scholarly journals Effects of two different emotion-inducing methods on the emotional memory of non-clinically depressed individuals

PLoS ONE ◽  
2021 ◽  
Vol 16 (5) ◽  
pp. e0249863
Author(s):  
Wuji Lin ◽  
Jingyuan Lin ◽  
Xiaoqing Cai ◽  
Jun Deng ◽  
Yuan Gao ◽  
...  

In the study of emotional memory bias in depressed individuals, most previous studies have used emotional materials, but there were significant differences in the effects of different emotion-inducing methods on face memory. In the present study, two experiments were conducted to explore the effects of different emotion-inducing methods on memory between healthy participants and non-clinically depressed participants. The results from experiment 1 showed that when feedback was used as induction, the memory performance of the non-clinical depression group was significantly higher than that of the healthy group under the condition of negative feedback. Under positive and neutral feedback, there were no significant differences between the two groups. In experiment 2, when emotional materials were used as a mode of induction, no significantly difference in each emotional condition between the healthy and depressed groups was found. The results of the present study show that different methods of emotional induction have different effects on depressed participants. Compared with the emotion induced by the emotional material, the non-clinical depressed participants had a better memory effect induced by negative emotional events.

2019 ◽  
Author(s):  
Leonore Bovy ◽  
Ruud M.W.J. Berkers ◽  
Julia Pottkämper ◽  
Rathiga Varatheesvaran ◽  
Guillén Fernández ◽  
...  

AbstractMemory bias for negative information is a critical characteristic of major depression, but the underlying neural mechanisms are largely unknown. The recently revived concept of memory schemas may shed new light on memory bias in depression: negative schemas might enhance the encoding and consolidation of negative experiences, thereby contributing to the genesis and perpetuation of depressive pathology. To investigate this relationship, we aimed to transiently perturb processing in the medial prefrontal cortex (mPFC), a core region involved in schema memory, using neuronavigated transcranial magnetic stimulation (TMS) targeting the mPFC. Forty healthy volunteers first underwent a negative mood induction to activate negative schema processing after which they received either active inhibitory (N = 20) or control (N = 20) stimulation to the mPFC. Then, all participants performed the encoding of an emotional false memory task. Recall and recognition performance was tested the following morning. Polysomnographic data was recorded continuously during the night before and after encoding. Secondary measures included sleep and mood questionnaires. We observed a significantly lower number of false recognition of negative critical lures following mPFC perturbation compared to the control group, whereas no differences in veridical memory performance were observed. These findings were supported by reaction time data. No relation between REM sleep and (false) emotional memory performance was observed. These findings support previous causal evidence for a role of the mPFC in schema memory processing and further suggest a role of the mPFC in memory bias.


SLEEP ◽  
2020 ◽  
Vol 43 (Supplement_1) ◽  
pp. A40-A40
Author(s):  
J F Holmes ◽  
M K Deighan ◽  
N W Miranda ◽  
G M Mason ◽  
R M Spencer

Abstract Introduction Naps are known to benefit emotional memory consolidation in preschoolers, though improvement is not evident until the following day. The mechanisms by which naps aid emotional memory, and how they differ from those facilitating more neutral declarative memory consolidation, are currently unknown. In this study, we used an emotional storybook task to assess change in memory for emotionally salient vs. neutral events across a nap and overnight sleep. PSG was included to explore sleep physiology correlates. Methods Preschool children (n = 9; Mage= 43.2 months) were read a novel storybook featuring negative and neutral events. Memory of story events was probed through sets of multiple-choice questions and assessed at three time points: immediately following the story, following a nap or equivalent wake period (within-subject; counterbalanced; separated by ~1 week), and 24h post-encoding. PSG was recorded during the nap period and both subsequent overnight sleep bouts. Results Memory performance across time points was assessed via change scores. Recall of story events did not differ between conditions from immediate to post-nap/wake assessment. When probed the following morning, children better remembered events when a nap took place the day prior (F(1,7) = 8.848, p=.021). This delayed nap benefit correlated with time spent in NREM2 during the nap (r=.91, p=.017). No differences were found between recall of negative vs. neutral events at any time point or between conditions. Conclusion Our results show a delayed benefit of napping on recall of a storybook, though at present no preference for emotional events is seen. Time spent in NREM2 during the nap was strongly associated with our finding, likely reflecting the declarative memory benefits conferred from this stage. Further analyses will include overnight sleep physiology to explore differential enhancement between event types, and possible interactions with nap microstructure. Support This work was supported by NIH R01 HL111695.


2011 ◽  
Author(s):  
Jason Swift ◽  
Andrew Garcia ◽  
Maura Pilotti ◽  
Salif Mahamane ◽  
Jennifer Almand

2013 ◽  
Vol 25 (10) ◽  
pp. 1597-1610 ◽  
Author(s):  
Erik J. Kaestner ◽  
John T. Wixted ◽  
Sara C. Mednick

Sleep affects declarative memory for emotional stimuli differently than it affects declarative memory for nonemotional stimuli. However, the interaction between specific sleep characteristics and emotional memory is not well understood. Recent studies on how sleep affects emotional memory have focused on rapid eye movement sleep (REM) but have not addressed non-REM sleep, particularly sleep spindles. This is despite the fact that sleep spindles are implicated in declarative memory as well as neural models of memory consolidation (e.g., hippocampal neural replay). Additionally, many studies examine a limited range of emotional stimuli and fail to disentangle differences in memory performance because of variance in valence and arousal. Here, we experimentally increase non-REM sleep features, sleep spindle density, and SWS, with pharmacological interventions using zolpidem (Ambien) and sodium oxybate (Xyrem) during daytime naps. We use a full spread of emotional stimuli to test all levels of valence and arousal. We find that increasing sleep spindle density increases memory discrimination (da) for highly arousing and negative stimuli without altering measures of bias (ca). These results indicate a broader role for sleep in the processing of emotional stimuli with differing effects based on arousal and valence, and they raise the possibility that sleep spindles causally facilitate emotional memory consolidation. These findings are discussed in terms of the known use of hypnotics in individuals with emotional mood disorders.


SLEEP ◽  
2021 ◽  
Vol 44 (Supplement_2) ◽  
pp. A21-A22
Author(s):  
Negin Sattari ◽  
Lauren Whitehurst ◽  
Sara Mednick

Abstract Introduction Aging is accompanied by deterioration in both working memory (WM) and long-term memory (LTM), though the reason is not well understood. Sleep may play a role in young adults, but the findings in older adults are not as clear. In addition, older adults show better memory for positive memories, whereas youngers tend to hold on to negative memories. The prefrontal cortex has been implicated in this emotional memory bias. The current study investigated the role of working memory (a prefrontal task) on emotional memory consolidation across sleep and wake in young and older adults. Methods In the morning, 93 younger (18–39) and 121 older (60–85) adults took a WM task and encoded neutral or negative word pairs, and gave valence and arousal ratings for each pair. After a wake or polysomnography-recorded sleep condition, memory for the word pairs was tested plus valence and arousal ratings. Results Youngers had better overall memory (p<.001), with older adults showing better memory for neutral compared to negative word pairs (p=.04), as well as increased positivity (p=.02), which was correlated with LTM performance (p=.009). In contrast, youngers performed better on the negative word pairs (p=.01), but no change in ratings and no association between emotional reactivity and LTM. Further, WM was positively related to memory in youngers (r=.38, p=.02), but not in older adults. Lastly, no role for sleep likely due to the lack of an immediate test. Conclusion we found that the positivity bias in aging in both memory and valence, with increasing positivity associated with better memory. We found a robust relation between WM and LTM in youngers but not older adults. Our findings are consistent with the socioemotional-selectivity theory that posits that aging is associated with a relative suppression of negative information while WM may play a role. Support (if any):


2020 ◽  
Vol 30 (6) ◽  
pp. 3608-3616 ◽  
Author(s):  
Leonore Bovy ◽  
Ruud M W J Berkers ◽  
Julia C M Pottkämper ◽  
Rathiga Varatheeswaran ◽  
Guillén Fernández ◽  
...  

Abstract Mood-congruent memory bias is a critical characteristic of depression, but the underlying neural mechanism is largely unknown. Negative memory schemas might enhance encoding and consolidation of negative experiences, thereby contributing to the genesis and perpetuation of depressive pathology. To investigate this relationship, we aimed to perturb medial prefrontal cortex (mPFC) processing, using neuronavigated transcranial magnetic stimulation (TMS) targeting the mPFC. Forty healthy volunteers first underwent a negative mood induction to activate negative schema processing after which they received either active inhibitory (N = 20) or control (N = 20) stimulation to the mPFC. Then, all participants performed the encoding of an emotional false memory task. Recall and recognition performance was tested the following morning. Polysomnographic data were recorded continuously during the night before and after encoding. We observed a significantly lower false recognition of negative critical lures following mPFC inhibition, but no differences in veridical memory. These findings were supported by reaction time data, showing a relative slower response to negative compared with positive critical lures. The current findings support previous causal evidence for a role of the mPFC in schema memory processing and further suggest a role of the mPFC in memory bias.


2018 ◽  
Vol 48 (10) ◽  
pp. 1608-1615 ◽  
Author(s):  
G. Donohoe ◽  
J. Holland ◽  
D. Mothersill ◽  
S. McCarthy-Jones ◽  
D. Cosgrove ◽  
...  

AbstractBackgroundThe longstanding association between the major histocompatibility complex (MHC) locus and schizophrenia (SZ) risk has recently been accounted for, partially, by structural variation at the complement component 4 (C4) gene. This structural variation generates varying levels ofC4RNA expression, and genetic information from the MHC region can now be used to predictC4RNA expression in the brain. Increased predictedC4ARNA expression is associated with the risk of SZ, andC4is reported to influence synaptic pruning in animal models.MethodsBased on our previous studies associating MHC SZ risk variants with poorer memory performance, we tested whether increased predictedC4ARNA expression was associated with reduced memory function in a large (n= 1238) dataset of psychosis cases and healthy participants, and with altered task-dependent cortical activation in a subset of these samples.ResultsWe observed that increased predictedC4ARNA expression predicted poorer performance on measures of memory recall (p= 0.016, corrected). Furthermore, in healthy participants, we found that increased predictedC4ARNA expression was associated with a pattern of reduced cortical activity in middle temporal cortex during a measure of visual processing (p< 0.05, corrected).ConclusionsThese data suggest that the effects ofC4on cognition were observable at both a cortical and behavioural level, and may represent one mechanism by which illness risk is mediated. As such, deficits in learning and memory may represent a therapeutic target for new molecular developments aimed at alteringC4’s developmental role.


2019 ◽  
Vol 50 (10) ◽  
pp. 1727-1735
Author(s):  
A. Kühnel ◽  
A. Widmann ◽  
L. Colic ◽  
L. Herrmann ◽  
L. R. Demenescu ◽  
...  

AbstractBackgroundPrevious research showed that automatic emotion regulation is associated with activation of subcortical areas and subsequent feedforward processes to cortical areas. In contrast, cognitive awareness of emotions is mediated by negative feedback from cortical to subcortical areas. Pregenual anterior cingulate cortex (pgACC) is essential in the modulation of both affect and alexithymia. We considered the interplay between these two mechanisms in the pgACC and their relationship with alexithymia.MethodIn 68 healthy participants (30 women, age = 26.15 ± 4.22) we tested associations of emotion processing and alexithymia with excitation/inhibition (E/I) balance represented as glutamate (Glu)/GABA in the pgACC measured via magnetic resonance spectroscopy in 7 T.ResultsAlexithymia was positively correlated with the Glu/GABA ratio (N = 41, p = 0.0393). Further, cognitive self-awareness showed an association with Glu/GABA (N = 52, p = 0.003), which was driven by a correlation with GABA. In contrast, emotion regulation was only correlated with glutamate levels in the pgACC (N = 49, p = 0.008).ConclusionOur results corroborate the importance of the pgACC as a mediating region of alexithymia, reflected in an altered E/I balance. Furthermore, we could specify that this altered balance is linked to a GABA-related modulation of cognitive self-awareness of emotions.


2007 ◽  
Vol 16 (4) ◽  
pp. 173-177 ◽  
Author(s):  
Kevin S. LaBar

Neurobiological accounts of emotional memory have been derived largely from animal models investigating the encoding and retention of memories for events that signal threat. This literature has implicated the amygdala, a structure in the brain's temporal lobe, in the learning and consolidation of fear memories. Its role in fear conditioning has been confirmed, but the human amygdala also interacts with cortical regions to mediate other aspects of emotional memory. These include the encoding and consolidation of pleasant and unpleasant arousing events into long-term memory, the narrowing of focus on central emotional information, the retrieval of prior emotional events and contexts, and the subjective experience of recollection and emotional intensity during retrieval. Along with other mechanisms that do not involve the amygdala, these functions ensure that significant life events leave a lasting impression in memory.


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