Abstract
Cortisol's effects on memory follow an inverted U-shaped function such that memory retrieval is impaired with very low concentrations, presumably due to insufficient activation of high-affine mineralocorticoid receptors (MR), or with very high concentrations, due to predominant low-affine glucocorticoid receptor (GR) activation. Through corresponding changes in re-encoding, the retrieval effect of cortisol might translate into a persistent change of the retrieved memory. We tested whether partial suppression of morning cortisol synthesis by metyrapone, leading to intermediate, circadian nadir-like levels with presumed predominant MR activation, improves retrieval, particularly of emotional memory, and persistently changes the memory. In a randomized, placebo-controlled, double-blind, within-subject cross-over design, 18 men were orally administered metyrapone (1. g) vs. placebo at 4:00. AM to suppress the morning cortisol rise. Retrieval of emotional and neutral texts and pictures (learned 3. days earlier) was assessed 4. h after substance administration and a second time one week later. Metyrapone suppressed endogenous cortisol release to circadian nadir-equivalent levels at the time of retrieval testing. Contrary to our expectations, metyrapone significantly impaired free recall of emotional texts (p< .05), whereas retrieval of neutral texts or pictures remained unaffected. One week later, participants still showed lower memory for emotional texts in the metyrapone than placebo condition (p< .05). Our finding that suppressing morning cortisol to nadir-like concentrations not only impairs acute retrieval, but also persistently weakens emotional memories corroborates the concept that retrieval effects of cortisol produce persistent memory changes, possibly by affecting re-encoding.
| Original language | English |
|---|---|
| Journal | Neurobiology of Learning and Memory |
| Volume | 119 |
| Pages (from-to) | 102-107 |
| Number of pages | 6 |
| ISSN | 1074-7427 |
| DOIs | |
| Publication status | Published - 01.03.2015 |
Funding
This research is supported by grants from the Deutsche Forschungsgemeinschaft DFG (RI 1894/2-1 and SFB 654 ‘‘Plasticity and Sleep’’), the Swiss National Science Foundation (PZ00P1_137126, to U.R.), and the European Community Seventh Framework Programme ([ FP7/2007–2013 ] [ FP7/2007–2011 ]) under grant agreement n° 334360. We thank Yvonne Riexinger and Despina Antypa for help with data analysis.
Research Areas and Centers
- Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)