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Related Experiment Video

Updated: Jun 8, 2026

Whisker-signaled Eyeblink Classical Conditioning in Head-fixed Mice
10:14

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Published on: March 30, 2016

Accelerated trace eyeblink conditioning after cortisol IV-infusion.

Linn K Kuehl1, Johanna Lass-Hennemann, Steffen Richter

  • 1Institute of Psychobiology, Department of Clinical Physiology, University of Trier, Germany. linnkuehl@gmail.com

Neurobiology of Learning and Memory
|September 21, 2010
PubMed
Summary
This summary is machine-generated.

Cortisol rapidly accelerates learning in trace eyeblink conditioning within minutes, suggesting a fast, non-genomic mechanism. This contrasts with previously known slower, genomic effects of cortisol on learning.

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Area of Science:

  • Neuroscience
  • Psychology
  • Endocrinology

Background:

  • Cortisol's impairing effects on learning are known, typically appearing 30 minutes to hours after administration, suggesting genomic mechanisms.
  • Previous research primarily focused on slower, genomic actions of cortisol on learning performance.

Purpose of the Study:

  • To investigate rapid, non-genomic effects of cortisol on human learning.
  • To examine cortisol's influence on the speed of trace eyeblink conditioning.

Main Methods:

  • Young healthy males (n=24) received metyrapone to block endogenous cortisol synthesis.
  • Intravenous infusion of 2mg cortisol or placebo preceded trace eyeblink conditioning.
  • Conditioned eyeblink responses were measured electromyographically.

Main Results:

  • Cortisol significantly accelerated the increase in conditioning probability (p=.02) within the first 10 minutes.
  • The accelerated conditioning reached placebo levels later in the task.
  • This indicates cortisol affects the speed, not just the amount, of learning.

Conclusions:

  • Cortisol can exert rapid effects on learning, observable within minutes.
  • A fast, non-genomic mechanism is proposed for cortisol's acceleration of trace eyeblink conditioning.
  • This rapid action may be an adaptive component of the early stress response.