scholarly journals The processing of color preference in the brain

2018 ◽  
Author(s):  
Chris Racey ◽  
Anna Franklin ◽  
Chris M. Bird

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.

2012 ◽  
Vol 107 (1) ◽  
pp. 126-133 ◽  
Author(s):  
Masahiko Haruno ◽  
Gowrishankar Ganesh ◽  
Etienne Burdet ◽  
Mitsuo Kawato

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.


2018 ◽  
Author(s):  
Evelyn MR Lake ◽  
Xinxin Ge ◽  
Xilin Shen ◽  
Peter Herman ◽  
Fahmeed Hyder ◽  
...  

ABSTRACTTo achieve a more comprehensive understanding of brain function requires simultaneous measurement of activity across a range of spatiotemporal scales. However, the appropriate tools to perform such studies are largely unavailable. Here, we present a novel approach for concurrent wide-field optical and functional magnetic resonance imaging (fMRI). By merging these two modalities, we are for the first time able to simultaneously acquire whole-brain blood-oxygen-level-dependent and whole-cortex calcium-sensitive fluorescent measures of brain activity. We describe the developments that allow us to combine these modalities without compromising the fidelity of either technique. In a transgenic murine model, we examine correspondences between activity measured using these modalities and identify unique and complementary features of each. Our approach links cell-type specific optical measurements of neural activity to the most widely used method for assessing human brain function. These data and approach directly establish the neural basis for the macroscopic connectivity patterns observed with fMRI.


2021 ◽  
Vol 15 ◽  
Author(s):  
Hans Albert Braun

If one accepts that decisions are made by the brain and that neuronal mechanisms obey deterministic physical laws, it is hard to deny what some brain researchers postulate, such as “We do not do what we want, but we want what we do” and “We should stop talking about freedom. Our actions are determined by physical laws.” This point of view has been substantially supported by spectacular neurophysiological experiments demonstrating action-related brain activity (readiness potentials, blood oxygen level–dependent signals) occurring up to several seconds before an individual becomes aware of his/her decision to perform the action. This report aims to counter the deterministic argument for the absence of free will by using experimental data, supplemented by computer simulations, to demonstrate that biological systems, specifically brain functions, are built on principle randomness, which is introduced already at the lowest level of neuronal information processing, the opening and closing of ion channels. Switching between open and closed states follows physiological laws but also makes use of randomness, which is apparently introduced by Brownian motion – principally unavoidable under all life-compatible conditions. Ion-channel stochasticity, manifested as noise, function is not smoothed out toward higher functional levels but can even be amplified by appropriate adjustment of the system’s non-linearities. Examples shall be given to illustrate how stochasticity can propagate from ion channels to single neuron action potentials to neuronal network dynamics to the interactions between different brain nuclei up to the control of autonomic functions. It is proposed that this intrinsic stochasticity helps to keep the brain in a flexible state to explore diverse alternatives as a prerequisite of free decision-making.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Young-Bo Kim ◽  
Nambeom Kim ◽  
Jae Jun Lee ◽  
Seo-Eun Cho ◽  
Kyoung-Sae Na ◽  
...  

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.


2016 ◽  
Vol 113 (17) ◽  
pp. 4853-4858 ◽  
Author(s):  
Robin L. Carhart-Harris ◽  
Suresh Muthukumaraswamy ◽  
Leor Roseman ◽  
Mendel Kaelen ◽  
Wouter Droog ◽  
...  

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.


2019 ◽  
Vol 40 (10) ◽  
pp. 2066-2080
Author(s):  
Yaoyu Zhang ◽  
Yayan Yin ◽  
Huanjie Li ◽  
Jia-Hong Gao

Cerebral blood flow (CBF) and cerebral metabolic rate of oxygen (CMRO2) are physiological parameters that not only reflect brain health and disease but also jointly contribute to blood oxygen level-dependent (BOLD) signals. Nevertheless, unsolved issues remain concerning the CBF–CMRO2 relationship in the working brain under various oxygen conditions. In particular, the CMRO2 responses to functional tasks in hypoxia are less studied. We extended the calibrated BOLD model to incorporate CMRO2 measurements in hypoxia. The extended model, which was cross-validated with a multicompartment BOLD model, considers the influences of the reduced arterial saturation level and increased baseline cerebral blood volume (CBV) and deoxyhemoglobin concentration on the changes of BOLD signals in hypoxia. By implementing a pulse sequence to simultaneously acquire the CBV-, CBF- and BOLD-weighted signals, we investigated the effects of mild hypoxia on the CBF and CMRO2 responses to graded visual stimuli. Compared with normoxia, mild hypoxia caused significant alterations in both the amplitude and the trend of the CMRO2 responses but did not impact the corresponding CBF responses. Our observations suggested that the flow-metabolism coupling strategies in the brain during mild hypoxia were different from those during normoxia.


2006 ◽  
Vol 96 (1) ◽  
pp. 259-275 ◽  
Author(s):  
Maria G. Knyazeva ◽  
Eleonora Fornari ◽  
Reto Meuli ◽  
Philippe Maeder

The early visual system processes different spatial frequencies (SFs) separately. To examine where in the brain the scale-specific information is integrated, we mapped the neural assemblies engaged in interhemispheric coupling with electroencephalographic (EEG) coherence and blood-oxygen-level dependent (BOLD) signal. During similar EEG and functional magnetic resonance imaging (fMRI) experiments, our subjects viewed centrally presented bilateral gratings of different SF (0.25–8.0 cpd), which either obeyed Gestalt grouping rules (iso-oriented, IG) or violated them (orthogonally oriented, OG). The IG stimuli (0.5–4.0 cpd) synchronized EEG at discrete beta frequencies (beta1, beta2) and increased BOLD (0.5 and 2.0 cpd tested) in ventral (around collateral sulcus) and dorsal (parieto-occipital fissure) regions compared with OG. At both SF, the beta1 coherence correlated with the ventral activations, whereas the beta2 coherence correlated with the dorsal ones. Thus distributed neural substrates mediated interhemispheric integration at single SF. The relative impact of the ventral versus dorsal networks was modulated by the SF of the stimulus.


2010 ◽  
Vol 104 (3) ◽  
pp. 1746-1757 ◽  
Author(s):  
R. S. Weil ◽  
N. Furl ◽  
C. C. Ruff ◽  
M. Symmonds ◽  
G. Flandin ◽  
...  

Reward can influence visual performance, but the neural basis of this effect remains poorly understood. Here we used functional magnetic resonance imaging to investigate how rewarding feedback affected activity in distinct areas of human visual cortex, separating rewarding feedback events after correct performance from preceding visual events. Participants discriminated oriented gratings in either hemifield, receiving auditory feedback at trial end that signaled financial reward after correct performance. Greater rewards improved performance for all but the most difficult trials. Rewarding feedback increased blood-oxygen-level-dependent (BOLD) signals in striatum and orbitofrontal cortex. It also increased BOLD signals in visual areas beyond retinotopic cortex, but not in primary visual cortex representing the judged stimuli. These modulations were seen at a time point in which no visual stimuli were presented or expected, demonstrating a novel type of activity change in visual cortex that cannot reflect modulation of response to incoming or anticipated visual stimuli. Rewarded trials led on the next trial to improved performance and enhanced visual activity contralateral to the judged stimulus, for retinotopic representations of the judged visual stimuli in V1. Our findings distinguish general effects in nonretinotopic visual cortex when receiving rewarding feedback after correct performance from consequences of reward for spatially specific responses in V1.


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