Behavioral assessment of the senescence-accelerated mouse (SAM P8 and R1)

被引:78
作者
Markowska, AL
Spangler, EL
Ingram, DK
机构
[1] Johns Hopkins Univ, Dept Psychol, Neuromnemon Lab, Baltimore, MD 21218 USA
[2] NIA, Mol Physiol & Genet Sect, Nathan W Shock Labs, Gerontol Res Ctr,NIH, Baltimore, MD 21224 USA
关键词
senescence-accelerated mouse (SAM); working memory; reference memory; water maze; sensor motor skills; exploratory activity; emotionality;
D O I
10.1016/S0031-9384(98)00011-0
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Senescence-accelerated mice (SAM P8 and R1) were behaviorally assessed in a cross-sectional study at 4 and 15 months of age. Behavioral measures included memory (place discrimination and repeated acquisition in a water maze), sensorimotor performance (turning in an alley, traversing bridges, wire rod hanging, and falls from a wire screen), psychomotor performance (open-field exploration), and emotionality (entries in a plus maze, grooming, and defecation in a plus maze and in an open field). In the water maze, aged P8 mice were impaired in place discrimination end in repeated acquisition tasks, demonstrating evidence of an age-related decline in spatial memory processing abilities. The demonstration of this impairment, however, was complicated by noncognitive factors, such as the tendency of many older P8 mice to float. Sensorimotor skill impairment was accelerated with age in P8 mice, but not in R1 mice, and this impairment vas present despite the lack of age-related changes in body weight in P8 mice. Although PS and R1 mice were not different in general activity at old age, P8 mice were substantially more hyperactive in an open field and in the plus maze than Ri mice when compared at young age. Independent of age, P8 mice demonstrated a reduction of anxiety-like behavior in the plus maze. Taken as a whole, the data suggest that although age-related behavioral alterations occur in the P8 mice, some of these changes are evident at 4 months of age. Thus, the behavioral abnormalities that exist not only represent an accelerated aging phenomenon but may also be considered a developmental pathology. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:15 / 26
页数:12
相关论文
共 43 条
[1]  
AKIGUCHI I, 1994, INT CONGR SER, V1062, P67
[2]   PERIODIC ACID-SCHIFF (PAS)-POSITIVE, ANTIGRANULOCYTES STRUCTURES INCREASE IN THE BRAIN OF SENESCENCE ACCELERATED MOUSE (SAM) [J].
AKIYAMA, H ;
KAMEYAMA, M ;
AKIGUCHI, I ;
SUGIYAMA, H ;
KAWAMATA, T ;
FUKUYAMA, H ;
KIMURA, H ;
MATSUSHITA, M ;
TAKEDA, T .
ACTA NEUROPATHOLOGICA, 1986, 72 (02) :124-129
[3]  
BONDI MW, 1994, ALZHEIMERS DIS, P38
[4]  
FLOOD JE, IN PRESS NEUROSCI BI
[5]  
FLOOD JE, 1994, SAM MODEL SENESCENCE, P113
[6]   AGE-RELATED-CHANGES IN FOOTSHOCK AVOIDANCE ACQUISITION AND RETENTION IN SENESCENCE ACCELERATED MOUSE (SAM) [J].
FLOOD, JF ;
MORLEY, JE .
NEUROBIOLOGY OF AGING, 1993, 14 (02) :153-157
[7]   EARLY ONSET OF AGE-RELATED IMPAIRMENT OF AVERSIVE AND APPETITIVE LEARNING IN THE SAM-P/8 MOUSE [J].
FLOOD, JF ;
MORLEY, JE .
JOURNALS OF GERONTOLOGY, 1992, 47 (02) :B52-B59
[8]   AGE-RELATED SPATIAL REFERENCE AND WORKING-MEMORY DEFICITS ASSESSED IN THE WATER MAZE [J].
FRICK, KM ;
BAXTER, MG ;
MARKOWSKA, AL ;
OLTON, DS ;
PRICE, DL .
NEUROBIOLOGY OF AGING, 1995, 16 (02) :149-160
[9]   EFFECTS OF INTERMITTENT FEEDING UPON BODY-WEIGHT AND LIFE-SPAN IN INBRED MICE - INTERACTION OF GENOTYPE AND AGE [J].
GOODRICK, CL ;
INGRAM, DK ;
REYNOLDS, MA ;
FREEMAN, JR ;
CIDER, N .
MECHANISMS OF AGEING AND DEVELOPMENT, 1990, 55 (01) :69-87
[10]  
HOSOKAWA M, 1994, INT CONGR SER, V1062, P23