Functional connectivity of the human insular cortex during noxious and innocuous thermal stimulation

The insula plays a key role in brain processing of noxious and innocuous thermal stimuli. The anterior and the posterior portions of the insular cortex are involved in different ways in nociceptive and thermoceptive processing. Therefore, their stimulus-specific functional connectivity may also differ. Here we used functional magnetic resonance imaging (fMRI) to investigate the activity and functional connectivity of insular cortex subregions during noxious and innocuous thermal stimulation. In 11 healthy subjects, psychophysically controlled noxious and innocuous warm and cold stimuli were applied to the left forearm. To differentiate between the subregions of the insular cortex involved in pain processing and those involved in temperature processing, a 2×2 factorial fMRI analysis was performed. Pain processing insular areas (main effect of pain) were detected in bilateral aINS and contralateral pINS. Temperature processing insular areas (main effect of temperature) were also found in bilateral aINS and contralateral pINS. The individual signal time courses from the pain- and temperature processing insular activation clusters were used for calculation and comparison of stimulus-specific functional connectivity of aINS and pINS by means of a correlation analysis. As expected, both aINS and pINS were functionally connected to a large brain network - which predominantly includes areas involved in nociception and thermoception: primary (S1) and secondary (S2) somatosensory cortices, cingulate gyrus, prefrontal cortex (PFC) and parietal association cortices (PA). When statistically compared, during both noxious and innocuous stimulation, aINS was more strongly connected to PFC and to ACC than was pINS; pINS meanwhile was more strongly connected to S1 and to the primary motor cortex (M1). Interestingly, S2 was more strongly connected to aINS than to pINS during painful stimulation but not during innocuous thermal stimulation. We conclude that aINS is more strongly functionally connected to areas known for affective and cognitive processing, whereas pINS is more strongly connected with areas known for sensory-discriminative processing of noxious and somatosensory stimuli.

[1]  Anthony K. P. Jones,et al.  The cortical representation of pain , 1999, PAIN.

[2]  A. Apkarian,et al.  Parsing pain perception between nociceptive representation and magnitude estimation. , 2009, Journal of neurophysiology.

[3]  A. Apkarian,et al.  Squirrel monkey lateral thalamus. I. Somatic nociresponsive neurons and their relation to spinothalamic terminals , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  M. Bushnell,et al.  Mood Influences Supraspinal Pain Processing Separately from Attention , 2009, The Journal of Neuroscience.

[5]  S. C. Gandevia,et al.  Somatotopic organization of the processing of muscle and cutaneous pain in the left and right insula cortex: A single-trial fMRI study , 2007, Pain.

[6]  Christian Maihöfner,et al.  Secondary somatosensory cortex is important for the sensory discriminative dimension of pain: a functional MRI-study , 2006 .

[7]  François Mauguière,et al.  Dual representation of pain in the operculo-insular cortex in humans. , 2003, Brain : a journal of neurology.

[8]  Roland Peyron,et al.  Role of Operculoinsular Cortices in Human Pain Processing: Converging Evidence from PET, fMRI, Dipole Modeling, and Intracerebral Recordings of Evoked Potentials , 2002, NeuroImage.

[9]  D. Kenshalo,et al.  Responses of primate SI cortical neurons to noxious stimuli. , 1983, Journal of neurophysiology.

[10]  M. Mesulam,et al.  Insula of the old world monkey. Architectonics in the insulo‐orbito‐temporal component of the paralimbic brain , 1982, The Journal of comparative neurology.

[11]  David Bowsher,et al.  Central Representation of Somatic Sensations in the Parietal Operculum (SII) and Insula , 2004, European Neurology.

[12]  Frank Seifert,et al.  Representation of cold allodynia in the human brain—A functional MRI study , 2007, NeuroImage.

[13]  R. Koeppe,et al.  Comparison of human cerebral activation pattern during cutaneous warmth, heat pain, and deep cold pain. , 1996, Journal of neurophysiology.

[14]  K. Davis,et al.  Two systems of resting state connectivity between the insula and cingulate cortex , 2009, Human brain mapping.

[15]  Raymond J. Dolan,et al.  Anxiety Reduction through Detachment: Subjective, Physiological, and Neural Effects , 2005, Journal of Cognitive Neuroscience.

[16]  M. Rowbotham,et al.  A new human experimental pain model: the heat/capsaicin sensitization model. , 1999, Neuroreport.

[17]  T. V. Sewards,et al.  The medial pain system: Neural representations of the motivational aspect of pain , 2002, Brain Research Bulletin.

[18]  J. Price,et al.  Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys , 1995, The Journal of comparative neurology.

[19]  M. Mesulam,et al.  Insula of the old world monkey. III: Efferent cortical output and comments on function , 1982, The Journal of comparative neurology.

[20]  M. Bushnell,et al.  Pain affect encoded in human anterior cingulate but not somatosensory cortex. , 1997, Science.

[21]  Philippe Kahane,et al.  Middle short gyrus of the insula implicated in pain processing , 2008, PAIN.

[22]  F. Benedetti,et al.  Neuropharmacological Dissection of Placebo Analgesia: Expectation-Activated Opioid Systems versus Conditioning-Activated Specific Subsystems , 1999, The Journal of Neuroscience.

[23]  S. Minoshima,et al.  Keeping pain out of mind: the role of the dorsolateral prefrontal cortex in pain modulation. , 2003, Brain : a journal of neurology.

[24]  David Yarnitsky,et al.  Thermal testing: normative data and repeatability for various test algorithms , 1994, Journal of the Neurological Sciences.

[25]  R. Peyron,et al.  Functional imaging of brain responses to pain. A review and meta-analysis (2000) , 2000, Neurophysiologie Clinique/Clinical Neurophysiology.

[26]  C. Büchel,et al.  Habituation to painful stimulation involves the antinociceptive system , 2007, Pain.

[27]  A. Craig How do you feel? Interoception: the sense of the physiological condition of the body , 2002, Nature Reviews Neuroscience.

[28]  Jason G. Craggs,et al.  Placebo analgesia is accompanied by large reductions in pain-related brain activity in irritable bowel syndrome patients , 2007, Pain.

[29]  Lumy Sawaki,et al.  Roles of the Insular Cortex in the Modulation of Pain: Insights from Brain Lesions , 2009, The Journal of Neuroscience.

[30]  Christian Maihöfner,et al.  Temporo-spatial analysis of cortical activation by phasic innocuous and noxious cold stimuli – a magnetoencephalographic study , 2002, Pain.

[31]  Nikolaus Weiskopf,et al.  Anterolateral Prefrontal Cortex Mediates the Analgesic Effect of Expected and Perceived Control over Pain , 2006, The Journal of Neuroscience.

[32]  C. L. Kwan,et al.  Functional MRI study of thalamic and cortical activations evoked by cutaneous heat, cold, and tactile stimuli. , 1998, Journal of neurophysiology.

[33]  Christian Maihöfner,et al.  Differential coding of hyperalgesia in the human brain: A functional MRI study , 2005, NeuroImage.

[34]  I. Tracey,et al.  The insula: A multidimensional integration site for pain , 2007, Pain.

[35]  A. Schnitzler,et al.  Differential coding of pain intensity in the human primary and secondary somatosensory cortex. , 2001, Journal of neurophysiology.

[36]  Krish D. Singh,et al.  fMRI of Thermal Pain: Effects of Stimulus Laterality and Attention , 2002, NeuroImage.

[37]  B. Vogt,et al.  The medial pain system, cingulate cortex, and parallel processing of nociceptive information. , 2000, Progress in brain research.

[38]  M. Bushnell,et al.  Cortical representation of the sensory dimension of pain. , 2001, Journal of neurophysiology.

[39]  M. Ingvar Pain and functional imaging. , 1999, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[40]  A. Craig,et al.  Cytoarchitectonic and immunohistochemical characterization of a specific pain and temperature relay, the posterior portion of the ventral medial nucleus, in the human thalamus. , 2000, Brain : a journal of neurology.

[41]  Brandall Y. Suyenobu,et al.  The neural correlates of placebo effects: a disruption account , 2004, NeuroImage.

[42]  R. Kraft,et al.  Brain Mechanisms Supporting Spatial Discrimination of Pain , 2007, The Journal of Neuroscience.

[43]  Jian Kong,et al.  Using fMRI to dissociate sensory encoding from cognitive evaluation of heat pain intensity , 2006, Human brain mapping.

[44]  E. Reiman,et al.  Thermosensory activation of insular cortex , 2000, Nature Neuroscience.

[45]  E. Disbrow,et al.  Brain processing of capsaicin-induced secondary hyperalgesia , 1999, Neurology.

[46]  D. Price Psychological and neural mechanisms of the affective dimension of pain. , 2000, Science.

[48]  Elena Peltz,et al.  Medial Prefrontal Cortex Activity Is Predictive for Hyperalgesia and Pharmacological Antihyperalgesia , 2009, The Journal of Neuroscience.

[49]  Ronald Melzack,et al.  From the gate to the neuromatrix , 1999, Pain.

[50]  Jonathan C. W. Brooks,et al.  Somatotopic organisation of the human insula to painful heat studied with high resolution functional imaging , 2005, NeuroImage.

[51]  Irene Tracey,et al.  The Cerebral Signature for Pain Perception and Its Modulation , 2007, Neuron.

[52]  F. Mauguière,et al.  Representation of pain and somatic sensation in the human insula: a study of responses to direct electrical cortical stimulation. , 2002, Cerebral cortex.

[53]  R. Peyron,et al.  An fMRI study of cortical representation of mechanical allodynia in patients with neuropathic pain , 2004, Neurology.

[54]  A. Craig,et al.  Pain mechanisms: labeled lines versus convergence in central processing. , 2003, Annual review of neuroscience.

[55]  G. Duncan,et al.  Is there a role for the parietal lobes in the perception of pain? , 2003, Advances in neurology.

[56]  Enrico Simonotto,et al.  The functional anatomy of inspection time: an event-related fMRI study , 2004, NeuroImage.

[57]  Richard J. Davidson,et al.  Individual Differences in the Effects of Perceived Controllability on Pain Perception: Critical Role of the Prefrontal Cortex , 2007, Journal of Cognitive Neuroscience.

[58]  J. Maisog,et al.  Pain intensity processing within the human brain: a bilateral, distributed mechanism. , 1999, Journal of neurophysiology.

[59]  Jason G. Craggs,et al.  Functional brain interactions that serve cognitive–affective processing during pain and placebo analgesia , 2007, NeuroImage.

[60]  M. Trimble,et al.  The insular Lobe of Reil–its Anatamico-Functional, behavioural and Neuropsychiatric attributes in humans–a review , 2004, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

[61]  C. Maihöfner,et al.  Central mechanisms of experimental and chronic neuropathic pain: Findings from functional imaging studies , 2009, Cellular and Molecular Life Sciences.

[62]  Sterling C. Johnson,et al.  Anteroposterior somatotopy of innocuous cooling activation focus in human dorsal posterior insular cortex. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.

[63]  R. Treede,et al.  Human brain mechanisms of pain perception and regulation in health and disease , 2005, European journal of pain.

[64]  Katrin Amunts,et al.  Cytoarchitecture and probabilistic maps of the human posterior insular cortex. , 2010, Cerebral cortex.

[65]  A. Craig,et al.  How do you feel — now? The anterior insula and human awareness , 2009, Nature Reviews Neuroscience.

[66]  Frank Seifert,et al.  Functional imaging of sensory decline and gain induced by differential noxious stimulation , 2008, NeuroImage.

[67]  Edward E. Smith,et al.  Placebo-Induced Changes in fMRI in the Anticipation and Experience of Pain , 2004, Science.

[68]  K. Yau,et al.  Interoception: the sense of the physiological condition of the body , 2003, Current Opinion in Neurobiology.

[69]  N. Costes,et al.  Haemodynamic brain responses to acute pain in humans: sensory and attentional networks. , 1999, Brain : a journal of neurology.

[70]  Ming-Tsung Tseng,et al.  Distinct and shared cerebral activations in processing innocuous versus noxious contact heat revealed by functional magnetic resonance imaging , 2009, Human brain mapping.