Does cortisol influence core executive functions? A meta-analysis of acute cortisol administration effects on working memory, inhibition, and set-shifting

Highlights • The fast, nongenomic effects of cortisol enhanced response inhibition. • The fast, nongenomic effects of cortisol impaired working memory. • Both of the above effects reversed over time. • Cortisol administration did not alter mental set-shifting.

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Bibliographic Details
Published inPsychoneuroendocrinology Vol. 58; pp. 91 - 103
Main Authors Shields, Grant S, Bonner, Joseph C, Moons, Wesley G
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.08.2015
Subjects
Animals
Attention - drug effects
Cognitive inhibition
Cortisol
Endocrinology & Metabolism
Executive attention
Executive function
Executive Function - drug effects
Humans
Hydrocortisone - pharmacology
Inhibition
Inhibition (Psychology)
Interference control
Memory, Short-Term - drug effects
Meta-analysis
Neuropsychological Tests
Psychiatry
Response inhibition
Set (Psychology)
Set-shifting
Working memory
Executive function
Response inhibition
Executive attention
Cortisol
Set-shifting
Working memory
Inhibition
Cognitive inhibition
Interference control
Meta-analysis
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Abstract Highlights • The fast, nongenomic effects of cortisol enhanced response inhibition. • The fast, nongenomic effects of cortisol impaired working memory. • Both of the above effects reversed over time. • Cortisol administration did not alter mental set-shifting.
AbstractList •The fast, nongenomic effects of cortisol enhanced response inhibition.•The fast, nongenomic effects of cortisol impaired working memory.•Both of the above effects reversed over time.•Cortisol administration did not alter mental set-shifting. The hormone cortisol is often believed to play a pivotal role in the effects of stress on human cognition. This meta-analysis is an attempt to determine the effects of acute cortisol administration on core executive functions. Drawing on both rodent and stress literatures, we hypothesized that acute cortisol administration would impair working memory and set-shifting but enhance inhibition. Additionally, because cortisol is thought to exert different nongenomic (rapid) and genomic (slow) effects, we further hypothesized that the effects of cortisol would differ as a function of the delay between cortisol administration and cognitive testing. Although the overall analyses were nonsignificant, after separating the rapid, nongenomic effects of cortisol from the slower, genomic effects of cortisol, the rapid effects of cortisol enhanced response inhibition, g+=0.113, p=.016, but impaired working memory, g+=−0.315, p=.008, although these effects reversed over time. Contrary to our hypotheses, there was no effect of cortisol administration on set-shifting. Thus, although we did not find support for the idea that increases in cortisol influence set-shifting, we found that acute increases in cortisol exert differential effects on working memory and inhibition over time.
Highlights • The fast, nongenomic effects of cortisol enhanced response inhibition. • The fast, nongenomic effects of cortisol impaired working memory. • Both of the above effects reversed over time. • Cortisol administration did not alter mental set-shifting.
The hormone cortisol is often believed to play a pivotal role in the effects of stress on human cognition. This meta-analysis is an attempt to determine the effects of acute cortisol administration on core executive functions. Drawing on both rodent and stress literatures, we hypothesized that acute cortisol administration would impair working memory and set-shifting but enhance inhibition. Additionally, because cortisol is thought to exert different nongenomic (rapid) and genomic (slow) effects, we further hypothesized that the effects of cortisol would differ as a function of the delay between cortisol administration and cognitive testing. Although the overall analyses were nonsignificant, after separating the rapid, nongenomic effects of cortisol from the slower, genomic effects of cortisol, the rapid effects of cortisol enhanced response inhibition, g+ = 0.113, p=.016, but impaired working memory, g+ = -0.315, p=.008, although these effects reversed over time. Contrary to our hypotheses, there was no effect of cortisol administration on set-shifting. Thus, although we did not find support for the idea that increases in cortisol influence set-shifting, we found that acute increases in cortisol exert differential effects on working memory and inhibition over time.
Author Moons, Wesley G
Bonner, Joseph C
Shields, Grant S
Author_xml – sequence: 1
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  fullname: Moons, Wesley G
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25973565$$D View this record in MEDLINE/PubMed
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Keywords Executive function
Response inhibition
Executive attention
Cortisol
Set-shifting
Working memory
Inhibition
Cognitive inhibition
Interference control
Meta-analysis
Language English
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Snippet Highlights • The fast, nongenomic effects of cortisol enhanced response inhibition. • The fast, nongenomic effects of cortisol impaired working memory. • Both...
•The fast, nongenomic effects of cortisol enhanced response inhibition.•The fast, nongenomic effects of cortisol impaired working memory.•Both of the above...
The hormone cortisol is often believed to play a pivotal role in the effects of stress on human cognition. This meta-analysis is an attempt to determine the...
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SubjectTerms Animals
Attention - drug effects
Cognitive inhibition
Cortisol
Endocrinology & Metabolism
Executive attention
Executive function
Executive Function - drug effects
Humans
Hydrocortisone - pharmacology
Inhibition
Inhibition (Psychology)
Interference control
Memory, Short-Term - drug effects
Meta-analysis
Neuropsychological Tests
Psychiatry
Response inhibition
Set (Psychology)
Set-shifting
Working memory
Title Does cortisol influence core executive functions? A meta-analysis of acute cortisol administration effects on working memory, inhibition, and set-shifting
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https://dx.doi.org/10.1016/j.psyneuen.2015.04.017
https://www.ncbi.nlm.nih.gov/pubmed/25973565
https://search.proquest.com/docview/1686996367
Volume 58
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