Is pain where you feel it in the body, or in the brain? Neurophenomenology and the spatial aspect of nociception

Pain is interesting, salient, mysterious. It may feel like it is in one specific place in or on the body. It may feel diffuse, with gradations, or it may seem referred from one area to another. What is happening in the brain and in the body as these spatial aspects of pain are experienced? How much of the causation of pain occurs where we feel it, and how much occurs in the brain? Below is a series of probes and thinking aloud about where pain is, with speculations to stimulate my thinking and yours.  I’m not a “pain expert”, nor a bodyworker that heals clients, nor a physiologist with a specialization in nociception, but a cognitive scientist, with clinical psychology training, interested in body phenomenology and the brain.  Please do post this essay to Facebook, share it, critique, respond, and comment (and it would be helpful to know if your background is in philosophy, neuroscience, bodywork, psychology, medicine, a student wanting to enter one of these or another field, etc). Pain should be looked at from multiple angles, with theoretical problems emphasized alongside clinical praxis, and with reductionistic accounts from neurophysiology juxtaposed against descriptions of the embodied phenomenology and existential structures.  As I have mentioned elsewhere, it is still early in the history of neurophenomenology…let a thousand flowers bloom when looking at pain. We need data, observations, insights and theories from both the experience side as well as the brain side. Francisco Varela aptly described how phenomenology and cognitive neuroscience should relate:

“The key point here is that by emphasizing a codetermination of both accounts one can explore the bridges, challenges, insights, and contradications between them. Both domains of phenomena have equal status in demanding full attention and respect for their specificity.”

We all know what pain is phenomenologically, what it feels like, but how to define it? The International Association for the Study of Pain offers this definition: “an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage.” Of particular interest to neurophenomenology and embodied cognitive science is their claim that “activity induced in the nociceptors and nociceptive pathways by a noxious stimulus is not pain, which is always a psychological state.” Good that they do not try to reduce the experience of pain to the strictly physiological dimension, but I wonder how Merleau-Ponty, with his non-dualistic ontology of the flesh would have responded. Pain seems to transgress the border of mind and body categories, does it not? I am slowly biting off chucks of the work on pain at the Stanford Encyclopedia of Philosophy. Lots of provocative angles, including this one:

“there appear to be reasons both for thinking that pains (along with other similar bodily sensations) are physical objects or conditions that we perceive in body parts, and for thinking that they are not. This paradox is one of the main reasons why philosophers are especially interested in pain.”

Right now I am particularly interested in the spatial aspect of where pain seems to be, what I might label the spatial phenomenology of nociception. When I introspect on aching parts of my feet, it seems as if the pain occupies a volume of space. Using manual pressure I can find places on my feel that are not sore, right next to areas that are slightly sore, which are in turn near focal areas of highest pain. It seems as if the pain is locatable “down there” in my body, and yet what we know about the nociceptive neural networks suggests the phenomenology is produced by complex interactions between flesh, nearby peripheral nerves, the central nervous system, and neurodynamics in the latter especially. A way of probing this this would be to examine the idea that the pain experience is the experiential correlate of bodily harm, a sort of map relating sensations to a corresponding nerve activated by damage to tissue. So, is the place in my body where I feel pain just the same as where the damage or strain is? Or, Is pain caused by pain-receptive nerves registering what is happening around them, via hormonal and electrical signals? Or is pain actually the nerve itself being “trapped” or damaged, yet in a volume of undamaged tissue one can feel hurts? Could the seeming volume of experienced pain-space be a partial illusion, produced by cognizing the tissue damage as some place near or overlapping with yet not spatially identical to where the “actual” damage is, in other words a case of existential-physiological discrepancy? One scenario could be, roughly, that pain “is” or “is made of” nerves getting signals about damage to tissue; another would be that pain “is” the nerves themselves being damaged or sustaining stress or injury. Maybe pain involves both? Maybe some pain is one, or the other? In terms of remembering how my heel pain started, it’s not so easy, but I love to walk an hour or two a day, and have done so for many years. I recall more than ten years ago playing football in the park, wearing what must have been the wrong sort of shoes, and upon waking the next day, having pretty serious pain in my heel. Here are some graphics that, intuitively, seem to map on to the areas where I perceive the pain to be most focal:

from bestfootdoc.com

from setup.tristatehand.com

from plantar-fasciitis-elrofeet.com

If I palpate my heel, I become aware of a phenomenologically complex, rich blend of pleasure and pain. I crave the sensation of pressure there, but it can be an endurance test when it happens. Does the sensation of pressure that I want reflect some body knowledge, some intuitive sense of what intervention will help my body heal? How could this be verified or falsified? It is not easy to describe the raw qualia of pain, actually. I can describe it as achey and moderately distressing when I walk around, and sharp upon palpating. Direct and forceful pressure on the heel area will make me wince, catch my breath, want to gasp or make sounds of pain/pleasure, and in general puts me in a state of heightened activation. But I love it when I can get a therapist to squeeze on it, producing what I call “pain-pleasure”:

from indyheelpaincenter.com

This diagram below helps me map the sensations to the neuroanatomy. We need to do more of this sort of thing. This kind of representation seems to me a new area for clinical neurophenomenological research (indeed, clinical neurophenomenology in general needs much more work, searching for those terms just leads back to my site, but see the Case History section in Sean Gallagher’s How the Body Shapes the Mind).

from reconstructivefootcaredoc.com

What is producing the pain-qualia, the particular feeling? Without going too far into varying differential diagnosis, it is commonly attributed to plantar fasciitis.  There the pain would be due to nociceptive nerve fibers activated by damage to the tough, fibrous fascia that attach to the calcaneus (heel bone) being strained, or sustaining small ripped areas, and/or local nerves being compressed or trapped. A 2012 article in Lower Extremity Review states that “evidence suggests plantar fasciitis is a noninflammatory degenerative condition in the plantar fascia caused by repetitive microtears at the medial tubercle of the calcaneus.” There are quite a few opinions out there about the role of bony calcium buildups, strain from leg muscles, specific trapped nerves and so forth, and it would be interesting to find out how different aspects of reported pain qualia map on to these. Below you can see the sheetlike fascia fiber, the posterior tibial nerve, and it’s branches that enable local sensations:

from aafp.org

Next: fascia and the innervation of the heel, from below:

from mollyjudge.com

Another view of the heel and innervation:

from mollyjudge.com

Below is a representation of the fascia under the skin:

from drwolgin.com

There is a very graphic,under the skin, maybe not SFW surgeon’s-eye perspective on these structures available here. Heel pain turns out to be very common, and is evidently one of the most frequently reported medical issues. Searching online for heel pain mapping brings up a representation purportedly of 2666 patients describing where they feel heel pain: I can’t find where this comes from originally and can’t speak to the methodology, rigor, or quality of the study, but the supposed data are interesting, as is the implicit idea of spatial qualia mapping:  the correspondence of experienced pain to a volume of space in the body. It also quite well represents where the pain is that I feel. The focal area seems to be where the fascia fibers attach to the calcaneus, an area that bears alot of weight, does alot of work, and is prone to overuse. So, where is the pain? Is it in the heel or the brain? Is it in the tissue, the nerve, or both? Is there a volume of flesh that contains the pain? I am going to have to think about these more, and welcome your input. What about the central nervous system that processes nociceptive afferents coming from the body? A good model of pain neurophenomenology should involve a number of cortical and subcortical areas that comprise the nociceptive neural network: -primary somatosensory cortex (S1) and secondary somatosensory cortex (S2): -insula -anterior cingulate cortex (ACC) -prefrontal cortex (PFC) -thalamus Here are some representations of the pain pathways, or the nociceptive neural network:

from Moisset and Bouhassira (2007)

Moisett el (2009)

 

from Tracey and Mantyh (2012)

Broadly speaking, pain seems to be generated by tissue damage, inflammation, compromising the integrity of tissue, stress on localized regions, and so forth being processed by peripheral afferent pain pathways in the body, then phylogenetically ancient subcortical structures, and then the aforementioned cortical regions or nociceptive neural network.  As I have mentioned many times, making a robust account of how various regions of the brain communicate such that a person experiences qualia or sensory phenomenology will need to reference neurodynamics, which integrates ideas from the physics of self-organization, complexity, chaos and non-linear dynamics into biology.  It is gradually becoming apparent to many if not most workers in the cognitive neurosciences that there are a host of mechanisms regions of the brain use to send signals, and many of these are as time dependent as space dependent. Michael Cohen puts it thusly: “The way we as cognitive neuroscientists typically link dynamics of the brain to dynamics of behavior is by correlating increases or decreases of some measure of brain activity with the cognitive or emotional state we hope the subject is experiencing at the time. The primary dependent measure in the majority of these studies is whether the average amount of activity – measured through spiking, event-related-potential or -field component amplitude, blood flow response, light scatter, etc. – in a region of the brain goes up or down. In this approach, the aim is to reduce this complex and enigmatic neural information processing system to two dimensions: Space and activation (up/down). The implicit assumption is that cognitive processes can be localized to specific regions of the brain, can be measured by an increase in average activity levels, and in different experimental conditions, either operate or do not. It is naïve to think that these two dimensions are sufficient for characterizing neurocognitive function. The range and flexibility of cognitive, emotional, perceptual, and other mental processes is huge, and the scale of typical functional localization claims – on the order of several cubic centimeters – is large compared to the number of cells with unique physiological, neurochemical, morphological, and connectional properties contained in each MRI voxel. Further, there are no one-to-one mappings between cognitive processes and brain regions: Different cognitive processes can activate the same brain region, and activation of several brain regions can be associated with single cognitive processes. In the analogy of Plato’s cave, our current approach to understanding the biological foundations of cognition is like looking at shadows cast on a region of the wall of the cave without observing how they change dynamically over time.” But what of the original question? Is pain where you feel it in the body, or in the brain? It seems to me the answer must be both.  The experience of pain being localized there or a little on the left is a product of local tissue signals and receptor activation, which produces peripheral afferent nerve firing, which gets processed by spinal afferent neurodynamics, brainstem activation, thalamic gating, and then somatosensory, insular, anterior cingulated, and prefrontal cortical regions. Yet the real model of pain, one that invokes mechanisms and causes, remains elusive. And a good model of pain must account for the possibility of pain without suffering as well! For now, what I can offer are probes to get us speculating, thinking critically, and eventually building a clinical neurophenomenology of pain. If that interests you, by all means get involved.

A complex mapping of the interior sense: why Damasio’s theory of embodied cognition focuses on the brainstem and viscera

If, like me,  you are interested in the biological dimensions of cognition, consciousness, and phenomenology, you tend to study the cortex.  Attention, decision-making, having a sense of self, perception, visual awareness, and many other key higher mental processes are modeled with data from cortical measurements, and especially with recent neurodynamics and computational neuroscience, there are increasingly sophisticated theories about the underlying mechanisms. But the cortex possibly gets too much attention compared to the rest of the brain and body.  This is partially because it indeed makes us human, but also for practical reasons, much of what we know about the brain comes from EEG research that with people is usually limited to scalp-based cortical signal acquisition. Dig a little deeper, say, when learning about emotions, and the student or scholar gets at least cursory introduction into the sub-cortical, emotion-regulating structures of the limbic system such as the hippocampus, thalamus, and hypothalamus. Our sense of salience, that things matter, our bodily sensations, our emotions and drives are associated especially with these sub-cortical structures. The study of how the brain processes emotions and bodily sensations has pointed some psychologists, neuroscientists, physicians, and philosophers in recent decades towards the idea of the experienced, phenomenologically lived body as the basis of consciousness and the self (or “self”). The growing sense for some of us about the limitations of traditional computationalist/cognitive theories has led to to the idea that mind and brain must be understood as “enactive“: via  evolutionarily and environmentally situated, physiological, embodied processes that “bring forth an experienced world”. Whatever cognition is, more than a few of us cognitive scientists nowadays think of it as somehow based in temporally ongoing, fleshy, existentially meaningful conscious life, or phenomenology. The mechanics of embodied mind, and the embodied basis of phenomenology, are very poorly understood by cognitive neuroscience, psychology, and medicine. Only very recently has there been a revival of interest especially in how visceral body states get processed by the peripheral nervous system and subsequently transformed by the central nervous system. One could understand this as a subfield of neurophenomenology:  how the brain and body enable “the bodily feelings I have now”, the experiential phenomenology of the internal body (if you have poked around this site you may have seen my own 2011 dissertation work was on this very subject). The rise of interest in embodied cognition has been hugely advanced through the work of the neurologist Antonio Damasio. This pioneer of embodied cognitive neuroscience has been focusing the attention of the psychology and cognitive neuroscience communities on the brainstem as the basis of consciousness.  The brainstem is not the usual topic when scientists bravely try to model conscious aspects of cognition, and my sense is that in the public mind it tends to register mostly when someone famous has medical problems as a result of brainstem damage causing loss of core visceral regulatory processes, such as with the death of Michael Jackson. In Damasios’ account, it is not merely a bit player in the grand drama of how body produces consciousness, but plays a starring role. Damasio (2010) states in Self Comes to Mind:Constructing the Conscious Brain , “I believe that the mind is not made by the cerebral cortex alone. Its first manifestations arise in the brain stem . ” (p. 75).

Courtesy Wikimedia Commons

Above is the brainstem, in red.  It receives inputs from the spinal cord, called “afferents”, that deliver signals from sensory nerves distributed throughout the body. These sensory nerves are affected by the homeostatic and visceral states of organs, such as our heart beating, the fullness of our bladder, blood sugar levels, the gas exchange in our lungs, and so forth. How much of the time these nerve signals resulting from visceral processes enter into conscious is a murky business. Cognitive scientists and others researching consciousness have not particularly referenced interior body psychophysiology and internal body-sensation in most theories about consciousness, but the work of Damasio is changing that. In general, research on the perception of visceral states or “inner psychophysics” goes in and out of scientific fashion, according to Gyorgy Adam’s wonderful overview of many decades of research, Visceral Perception: Understanding Internal Cognition.

Courtesy Wikimedia Commons

Below is an MRI of a beating heart and other visceral organs, with the spine visible. Afferent nerves “encode” information (or “information”) about the homeostatic and other dynamics of these systems, and send signals to the spinal cord and brain.

Courtesy Wikimedia Commons

While the idea that the brainstem produces the first manifestations of consciousness may seem radical, Damasio cites experimental evidence that perception of visceral states is mediated by the brainstem’s nucleus of the solitary tract and the pons. This gives us a window into understanding interoception:  the awareness of our visceral organs and internal body (though I think interoception also refers to unconscious signals from bodily organs affecting the brain and possibly influencing unconscious cognition). Building on generations of basic research on the neurophysiology of visceral perception, Damasio (2010) defines interoception as a “complex mapping of the interior sense” (p. 97). He emphasizes this occurs through an interoceptive network involving significant processing by the brainstem, which, unlike a mere relay, receives, processes and integrates afferents from the state of the visceral organs, and in turn projects to the thalamus. Through the work of Damasio, Bud Craig and others, we can model cognition as based in a central nervous system which filters and transforms signals from the lifegiving organs of the body. Building on their contributions, here is how I understand the neurophenomenology of visceral perception to work: our body organs are responding to existential life needs, our brainstem gets signals from the body organs and actively filters and transforms the signals, and in turn projects to the thalamus. Thalamo-cortical fibers then make synapses with neurons in the insula, cingulum, and somatosensory and orbitofrontal cortices, regions implicated in interoceptive activity and cognitive processes handling internal body information.  These areas all contribute to both consciousness in the foundational sense Damasio is investigating, and also produces specific awareness of our emotions and of our interior bodily sensations, such as feeling hungry. What goes on at the final stage, when cortical regions take the transformed bodily signal from the brainstem and thalamo-cortical processing, and somehow produce changes in consciousness? That gets into very complicated territory, and nowadays some of our most progressive thinkers use ideas and mechanisms from physics, such as Walter Freeman’s work on cortical neurodynamics, or that of Varela and colleagues. As of 2013 the dynamical aspects of interoception do not seem to be on many people’s radar besides mine and maybe a few others. What does it all mean for theories about the mind? If we accept that thalamic relay nuclei, activated by processed bodily interoceptive inputs in the brainstem, engage in further processing, and subsequently synapse on to (probably) dynamically interactive interoceptive centers in the insula and orbitofrontal, sensory, and cingulated cortical regions, what do we then understand about consciousness and cognition? As far as I can tell, the heart of Damasio’s theory is that visceral and homeostatic body states are “mapped” on to the brain via the brainstem,  and this mapping is what consciousness and the sense of self is “made of”. As we are organisms needing to engage in the right sort of behavior to survive, we depend on our sensory and visceral organs functioning appropriately. Our minds are thus built out of an evolutionarily developed machinery of life preservation. Put another way: the interior chemical milieu in our viscera affects nerve signals into the brainstem, and brainstem-mediated afferent signals tell our brain and mind about the state of our organs by projecting to the “gateway of the cortex”: the thalamus. A series of cortical regions process the thalamus gated body-signals, some of which are  cognitively and phenomenologically processed by a person as more emotionally and behaviorally salient, such as signals associated with food and thirst, pain and sex, and fighting or fleeing. Damasio, never one to shy away from big ideas and bold claims, sums up the state of his thinking in a 2010 interview:

Feelings, especially the kind that I call primordial feelings, portray the state of the body in our own brain. They serve notice that there is life inside the organism and they inform the brain (and its mind, of course), of whether such life is in balance or not. That feeling is the foundation of the edifice we call conscious mind. When the machinery that builds that foundation is disrupted by disease, the whole edifice collapses. Imagine pulling out the ground floor of a high-rise building and you get the picture. That is, by the way, precisely what happens in certain cases of coma or vegetative state. Now, where in the brain is that “feel-making” machinery? It is located in the brain stem and it enjoys a privileged situation. It is part of the brain, of course, but it is so closely interconnected with the body that it is best seen as fused with the body. I suspect that one reason why our thoughts are felt comes from that obligatory fusion of body and brain at brain stem level.

Can we not agree, that this is a profound way of thinking about the human condition?   Buy me a beer!

Neurodynamicist Walter Freeman on globalist vs. modularist approaches to EEG

Walter Freeman (http://sulcus.berkeley.edu/) is very prominent within the neurodynamics  world, but is perhaps not as well known to the neurophenomenology and emobodied cognition communities as he should be. This is possibly because of the forebodingly technical nature of the physics concepts he employs. He told me at a conference some years ago that his views were very close to those of Francisco Varela, who himself was a dynamical systems neuroscientist. He is quite possibly the world’s foremost expert modeling cognitive neurodynamics with EEG. I am examining his work again as I am in the process of designing an EEG study.  Our Science Club in Austin has been wrestling with his paper “Metastability, Instability, and State Tranistions in Neocortex” (Freeman and Holmes, 2005) where he presents a “globalist” alternative to researchers who focus on “modules lighting up:”

“Humans observe and grasp complex events and situations by means of expectations that have the form of theories. A theory determines the techniques of observation, which in turn shape what is observed and
understood. The classic case in physics is the wave–particle duality, in which the choice of one or two slits determines the outcome of the observation. A similar situation holds for the classic debates among proponents of competing theories about neocortical dynamics: localization vs. mass action. In one view, cortex is a collection of modules like a piano keyboard, each with its structure, signal, and contribution to behavior. In the other view, the neocortex is a continuous sheet of neuropil in each cerebral hemisphere, which embeds specialized architectures that were induced by axon tips arriving from extracortical sources during embryological development. Cooperative domains of varying size emerge within each hemisphere during behavior that includes the specialized.

Observers of both kinds use electroencephalograms (EEGs) and units to test their models. Localizationists (e.g. Calvin, 1996; Houk, 2001; Llina´s & Ribary, 1993; Makeig et al., 2002; Singer & Gray, 1995) analogize the neocortex to a cocktail party with standing speakers; each
module gives a signal that, when activated like a voice in a room, by volume conduction occupies the whole head and overlaps other signals. On the assumption of stationarity, the signals can be separated by independent components analysis (ICA) of multichannel EEG recordings. Globalists (e.g. Amit, 1989; Basar, 1998; Freeman, 2000) analogize neocortex to a planetary surface, the storms of which are generated by intrinsic dynamics and modified by the structural features of the surface.

These analogies throw into sharp relief the contrasting assumptions and inferences on which the two theories are based. Further, they justify the different methods by which the EEGs are processed, so that after the processing the two forms of the postprocessed EEG data differ dramatically, each legitimately in support of the parent theory. This is
why any description of a brain theory should be prefaced by a review of the methods used to get the data that supports the theory

Raw EEG data must be preprocessed prior to measurement. Here six decisions are summarized that have to be made by localizationists and globalists before they acquire EEG data. The choices are diametrically opposed (Freeman, Burke, & Holmes, 2003; Freeman & Holmes, 2005).

(i) According to localizationists, specified behaviors require activation of selected cortical modules that give signals at specific stages of the behaviors and are otherwise silent. The background EEG is incompatible
with this expectation, so they adopt the theory established years ago by Bullock (1969) and Elul (1972) that background EEG is dendritic noise, which is so smoothed by volume conduction, particularly at the scalp, that it has no identifiable spatiotemporal structure. They use time ensemble averaging (TEA) to attenuate the noise in proportion to the square root of the number of repeated stimuli that activate the modules, and to extract the expected signals as event related
potentials (ERPs). Globalists view the background
activity as the necessary pre-condition for execution of the specified behavior. That activity is modified by conditioned stimuli in differing ways in various areas of neocortex. The induced modifications are not time-locked to triggering stimuli, so that TEA cannot be used. Instead, spatial ensemble averaging (SEA) is used to extract reference values for sets of
phase and amplitude values from multiple EEGs.

(ii) The sensor of choice for localization is the depth microelectrode, because the size of the tip determines the acuity of spatial resolution. For globalization the spatial resolution is determined by the interelectrode
distances, so the electrode face to minimize noise should be as large as possible without touching neighbor electrodes.

(iii) Both observers use as many electrodes as possible. Localizationists space their electrodes as far apart as possible to sample from as many modules as they can. Globalists space them closely to avoid spatial aliasing and undersampling of spatial patterns of cortical activity.

(iv) Localizationists sharpen the spatial focus of the signals by high-pass spatial filters such as the Laplacian to correct the smoothing by volume
conduction. Globalists use low-pass spatial filters to attenuate contributions that are unique to individual electrodes and enhance the sampling of synchronized field potential activity.

(v) Narrow band-pass filters are favored by localizationists on the premise that modular signals are likely to be bursts at definite frequencies such as 40 Hz. Globalists prefer broad-band filters in expectation that oscillatory signals in EEGs are aperiodic (chaotic).

(vi) Signal sources are localized to modules by fitting equivalent dipoles to the filtered data in order to solve the inverse problem. Global signals are not confined to specific anatomical sites; they are localized not in
the Euclidean space of the forebrain but in multidimensional N-space, where N is the number of available electrodes. These diametrically opposed choices in data processing lead to widely divergent EEG data, and the data lead to theories that are skew. The two theoretical positions are more complementary than conflicting”

Modularism vs. globalism in cognitive neuroscience: implications for a science of body-knowledge

Models of how people are able to access physiological state information should take into account a long-running divide in cognitive neuroscience about to what extent explanations, models, and purported mechanisms privilege local, reductionistic, and/or modular theories, as opposed to global and holistic theories that emphasize connectedness with and interdependence of particular systems to the entire brain. The debate is described by the dynamicist Walter Freeman (Freeman and Holmes, 2005) :

“In one view, cortex is a collection of modules like a piano keyboard, each with its structure, signal, and contribution to behavior. In the other view, the neocortex is a continuous sheet of neuropil in each cerebral hemisphere, which embeds specialized architectures that were induced by axon tips arriving from extracortical sources during embryological development. Localizationists analogize the neocortex to a cocktail party with standing speakers; each module gives a signal that, when activated like a voice in a room, by volume conduction occupies the whole head and overlaps other signals… Globalists analogize neocortex to a planetary surface, the storms of which are generated by intrinsic dynamics and modified by the structural features of the surface”

The issue of “module activation” vs. “global pattern dynamics” should be kept in mind while reviewing the evidence for specific regions as crucial to biological models of sensation or perception. Nonetheless, for researchers investigating the neurophysiological basis of access to interoceptive information or body-knowledge focus on a number of cortical areas of interest, particularly somatosensory cortex, orbitofrontal cortex, insular cortex, and cingular cortex/cingulate gyrus. The somatosensory cortex or (S1) is conceived as containing “maps” of body surface areas. A standard interpretation would explain the perception of touch, temperature, and pain as occurring through sensory nerves, which are joined into the spinal cord, and which eventually route through the thalamus, and then the cortical region known as the postcentral gyrus.

One standard refinement to the traditional model gives the label “primary somatosensory cortex” only to the area shown in red, Brodmann area 3 (Kaas, 1983). In any event, primary somatosensory cortex/S1 is conventionally modeled as having four complete maps of the body surface. Arguably, the biological/anatomical grounding of this concept allows one to state that the somatosensory cortex/SI contains “multiple representations of the sensory surface of the body,” without running the risk of invoking representationalist epistemologies, with their polymorphous and “mentalistic” significations. Over time, a picture has emerged of sensation occurring on the outer surface of the body, and then activating S1: neurons in these regions are firing (generating electrical discharges and secreting “signaling” molecules across synapses) at a higher amplitude. Any model that accounts for how perception and awareness of the body is possible will likely need to reference the role of somatosensory cortex.

Another cortical region implicated in interoception or internal perception is that part of the frontal lobes known as the orbitofrontal cortex, which can be defined as that part of the prefrontal cortex that receives certain key afferent projections from the thalamus (the so-called “gateway to the cortex), which receives afferent projections from the body, including the visceral organs. In theory, enhanced activation of physiological state (such as heart rate increase) should be reflected in increased activation of orbitofrontal cortices.

Studies of the role of cortex in processing internal body state often emphasize the role of the (formerly) obscure structure known as the insula, a cortical structure which is nonetheless tucked away underneath the visible cortical layers. The anterior portion of the insula is especially implicated in interoception and internal body-state “information gain”.

Yet another specialized brain area becomes more active in those psychophysiological processes involving internal body state dynamics: a collection of white-matter fibers known as the cingulate gyrus of the cortex.

Again, it should be stressed that neuroscientists may debate the extent to which any one region’s activity should be privileged against global overall processes. Certainly, S1, orbitofrontal cortices, anterior insula and anterior cingulate gyrus are only one of a series of regions that play a part in allowing visceral perception, interoception, or a gain in information about the inside of the body. Emphasizing the contribution of such discreet areas carries forward the “modularist” tradition, while other models will stress more of a global or holistic system of interactions, which is a classic debate in psychology and neurology (Gardner, 1985). Arguably, the pre-understanding of how much processing is done by local “modules” as opposed to collective and global activities influences the very means of data collection (Freeman and Holmes, 2005).