scholarly journals Toward understanding the neural code of the brain

Author(s):  
Christoph von der Malsburg
Keyword(s):  
2000 ◽  
Vol 69 (1-2) ◽  
pp. 87-96 ◽  
Author(s):  
Patricia M Di Lorenzo
Keyword(s):  

2017 ◽  
Author(s):  
Joe Z. Tsien ◽  
Meng Li

AbstractOne important goal of BRAIN projects is to crack the neural code — to understand how information is represented in patterns of electrical activity generated by ensembles of neurons. Yet the major stumbling block in the understanding of neural code isneuronal variability- neurons in the brain discharge their spikes with tremendous variability in both thecontrolresting states and across trials within the same experiments. Such on-going spike variability imposes a great conceptual challenge to the classic rate code and/or synchrony-based temporal code. In practice, spike variability is typically removed via over-the-trial averaging methods such as peri-event spike histogram. In contrast to view neuronal variability as a noise problem, here we hypothesize that neuronal variability should be viewed as theself-information processor. Under this conceptual framework, neurons transmit their information by conforming to the basic logic of the statistical Self-Information Theory: spikes with higher-probability inter-spike-intervals (ISI) contain less information, whereas spikes with lower-probability ISIs convey more information, termed assurprisal spikes. In other words, real-time information is encoded not by changes in firing frequency per se, but rather by spike’s variability probability. When these surprisal spikes occur as positive surprisals or negative surprisals in a temporally coordinated manner across populations of cells, they generate cell-assembly neural code to convey discrete quanta of information in real-time. Importantly, such surprisal code can afford not only robust resilience to interference, but also biochemical coupling to energy metabolism, protein synthesis and gene expression at both synaptic sites and cell soma. We describe how this neural self-information theory might be used as a general decoding strategy to uncover the brain’s various cell assemblies in an unbiased manner.


2021 ◽  
Author(s):  
Bruce C. Hansen ◽  
Michelle R. Greene ◽  
David J. Field

AbstractA chief goal of systems neuroscience is to understand how the brain encodes information in our visual environments. Understanding that neural code is crucial to explaining how visual content is transformed via subsequent semantic representations to enable intelligent behavior. Although the visual code is not static, this reality is often obscured in voxel-wise encoding models of BOLD signals due to fMRI’s poor temporal resolution. We leveraged the high temporal resolution of EEG to develop an encoding technique based in state-space theory. This approach maps neural signals to each pixel within a given image and reveals location-specific transformations of the visual code, providing a spatiotemporal signature for the image at each electrode. This technique offers a spatiotemporal visualization of the evolution of the neural code of visual information thought impossible to obtain from EEG and promises to provide insight into how visual meaning is developed through dynamic feedforward and recurrent processes.


2018 ◽  
Author(s):  
Beau Sievers ◽  
Carolyn Parkinson ◽  
Peter J. Kohler ◽  
James Hughes ◽  
Sergey V. Fogelson ◽  
...  

AbstractEmotional music and movement are human universals. Further, music and movement are subjectively linked: it is hard to imagine one without the other. One possible reason for the fundamental link between music and movement is that they are represented the same way in the brain, using a shared neural code. To test this, we created emotional music and animation stimuli that were precisely matched on all time-varying structural features. Participants viewed these stimuli while undergoing fMRI of the brain. Using representational similarity analysis (Kriegeskorte & Kievit, 2013), we show that a single model of stimulus features and emotion content fit activity in both auditory and visual brain areas, providing evidence that these regions share a neural code. Further, this code was used in posterior superior temporal cortex during both audition and vision. Across all regions, the shared code represented both prototypical and mixed emotions (e.g., Happy–Sad). Finally, exploratory analysis revealed that stimulus features and emotion content were represented in early visual areas even when stimuli were presented auditorily. This evidence for a shared neural code is consistent with an adaptive signaling account of emotion perception, where perceivers specifically adapted to perceive cross-sensory redundancy accrue an evolutionary advantage.


2016 ◽  
Vol 27 (1) ◽  
pp. 34 ◽  
Author(s):  
Victor M. Erlich

Extensive investigation of the brain’s synaptic connectivity, the presumed material basis of cognition, has failed toexplain how the brain thinks. Further, the neural code that purportedly allows the brain to coordinate synapticmodulation over wide areas of cortex has yet to be found and may not exist. An alternative approach, focusing onthe possibility that the brain’s internally generated electromagnetic fields might be biologically effective, leads to amodel that solves this “binding problem.” The model of cognition proposed here permits mind and consciousness toarise naturally from the brain as trains of signifying states, or stationarities. Neuronal circuits in suitably constructedhierarchies produce thought by reconciling themselves with each other through the forward- and back-broadcast ofspecific electromagnetic fields, executing a natural algorithm as a harmonized set is selected. Beyond the postulationthat information is encoded in specifically organized electromagnetic fields, the only other “code” necessary is topographic,one that is already known. That the brain might use its own fields to think is supported by the literature onthe widespread sensitivity of biological organisms to small, windowed fields. This model may help explain the coherenceof the brain’s fields, the conservation of the folded cortex, and, in its emphasis on a self-harmonizing process,the universality of the esthetic impulse as a projection of the brain’s basic mechanism of thought.


2019 ◽  
Vol 42 ◽  
Author(s):  
Chloé Huetz ◽  
Samira Souffi ◽  
Victor Adenis ◽  
Jean-Marc Edeline

Abstract Brette presents arguments that query the existence of the neural code. However, he has neglected certain evidence that could be viewed as proof that a neural code operates in the brain. Albeit these proofs show a link between neural activity and cognition, we discuss why they fail to demonstrate the existence of an invariant neural code.


eLife ◽  
2015 ◽  
Vol 4 ◽  
Author(s):  
Elad Ganmor ◽  
Ronen Segev ◽  
Elad Schneidman

Information is carried in the brain by the joint spiking patterns of large groups of noisy, unreliable neurons. This noise limits the capacity of the neural code and determines how information can be transmitted and read-out. To accurately decode, the brain must overcome this noise and identify which patterns are semantically similar. We use models of network encoding noise to learn a thesaurus for populations of neurons in the vertebrate retina responding to artificial and natural videos, measuring the similarity between population responses to visual stimuli based on the information they carry. This thesaurus reveals that the code is organized in clusters of synonymous activity patterns that are similar in meaning but may differ considerably in their structure. This organization is highly reminiscent of the design of engineered codes. We suggest that the brain may use this structure and show how it allows accurate decoding of novel stimuli from novel spiking patterns.


2019 ◽  
Author(s):  
jean-marc Edeline ◽  
Chloe Huetz ◽  
SOUFFI Samira ◽  
Victor Adenis

Brette presents arguments that query the existence of the neural code. However he has neglected certain evidence that could be viewed as proof that a neural code operates in the brain. Albeit these proofs show a link between neural activity and cognition, we discuss why they fail to demonstrate the existence of an invariant neural code


2017 ◽  
Author(s):  
Romain Brette

Short abstractI argue that the popular neural coding metaphor is often misleading. First, the “neural code” often spans both the experimental apparatus and the brain. Second, a neural code is information only by reference to something with a known meaning, which is not the kind of information relevant for a perceptual system. Third, the causal structure of neural codes (linear, atemporal) is incongruent with the causal structure of the brain (circular, dynamic). I conclude that a causal description of the brain cannot be based on neural codes, because spikes are more like actions than hieroglyphs.Long abstract“Neural coding” is a popular metaphor in neuroscience, where objective properties of the world are communicated to the brain in the form of spikes. Here I argue that this metaphor is often inappropriate and misleading. First, when neurons are said to encode experimental parameters, the neural code depends on experimental details that are not carried by the coding variable. Thus, the representational power of neural codes is much more limited than generally implied. Second, neural codes carry information only by reference to things with known meaning. In contrast, perceptual systems must build information from relations between sensory signals and actions, forming a structured internal model. Neural codes are inadequate for this purpose because they are unstructured. Third, coding variables are observables tied to the temporality of experiments, while spikes are timed actions that mediate coupling in a distributed dynamical system. The coding metaphor tries to fit the dynamic, circular and distributed causal structure of the brain into a linear chain of transformations between observables, but the two causal structures are incongruent. I conclude that the neural coding metaphor cannot provide a basis for theories of brain function, because it is incompatible with both the causal structure of the brain and the informational requirements of cognition.


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