Emotion regulation ( ).
VLPFC | 44, 45, 47 | Left VLPFC supports mnemonic control (i.e., task switching, WM and semantic retrieval), and supports access to stored conceptual representations ( ). | Emotion regulation ( ). |
| | Left VLPFC is involved in elaborative (semantic/phonological) encoding of information into episodic memory, the specification of retrieval cues and the maintenance of LTM retrieval ( ; ). Right VLPFC supports memory encoding and retrieval of visuospatial stimuli, action imitation and motor inhibition ( ). | Inhibition of distracting emotions (right VLPFC for inhibition of negative emotions) ( ). |
mPFC | 25, 32 | Learning, memory, and decision-making ( ; ). | Dorsal-caudal mPFC involved in appraisal-expression of negative emotion; ventral-rostral PFC generates emotional regulation-responses ( ). |
OFC | 11, 12, 14 | Decision making ( ). | Emotional processing and responses ( ), social and emotional judgment ( ), facilitation of regret ( ). |
| | | Reward processing and reinforcement learning ( ). |
Effects Deriving From Different Modalities of Emotional Stimuli on Learning and Memory
As discussed above, evidence indicates the neural mechanisms underlying the emotional processing of valence and arousal involve the amygdala and PFC, where the amygdala responds to emotionally arousing stimuli and the PFC responds to the emotional valence of non-arousing stimuli. We have thus far primarily discussed studies examining neural mechanisms underlying the processing of emotional images. However, recent neuroimaging studies have investigated a wider range of visual emotional stimuli. These include words ( Sharot et al., 2004 ), pictures ( Dolcos et al., 2005 ; Weymar et al., 2011 ), film clips ( Cahill et al., 1996 ), and faces ( González-Roldan et al., 2011 ), to investigate neural correlates of emotional processing and the impact of emotion on subsequent memory. These studies provided useful supplemental information for future research on emotional effects of educational multimedia content (combination of words and pictures), an increasingly widespread channel for teaching and learning.
An event-related fMRI study examined the neural correlates of responses to emotional pictures and words in which both were manipulated in terms of positive and negative valence, and where neutral emotional content served as a baseline (“conditioned stimuli”/no activating emotion with valence rating of 5 that spans between 1/negative valence-9/positive valence), even though all stimuli were consistent in terms of arousal levels ( Kensinger and Schacter, 2006 ). Subjects were instructed to rate each stimulus as animate or inanimate and common or uncommon . The results revealed the activation of the amygdala in response to positive and negative valence (valence-independent) for pictures and words. A lateralization effect was observed in the amygdala when processing different emotional stimuli types. The left amygdala responded to words while either the right and/or bilateral amygdala activation regions responded to pictures. In addition, participants were more sensitive to emotional pictures than to emotional words. The mPFC responded more rigorously during the processing of positive than to that of negative stimuli, while the VLPFC responded more to negative stimuli. The researchers concluded that arousal-related responses occur in the amygdala, dmPFC, vmPFC, anterior temporal lobe and temporo-occipital junction, whereas valence-dependent responses were associated with the lateral PFC for negative stimuli and the mPFC for positive stimuli. The lateralization of the amygdala’s activation was consistent with that in other studies that also showed left-lateralized amygdala responses for words ( Hamann and Mao, 2002 ) vs. right-lateralized amygdala responses for images ( Pegna et al., 2005 ). However, a wide range of studies suggest that lateralization likely differs with sex ( Hamann, 2005 ), individual personality ( Hamann and Canli, 2004 ), mood ( Rusting, 1998 ), age ( Allard and Kensinger, 2014 ), sleep ( Walker, 2009 ), subject’s awareness of stimuli ( Morris et al., 1998 ), stress ( Payne et al., 2007 ) and other variables. Hence, these factors should be considered in future studies.
Event-related potentials (ERPs) were used to investigate the modality effects deriving from emotional words and facial expressions as stimuli in healthy, native German speakers ( Schacht and Sommer, 2009a ). German verbs or pseudo-words associated with positive, negative or neutral emotions were used, in addition to happy vs. angry faces, as well as neutral and slightly distorted faces. The results revealed that negative posterior ERPs were evoked in the temporo-parieto-occipital regions, while enhanced positive ERPs were evoked in the fronto-central regions (positive verbs and happy faces) when compared with neutral and negative stimuli. These findings were in agreement with the previous findings ( Schupp et al., 2003 ; Schacht and Sommer, 2009b ). While the same neuronal mechanisms appear to be involved in response to both emotional stimuli types, latency differences were also reported with faster responses to facial stimuli than to words, likely owing to more direct access to neural circuits-approximately 130 ms for happy faces compared to 380 ms for positive verbs ( Schacht and Sommer, 2009a ). Moreover, augmented responses observed in the later positive complex (LPP), i.e., larger late positive waves in response to emotional verbs (both positive and negative) and angry faces, all associated with the increased motivational significance of emotional stimuli ( Schupp et al., 2000 ) and increased selective attention to pictures ( Kok, 2000 ).
Khairudin et al. (2011) investigated effects of emotional content on explicit memory with two standardized stimuli: emotional words from the Affective Norms for English Words (ANEW) and emotional pictures from the IAPS. All stimuli were categorized as positive, negative or neutral, and displayed in two different trials. Results revealed that better memory for emotional images than for emotional words. Moreover, a recognition test demonstrated that positive emotional content was remembered better than negative emotional content. Researchers concluded that emotional valence significantly impacts memory and that negative valence suppressed the explicit memory. Another study by Khairudin et al. (2012) investigated the effects of emotional content on explicit verbal memory by assessing recall and recognition for emotionally positive, negative and neutral words. The results revealed that emotion substantially influences memory performance and that both positive and negative words were remembered more effectively than neutral words. Moreover, emotional words were remembered better in recognition vs. recall test.
Another group studied the impacts of emotion on memory using emotional film clips that varied in emotion with neutral, positive, negative and arousing contents ( Anderson and Shimamura, 2005 ). A subjective experiment for word recall and context recognition revealed that memory, for words associated with emotionally negative film clips, was lower than emotionally neutral, positive and arousing films. Moreover, emotionally arousing film clips were associated with enhanced context recognition memory but not during a free word recall test. Therefore, clarifying whether emotional stimuli enhance recognition memory or recall memory requires further investigation, as it appears that emotional information was better remembered for recognition compared to recall. In brief, greater attentional resource toward emotional pictures with large late positive waves of LPP in the posterior region, the amygdala responds to emotional stimuli (both words and pictures) independent on its valence, leading to enhanced memory. Table Table2 2 summarizes studies on the brain regions that respond to standardized stimuli as cited above, and also for pictures of emotional facial expression or Pictures of Facial Affect (POFA), Affective Norms for English Words (ANEW) for emotional words, as well as for the International Affective Digitized Sound System (IDAS) for emotional sounds.
Comparison of different emotional stimulus categories.
Study | Stimulus types | Emotion categories | Investigation | Brain imaging modality | Brain regions of interest | Findings | Subjects | Status | Age |
---|
| Pictures (IAPS) and words (ANEW) | Positive, negative, and neutral | Brain responses to emotionally positive, negative, and arousing words | Event-related fMRI | Amygdala, PFC, anterior temporal lobe, and temporooccipital junction | ∙ Amygdala, dmPFC, and vmPFC responded equally to both pictures and words regardless of valence. ∙ mPFC was more activated for positive content. ∙ VLPFC was more activated for negative content. ∙ Greater sensitivity for emotional pictures than words. | 21 adults (10 Female, 11 Male) | Healthy | 18–35 years |
| Words (ANEW) | High-arousal positive, high-arousal negative, and neutral | Brain responses to positive and negative emotionally arousing words | Event-related fMRI | Amygdala, vmPFC | ∙ Left amygdala activated for both positive and negative words. ∙ No activation observed in the vmPFC in response to positive or negative words. | 14 adults (All) | Healthy | 20–31 years |
| Faces | Positive, negative, and neutral | Responses to emotional face expression without primary visual areas | Event-related fMRI | Amygdala | ∙ Right amygdala activated for all emotional faces (anger, happiness, and fear). | 1 Male | Blind sight patient | 52 years |
| Pictures (IAPS) | Negative and neutral | Amygdala response to emotional experience during study and LTM | Event-related fMRI | Amygdala | ∙ Left amygdala activation during encoding was a predictor of subsequent recognition memory for pictures with high emotional intensity ratings. | 10 Female | Healthy | – |
| Film clips | Aggressive, sad, and neutral | Responses of EEG frequency bands on the emotional film content | EEG | Occipital (Posterior), central and frontal (anterior) | ∙ EEG theta (4–6 Hz) was more synchronized in occipital and frontal regions for the aggressive films compared with neutral films. ∙ EEG theta (4–6 Hz) respond specifically to visual emotional stimulus. ∙ EEG alpha is associated with attention and habituation. | 18 adults (All Female) | Healthy | 20–33 years |
| Pictures (IAPS) | Pleasant, neutral, and unpleasant | Brain responses to emotional pictures | ERP | Midline (Fz, Cz, and Pz) | ∙ More positivity for pleasant and unpleasant pictures than neutral pictures in the posterior regions. ∙ An indication of selective emotional processing (resulted from the motivational relevance of emotional pictures compared to neutral ones). | 14 Female | – | 18–24 years |
| Words (Spanish nouns)
Pictures (IAPS) | Negative, positive, neutral, and relaxing | Processing of emotional information in words and pictures | ERP | Frontal and parieto-occipital
Centro-parietal and frontal regions | ∙ Both emotional words and pictures were associated with an early posterior negativity and LPC. ∙ Emotional pictures elicited greater amplitude of early posterior negativity after stimulus presentation at the frontal and parieto-occipital regions. ∙ Positive pictures were associated with enhanced early posterior negativity amplitude in the right parieto-occipital regions. ∙ An arousal-dependent effect was observed in the left parieto-occipital regions for both positive and negative stimuli. | 21 volunteers (19 Female, 2 Male) 28 volunteers (21 Female, 7 Male) | Healthy Healthy | 19–27 years 19–29 years |
| Facial expression (POFA) | Fearful vs. neutral | Spatial attention effects on emotional face processing. | ERP | Frontal, central and posterior regions | Faces enhanced N170 amplitude reflecting that spatial attention modulates face encoding at lateral posterior electrodes. However, N170 was insensitive to emotional expression. | 20 subjects (11 Female, 7 Male, 2 excluded due to excess artifacts) | Healthy | 18–32 years |
| Sentence | Negative/high arousal and Neutral/ low arousal | Impact of emotional verb processing in short sentences (Reading) | ERP | Centro-parietal regions | Effect on LPC of negative and high-arousal words, while LPC was not affected by arousal-related words alone. Reported the importance of valence and arousal in emotion-related ERP effects. | 21 participants (11 Female, 10 Male) | Healthy | – |
| Sound (IADS) | Pleasant, unpleasant, and neutral | Auditory cortex response to emotional stimuli | fNIRS | Auditory cortex | Both pleasant and unpleasant sounds led to greater activation in the left and right auditory cortex compared with neutral sound. | 17 participants (10 Female, 7 Male) | Healthy | – |
Neuroimaging Techniques for the Investigation of Emotional-Cognitive Interactions
The brain regions associated with cognitive-emotional interactions can be studied with different functional neuroimaging techniques (fMRI, PET, and fNIRS) to examine hemodynamic responses (indirect measurement). EEG is used to measure brain electrical dynamics (direct measurement) associated with responses to cognitive and emotional tasks. Each technique has particular strengths and weaknesses, as described below.
Functional Magnetic Resonance Imaging (fMRI)
Functional magnetic resonance imaging is a widely used functional neuroimaging tool for mapping of brain activation as it provides a high spatial resolution (a few millimeters). fMRI is an indirect measure of hemodynamic response by measuring changes in local ratios of oxy-hemoglobin vs. deoxy-hemoglobin, typically known as a blood oxygenation level dependent (BOLD) signal ( Cabeza and Nyberg, 2000 ). Dolcos et al. (2005) examined the effects of emotional content on memory enhancement during retrieval process using event-related fMRI to measure retrieval-related activity after a retention interval of 1 year. The researchers concluded that successful retrieval of emotional pictures involved greater activation of the amygdala as well as the entorhinal cortex and hippocampus than that of neutral pictures. Both the amygdala and hippocampus were rigorously activated during recollection compared to familiarity recognition, whereas no differences were found in the entorhinal cortex for either recollection or familiarity recognition. Moreover, a study investigates motivation effect (low vs. high monetary reward) on episodic retrieval by manipulating task difficulty, fMRI data reports that increased activation in the substantia nigra/VTA, MTL, dmPFC, and DLPFC when successful memory retrieval with high difficulty than with low difficulty. Moreover, reward-related of functional connectivities between the (i) SN/VTA–MTL and (ii) SN/VTA–dmPFC appear to increases significantly with increases retrieval accuracy and subjective motivation. Thus, Shigemune et al. (2017) suggest that reward/motivation-related memory enhancement modulated by networking between the SN/VTA (reward-related), dmPFC (motivation-related) and MTL (memory-related) network as well as DLPFC (cognitive controls) with high task difficulty.
Taken together, these findings indicate that the amygdala and MTL have important roles in the recollection of emotional and motivational memory. Another fMRI study reported that greater success for emotional retrieval (emotional hits > misses ) was associated with neural activation of the bilateral amygdala, hippocampus, and parahippocampus, whereas a higher success rate for neutral retrieval is associated with a greater activity in right posterior parahippocampus regions ( Shafer and Dolcos, 2014 ). Hence, fMRI has clearly revealed interactions between cognitive and emotional neural networks during information processing, particularly in response to emotion-related content. Such interactions appear to modulate memory consolidation while also mediating encoding and retrieval processes that underlie successful LTM formation and memory recall. More specifically, it appears that amygdala activation modulates both the hippocampus and visual cortex during visual perception and enhances the selection and organization of salient information via the “bottom-up” approach to higher cognitive functions directed at awareness. Although fMRI is widely used, it poses several limitations such as poor temporal resolution, expensive setup costs, plus the difficulty of having a subject hold still during the procedure in an electromagnetically shielded room (immobility). Furthermore, fMRI is slightly more metabolically sluggish, as BOLD signal exhibits an initial dip, where the increase of subsequent signal is delayed by 2–3 s and it takes approximately 6–12 s to reach to a peak value that reflects the neural responses elicited by a stimulus ( Logothetis et al., 2001 ). This means that fMRI having a coarse temporal resolution (several seconds) when compared with electrophysiological techniques (a few milliseconds) and also not a great technique for visualizing subcortical regions (mesencephalon and brainstem) due to metabolically sluggish compared to PET.
Positron Emission Tomography (PET)
Positron emission tomography is another functional neuroimaging tool that maps CNS physiology and neural activation by measuring glucose metabolism or regional cerebral blood flow (rCBF). PET uses positron-emitting radionuclides such as 18 F-fluorodeoxyglucose (FDG) and positron-emitting-oxygen isotope tagged with water ([ 15 O] H 2 O), etc. This technique identifies different neural networks involving pleasant, unpleasant and neutral emotions ( Lane et al., 1997 ). It thus far appears that increased rCBF in the mPFC, thalamus, hypothalamus, and midbrain associated with pleasant and unpleasant emotional processing, while unpleasant emotions are more specifically associated with the bilateral OTC, cerebellum, left parahippocampal gyrus, hippocampus, and amygdala; moreover, the caudate nucleus is associated with pleasant emotions.
Using PET scanning demonstrated that emotional information enhances visual memory recognition via interactions between perception and memory systems, specifically with greater activation of the lingual gyrus for visual stimuli ( Taylor et al., 1998 ). The results also showed that strong negative emotional valence appeared to enhance the processing of early sensory input. Moreover, differences in neural activation appeared in the left amygdaloid complex (AC) during encoding, while the right PFC and mPFC responded during recognition memory. Similarly, Tataranni et al. (1999) identified CNS regions associated with appetitive states (hunger and satiation) ( Tataranni et al., 1999 ). Hunger stimulated increased rCBF uptake in multiple regions including the hypothalamus, insular cortex, limbic and paralimbic regions (anterior cingulate cortex, parahippocampal and hippocampal formation, the anterior temporal and posterior orbitofrontal cortex), as well as the thalamus, caudate, precuneus, putamen, and cerebellum. Satiation was associated with increased rCBF uptake in the bilateral vmPFC, the DLPFC, and the inferior parietal lobule. These results imply that (i) subcortical regions associated with emotion/motivation involved in hunger that signals distressing feeling (discomfort, pain and anxiety) for the regulation of food intake; and (ii) the PFC associated with inhibition of inappropriate behavioral response involved in satiation that signals excessive food consumption for a termination of meal.
In a study of emotional self-generation using PET noted that the insular cortex, secondary somatosensory cortex, and hypothalamus, as well as the cingulate cortex and nuclei in the brainstem’s tegmentum, including PAG, parabrachial nucleus, and substantia nigra maintained current homeostasis by generating regulatory signals ( Damasio et al., 2000 ). PET scanning has also been used for neuroanatomical mapping of emotions ( Davidson and Irwin, 1999 ), emotional processing ( Choudhary et al., 2015 ), and cognitive functions ( Cabeza and Nyberg, 2000 ). Although PET scanning has a relatively good spatial resolution for both the brain and bodily functions, it is costly and yields lower temporal resolution than does EEG and is invasive as opposed to fMRI. Moreover, PET tends to show better activation of more ancient brain regions in the mesencephalon and brainstem when compared to fMRI. Hence, it is generally reserved for the clinical diagnoses of cancers, neurological diseases processes (e.g., epilepsy and Alzheimer’s disease), and heart diseases.
Electroencephalography (EEG)
Electroencephalography obtains high temporal resolution in milliseconds, portable, less expensive, and non-invasive techniques by attaching scalp electrodes to record brain electrical activity. Moreover, numerous studies reported that EEG is useful in mapping CNS cognitive and emotional processing. The technique offers a comprehensive range of feature extraction and analysis methods, including power spectral analysis, EEG coherence, phase delay, and cross-power analysis. One study examined changes in EEG oscillations in the amygdala during the consolidation of emotionally aroused memory processing that exhibited theta (4–8 Hz) activity ( Paré et al., 2002 ), indicating the facilitation of memory consolidation, improved retention of emotional content, and enhanced memory recall. This finding was later supported by the revelation of increased theta activity in the right frontal ( Friese et al., 2013 ) and right temporal cortices ( Sederberg et al., 2003 ) and consequently associated with the successful encoding of new information. Another study ( Buzsáki, 2002 ) revealed that theta oscillations were positively related to the activation of the hippocampus represent the active brain state during sensory, motor and memory-related processing. The theta waves are generated through an interaction between the entorhinal cortex, the Schaffer collateral (CA3 region) and the pyramidal cell dendrites (both CA3 and CA1 regions) that result in a synaptic modification underlie learning and memory. Thus, theta oscillation is thought to be associated with the encoding of new memories.
Increased gamma oscillation in the neocortex and right amygdala have been reported in response to emotionally arousing pictures during learning and memory tasks undertaken by 148 right-handed female participants ( Headley and Paré, 2013 ). A more detailed study by Müller et al. (1999) reported increased gamma potentials in the left frontal and temporal regions in response to images having a negative valence, whereas increased gamma-bands in the right frontal regions were observed in responses to images with positive valence for 11 right-handed male participants. During an emotionally positive experience, another study reported significantly increased EEG theta-alpha coherence between prefrontal and posterior parietal regions ( Aftanas and Golocheikine, 2001 ). They concluded the change was associated with heightened attention in association with improved performance in memory and emotional processing. Thus, we have a number of EEG investigations of left and right hemispheric activity while processing positive (pleasant) and negative (unpleasant) stimuli that revealed differences in regional electrophysiological activation. Nonetheless, EEG exhibits a relatively poor spatial resolution approximately 5 to 9 cm compared with fMRI and PET ( Babiloni et al., 2001 ). Thus, scalp EEG unable to measure activation much below cortex owing to the distortion of scalp potentials where different volume conduction effects of the cortex, dura mater, skull, and scalp resulting in imprecise localization of the electromagnetic field patterns associated with neural current flow. Subsequent studies have demonstrated that the EEG spatial resolution can be improved using high-resolution EEG (high-density electrode arrays to increase spatial sampling) with surface Laplacian estimation and cortical imaging (details discussion of this area is beyond the scope of this review, see ( Nunez et al., 1994 ) for theoretical and experimental study) or integrating multiple imaging modalities that provide complement information, for instance EEG-fMRI and EEG-fNIRS ( Dale and Halgren, 2001 ).
Functional Near-Infrared Spectroscopy (fNIRS)
Functional near-infrared spectroscopy is an emerging and relatively low-cost imaging technique that is also portable and non-invasive. It can be used to map the hemodynamic responses associated with brain activation. This technology measures cerebral changes in the concentration of oxygenated hemoglobin (oxy-Hb) vs. deoxygenated hemoglobin (deoxy-Hb) using optodes (light emitters and detectors) placed on the scalp ( Villringer et al., 1993 ). It is limited to visualizations of cortical activity compared to the subcortical regions, and findings only imply increased brain activity associated with increased glucose and oxygen consumption. Elevations in cerebral blood flow and oxygen delivery exceed quo oxygen consumption, thereby enabling changes in local cerebral blood oxygenation to be measured by optic penetration.
The number of studies that have implemented this investigative technique are associated with task performance ( Villringer et al., 1993 ), including exercise ( Perrey, 2008 ), cognitive workload ( Durantin et al., 2014 ), psychiatric disorders ( Ehlis et al., 2014 ), emotional processing ( Bendall et al., 2016 ), and aging ( Hock et al., 1995 ). One study used fNIRS to examine the relationship between subjective happiness and emotional changes ( Oonishi et al., 2014 ). The results revealed that the level of subjective happiness influenced the pattern of left-right PFC activation during the emotion-related task, showing increased oxy-Hb in the left PFC when viewing pleasant pictures, and increased oxy-Hb in the right PFC when viewing unpleasant pictures. Viewing unpleasant emotional stimuli accompanied increased in oxy-Hb levels in the bilateral VLPFC while also activating several regions in both the right VLPFC (BA45/47) and left VLPFC (BA10/45/46/47). However, another fNIRS study reported that viewing pleasant emotional stimuli was associated with decreased oxy-Hb in the left DLPFC (BA46/10) when affective images were presented for 6 s ( Hoshi et al., 2011 ). Thus, this study found an opposite pattern indicating left hemisphere involvement in positive/approach processing and right hemisphere involvement in negative/withdrawal processing ( Davidson, 1992 ; Davidson and Irwin, 1999 ). This inconsistent finding of frontal hemispheric asymmetric might result from the comparison of state-related changes rather than baseline levels of asymmetric. Thus, several issues should take into consideration: (i) methodological issues to assess hemispheric asymmetry, including requires repeat measures of anterior asymmetry for at least two sessions, stimulus content should comprise both positive valence and negative valence while maintaining at a similar level of arousal and with a baseline resting condition, appropriate selection of reference electrode and individual differences, etc; and (ii) conceptual issues is related to the fact that prefrontal cortex is an anatomically and functionally heterogeneous and complex region interacts with other cortical and subcortical structures during emotional processing ( Davidson, 2004 ). Another fNIRS study examined the relationship between PFC function and cognitive control of emotion ( Ozawa et al., 2014 ). This was done by presenting emotional IAPS pictures for 5.2 s, followed by the n -back task. The results revealed a significantly greater increase in oxy-HB in the mPFC and left superior frontal gyrus in response to negative pictures compared with neutral pictures. Meanwhile, no significant hemodynamic changes were observed during image presentation and the n -back task, indicating the need for further investigation.
Factors Affecting the Effect of Emotion on Learning and Memory
The preceding section described neuroimaging techniques used to examine brain responses to emotional stimuli during WM processing leading to LTM. This section presents six key factors that are recommended for consideration in the experimental design and appropriate protocol.
Individual Differences
A number of studies have reported numerous influences in addition to a range of individual differences in emotional processing. These include personality traits ( Montag and Panksepp, 2017 ), intellectual ability ( Brackett et al., 2004 ), and sex ( Cahill, 2003 ). Moreover, sex hormones and personality traits (e.g., extraversion and neuroticism) appear to influence individual responses to emotional stimuli as well as modulate emotional processing. Appropriate screening with psychological testing as well as balancing experimental cohorts in terms of sex can help reduce spurious results owing to individual differences.
Age-Related Differences
Studies have also shown that older adults are associated with the greater familiarity with psychological stress and emotional experiences, thus causing positivity biases in emotional processing and better emotional control than in younger adults ( Urry and Gross, 2010 ; Allard and Kensinger, 2014 ). Consequently, the age of participants in a sample population should be considered for both cognitive and emotional studies.
Emotional Stimulus Selection
The selection of emotional stimuli for experimental studies is generally divided into two streams: (1) discrete emotional, and (2) dimensional emotions of valence, arousal, dominance and familiarity ( Russell, 1980 ; Barrett, 1998 ). The latter include pictures from the IAPS database and words from the ANEW database, which are both available for non-commercial research. Appropriate selection of emotional stimuli is another important consideration that ensures experimental tasks are suitable for the investigation of emotional processing in learning and memory. Furthermore, the type of stimulus determines stimulus presentation duration, especially for experimental tasks involving the induction of emotions.
Self-assessment Techniques
There are numerous self-assessment techniques used to measure individual emotional states ( Bradley and Lang, 1994 ). The most widely used techniques are the Self-Assessment Manikin (SAM), the Semantic Differential (SD) scale, and the Likert scale. The SAM is a non-verbal pictorial assessment technique directly measures emotional responses to emotional stimuli for valence, arousal, and dominance. The SD scale consists of a set of bipolar adjective pairs for the subjective rating of image stimuli. The Likert’s “ x -point” scale allows participants to rate their own emotional responses. If a study does not seek to assess distinct emotional states but rather involves the assessment of two primary dimensions of emotion (positive and negative valence), then the Positive and Negative Affect Schedule (PANAS) is a recommended method ( Watson et al., 1988 ). Thus, selection of the most appropriate self-assessment technique is an important part of the experimental design but can also become an overwhelming task.
Selection of Brain Imaging Techniques
As mentioned above, the two major types of brain imaging techniques EEG (direct) and fMRI/PET/fNIRS (indirect) have respective advantages and disadvantages. To overcome these limitations, simultaneous or combined dual-modality imaging (EEG-fMRI or EEG-fNIRS) can now be implemented for complementary data collection. Although functional neuroimaging works to identify the neural correlates of emotional states, technologies such as deep brain stimulation (DBS) and connectivity maps might provide new opportunities to seek understanding of emotions and its corresponding psychological responses.
Neurocognitive Research Design
The neuroscience of cognition and emotion requires appropriate task designs to accomplish specific study objectives ( Amin and Malik, 2013 ). Environmental factors, ethical issues, memory paradigms, cognitive task difficulty, and emotional induction task intensity must be considered for this.
Numerous neuroimaging studies cited thus far have indicated that emotions influence memory processes, to include memory encoding, memory consolidation, and memory retrieval. Emotional attentional and motivational components might explain why emotional content exhibits privileged information processing. Emotion has a “pop-out” effect that increases attention and promotes bottom-up instinctual impact that enhances awareness. Significant emotional modulation affects memory consolidation in the amygdala, and emotional content also appears to mediate memory encoding and retrieval in the PFC, leading to slow rates of memory lapse accompanied by the accurate recall. Moreover, cognitive and emotional interactions also appear to modulate additional memory-related CNS regions, such as the frontal, posterior parietal and visual cortices. The latter are involved in attentional control, association information, and the processing of visual information, respectively. Therefore, higher-level cognitive functions such as learning and memory, appear to be generally guided by emotion, as outlined in the Panksepp’s framework of brain processing ( Panksepp, 1998 ).
Neuroimaging findings also indicate the involvement of the PFC in emotional processing by indirectly influencing WM and semantic memory ( Kensinger and Corkin, 2003 ). This is reflected by the involvement of the DLPFC in WM and the role played by VLPFC in semantic processing, both of which have been found to enhance or impair semantic encoding task performance when emotion is involved. Various parts of the lateral PFC (ventrolateral, dorsolateral and medial prefrontal cortical regions) are suspected of having key roles that support memory retrieval ( Simons and Spiers, 2003 ). All of these findings suggest that PFC-MTL interactions underlie effective semantic memory encoding and thus strategically mediate information processing with increased transfer to the hippocampus, consequently enhancing memory retrieval. Accordingly, learning strategies that emphasize emotional factors are more likely to result in long-term knowledge retention. This consideration is potentially useful in the design of educational materials for academic settings and informed intelligent tutoring systems.
Based on numerous previous findings, future research might take emotional factors more seriously and more explicitly in terms of their potential impact on learning. By monitoring the emotional state of students, the utilization of scientifically derived knowledge of stimulus selection can be particularly useful in the identification of emotional states that advance learning performance and outcomes in educational settings. Moreover, functional neuroimaging investigations now include single and/or combined modalities that obtain complementary datasets that inform a more comprehensive overview of neuronal activity in its entirety. For example, curiosity and motivation promote learning, as it appears cognitive network become energized by the mesolimbic-mesocortical dopamine system (generalized motivational arousal/SEEKING system). In addition, the identification of emotional impact on learning and memory potentially has direct implications for healthy individuals as well as patients with psychiatric disorders such as depression, anxiety, schizophrenia, autism, mania, obsessive-compulsive disorder and post-traumatic stress disorder (PTSD) ( Panksepp, 2011a ). To emphasize, depression and anxiety are the two most commonly diagnosed psychiatric disorders associated with learning/memory impairment and pose negative consequences that (i) limit the total amount of information that can otherwise be learned, and (ii) inhibit immediate recall as well as memory retention and retrieval of newly learned information. Depression and anxiety are also associated with negative emotions such as hopelessness, anxiety, apathy, attention deficit, lack of motivation, and motor and mental insufficiencies. Likewise, neuroscience studies report that decreased activation of the dorsal limbic (the anterior and posterior cingulate) as well as in the prefrontal, premotor and parietal cortices causes attentional disturbance, while increased neural activation in the ventral paralimbic region (the subgenual cingulate, anterior insula, hypothalamus and caudate) is associated with emotional and motivational disorders ( Mayberg, 1997 ).
Concluding Remarks, Open Questions, and Future Directions
Substantial evidence has established that emotional events are remembered more clearly, accurately and for longer periods of time than are neutral events. Emotional memory enhancement appears to involve the integration of cognitive and emotional neural networks, in which activation of the amygdala enhances the processing of emotionally arousing stimuli while also modulating enhanced memory consolidation along with other memory-related brain regions, particularly the amygdala, hippocampus, MTL, as well as the visual, frontal and parietal cortices. Similarly, activation of the PFC enhances cognitive functions, such as strategic and semantic processing that affect WM and also promote the establishment of LTM. Previous studies have primarily used standardized emotional visual, or auditory stimuli such as pictures, words, facial expression, and film clips, often based on the IAPS, ANEW, and POFA databases for emotional pictures, words and facial expressions, respectively. Further studies have typically focused on the way individuals memorize (intentional or incidental episodic memory paradigm) emotional stimuli in controlled laboratory settings. To our knowledge, there are few objective studies that employed brain-mapping techniques to examine semantic memory of learning materials (using subject matter) in the education context. Furthermore, influences derived from emotional factors in human learning and memory remains unclear as to whether positive emotions facilitate learning or negative emotions impair learning and vice versa. Thus, several remaining questions should be addressed in future studies, including (i) the impact of emotion on semantic knowledge encoding and retrieval, (ii) psychological and physiological changes associated with semantic learning and memory, and (iii) the development of methods that incorporate emotional and motivational aspects that improve educational praxes, outcomes, and instruments. The results of studies on emotion using educational learning materials can indeed provide beneficial information for informed designs of new educational courses that obtain more effective teaching and help establish better informed learning environments. Hence, to understand how emotion influence learning and memory requires understanding of an evolutionary consideration of the nested hierarchies of CNS emotional-affective processes as well as a large-scale network, including the midbrain’s PAG and VTA, basal ganglia (amygdala and NAc), and insula, as well as diencephalon (the cingulate and medial frontal cortices through the lateral and medial hypothalamus and medial thalamus) together with the MTL, including the hippocampus as well as the entorhinal cortex, perirhinal cortex, and parahippocampal cortices that responsible for declarative memories. Moreover, the SEEKING system generates positive subjective emotional states-positive expectancy, enthusiastic exploration, and hopefulness, apparently, initiates learning and memory in the brain. All cognitive activity is motivated from ‘underneath’ by basic emotional and homeostatic needs (motivational drives) that explore environmental events for survival while facilitating secondary processes of learning and memory.
Author Contributions
CMT drafted this manuscript. CMT, HUA, MNMS, and ASM revised this draft. All authors reviewed and approved this manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to thank Ministry of Education (MOE), Malaysia for the financial support. We gratefully thank Frontiers in Psychology, Specialty Section Emotion Sciences reviewers and the journal Associate Editor, for their helpful input and feedback on the content of this manuscript.
Funding. This research work was supported by the HiCoE grant for CISIR (Ref No. 0153CA-002), Ministry of Education (MOE), Malaysia.
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IMAGES
COMMENTS
Memory retrieval involves the interaction between external sensory or internally generated cues and stored memory traces (or engrams) in a process termed 'ecphory'. While ecphory has been examined in human cognitive neuroscience research, its neurobiological foundation is less understood. To the extent that ecphory involves 'reawakening ...
Memory is the term given to the structures and processes involved in the storage and subsequent retrieval of information. Memory is essential to all our lives. Without a memory of the past, we cannot operate in the present or think about the future. We would not be able to remember what we did yesterday, what we have done today, or what we plan ...
Memory also gives individuals a framework through which to make sense of the present and future. As such, memory plays a crucial role in teaching and learning. There are three main processes that characterize how memory works. These processes are encoding, storage, and retrieval (or recall).
Our memory has three basic functions: encoding, storing, and retrieving information. Encoding is the act of getting information into our memory system through automatic or effortful processing. Storage is retention of the information, and retrieval is the act of getting information out of storage and into conscious awareness through recall ...
Abstract "Memory" is a single term but it reflects a number of different abilities—holding information briefly while working with it (working memory), remembering episodes of one's life (episodic memory), and our general knowledge of facts of the world (semantic memory), among other types. Remembering episodes involves three processes: encoding information (perceiving it and relating ...
While the assessment of memory has greatly improved, we are only beginning to understand the underlying mechanisms. Keywords: Amnesia, declarative/explicit memory, encoding, long-term potentiation, memory, neural plasticity, procedural/implicit memories, recall, retrieval, storage Go to:
Pervasive Role of Memory in Everyday Life Until recently, memory has been compared to a computer and defined by an information-processing model in which information goes through three discrete stages: encoding, storage, and retrieval. Additionally, Atkinson and Shiffrin (1968) posited that information goes through three stages: sensory, short-term memory, and long-term memory. Today ...
Memory is the set of processes used to encode, store, and retrieve information over different periods of time ( Figure 8.2 ). Figure 8.2 Encoding involves the input of information into the memory system. Storage is the retention of the encoded information.
The learning and memory process consists of four stages, with retrieval as the final stage (Fig. 1 ). The life of a memory starts with encoding, a process in which information enters the cognitive ...
Psychology essay sample: The paper aims to study the current research on encoding, storage, and retrieval processes, short- and long-term memory, providing practical essences for experts in related fields.
This paper explores memory from a cognitive neuroscience perspective and examines associated neural mechanisms. It examines the different types of memory: working, declarative, and non-declarative, and the brain regions involved in each type. The paper highlights the role of different brain regions, such as the prefrontal cortex in working ...
"Memory" is a single term that reflects a number of different abilities: holding information briefly while working with it (working memory), remembering episodes of one's life (episodic memory), and our general knowledge of facts of the world (semantic memory), among other types. Remembering episodes involves three processes: encoding information (learning it, by perceiving it and ...
We get information into our brains through a process called encoding, which is the input of information into the memory system. Once we receive sensory ...
After the encoding process information is stored so that it can be retrieved when needed (Brem, Ran & Pascual-leone, 2013). This essay will explore the three different types of memory mentioned earlier and how the encoding, storage and retrieval model explains the process of forming, maintaining and recalling memories.
Stage 1: Encoding Encoding is the first stage of memory, and it refers to the process of converting information into a format that can be stored in our memory: Encoding occurs when we pay attention to information. For example, if you are trying to remember a list of groceries, you will need to pay attention to the items on the list in order to encode them into your memory. Information is ...
Psychologists who study memory generally recognize three stages in memory: 1) an encoding phase, where the information is first learned and prepared to be remembered; 2) a storage or consolidation phase, in which the information is allowed to "gel" in the brain. Drugs, alcohol, and head trauma can all disrupt this consolidation phase; and, 3) a retrieval phase, where the stored information ...
How Memory Works. Memory is a continually unfolding process. Initial details of an experience take shape in memory; the brain's representation of that information then changes over time. With ...
The effects of acute stress on memory encoding are complex. Recent work has suggested that both the delay between stress and encoding and the relevance of the information learned to the stressor may modulate the effects of stress on memory encoding, but ...
Summary We outline a theoretical framework encompassing the relationship between encoding and retrieval processes in episodic memory. There are no cortical regions or networks that are specialized for encoding; rather, successful encoding depends on the same regions that are engaged during on-line processing.
Memory is an essential brain mechanism that works alongside visual stimuli. During a vision-memory cognitive task, we found the non-visual brain is largely predictable using previously seen images. Our Memory Encoding Model (Mem) won the Algonauts 2023 visual brain competition even without model ensemble (single model score 66.8, ensemble score ...
First, we examine the evidence for the architecture of short-term memory, with special attention to questions of capacity and how—or whether—short-term memory can be separated from long-term memory. Second, we ask how the components of that architecture enact processes of encoding, maintenance, and retrieval. Third, we describe the debate ...
However, for Pauli channels, having access to an ideal quantum memory and entangling operations allows encoding parameters in commuting observables, thereby exponentially reducing measurement complexity.
Emotion also facilitates encoding and helps retrieval of information efficiently. However, the effects of emotion on learning and memory are not always univalent, as studies have reported that emotion either enhances or impairs learning and long-term memory (LTM) retention, depending on a range of factors.