether osteoporotic SAMP6 mice have cognitive deficits remains largely unexplored. Here, we used Morris water maze to assess reference memory and working memory performance in SAMP6 mice and SAMR1 controls, at 4 and 8 months of age. In addition, unbiased stereological techniques were used to estimate total neuron number in hippocampal CA1 subfield of the mice used in the behavioral study. Morris water maze test revealed impairments in working memory but not in reference memory of the 4- and 8-month-old SAMP6 mice compared with the SAMR1 mice at the same age. However, there were no significant differences in the total numbers of neurons in hippocampal CA1 subfield when comparing 4-month-old SAMR1 and 4-month-old SAMP6 and 8-month-old SAMR1 and 8-month-old SAMP6, which indicate that, in SAMP6 mice, the structural correlates of working memory deficits are to be found in parameters other than the number of neurons in hippocampal CA1 subfield. These findings suggest that SAMP6 mice exhibit selective cognitive deficits and highlight the importance of this mouse model for studying the brain alterations associated with osteoporosis.