Browse
Submit Data
Databases
API
Help

Dataset Information

26 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Inhibition-induced forgetting: when more control leads to less memory.

ABSTRACT: The ability to inhibit prepotent responses is a core executive function, but the relation of response inhibition to other cognitive operations is poorly understood. In the study reported here, we examined inhibitory control through the lens of incidental memory. Participants categorized face stimuli by gender in a go/no-go task (Experiments 1 and 2) or a stop-signal task (Experiment 3) and, after a short delay, performed a surprise recognition memory task for those faces. Memory was impaired for stimuli presented during no-go and stop trials compared with those presented during go trials. Experiment 4 showed that this inhibition-induced forgetting was not attributable to event congruency. In Experiment 5, we combined a go/no-go task with a dot-probe test and found that probe detection during no-go trials was inferior to that on go trials. This result supports the hypothesis that inhibition-induced forgetting occurs when response inhibition shunts attentional resources from perceptual stimulus encoding to action control.

SUBMITTER: Chiu YC

PROVIDER: S-EPMC4353579 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Inhibition-induced forgetting: when more control leads to less memory.

Chiu Yu-Chin YC Egner Tobias T

Psychological science 20141114 1

The ability to inhibit prepotent responses is a core executive function, but the relation of response inhibition to other cognitive operations is poorly understood. In the study reported here, we examined inhibitory control through the lens of incidental memory. Participants categorized face stimuli by gender in a go/no-go task (Experiments 1 and 2) or a stop-signal task (Experiment 3) and, after a short delay, performed a surprise recognition memory task for those faces. Memory was impaired for ...[more]

PMID: 25398560

Similar Datasets

High working memory capacity predicts less retrieval induced forgetting.

Project description:BackgroundWorking Memory Capacity (WMC) is thought to be related to executive control and focused memory search abilities. These two hypotheses make contrasting predictions regarding the effects of retrieval on forgetting. Executive control during memory retrieval is believed to lead to retrieval induced forgetting (RIFO) because inhibition of competing memory traces during retrieval renders them temporarily less accessible. According to this suggestion, superior executive control should increase RIFO. Alternatively, superior focused search abilities could diminish RIFO, because delimiting the search set reduces the amount of competition between traces and thus the need for inhibition. Some evidence suggests that high WMC is related to more RIFO, which is inconsistent with the focused search hypothesis.Methodology/principal findingsUsing the RIFO paradigm, we created distinct and overlapping categories to manipulate the amount of competition between them. This overlap increased competition between some categories while exclusive use of weak exemplars ensured negligible effects of output interference and integration. Low WMC individuals exhibited RIFO within and between overlapping categories, indicating the effect of resolving competition during retrieval. High WMC individuals only exhibited between-category RIFO, suggesting they experienced reduced competition resolution demands. Low WMC Individuals exhibited the strongest RIFO and no retrieval benefits when interference resolution demands were high.Conclusions/significanceOur findings qualify the inhibitory explanation for RIFO by incorporating the focused search hypothesis for materials that are likely to pose extraordinary challenges at retrieval. The results highlight the importance of considering individual differences in retrieval-induced effects and qualify existing models of these effects.

| S-EPMC3543406 | biostudies-literature

Competition between items in working memory leads to forgetting.

Project description:Switching attention from one thought to the next propels our mental lives forward. However, it is unclear how this thought-juggling affects our ability to remember these thoughts. Here we show that competition between the neural representations of pictures in working memory can impair subsequent recognition of those pictures. We use pattern classifiers to decode functional magnetic resonance imaging (fMRI) data from a retro-cueing task where participants juggle two pictures in working memory. Trial-by-trial fluctuations in neural dynamics are predictive of performance on a surprise recognition memory test: trials that elicit similar levels of classifier evidence for both pictures (indicating close competition) are associated with worse memory performance than trials where participants switch decisively from thinking about one picture to the other. This result is consistent with the non-monotonic plasticity hypothesis, which predicts that close competition can trigger weakening of memories that lose the competition, leading to subsequent forgetting.

| S-EPMC4284654 | biostudies-other

EphB2 mediates social isolation-induced memory forgetting.

Project description:Social isolation in adolescence leads to lasting deficits, including emotional and cognitive dysregulation. It remains unclear, however, how social isolation affects certain processes of memory and what molecular mechanisms are involved. In this study, we found that social isolation during the post-weaning period resulted in forgetting of the long-term fear memory, which was attributable to the downregulation of synaptic function in the hippocampal CA1 region mediated by EphB2, a receptor tyrosine kinase which involves in the glutamate receptor multiprotein complex. Viral-mediated EphB2 knockdown in CA1 mimicked the memory defects in group-housed mice, whereas restoration of EphB2 by either viral overexpression or resocialization reversed the memory decline in isolated mice. Taken together, our finding indicates that social isolation gives rise to memory forgetting by disrupting EphB2-mediated synaptic plasticity, which may provide a potential target for preventing memory loss caused by social isolation or loneliness.

| S-EPMC7653962 | biostudies-literature

More attention with less working memory: The active inhibition of attended but outdated information.

Project description:Attention has traditionally been regarded as a gateway to working memory, and almost all theoretical frameworks of attention and working memory assume that individuals always have a better memory for information that has received more attention. Here, we provide a series of counterintuitive demonstrations that show that paying more attention to a piece of information impedes, rather than enhances, the selection of this information into working memory. Experiments 1 to 5 provide converging evidence for an even weaker working memory trace of fully attended but outdated features, compared with baseline irrelevant features that were completely ignored. This indicates that the brain actively inhibits attended but outdated information to prevent it from entering working memory. Experiment 6 demonstrates that this inhibition processing is subject to executive control. These findings lead to a substantial reinterpretation of the relationship between attention and working memory.

| S-EPMC8604409 | biostudies-literature

On the role of inhibition in suppression-induced forgetting.

Project description:Suppressing retrieval of unwanted memories can cause forgetting, an outcome often attributed to the recruitment of inhibitory control. This suppression-induced forgetting (SIF) generalizes to different cues used to test the suppressed content (cue-independence), a property taken as consistent with inhibition. But does cue-independent forgetting necessarily imply that a memory has been inhibited? Tomlinson et al. (Proc Natl Acad Sci 106:15588-15593, 2009) reported a surprising finding that pressing a button also led to cue-independent forgetting, which was taken as support for an alternative interference account. Here we investigated the role of inhibition in forgetting due to retrieval suppression and pressing buttons. We modified Tomlinson et al.'s procedure to examine an unusual feature they introduced that may have caused memory inhibition effects in their experiment: the omission of explicit task-cues. When tasks were uncued, we replicated the button-press forgetting effect; but when cued, pressing buttons caused no forgetting. Moreover, button-press forgetting partially reflects output-interference effects at test and not a lasting effect of interference. In contrast, SIF occurred regardless of these procedural changes. Collectively, these findings indicate that simply pressing a button does not induce forgetting, on its own, without confounding factors that introduce inhibition into the task and that inhibition likely underlies SIF.

| S-EPMC10015003 | biostudies-literature

Are stronger memories forgotten more slowly? No evidence that memory strength influences the rate of forgetting.

Project description:Information stored in visual short-term memory is used ubiquitously in daily life; however, it is forgotten rapidly within seconds. When more items are to be remembered, they are forgotten faster, potentially suggesting that stronger memories are forgotten less rapidly. Here we tested this prediction with three experiments that assessed the influence of memory strength on the rate of forgetting of visual information without manipulating the number of items. Forgetting rate was assessed by comparing the accuracy of reports in a delayed-estimation task following relatively short and long retention intervals. In the first experiment, we compared the forgetting rate of items that were directly fixated, to items that were not. In Experiments 2 and 3 we manipulated memory strength by extending the exposure time of one item in the memory array. As expected, direct fixation and longer exposure led to better accuracy of reports, reflecting stronger memory. However, in all three experiments, we did not find evidence that increased memory strength moderated the forgetting rate.

| S-EPMC6044536 | biostudies-literature

Inhibition of Rac1-dependent forgetting alleviates memory deficits in animal models of Alzheimer's disease.

Project description:Accelerated forgetting has been identified as a feature of Alzheimer's disease (AD), but the therapeutic efficacy of the manipulation of biological mechanisms of forgetting has not been assessed in AD animal models. Ras-related C3 botulinum toxin substrate 1 (Rac1), a small GTPase, has been shown to regulate active forgetting in Drosophila and mice. Here, we showed that Rac1 activity is aberrantly elevated in the hippocampal tissues of AD patients and AD animal models. Moreover, amyloid-beta 42 could induce Rac1 activation in cultured cells. The elevation of Rac1 activity not only accelerated 6-hour spatial memory decay in 3-month-old APP/PS1 mice, but also significantly contributed to severe memory loss in aged APP/PS1 mice. A similar age-dependent Rac1 activity-based memory loss was also observed in an AD fly model. Moreover, inhibition of Rac1 activity could ameliorate cognitive defects and synaptic plasticity in AD animal models. Finally, two novel compounds, identified through behavioral screening of a randomly selected pool of brain permeable small molecules for their positive effect in rescuing memory loss in both fly and mouse models, were found to be capable of inhibiting Rac1 activity. Thus, multiple lines of evidence corroborate in supporting the idea that inhibition of Rac1 activity is effective for treating AD-related memory loss.

| S-EPMC6776562 | biostudies-literature

Forgetting emotional material in working memory.

Project description:Proactive interference (PI) is the tendency for information learned earlier to interfere with more recently learned information. In the present study, we induced PI by presenting items from the same category over several trials. This results in a build-up of PI and reduces the discriminability of the items in each subsequent trial. We introduced emotional (e.g. disgust) and neutral (e.g. furniture) categories and examined how increasing levels of PI affected performance for both stimulus types. Participants were scanned using functional magnetic resonance imaging (fMRI) performing a 5-item probe recognition task. We modeled responses and corresponding response times with a hierarchical diffusion model. Results showed that PI effects on latent processes (i.e. reduced drift rate) were similar for both stimulus types, but the effect of PI on drift rate was less pronounced PI for emotional compared to neutral stimuli. The decline in the drift rate was accompanied by an increase in neural activation in parahippocampal regions and this relationship was more strongly observed for neutral stimuli compared to emotional stimuli.

| S-EPMC5836275 | biostudies-literature

Less imageable words lead to more looks to blank locations during memory retrieval.

Project description:People revisit spatial locations of visually encoded information when they are asked to retrieve that information, even when the visual image is no longer present. Such "looking at nothing" during retrieval is likely modulated by memory load (i.e., mental effort to maintain and reconstruct information) and the strength of mental representations. We investigated whether words that are more difficult to remember also lead to more looks to relevant, blank locations. Participants were presented four nouns on a two by two grid. A number of lexico-semantic variables were controlled to form high-difficulty and low-difficulty noun sets. Results reveal more frequent looks to blank locations during retrieval of high-difficulty nouns compared to low-difficulty ones. Mixed-effects modelling demonstrates that imagery-related semantic factors (imageability and concreteness) predict looking at nothing during retrieval. Results provide the first direct evidence that looking at nothing is modulated by word difficulty and in particular, word imageability. Overall, the research provides substantial support to the integrated memory account for linguistic stimuli and looking at nothing as a form of mental imagery.

| S-EPMC7109172 | biostudies-literature

Sleep-dependent memory consolidation and accelerated forgetting.

Project description:Accelerated long-term forgetting (ALF) is a form of memory impairment in which learning and initial retention of information appear normal but subsequent forgetting is excessively rapid. ALF is most commonly associated with epilepsy and, in particular, a form of late-onset epilepsy called transient epileptic amnesia (TEA). ALF provides a novel opportunity to investigate post-encoding memory processes, such as consolidation. Sleep is implicated in the consolidation of memory in healthy people and a deficit in sleep-dependent memory consolidation has been proposed as an explanation for ALF. If this proposal were correct, then sleep would not benefit memory retention in people with ALF as much as in healthy people, and ALF might only be apparent when the retention interval contains sleep. To test this theory, we compared performance on a sleep-sensitive memory task over a night of sleep and a day of wakefulness. We found, contrary to the hypothesis, that sleep benefits memory retention in TEA patients with ALF and that this benefit is no smaller in magnitude than that seen in healthy controls. Indeed, the patients performed significantly more poorly than the controls only in the wake condition and not the sleep condition. Patients were matched to controls on learning rate, initial retention, and the effect of time of day on cognitive performance. These results indicate that ALF is not caused by a disruption of sleep-dependent memory consolidation. Instead, ALF may be due to an encoding abnormality that goes undetected on behavioural assessments of learning, or by a deficit in memory consolidation processes that are not sleep-dependent.

| S-EPMC4007033 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data