scholarly journals Spontaneous Beta Band Rhythms in the Predictive Coding of Natural Stimuli

2020 ◽  
pp. 107385842092898 ◽  
Author(s):  
Viviana Betti ◽  
Stefania Della Penna ◽  
Francesco de Pasquale ◽  
Maurizio Corbetta

The regularity of the physical world and the biomechanics of the human body movements generate distributions of highly probable states that are internalized by the brain in the course of a lifetime. In Bayesian terms, the brain exploits prior knowledge, especially under conditions when sensory input is unavailable or uncertain, to predictively anticipate the most likely outcome of upcoming stimuli and movements. These internal models, formed during development, yet still malleable in adults, continuously adapt through the learning of novel stimuli and movements. Traditionally, neural beta (β) oscillations are considered essential for maintaining sensorimotor and cognitive representations, and for temporal coding of expectations. However, recent findings show that fluctuations of β band power in the resting state strongly correlate between cortical association regions. Moreover, central (hub) regions form strong interactions over time with different brain regions/networks (dynamic core). β band centrality fluctuations of regions of the dynamic core predict global efficiency peaks suggesting a mechanism for network integration. Furthermore, this temporal architecture is surprisingly stable, both in topology and dynamics, during the observation of ecological natural visual scenes, whereas synthetic temporally scrambled stimuli modify it. We propose that spontaneous β rhythms may function as a long-term “prior” of frequent environmental stimuli and behaviors.

Meditation refers to a state of mind of relaxation and concentration, where generally the mind and body is at rest. The process of meditation reflects the state of the brain which is distinct from sleep or typical wakeful states of consciousness. Meditative practices usually involve regulation of emotions and monitoring of attention. Over the past decade there has been a tremendous increase in an interest to study the neural mechanisms involved in meditative practices. It could also be beneficial to explore if the effect of meditation is altered by the number of years of meditation practice. Functional Magnetic Resonance Imaging (fMRI) is a very useful imaging technique which can be used to perform this analysis due to its inherent benefits, mainly it being a non-invasive technique. Functional activation and connectivity analysis can be performed on the fMRI data to find the active regions and the connectivity in the brain regions. Functional connectivity is defined as a simple temporal correlation between anatomically separate, active neural regions. Functional connectivity gives the statistical dependencies between regional time series. It is a statistical concept and is quantified using metrics like Correlation. In this study, a comparison is made between functional connectivity in the brain regions of long term meditation practitioners (LTP) and short-term meditation practitioners (STP) to see the differences and similarities in the connectivity patterns. From the analysis, it is evident that in fact there is a difference in connectivity between long term and short term practitioners and hence continuous practice of meditation can have long term effects.


2019 ◽  
Vol 12 (3) ◽  
pp. 138 ◽  
Author(s):  
Robert R. Crichton ◽  
Roberta J. Ward ◽  
Robert C. Hider

Iron chelation therapy, either subcutaneous or orally administered, has been used successfully in various clinical conditions. The removal of excess iron from various tissues, e.g., the liver spleen, heart, and the pituitary, in beta thalassemia patients, has become an essential therapy to prolong life. More recently, the use of deferiprone to chelate iron from various brain regions in Parkinson’s Disease and Friederich’s Ataxia has yielded encouraging results, although the side effects, in <2% of Parkinson’s Disease(PD) patients, have limited its long-term use. A new class of hydroxpyridinones has recently been synthesised, which showed no adverse effects in preliminary trials. A vital question remaining is whether inflammation may influence chelation efficacy, with a recent study suggesting that high levels of inflammation may diminish the ability of the chelator to bind the excess iron.


2020 ◽  
Vol 6 (1) ◽  
pp. 103-111 ◽  
Author(s):  
Yosef Avchalumov ◽  
Chitra D. Mandyam

Alcohol is one of the oldest pharmacological agents used for its sedative/hypnotic effects, and alcohol abuse and alcohol use disorder (AUD) continues to be major public health issue. AUD is strongly indicated to be a brain disorder, and the molecular and cellular mechanism/s by which alcohol produces its effects in the brain are only now beginning to be understood. In the brain, synaptic plasticity or strengthening or weakening of synapses, can be enhanced or reduced by a variety of stimulation paradigms. Synaptic plasticity is thought to be responsible for important processes involved in the cellular mechanisms of learning and memory. Long-term potentiation (LTP) is a form of synaptic plasticity, and occurs via N-methyl-D-aspartate type glutamate receptor (NMDAR or GluN) dependent and independent mechanisms. In particular, NMDARs are a major target of alcohol, and are implicated in different types of learning and memory. Therefore, understanding the effect of alcohol on synaptic plasticity and transmission mediated by glutamatergic signaling is becoming important, and this will help us understand the significant contribution of the glutamatergic system in AUD. In the first part of this review, we will briefly discuss the mechanisms underlying long term synaptic plasticity in the dorsal striatum, neocortex and the hippocampus. In the second part we will discuss how alcohol (ethanol, EtOH) can modulate long term synaptic plasticity in these three brain regions, mainly from neurophysiological and electrophysiological studies. Taken together, understanding the mechanism(s) underlying alcohol induced changes in brain function may lead to the development of more effective therapeutic agents to reduce AUDs.


2016 ◽  
Author(s):  
Alla Brodski-Guerniero ◽  
Georg-Friedrich Paasch ◽  
Patricia Wollstadt ◽  
Ipek Özdemir ◽  
Joseph T. Lizier ◽  
...  

AbstractPredictive coding suggests that the brain infers the causes of its sensations by combining sensory evidence with internal predictions based on available prior knowledge. However, the neurophysiological correlates of (pre-)activated prior knowledge serving these predictions are still unknown. Based on the idea that such pre-activated prior knowledge must be maintained until needed we measured the amount of maintained information in neural signals via the active information storage (AIS) measure. AIS was calculated on whole-brain beamformer-reconstructed source time-courses from magnetoencephalography (MEG) recordings of 52 human subjects during the baseline of a Mooney face/house detection task. Pre-activation of prior knowledge for faces showed as alpha- and beta-band related AIS increases in content specific areas; these AIS increases were behaviourally relevant in brain area FFA. Further, AIS allowed decoding of the cued category on a trial-by-trial basis. Moreover, top-down transfer of predictions estimated by transfer entropy was associated with beta frequencies. Our results support accounts that activated prior knowledge and the corresponding predictions are signalled in low-frequency activity (<30 Hz).Significance statementOur perception is not only determined by the information our eyes/retina and other sensory organs receive from the outside world, but strongly depends also on information already present in our brains like prior knowledge about specific situations or objects. A currently popular theory in neuroscience, predictive coding theory, suggests that this prior knowledge is used by the brain to form internal predictions about upcoming sensory information. However, neurophysiological evidence for this hypothesis is rare – mostly because this kind of evidence requires making strong a-priori assumptions about the specific predictions the brain makes and the brain areas involved. Using a novel, assumption-free approach we find that face-related prior knowledge and the derived predictions are represented and transferred in low-frequency brain activity.


2020 ◽  
Author(s):  
Charidimos Tzagarakis ◽  
Sarah West ◽  
Giuseppe Pellizzer

AbstractVisual information about an upcoming target can be used to prepare an appropriate motor response and reduce its reaction time. However, when the anticipation is incorrect and the planned response must be changed, the reaction time is lengthened. Here, we investigated the brain mechanisms associated with the reliability and validity of visual information used for motor preparation. We recorded brain activity using magnetoencephalography (MEG) during a delayed reaching task in which a visual cue provided valid information about the location of the upcoming target with 50, 75 or 100% reliability. We found that reaction time increased as cue reliability decreased and that trials with invalid cues had longer reaction times than trials with valid cues. MEG channel analysis showed that beta-band power from left mid-anterior channels correlated with the reliability of the cue after cue onset but before target onset. This effect was source localized over a large motor-related cortical and subcortical network. In addition, during invalid-cue trials there was a phasic increase of theta-band power following target onset from left posterior channels, localized to the left occipito-parietal cortex. Furthermore, the theta-beta cross-frequency coupling between left mid-occipital and motor cortex also transiently increased before responses to invalid-cue trials. In conclusion, beta-band power in motor-related areas reflected the reliability of visual information used during motor preparation, whereas phasic theta-band activity signaled whether the target was at the expected location or not. These results elucidate mechanisms of interaction between attentional and motor processes.Significance StatementWe used magnetoencephalography to investigate how the brain mechanisms preparing a motor response take into account the reliability of information about the upcoming location of a target to reach, and how these mechanisms adjust when that information turns out to be incorrect. We found that during the response preparation, the power of motor-related beta-band oscillations changed with the reliability of the visual information. In addition, we found that after the onset of the target the power of the left occipito-parietal theta-band signaled whether the prior information was correct or not. The pattern of activity of the beta-band and theta-band explain the pattern of latency of responses in the task, and demonstrate how attentional and motor processes interact.


2020 ◽  
Author(s):  
Alejandro Lerer ◽  
Hans Supèr ◽  
Matthias S.Keil

AbstractThe visual system is highly sensitive to spatial context for encoding luminance patterns. Context sensitivity inspired the proposal of many neural mechanisms for explaining the perception of luminance (brightness). Here we propose a novel computational model for estimating the brightness of many visual illusions. We hypothesize that many aspects of brightness can be explained by a predictive coding mechanism, which reduces the redundancy in edge representations on the one hand, while non-redundant activity is enhanced on the other (response equalization). Response equalization is implemented with a dynamic filtering process, which (dynamically) adapts to each input image. Dynamic filtering is applied to the responses of complex cells in order to build a gain control map. The gain control map then acts on simple cell responses before they are used to create a brightness map via activity propagation. Our approach is successful in predicting many challenging visual illusions, including contrast effects, assimilation, and reverse contrast.Author summaryWe hardly notice that what we see is often different from the physical world “outside” of the brain. This means that the visual experience that the brain actively constructs may be different from the actual physical properties of objects in the world. In this work, we propose a hypothesis about how the visual system of the brain may construct a representation for achromatic images. Since this process is not unambiguous, sometimes we notice “errors” in our perception, which cause visual illusions. The challenge for theorists, therefore, is to propose computational principles that recreate a large number of visual illusions and to explain why they occur. Notably, our proposed mechanism explains a broader set of visual illusions than any previously published proposal. We achieved this by trying to suppress predictable information. For example, if an image contained repetitive structures, then these structures are predictable and would be suppressed. In this way, non-predictable structures stand out. Predictive coding mechanisms act as early as in the retina (which enhances luminance changes but suppresses uniform regions of luminance), and our computational model holds that this principle also acts at the next stage in the visual system, where representations of perceived luminance (brightness) are created.


2021 ◽  
Vol 12 ◽  
Author(s):  
Xinzhen Pei ◽  
Xiaoying Qi ◽  
Yuzhou Jiang ◽  
Xunzhang Shen ◽  
An-Li Wang ◽  
...  

Human brains are extremely energy costly in neural connections and activities. However, it is unknown what is the difference in the brain connectivity between top athletes with long-term professional trainings and age-matched controls. Here we ask whether long-term training can lower brain-wiring cost while have better performance. Since elite swimming requires athletes to move their arms and legs at different tempos in time with high coordination skills, we selected an eye-hand-foot complex reaction (CR) task to examine the relations between the task performance and the brain connections and activities, as well as to explore the energy cost-efficiency of top athletes. Twenty-one master-level professional swimmers and 23 age-matched non-professional swimmers as controls were recruited to perform the CR task with concurrent 8-channel EEG recordings. Reaction time and accuracy of the CR task were recorded. Topological network analysis of various frequency bands was performed using the phase lag index (PLI) technique to avoid volume conduction effects. The wiring number of connections and mean frequency were calculated to reflect the wiring and activity cost, respectively. Results showed that professional athletes demonstrated better eye-hand-foot coordination than controls when performing the CR task, indexing by faster reaction time and higher accuracy. Comparing to controls, athletes' brain demonstrated significantly less connections and weaker correlations in upper beta frequency band between the frontal and parietal regions, while demonstrated stronger connectivity in the low theta frequency band between sites of F3 and Cz/C4. Additionally, athletes showed highly stable and low eye-blinking rates across different reaction performance, while controls had high blinking frequency with high variance. Elite athletes' brain may be characterized with energy efficient sparsely wiring connections in support of superior motor performance and better cognitive performance in the eye-hand-foot complex reaction task.


Author(s):  
Sahib S. Khalsa ◽  
Justin S. Feinstein

A regulatory battle for control ensues in the central nervous system following a mismatch between the current physiological state of an organism as mapped in viscerosensory brain regions and the predicted body state as computed in visceromotor control regions. The discrepancy between the predicted and current body state (i.e. the “somatic error”) signals a need for corrective action, motivating changes in both cognition and behavior. This chapter argues that anxiety disorders are fundamentally driven by somatic errors that fail to be adaptively regulated, leaving the organism in a state of dissonance where the predicted body state is perpetually out of line with the current body state. Repeated failures to quell somatic error can result in long-term changes to interoceptive circuitry within the brain. This chapter explores the neuropsychiatric sequelae that can emerge following chronic allostatic dysregulation of somatic errors and discusses novel therapies that might help to correct this dysregulation.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Seongmin A. Park ◽  
Mariateresa Sestito ◽  
Erie D. Boorman ◽  
Jean-Claude Dreher

AbstractWhen making decisions in groups, the outcome of one’s decision often depends on the decisions of others, and there is a tradeoff between short-term incentives for an individual and long-term incentives for the groups. Yet, little is known about the neurocomputational mechanisms at play when weighing different utilities during repeated social interactions. Here, using model-based fMRI and Public-good-games, we find that the ventromedial prefrontal cortex encodes immediate expected rewards as individual utility while the lateral frontopolar cortex encodes group utility (i.e., pending rewards of alternative strategies beneficial for the group). When it is required to change one’s strategy, these brain regions exhibited changes in functional interactions with brain regions engaged in switching strategies. Moreover, the anterior cingulate cortex and the temporoparietal junction updated beliefs about the decision of others during interactions. Together, our findings provide a neurocomputational account of how the brain dynamically computes effective strategies to make adaptive collective decisions.


2012 ◽  
Vol 2012 ◽  
pp. 1-16 ◽  
Author(s):  
Sylvia Navailles ◽  
Philippe De Deurwaerdère

L-DOPA-induced dyskinesias (LIDs) are one of the main motor side effects of L-DOPA therapy in Parkinson's disease. The review will consider the biochemical evidence indicating that the serotonergic neurons are involved in the dopaminergic effects of L-DOPA in the brain. The consequences are an ectopic and aberrant release of dopamine that follows the serotonergic innervation of the brain. After mid- to long-term treatment with L-DOPA, the pattern of L-DOPA-induced dopamine release is modified. In several brain regions, its effect is dramatically reduced while, in the striatum, its effect is quite preserved. LIDs could appear when the dopaminergic effects of L-DOPA fall in brain areas such as the cortex, enhancing the subcortical impact of dopamine and promoting aberrant motor responses. The consideration of the serotonergic system in the core mechanism of action of L-DOPA opens an important reserve of possible strategies to limit LIDs.


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