Age-related changes in working and reference memory performance and locomotor activity in the Wistar rat

1988 ◽  
Vol 50 (1) ◽  
pp. 24-36 ◽  
Author(s):  
Mathias Jucker ◽  
Roland Oettinger ◽  
Karl Battig
2004 ◽  
Vol 360 (3) ◽  
pp. 157-160 ◽  
Author(s):  
Thomas Schiffelholz ◽  
Dunja Hinze-Selch ◽  
Josef B Aldenhoff

2021 ◽  
Vol 4 (Supplement_1) ◽  
pp. 288-289
Author(s):  
N Kraimi ◽  
G De Palma ◽  
J Lu ◽  
D Bowdish ◽  
E Verdu ◽  
...  

Abstract Background Age-associated deterioration of cognitive function and memory capacity occur in a variety of mammals, from humans to rodents. For example, significant memory deficits have been reported in conventionally raised (SPF) old mice compared to conventionally raised young mice submitted to a spatial memory task (Prevot et al., Mol Neuropsychiatry 2019). Microbiota to brain signaling is now well established in mice, but the extent to which this influences age-related memory decline is unknown. Aims Our project aims to determine whether the intestinal microbiota contributes to age-related changes in brain function. We address the hypothesis that age-related cognitive decline is attenuated in the absence of the intestinal microbiota. Methods We studied locomotor behavior and spatial memory performance in young germ-free (GF) mice (2–3 months of age, n=24) and senescent GF mice (13–27 months old, n=22) maintained in axenic conditions, and compared them to conventionally raised (SPF) mice. We used the Y-maze test based on a spontaneous alternations task to assess cognition, with alternation rate as a proxy of spatial working memory performance. The locomotor activity was measured using the open-field test. Results GF old mice traveled less distance (458.9 cm) than GF young mice (875.7 cm, p < 0.001) but these differences in locomotor activity did not influence spatial memory performance. Indeed, both GF old and GF young mice had an identical alternation rate of 73.3% (p > 0.05). This contrasted with the memory impairment found in old SPF mice that displayed lower alternation rate of 58.3%, compared to that found in young SPF mice (76.2%, p = 0.13). Conclusions We conclude that the absence of age-related memory decline in germ-free mice is consistent with a role for the microbiota in the cognitive decline associated with aging, likely through action on the immune system, well documented in SPF mice (Thevaranjan et al., Cell Host & Microbe 2017). We propose that novel microbiota-targeted therapeutic strategies may delay or prevent the cognitive decline of aging. Funding Agencies CIHRBalsam Family Foundation


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Stephan Heinzel ◽  
Thomas G. Riemer ◽  
Stefanie Schulte ◽  
Johanna Onken ◽  
Andreas Heinz ◽  
...  

Objectives. Recent work suggests that a genetic variation associated with increased dopamine metabolism in the prefrontal cortex (catechol-O-methyltransferase Val158Met; COMT) amplifies age-related changes in working memory performance. Research on younger adults indicates that the influence of dopamine-related genetic polymorphisms on working memory performance increases when testing the cognitive limits through training. To date, this has not been studied in older adults.Method. Here we investigate the effect of COMT genotype on plasticity in working memory in a sample of 14 younger (aged 24–30 years) and 25 older (aged 60–75 years) healthy adults. Participants underwent adaptive training in then-back working memory task over 12 sessions under increasing difficulty conditions.Results. Both younger and older adults exhibited sizeable behavioral plasticity through training (P<.001), which was larger in younger as compared to older adults (P<.001). Age-related differences were qualified by an interaction with COMT genotype (P<.001), and this interaction was due to decreased behavioral plasticity in older adults carrying the Val/Val genotype, while there was no effect of genotype in younger adults.Discussion. Our findings indicate that age-related changes in plasticity in working memory are critically affected by genetic variation in prefrontal dopamine metabolism.


1998 ◽  
Vol 274 (3) ◽  
pp. R830-R839 ◽  
Author(s):  
Susan E. Labyak ◽  
Fred W. Turek ◽  
Edward P. Wallen ◽  
Phyllis C. Zee

Syrian hamsters display age-related changes in the expression of circadian rhythms and in responsiveness of the circadian system to photic and nonphotic stimuli. This study characterized the effects of age on the locomotor activity rhythm of middle-aged and old hamsters and evaluated the effects of strengthening the entraining light signal. Compared with young (4.5 mo) animals, middle-aged (11.25 mo) and old (16 mo) animals displayed increased daily bouts of activity ( P < 0.001) and reduced total daily activity and activity rhythm amplitude ( P < 0.05) in 14:10-h light-dark cycles. After the light intensity was increased from 300 to 1,500 lx during the light cycle, middle-aged hamsters demonstrated decreased daily activity bouts ( P < 0.05) and increased total daily activity ( P ≤ 0.01) and activity rhythm amplitude ( P≤ 0.001) compared with controls maintained in 300 lx. The pattern of changes in the activity rhythm of old experimental animals was similar to trends observed in middle-aged experimental hamsters, although not as robust. Thus age-related changes in the activity rhythm are occurring by middle age in hamsters, and the provision of stronger entraining signals may lead to more stable circadian organization.


2002 ◽  
Vol 49 (3) ◽  
pp. 341-362 ◽  
Author(s):  
Werner W.A. Vogels ◽  
Mark R. Dekker ◽  
Wiebo H. Brouwer ◽  
Ritske de Jong

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