scholarly journals Sensing and seeing associated with overlapping occipitoparietal activation in simultaneous EEG-fMRI

2021 ◽  
Vol 2021 (1) ◽  
Author(s):  
Catriona L Scrivener ◽  
Asad Malik ◽  
Michael Lindner ◽  
Etienne B Roesch
Keyword(s):  
Brain Activity ◽  
Change Blindness ◽  
Colour Change ◽  
Visual Display ◽  
Blood Oxygen Level Dependent ◽  
Anterior Cingulate ◽  
Blood Oxygen Level ◽  
Fmri Analysis ◽  
And Behavior ◽  
Blind Trials

Abstract The presence of a change in a visual scene can influence brain activity and behavior, even in the absence of full conscious report. It may be possible for us to sense that such a change has occurred, even if we cannot specify exactly where or what it was. Despite existing evidence from electroencephalogram (EEG) and eye-tracking data, it is still unclear how this partial level of awareness relates to functional magnetic resonance imaging (fMRI) blood oxygen level dependent (BOLD) activation. Using EEG, fMRI, and a change blindness paradigm, we found multi-modal evidence to suggest that sensing a change is distinguishable from being blind to it. Specifically, trials during which participants could detect the presence of a colour change but not identify the location of the change (sense trials), were compared to those where participants could both detect and localise the change (localise or see trials), as well as change blind trials. In EEG, late parietal positivity and N2 amplitudes were larger for localised changes only, when compared to change blindness. However, ERP-informed fMRI analysis found no voxels with activation that significantly co-varied with fluctuations in single-trial late positivity amplitudes. In fMRI, a range of visual (BA17,18), parietal (BA7,40), and mid-brain (anterior cingulate, BA24) areas showed increased fMRI BOLD activation when a change was sensed, compared to change blindness. These visual and parietal areas are commonly implicated as the storage sites of visual working memory, and we therefore argue that sensing may not be explained by a lack of stored representation of the visual display. Both seeing and sensing a change were associated with an overlapping occipitoparietal network of activation when compared to blind trials, suggesting that the quality of the visual representation, rather than the lack of one, may result in partial awareness during the change blindness paradigm.

scholarly journals Sensing and seeing associated with overlapping occipitoparietal activation in simultaneous EEG-fMRI

2020 ◽  
Author(s):  
Catriona L. Scrivener ◽  
Asad Malik ◽  
Michael Lindner ◽  
Etienne B. Roesch
Keyword(s):  
Brain Activity ◽  
Change Blindness ◽  
Colour Change ◽  
Visual Display ◽  
Anterior Cingulate ◽  
Functional Magnetic Resonance ◽  
Late Positivity ◽  
Fmri Analysis ◽  
Electroencephalogram Eeg

AbstractThe presence of a change in a visual scene can influence brain activity and behaviour, even in the absence of full conscious report. It may be possible for us to sense that such a change has occurred, even if we cannot specify exactly where or what it was. Despite existing evidence from electroencephalogram (EEG) and eye-tracking data, it is still unclear how this partial level of awareness relates to fMRI BOLD activation. Using EEG, functional magnetic resonance imaging (fMRI), and a change blindness paradigm, we found multi-modal evidence to suggest that sensing a change is distinguishable from being blind to it. Specifically, trials during which participants could detect the presence of a colour change but not identify the location of the change (sense trials), were compared to those where participants could both detect and localise the change (localise or see trials), as well as change blind trials. In EEG, late parietal positivity and N2 amplitudes were larger for localised changes only, when compared to change blindness. However, ERP-informed fMRI analysis found no voxels with activation that significantly co-varied with fluctuations in single-trial late positivity amplitudes. In fMRI, a range of visual (BA17,18), parietal (BA7,40), and midbrain (anterior cingulate, BA24) areas showed increased fMRI BOLD activation when a change was sensed, compared to change blindness. These visual and parietal areas are commonly implicated as the storage sites of visual working memory, and we therefore argue that sensing may not be explained by a lack of stored representation of the visual display. Both seeing and sensing a change were associated with an overlapping occipitoparietal network of activation when compared to blind trials, suggesting that the quality of the visual representation, rather than the lack of one, may result in partial awareness during the change blindness paradigm.

scholarly journals Brain reactivity using fMRI to insomnia stimuli in insomnia patients with discrepancy between subjective and objective sleep

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Young-Bo Kim ◽  
Nambeom Kim ◽  
Jae Jun Lee ◽  
Seo-Eun Cho ◽  
Kyoung-Sae Na ◽  
...  
Keyword(s):  
Brain Activity ◽  
Blood Oxygen Level Dependent ◽  
Brain Regions ◽  
Cognitive Distortion ◽  
Sleep Diary ◽  
Bold Signal ◽  
Blood Oxygen Level ◽  
General Anxiety ◽  
Sleep Deficit ◽  
Perception Of Sleep

AbstractSubjective–objective discrepancy of sleep (SODS) might be related to the distorted perception of sleep deficit and hypersensitivity to insomnia-related stimuli. We investigated differences in brain activation to insomnia-related stimuli among insomnia patients with SODS (SODS group), insomnia patients without SODS (NOSODS group), and healthy controls (HC). Participants were evaluated for subjective and objective sleep using sleep diary and polysomnography. Functional magnetic resonance imaging was conducted during the presentation of insomnia-related (Ins), general anxiety-inducing (Gen), and neutral (Neu) stimuli. Brain reactivity to the contrast of Ins vs. Neu and Gen vs. Neu was compared among the SODS (n = 13), NOSODS (n = 15), and HC (n = 16) groups. In the SODS group compared to other groups, brain areas including the left fusiform, bilateral precuneus, right superior frontal gyrus, genu of corpus callosum, and bilateral anterior corona radiata showed significantly increased blood oxygen level dependent (BOLD) signal in the contrast of Ins vs. Neu. There was no brain region with significantly increased BOLD signal in the Gen vs. Neu contrast in the group comparisons. Increased brain activity to insomnia-related stimuli in several brain regions of the SODS group is likely due to these individuals being more sensitive to sleep-related threat and negative cognitive distortion toward insomnia.

scholarly journals The role of the mesolimbic dopamine system in the formation of blood-oxygen-level dependent responses in the medial prefrontal/anterior cingulate cortex during high-frequency stimulation of the rat perforant pathway

2016 ◽  
Vol 36 (12) ◽  
pp. 2177-2193 ◽  
Author(s):  
Cornelia Helbing ◽  
Marta Brocka ◽  
Thomas Scherf ◽  
Michael T Lippert ◽  
Frank Angenstein
Keyword(s):  
Magnetic Resonance Imaging ◽  
Anterior Cingulate Cortex ◽  
Cingulate Cortex ◽  
Blood Oxygen Level Dependent ◽  
Anterior Cingulate ◽  
Blood Oxygen ◽  
Oxygen Level ◽  
Functional Magnetic Resonance ◽  
Resonance Imaging ◽  
Blood Oxygen Level

Several human functional magnetic resonance imaging studies point to an activation of the mesolimbic dopamine system during reward, addiction and learning. We previously found activation of the mesolimbic system in response to continuous but not to discontinuous perforant pathway stimulation in an experimental model that we now used to investigate the role of dopamine release for the formation of functional magnetic resonance imaging responses. The two stimulation protocols elicited blood-oxygen-level dependent responses in the medial prefrontal/anterior cingulate cortex and nucleus accumbens. Inhibition of dopamine D1/5 receptors abolished the formation of functional magnetic resonance imaging responses in the medial prefrontal/anterior cingulate cortex during continuous but not during discontinuous pulse stimulations, i.e. only when the mesolimbic system was activated. Direct electrical or optogenetic stimulation of the ventral tegmental area caused strong dopamine release but only electrical stimulation triggered significant blood-oxygen level-dependent responses in the medial prefrontal/anterior cingulate cortex and nucleus accumbens. These functional magnetic resonance imaging responses were not affected by the D1/5 receptor antagonist SCH23390 but reduced by the N-methyl-D-aspartate receptor antagonist MK801. Therefore, glutamatergic ventral tegmental area neurons are already sufficient to trigger blood-oxygen-level dependent responses in the medial prefrontal/anterior cingulate cortex and nucleus accumbens. Although dopamine release alone does not affect blood-oxygen-level dependent responses it can act as a switch, permitting the formation of blood-oxygen-level dependent responses.

scholarly journals Neural correlates of the LSD experience revealed by multimodal neuroimaging

2016 ◽  
Vol 113 (17) ◽  
pp. 4853-4858 ◽  
Author(s):  
Robin L. Carhart-Harris ◽  
Suresh Muthukumaraswamy ◽  
Leor Roseman ◽  
Mendel Kaelen ◽  
Wouter Droog ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Visual Processing ◽  
Brain Activity ◽  
Blood Oxygen Level Dependent ◽  
Retrosplenial Cortex ◽  
Alpha Power ◽  
Blood Oxygen Level ◽  
Psychedelic Drugs ◽  
Cortex Cérébral ◽  
Intrinsic Brain Activity

Lysergic acid diethylamide (LSD) is the prototypical psychedelic drug, but its effects on the human brain have never been studied before with modern neuroimaging. Here, three complementary neuroimaging techniques: arterial spin labeling (ASL), blood oxygen level-dependent (BOLD) measures, and magnetoencephalography (MEG), implemented during resting state conditions, revealed marked changes in brain activity after LSD that correlated strongly with its characteristic psychological effects. Increased visual cortex cerebral blood flow (CBF), decreased visual cortex alpha power, and a greatly expanded primary visual cortex (V1) functional connectivity profile correlated strongly with ratings of visual hallucinations, implying that intrinsic brain activity exerts greater influence on visual processing in the psychedelic state, thereby defining its hallucinatory quality. LSD’s marked effects on the visual cortex did not significantly correlate with the drug’s other characteristic effects on consciousness, however. Rather, decreased connectivity between the parahippocampus and retrosplenial cortex (RSC) correlated strongly with ratings of “ego-dissolution” and “altered meaning,” implying the importance of this particular circuit for the maintenance of “self” or “ego” and its processing of “meaning.” Strong relationships were also found between the different imaging metrics, enabling firmer inferences to be made about their functional significance. This uniquely comprehensive examination of the LSD state represents an important advance in scientific research with psychedelic drugs at a time of growing interest in their scientific and therapeutic value. The present results contribute important new insights into the characteristic hallucinatory and consciousness-altering properties of psychedelics that inform on how they can model certain pathological states and potentially treat others.

Differential neural correlates of reciprocal activation and cocontraction control in dorsal and ventral premotor cortices

2012 ◽  
Vol 107 (1) ◽  
pp. 126-133 ◽  
Author(s):  
Masahiko Haruno ◽  
Gowrishankar Ganesh ◽  
Etienne Burdet ◽  
Mitsuo Kawato
Keyword(s):  
Brain Activity ◽  
Premotor Cortex ◽  
Neural Correlates ◽  
Blood Oxygen Level Dependent ◽  
Blood Oxygen ◽  
Dorsal Premotor Cortex ◽  
Blood Oxygen Level ◽  
Efficient Control ◽  
Dependent Activity ◽  
The Brain

Efficient control of reciprocal activation and cocontraction of the muscles are critical to perform skillful actions with suitable force and impedance. However, it remains unclear how the brain controls force and impedance while recruiting the same set of muscles as actuators. Does control take place at the single muscle level leading to force and impedance, or are there higher-order centers dedicated to controlling force and impedance? We addressed this question using functional MRI during voluntary isometric wrist contractions with online electromyogram feedback. Comparison of the brain activity between the conditions requiring control of either wrist torque or cocontraction demonstrates that blood oxygen level-dependent activity in the caudo-dorsal premotor cortex (PMd) correlates well with torque, whereas the activity in the ventral premotor cortex (PMv) correlates well with the level of cocontraction. This suggests distinct roles of the PMd and PMv in the voluntary control of reciprocal activation and cocontraction of muscles, respectively.

scholarly journals Analogous responses in the nucleus accumbens and cingulate cortex to pain onset (aversion) and offset (relief) in rats and humans

2013 ◽  
Vol 110 (5) ◽  
pp. 1221-1226 ◽  
Author(s):  
L. Becerra ◽  
E. Navratilova ◽  
F. Porreca ◽  
D. Borsook
Keyword(s):  
Nucleus Accumbens ◽  
Cingulate Cortex ◽  
Blood Oxygen Level Dependent ◽  
Anterior Cingulate ◽  
Activity Change ◽  
Blood Oxygen Level ◽  
Noxious Heat ◽  
Brain Circuits ◽  
Mechanistic Investigation ◽  
Brain Processing

In humans, functional magnetic resonance imaging (fMRI) activity in the anterior cingulate cortex (ACC) and the nucleus accumbens (NAc) appears to reflect affective and motivational aspects of pain. The responses of this reward-aversion circuit to relief of pain, however, have not been investigated in detail. Moreover, it is not clear whether brain processing of the affective qualities of pain in animals parallels the mechanisms observed in humans. In the present study, we analyzed fMRI blood oxygen level-dependent (BOLD) activity separately in response to an onset (aversion) and offset (reward) of a noxious heat stimulus to a dorsal part of a limb in both humans and rats. We show that pain onset results in negative activity change in the NAc and pain offset produces positive activity change in the ACC and NAc. These changes were analogous in humans and rats, suggesting that translational studies of brain circuits modulated by pain are plausible and may offer an opportunity for mechanistic investigation of pain and pain relief.

scholarly journals Cognitive control associated with irritability induction: an autobiographical recall fMRI study

2010 ◽  
Vol 32 (2) ◽  
pp. 109-118 ◽  
Author(s):  
Carlos T. Cerqueira ◽  
Jorge R. C. Almeida ◽  
João R. Sato ◽  
Clarice Gorenstein ◽  
Valentim Gentil ◽  
...  
Keyword(s):  
Magnetic Resonance ◽  
Cognitive Control ◽  
Blood Oxygen Level Dependent ◽  
Anterior Cingulate ◽  
Auditory Presentation ◽  
Imaging Method ◽  
Blood Oxygen ◽  
Oxygen Level ◽  
Blood Oxygen Level ◽  
Dependent Signal

OBJECTIVE: Despite the relevance of irritability emotions to the treatment, prognosis and classification of psychiatric disorders, the neurobiological basis of this emotional state has been rarely investigated to date. We assessed the brain circuitry underlying personal script-driven irritability in healthy subjects (n = 11) using functional magnetic resonance imaging. METHOD: Blood oxygen level-dependent signal changes were recorded during auditory presentation of personal scripts of irritability in contrast to scripts of happiness or neutral emotional content. Self-rated emotional measurements and skin conductance recordings were also obtained. Images were acquired using a 1,5T magnetic resonance scanner. Brain activation maps were constructed from individual images, and between-condition differences in the mean power of experimental response were identified by using cluster-wise nonparametric tests. RESULTS: Compared to neutral scripts, increased blood oxygen level-dependent signal during irritability scripts was detected in the left subgenual anterior cingulate cortex, and in the left medial, anterolateral and posterolateral dorsal prefrontal cortex (cluster-wise p-value < 0.05). While the involvement of the subgenual cingulate and dorsal anterolateral prefrontal cortices was unique to the irritability state, increased blood oxygen level-dependent signal in dorsomedial and dorsal posterolateral prefrontal regions were also present during happiness induction. CONCLUSION: Irritability induction is associated with functional changes in a limited set of brain regions previously implicated in the mediation of emotional states. Changes in prefrontal and cingulate areas may be related to effortful cognitive control aspects that gain salience during the emergence of irritability.

scholarly journals The processing of color preference in the brain

2018 ◽  
Author(s):  
Chris Racey ◽  
Anna Franklin ◽  
Chris M. Bird
Keyword(s):  
Brain Activity ◽  
Blood Oxygen Level Dependent ◽  
Color Preference ◽  
Blood Oxygen Level ◽  
Neural Basis ◽  
Color Preferences ◽  
Subjective Value ◽  
Value Judgements ◽  
Automatic Encoding ◽  
The Brain

AbstractDecades of research has established that humans have preferences for some colors (e.g., blue) and a dislike of others (e.g., dark chartreuse), with preference varying systematically with variation in hue (e.g., Hurlbert & Owen, 2015). Here, we used functional MRI to investigate why humans have likes and dislikes for simple patches of color, and to understand the neural basis of preference, aesthetics and value judgements more generally. We looked for correlations of a behavioural measure of color preference with the blood oxygen level-dependent (BOLD) response when participants performed an irrelevant orientation judgement task on colored squares. A whole brain analysis found a significant correlation between BOLD activity and color preference in the posterior midline cortex (PMC), centred on the precuneus but extending into the adjacent posterior cingulate and cuneus. These results demonstrate that brain activity is modulated by color preference, even when such preferences are irrelevant to the ongoing task the participants are engaged. They also suggest that color preferences automatically influence our processing of the visual world. Interestingly, the effect in the PMC overlaps with regions identified in neuroimaging studies of preference and value judgements of other types of stimuli. Therefore, our findings extends this literature to show that the PMC is related to automatic encoding of subjective value even for basic visual features such as color.

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