scholarly journals Are All Remote Associates Tests Equal? An Overview of the Remote Associates Test in Different Languages

2020 ◽  
Vol 11 ◽  
Author(s):  
Jan Philipp Behrens ◽  
Ana-Maria Olteţeanu
2020 ◽  
Author(s):  
Carola Salvi ◽  
Giulio Costantini ◽  
Adriana Pace ◽  
Massimiliano Palmiero

2012 ◽  
Vol 4 (2) ◽  
Author(s):  
Steven M. Smith ◽  
Cynthia M. Sifonis ◽  
Genna Angello

2016 ◽  
Vol 113 (26) ◽  
pp. 7272-7277 ◽  
Author(s):  
Lauren N. Whitehurst ◽  
Nicola Cellini ◽  
Elizabeth A. McDevitt ◽  
Katherine A. Duggan ◽  
Sara C. Mednick

Throughout history, psychologists and philosophers have proposed that good sleep benefits memory, yet current studies focusing on the relationship between traditionally reported sleep features (e.g., minutes in sleep stages) and changes in memory performance show contradictory findings. This discrepancy suggests that there are events occurring during sleep that have not yet been considered. The autonomic nervous system (ANS) shows strong variation across sleep stages. Also, increases in ANS activity during waking, as measured by heart rate variability (HRV), have been correlated with memory improvement. However, the role of ANS in sleep-dependent memory consolidation has never been examined. Here, we examined whether changes in cardiac ANS activity (HRV) during a daytime nap were related to performance on two memory conditions (Primed and Repeated) and a nonmemory control condition on the Remote Associates Test. In line with prior studies, we found sleep-dependent improvement in the Primed condition compared with the Quiet Wake control condition. Using regression analyses, we compared the proportion of variance in performance associated with traditionally reported sleep features (model 1) vs. sleep features and HRV during sleep (model 2). For both the Primed and Repeated conditions, model 2 (sleep + HRV) predicted performance significantly better (73% and 58% of variance explained, respectively) compared with model 1 (sleep only, 46% and 26% of variance explained, respectively). These findings present the first evidence, to our knowledge, that ANS activity may be one potential mechanism driving sleep-dependent plasticity.


2013 ◽  
Vol 84 (4) ◽  
pp. 419-428 ◽  
Author(s):  
Hitoshi Terai ◽  
Kazuhisa Miwa ◽  
Kazuaki Asami

2007 ◽  
Vol 19 (3) ◽  
pp. 468-478 ◽  
Author(s):  
Jessica K. Alexander ◽  
Ashleigh Hillier ◽  
Ryan M. Smith ◽  
Madalina E. Tivarus ◽  
David Q. Beversdorf

Stress-induced activation of the locus ceruleus-norepinephrine (LC-NE) system produces significant cognitive and behavioral effects, including enhanced arousal and attention. Improvements in discrimination task performance and memory have been attributed to this stress response. In contrast, for other cognitive functions that require cognitive flexibility, increased activity of the LC-NE system may produce deleterious effects. The aim of the present study was to determine the effect of pharmacological modulation of the LC-NE system on stress-induced impairments in cognitive flexibility performance in healthy individuals. Cognitive performance, plus psychological and physiological parameters for 16 adults without any history of anxiety disorders, was assessed during four test sessions: stress and no-stress, with each condition tested after administration of propranolol and placebo. The Trier Social Stress Test, a public-speaking and mental arithmetic stressor, was presented to participants for the stress sessions, whereas a similar, but nonstressful, control task (reading, counting) was utilized for the no-stress sessions. Tests of cognitive flexibility included lexical-semantic and associative problem-solving tasks (anagrams, Compound Remote Associates Test). Visuo-spatial memory and motor processing speed tests served as control tasks. Results indicate that (1) stress impaired performance on cognitive flexibility tasks, but not control tasks; (2) compared to placebo, cognitive flexibility improved during stress with propranolol. Therefore, psychological stress, such as public speaking, negatively impacts performance on tasks requiring cognitive flexibility in normal individuals, and this effect is reversed by beta-adrenergic antagonism. This may provide support for the hypothesis that stress-related impairments in cognitive flexibility are related to the noradrenergic system.


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