The COMT Val158Met polymorphism modulates working memory performance under acute stress

2012 ◽  
Vol 37 (11) ◽  
pp. 1810-1821 ◽  
Author(s):  
Magdalena Buckert ◽  
Brigitte M. Kudielka ◽  
Martin Reuter ◽  
Christian J. Fiebach
NeuroImage ◽  
2014 ◽  
Vol 100 ◽  
pp. 489-497 ◽  
Author(s):  
C.W.N. Saville ◽  
T.M. Lancaster ◽  
M.E. Stefanou ◽  
G. Salunkhe ◽  
I. Lourmpa ◽  
...  

Author(s):  
Petra Luers ◽  
Malgorzata Schloeffel ◽  
Jens C. Prüssner

Abstract. Acute stress and chronic stress change the physiology and function of the individual. As one facet, stress and its neuroendocrine correlates – with glucocorticoids in particular – modulate memory in a concerted action. With respect to working memory, impairing effects of acute stress and increased levels of glucocorticoids could be expected, but empirical evidence on moderating effects of cortisol on working memory is ambiguous in human studies. In the current study, we thus aimed to investigate cortisol stress responses and memory performance. Older men and women (32 men, 43 women, aged 61–67 years) underwent the Trier Social Stress Test (TSST) and performed the 2-back task before and after exposure to acute stress. In line with theoretical assumptions, we found that higher cortisol stress responses led to a decline of working memory performance in men. However, the opposite was evident for women, who appeared to benefit from higher stress responses. This effect was evident for accuracy, but not for reaction time. In conclusion, cortisol might mediate working memory alterations with stress in a sex-specific manner in older people. Possible mechanisms and causes for these sex differences put a focus on endocrine changes in the aging population that might lead to differential effects across the lifespan.


2019 ◽  
Vol 29 (12) ◽  
pp. 4948-4957 ◽  
Author(s):  
Laura Musazzi ◽  
Nathalie Sala ◽  
Paolo Tornese ◽  
Francesca Gallivanone ◽  
Sara Belloli ◽  
...  

Abstract Brain energy metabolism actively regulates synaptic transmission and activity. We have previously shown that acute footshock (FS)-stress induces fast and long-lasting functional and morphological changes at excitatory synapses in prefrontal cortex (PFC). Here, we asked whether FS-stress increased energy metabolism in PFC, and modified related cognitive functions. Using positron emission tomography (PET), we found that FS-stress induced a redistribution of glucose metabolism in the brain, with relative decrease of [18F]FDG uptake in ventro-caudal regions and increase in dorso-rostral ones. Absolute [18F]FDG uptake was inversely correlated with serum corticosterone. Increased specific hexokinase activity was also measured in purified PFC synaptosomes (but not in total extract) of FS-stressed rats, which positively correlated with 2-Deoxy [3H] glucose uptake by synaptosomes. In line with increased synaptic energy demand, using an electron microscopy-based stereological approach, we found that acute stress induced a redistribution of mitochondria at excitatory synapses, together with an increase in their volume. The fast functional and metabolic activation of PFC induced by acute stress, was accompanied by rapid and sustained alterations of working memory performance in delayed response to T-maze test. Taken together, the present data suggest that acute stress increases energy consumption at PFC synaptic terminals and alters working memory.


2015 ◽  
Vol 28 (5) ◽  
pp. 545-562 ◽  
Author(s):  
Anna Hood ◽  
Kim Pulvers ◽  
Thomas J. Spady ◽  
Alexa Kliebenstein ◽  
Jennifer Bachand

Medicina ◽  
2019 ◽  
Vol 55 (5) ◽  
pp. 119
Author(s):  
Pamela Ponce ◽  
Alberto del Arco ◽  
Paul Loprinzi

Background and Objective: The present study was designed to investigate whether acute physical activity and psychological stress produce different effects on cortisol release and working memory performance. Materials and Methods: Male subjects (N = 12; 18–35 years) were recruited and scheduled to come four times to our lab (within-subject design). For each counterbalanced visit, they performed one of the following four protocols: control, moderate physical activity (MOD), vigorous physical activity (VIG), and acute stress. Heart rate was monitored during every protocol. MOD and VIG were performed for 15 min and were defined as 40–50% and 70–80%, respectively, of their maximum heart rate. Acute stress was imposed via the Trier Social Stress Test (TSST). Salivary samples were collected before and after every protocol to assess cortisol concentrations. Working memory (WM) performance was evaluated through the 2N-Back task right after ending the protocol (early WM) and after a delay of 35 min (late WM). Results: VIG and stress, but not MOD, increased salivary cortisol concentrations. However, the increases of cortisol produced by VIG and stress were not significantly different. Also, there were no significant differences in working memory performance (late and early) in any of the experimental protocols tested. Conclusions: These results show that exercise (VIG) and stress produce similar effects on cortisol release and do not support the hypothesis that working memory capacity is influenced by elevated cortisol levels, either from varying exercise intensities or psychological stress.


2021 ◽  
pp. 1-9
Author(s):  
Simon B. Goldberg ◽  
Lisa Flook ◽  
Matthew J. Hirshberg ◽  
Richard J. Davidson ◽  
Stacey M. Schaefer

Intelligence ◽  
2017 ◽  
Vol 65 ◽  
pp. 75-92 ◽  
Author(s):  
Susann Geller ◽  
Oliver Wilhelm ◽  
Jan Wacker ◽  
Alfons Hamm ◽  
Andrea Hildebrandt

Sign in / Sign up

Export Citation Format

Share Document