Tuning hippocampal synapses by stress-hormones: Relevance for emotional memory formation

2015 ◽  
Vol 1621 ◽  
pp. 114-120 ◽  
Author(s):  
Hui Xiong ◽  
Harm J. Krugers
NeuroImage ◽  
2011 ◽  
Vol 56 (3) ◽  
pp. 1783-1790 ◽  
Author(s):  
Daniel A. Fitzgerald ◽  
Jennifer F. Arnold ◽  
Eni S. Becker ◽  
Anne E.M. Speckens ◽  
Mike Rinck ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (2) ◽  
pp. e0117062 ◽  
Author(s):  
Michael E. Ballard ◽  
Jessica Weafer ◽  
David A. Gallo ◽  
Harriet de Wit

Author(s):  
Jessica D. Payne

Memory consolidation processes can be highly selective. For example, negative emotional aspects of events tend to be consolidated more readily than other, more neutral, aspects. This chapter discusses evidence that the sleeping brain provides an ideal environment for memory consolidation, and that active, as opposed to passive, sleep-based consolidation processes are particularly important in explaining why emotional memories are retained so well. I also review evidence that elevated levels of stress hormones (cortisol, norepinephrine), particularly during the time of the initial experience, support downstream emotional memory consolidation. The chapter then proposes a working model that describes why arousal and stress at encoding may set the stage for sleep to etch emotional memories in the brain on a long-lasting basis and presents recent data to support this model. However, in addition to promoting the consolidation and stabilization of emotional memories, evidence suggests that sleep and stress also transform memories—in both adaptive and maladaptive ways. Memory for negative emotional experiences, while adaptive in general, can also contribute to the etiology and perpetuation of clinical conditions such as depression and anxiety. Thus, I argues that it is possible to have “too much of a good thing” and suggests ways that the transformative nature of stress and sleep might be used to restructure maladaptive memories in the clinic.


2011 ◽  
Vol 32 (12) ◽  
pp. 2096-2103 ◽  
Author(s):  
Maren Urner ◽  
Guido van Wingen ◽  
Barbara Franke ◽  
Mark Rijpkema ◽  
Guillén Fernández ◽  
...  

2019 ◽  
Vol 50 (8) ◽  
pp. 1316-1326 ◽  
Author(s):  
Hui Ai ◽  
Esther M. Opmeer ◽  
Jan-Bernard C. Marsman ◽  
Dick J. Veltman ◽  
Nic J. A. van der Wee ◽  
...  

AbstractBackgroundThe importance of the hippocampus and amygdala for disrupted emotional memory formation in depression is well-recognized, but it remains unclear whether functional abnormalities are state-dependent and whether they are affected by the persistence of depressive symptoms.MethodsThirty-nine patients with major depressive disorder and 28 healthy controls were included from the longitudinal functional magnetic resonance imaging (fMRI) sub-study of the Netherlands Study of Depression and Anxiety. Participants performed an emotional word-encoding and -recognition task during fMRI at baseline and 2-year follow-up measurement. At baseline, all patients were in a depressed state. We investigated state-dependency by relating changes in brain activation over time to changes in symptom severity. Furthermore, the effect of time spent with depressive symptoms in the 2-year interval was investigated.ResultsSymptom change was linearly associated with higher activation over time of the left anterior hippocampus extending to the amygdala during positive and negative word-encoding. Especially during positive word encoding, this effect was driven by symptomatic improvement. There was no effect of time spent with depression in the 2-year interval on change in brain activation. Results were independent of medication- and psychotherapy-use.ConclusionUsing a longitudinal within-subjects design, we showed that hippocampal–amygdalar activation during emotional memory formation is related to depressive symptom severity but not persistence (i.e. time spent with depression or ‘load’), suggesting functional activation patterns in depression are not subject to functional ‘scarring’ although this hypothesis awaits future replication.


Author(s):  
Dan Denis ◽  
Sara Y. Kim ◽  
Sarah M. Kark ◽  
Ryan T. Daley ◽  
Elizabeth A. Kensinger ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document