The Brain

 

 

 

The neural correlates of consciousness (NCC) constitute the minimal set of neuronal events and mechanisms sufficient for a specific conscious percept.[2] Neuroscientists use empirical approaches to discover neural correlates of subjective phenomena.[3] The set should be minimal because, under the assumption that the brain is sufficient to give rise to any given conscious experience, the question is which of its components is necessary to produce it.

 

Contents

1 Neurobiological approach to consciousness

2 Level of arousal and content of consciousness

3 The neuronal basis of perception

4 Global disorders of consciousness

5 Forward versus feedback projections

 

 

1 Neurobiological approach to consciousness

A science of consciousness must explain the exact relationship between subjective mental states and brain states, the nature of the relationship between the conscious mind and the electro-chemical interactions in the body (mind–body problem). Progress in neuropsychology and neurophilosophy has come from focusing on the body rather than the mind. In this context the neuronal correlates of consciousness may be viewed as its causes, and consciousness may be thought of as a state-dependent property of some undefined complex, adaptive, and highly interconnected biological system.[4]

Discovering and characterizing neural correlates does not offer a theory of consciousness that can explain how particular systems experience anything at all, or how and why they are associated with consciousness, the so-called hard problem of consciousness,[5] but understanding the NCC may be a step toward such a theory. Most neurobiologists assume that the variables giving rise to consciousness are to be found at the neuronal level, governed by classical physics, though a few scholars have proposed theories of quantum consciousness based on quantum mechanics.[6] [7]

There is great apparent redundancy and parallelism in neural networks so, while activity in one group of neurons may correlate with a percept in one case, a different population might mediate a related percept if the former population is lost or inactivated. It may be that every phenomenal, subjective state has a neural correlate. Where the NCC can be induced artificially the subject will experience the associated percept, while perturbing or inactivating the region of correlation for a specific percept will affect the percept or cause it to disappear, giving a cause-effect relationship from the neural region to the nature of the percept.

What characterizes the NCC? What are the commonalities between the NCC for seeing and for hearing? Will the NCC involve all the pyramidal neurons in the cortex at any given point in time? Or only a subset of long-range projection cells in the frontal lobes that project to the sensory cortices in the back? Neurons that fire in a rhythmic manner? Neurons that fire in a synchronous manner? These are some of the proposals that have been advanced over the years.[8]

The growing ability of neuroscientists to manipulate neurons using methods from molecular biology in combination with optical tools (e.g., Adamantidis et al. 2007) depends on the simultaneous development of appropriate behavioral assays and model organisms amenable to large-scale genomic analysis and manipulation. It is the combination of such fine-grained neuronal analysis in animals with ever more sensitive psychophysical and brain imaging techniques in humans, complemented by the development of a robust theoretical predictive framework, that will hopefully lead to a rational understanding of consciousness, one of the central mysteries of life.

 

2 Level of arousal and content of consciousness

There are two common but distinct dimensions of the term consciousness,[9] one involving arousal and states of consciousness and the other involving content of consciousness and conscious states. To be conscious of anything the brain must be in a relatively high state of arousal (sometimes called vigilance), whether in wakefulness or REM sleep, vividly experienced in dreams although usually not remembered. Brain arousal level fluctuates in a circadian rhythm but may be influenced by lack of sleep, drugs and alcohol, physical exertion, etc. Arousal can be measured behaviorally by the signal amplitude that triggers some criterion reaction (for instance, the sound level necessary to evoke an eye movement or a head turn toward the sound source). Clinicians use scoring systems such as the Glasgow Coma Scale to assess the level of arousal in patients.

High arousal states are associated with conscious states that have specific content, seeing, hearing, remembering, planning or fantasizing about something. Different levels or states of consciousness are associated with different kinds of conscious experiences. The "awake" state is quite different from the "dreaming" state (for instance, the latter has little or no self-reflection) and from the state of deep sleep. In all three cases the basic physiology of the brain is affected, as it also is in altered states of consciousness, for instance after taking drugs or during meditation when conscious perception and insight may be enhanced compared to the normal waking state.

Clinicians talk about impaired states of consciousness as in "the comatose state", "the persistent vegetative state" (PVS), and "the minimally conscious state" (MCS). Here, "state" refers to different "amounts" of external/physical consciousness, from a total absence in coma, persistent vegetative state and general anesthesia, to a fluctuating and limited form of conscious sensation in a minimally conscious state such as sleep walking or during a complex partial epileptic seizure.[10] The repertoire of conscious states or experiences accessible to a patient in a minimally conscious state is comparatively limited. In brain death there is no arousal, but it is unknown whether the subjectivity of experience has been interrupted, rather than its observable link with the organism.

The potential richness of conscious experience appears to increase from deep sleep to drowsiness to full wakefulness, as might be quantified using notions from complexity theory that incorporate both the dimensionality as well as the granularity of conscious experience to give an integrated-information-theoretical account of consciousness.[11] As behavioral arousal increases so does the range and complexity of possible behavior. Yet in REM sleep there is a characteristic atonia, low motor arousal and the person is difficult to wake up, but there is still high metabolic and electric brain activity and vivid perception.

Many nuclei with distinct chemical signatures in the thalamusmidbrain and pons must function for a subject to be in a sufficient state of brain arousal to experience anything at all. These nuclei therefore belong to the enabling factors for consciousness. Conversely it is likely that the specific content of any particular conscious sensation is mediated by particular neurons in cortex and their associated satellite structures, including the amygdalathalamusclaustrum and the basal ganglia.

 

3 The neuronal basis of perception

The possibility of precisely manipulating visual percepts in time and space has made vision a preferred modality in the quest for the NCC. Psychologists have perfected a number of techniques – maskingbinocular rivalrycontinuous flash suppressionmotion induced blindnesschange blindnessinattentional blindness – in which the seemingly simple and unambiguous relationship between a physical stimulus in the world and its associated percept in the privacy of the subject's mind is disrupted.[12] In particular a stimulus can be perceptually suppressed for seconds or even minutes at a time: the image is projected into one of the observer's eyes but is invisible, not seen. In this manner the neural mechanisms that respond to the subjective percept rather than the physical stimulus can be isolated, permitting visual consciousness to be tracked in the brain. In a perceptual illusion, the physical stimulus remains fixed while the percept fluctuates. The best known example is the Necker cube whose 12 lines can be perceived in one of two different ways in depth.

 

A perceptual illusion that can be precisely controlled is binocular rivalry. Here, a small image, e.g., a horizontal grating, is presented to the left eye, and another image, e.g., a vertical grating, is shown to the corresponding location in the right eye. In spite of the constant visual stimulus, observers consciously see the horizontal grating alternate every few seconds with the vertical one. The brain does not allow for the simultaneous perception of both images.

Logothetis and colleagues[14] recorded a variety of visual cortical areas in awake macaque monkeys performing a binocular rivalry task. Macaque monkeys can be trained to report whether they see the left or the right image. The distribution of the switching times and the way in which changing the contrast in one eye affects these leaves little doubt that monkeys and humans experience the same basic phenomenon. In the primary visual cortex (V1) only a small fraction of cells weakly modulated their response as a function of the percept of the monkey while most cells responded to one or the other retinal stimulus with little regard to what the animal perceived at the time. But in a high-level cortical area such as the inferior temporal cortex along the ventral stream almost all neurons responded only to the perceptually dominant stimulus, so that a "face" cell only fired when the animal indicated that it saw the face and not the pattern presented to the other eye. This implies that NCC involve neurons active in the inferior temporal cortex: it is likely that specific reciprocal actions of neurons in the inferior temporal and parts of the prefrontal cortex are necessary.

A number of fMRI experiments that have exploited binocular rivalry and related illusions to identify the hemodynamic activity underlying visual consciousness in humans demonstrate quite conclusively that BOLD activity in the upper stages of the ventral pathway (e.g., the fusiform face area and the parahippocampal place area) as well as in early regions, including V1 and the lateral geniculate nucleus (LGN), follow the percept and not the retinal stimulus.[15] Further, a number of fMRI[16][17] and DTI experiments[18] suggest V1 is necessary but not sufficient for visual consciousness.[19]

In a related perceptual phenomenon, flash suppression, the percept associated with an image projected into one eye is suppressed by flashing another image into the other eye while the original image remains. Its methodological advantage over binocular rivalry is that the timing of the perceptual transition is determined by an external trigger rather than by an internal event. The majority of cells in the inferior temporal cortex and the superior temporal sulcus of monkeys trained to report their percept during flash suppression follow the animal's percept: when the cell's preferred stimulus is perceived, the cell responds. If the picture is still present on the retina but is perceptually suppressed, the cell falls silent, even though primary visual cortex neurons fire.[20][21] Single-neuron recordings in the medial temporal lobe of epilepsy patients during flash suppression likewise demonstrate abolishment of response when the preferred stimulus is present but perceptually masked.[22]

 

4 Global disorders of consciousness

Given the absence of any accepted criterion of the minimal neuronal correlates necessary for consciousness, the distinction between a persistently vegetative patient who shows regular sleep-wave transitions and may be able to move or smile, and a minimally conscious patient who can communicate (on occasion) in a meaningful manner (for instance, by differential eye movements) and who shows some signs of consciousness, is often difficult. In global anesthesia the patient should not experience psychological trauma but the level of arousal should be compatible with clinical exigencies.

 

Blood-oxygen-level-dependent fMRI (BOLD fMRI) have demonstrated normal patterns of brain activity in a patient in a vegetative state following a severe traumatic brain injury when asked to imagine playing tennis or visiting rooms in his/her house.[24] Differential brain imaging of patients with such global disturbances of consciousness (including akinetic mutism) reveal that dysfunction in a widespread cortical network including medial and lateral prefrontal and parietal associative areas is associated with a global loss of awareness.[25] Impaired consciousness in epileptic seizures of the temporal lobe was likewise accompanied by a decrease in cerebral blood flow in frontal and parietal association cortex and an increase in midline structures such as the mediodorsal thalamus.[26]

Relatively local bilateral injuries to midline (paramedian) subcortical structures can also cause a complete loss of awareness.These structures therefore enable and control brain arousal (as determined by metabolic or electrical activity) and are necessary neural correlates. One such example is the heterogeneous collection of more than two dozen nuclei on each side of the upper brainstem (pons, midbrain and in the posterior hypothalamus), collectively referred to as the reticular activating system (RAS). Their axons project widely throughout the brain. These nuclei – three-dimensional collections of neurons with their own cyto-architecture and neurochemical identity – release distinct neuromodulators such as acetylcholine, noradrenaline/norepinephrine, serotonin, histamine and orexin/hypocretin to control the excitability of the thalamus and forebrain, mediating alternation between wakefulness and sleep as well as general level of behavioral and brain arousal. After such trauma, however, eventually the excitability of the thalamus and forebrain can recover and consciousness can return.[27] Another enabling factor for consciousness are the five or more intralaminar nuclei (ILN) of the thalamus. These receive input from many brainstem nuclei and project strongly, directly to the basal ganglia and, in a more distributed manner, into layer I of much of the neocortex. Comparatively small (1 cm3 or less) bilateral lesions in the thalamic ILN completely knock out all awareness.[28]

 

5 Forward versus feedback projections

Many actions in response to sensory inputs are rapid, transient, stereotyped, and unconscious.[29] They could be thought of as cortical reflexes and are characterized by rapid and somewhat stereotyped responses that can take the form of rather complex automated behavior as seen, e.g., in complex partial epileptic seizures. These automated responses, sometimes called zombie behaviors,[30] could be contrasted by a slower, all-purpose conscious mode that deals more slowly with broader, less stereotyped aspects of the sensory inputs (or a reflection of these, as in imagery) and takes time to decide on appropriate thoughts and responses. Without such a consciousness mode, a vast number of different zombie modes would be required to react to unusual events.

A feature that distinguishes humans from most animals is that we are not born with an extensive repertoire of behavioral programs that would enable us to survive on our own ("physiological prematurity"). To compensate for this, we have an unmatched ability to learn, i.e., to consciously acquire such programs by imitation or exploration. Once consciously acquired and sufficiently exercised, these programs can become automated to the extent that their execution happens beyond the realms of our awareness. Take, as an example, the incredible fine motor skills exerted in playing a Beethoven piano sonata or the sensorimotor coordination required to ride a motorcycle along a curvy mountain road. Such complex behaviors are possible only because a sufficient number of the subprograms involved can be executed with minimal or even suspended conscious control. In fact, the conscious system may actually interfere somewhat with these automated programs.[31]

From an evolutionary standpoint it clearly makes sense to have both automated behavioral programs that can be executed rapidly in a stereotyped and automated manner, and a slightly slower system that allows time for thinking and planning more complex behavior. This latter aspect may be one of the principal functions of consciousness.

It seems possible that visual zombie modes in the cortex mainly use the dorsal stream in the parietal region.[29] However, parietal activity can affect consciousness by producing attentional effects on the ventral stream, at least under some circumstances. The conscious mode for vision depends largely on the early visual areas (beyond V1) and especially on the ventral stream.

Seemingly complex visual processing (such as detecting animals in natural, cluttered scenes) can be accomplished by the human cortex within 130–150 ms,[32][33] far too brief for eye movements and conscious perception to occur. Furthermore, reflexes such as the oculovestibular reflex take place at even more rapid time-scales. It is quite plausible that such behaviors are mediated by a purely feed-forward moving wave of spiking activity that passes from the retina through V1, into V4, IT and prefrontal cortex, until it affects motorneurons in the spinal cord that control the finger press (as in a typical laboratory experiment). The hypothesis that the basic processing of information is feedforward is supported most directly by the short times (approx. 100 ms) required for a selective response to appear in IT cells.

Conversely, conscious perception is believed to require more sustained, reverberatory neural activity, most likely via global feedback from frontal regions of neocortex back to sensory cortical areas[19] that builds up over time until it exceeds a critical threshold. At this point, the sustained neural activity rapidly propagates to parietal, prefrontal and anterior cingulate cortical regions, thalamus, claustrum and related structures that support short-term memory, multi-modality integration, planning, speech, and other processes intimately related to consciousness. Competition prevents more than one or a very small number of percepts to be simultaneously and actively represented. This is the core hypothesis of the global workspace theory of consciousness.[34][35]

In brief, while rapid but transient neural activity in the thalamo-cortical system can mediate complex behavior without conscious sensation, it is surmised that consciousness requires sustained but well-organized neural activity dependent on long-range cortico-cortical feedback.

 

 

References

  • Adamantidis A.R., Zhang F., Aravanis A.M., Deisseroth K. and de Lecea L. (2007) Neural substrates of awakening probed with optogenetic control of hypocretin neurons. Nature. advanced online publication.
  • Baars B.J. (1988) A cognitive theory of consciousness. Cambridge University Press: New York, NY.
  • Sian Beilock, Carr T.H., MacMahon C. and Starkes J.L. (2002) When paying attention becomes counterproductive: impact of divided versus skill-focused attention on novice and experienced performance of sensorimotor skills. J. Exp. Psychol. Appl. 8: 6–16.
  • Blumenfeld H., McNally K.A., Vanderhill S.D., Paige A.L., Chung R., Davis K., Norden A.D., Stokking R., Studholme C., Novotny E.J. Jr., Zubal I.G. and Spencer S.S. (2004) Positive and negative network correlations in temporal lobe epilepsy. Cereb. Cort. 14: 892–902.
  • Bogen J.E. (1995) On the neurophysiology of consciousness: I. An Overview. Consciousness & Cognition 4: 52–62.
  • Chalmers, David J. (June 1998), "What is a neural correlate of consciousness?", in Metzinger, ThomasNeural Correlates of Consciousness:Empirical and Conceptual Questions

 

, MIT Press (published September 2000), ISBN 0-262-13370-9

  • Crick F. and Koch C. (1990) Towards a neurobiological theory of consciousness. Seminars in Neuroscience Vol2, 263–275.
  • Crick F.C. and Koch C. (1995) Are we aware of neural activity in primary visual cortex? Nature 375: 121–3.
  • Dehaene S., Sergent C. and Changeux J.P. (2003) A neuronal network model linking subjective reports and objective physiological data during conscious perception. Proc. Natl. Acad. Sci. USA 100: 8520–5.
  • Haynes J.D. and Rees G. (2005) Predicting the orientation of invisible stimuli from activity in human primary visual cortex. Nat. Neurosci. 8: 686–91.
  • Kandel Eric R. (2007). In search of memory: The emergence of a new science of mind

 

. W. W. Norton & Company. ISBN 0393329372.

 

. Englewood, US-CO: Roberts & Company Publishers. ISBN 0-9747077-0-8.

 

 (2007))

  • Kreiman G., Fried I. and Koch C. (2002) Single-neuron correlates of subjective vision in the human medial temporal lobe. Proc Natl. Acad. Sci. USA 99: 8378–83.
  • Laureys S. (2005) The neural correlate of (un)awareness: Lessons from the vegetative state. Trends Cogn. Sci. 9: 556–9.
  • Lee S.H., Blake R. and Heeger D.J. (2007) Hierarchy of cortical responses underlying binocular rivalry. Nat. Neurosci. 10: 1048–54.
  • Leopold D.A. and Logothetis N.K. (1996) Activity changes in early visual cortex reflects monkeys' percepts during binocular rivalry. Nature 379: 549–53.
  • Logothetis N. (1998) Single units and conscious vision. Philos. Trans. R. Soc. Lond. B, 353: 1801–18.
  • Milner A.D. and Goodale M.A. (1995) The visual brain in action. Oxford University Press, Oxford, UK.
  • Owen A.M., Cleman M.R., Boly M., Davis M.H., Laureys S. and Pickard J.D. (2006) Detecting awareness in the vegetative state. Science 313: 1402.
  • Rees G. and Frith C. (2007) Methodologies for identifying the neural correlates of consciousness. In: The Blackwell Companion to Consciousness. Velmans M and Schneider S, eds., pp. 553–66. Blackwell: Oxford, UK.
  • Sheinberg D.L. and Logothetis N.K. (1997) The role of temporal cortical areas in perceptual organization. Proc. Natl. Acad. Sci. USA 94: 3408–13.
  • Schiff, Nicholas D. (November 2004), "The neurology of impaired consciousness: Challenges for cognitive neuroscience.", in Gazzaniga, Michael S., The Cognitive Neurosciences (3rd ed.), MIT Press, ISBN 0-262-07254-8
  • Shimono M. and Niki K. (2013) Global Mapping of the Whole-Brain Network Underlining Binocular Rivalry. Brain connectivity 3: 212-221.
  • Thorpe S., Fize D. and Marlot C. (1996) Speed of processing in the human visual system. Nature 381: 520–2.
  • Squire, Larry R. (2008). Fundamental neuroscience (3rd ed.). Academic Press. p. 1256. ISBN 0-12-374019-3.
  • Tononi G. (2004) An information integration theory of consciousness. BMC Neuroscience. 5: 42–72.
  • VanRullen R. and Koch C. (2003) Visual selective behavior can be triggered by a feed-forward process. J. Cogn. Neurosci. 15: 209–17.
  • Villablanca J.R. (2004) Counterpointing the functional role of the forebrain and of the brainstem in the control of the sleep-waking system. J. Sleep Res. 13: 179–208.
  • Zeman A. (2001) Consciousness

 

. Brain. 7: 1263-1289.