Key Points
-
Observational evidence has highlighted similarities between physical pain and 'social pain' — the painful feelings associated with actual or potential damage to social bonds. Thus, experiences of social rejection or loss are often described with physical pain words ('hurt feelings' and 'broken heart'), and both physical and social pain are highly noxious experiences.
-
Research on the neurochemical substrates of physical and social pain has demonstrated that both rely on opioid processes. Thus, opiates, which are potent analgesics, have also been shown to reduce separation distress behaviours in animals.
-
Neuroimaging research has demonstrated that experiences of social exclusion predominantly activate the dorsal anterior cingulate cortex (dACC) and anterior insula (AI) — regions known to have a role in the distressing experience of physical pain.
-
In addition, several lines of research have shown that experiences of negative social evaluation, rejection from a romantic partner and bereavement also lead to activity in the dACC and AI. A few studies have also shown neural activity in regions associated with the sensory component of pain (posterior insula); additional research will be needed to determine the types of social pain that elicit sensory-related processing.
-
On the basis of the shared neural circuitry associated with physical and social pain, research has shown that individuals who are more sensitive to one kind of pain are also more sensitive to the other. Thus, greater physical pain experience or sensitivity is associated with greater social pain sensitivity (rejection sensitivity or anxious attachment).
-
Another consequence of a physical–social pain overlap is that factors that alter one type of pain have a similar effect on the other. For example, social support, which is known to reduce social pain, can also reduce physical pain, and Tylenol (paracetamol; Johnson and Johnson), which is known to reduce physical pain, can also reduce social pain.
-
On the basis of the role of the dACC and AI in responding to socially painful experience, these regions may be crucial for translating experiences of social disconnection into downstream physiological responses, which have implications for health. Indeed, the dACC and AI may have a mediating role in the links between social rejection and both inflammatory activity and depression.
Abstract
Experiences of social rejection, exclusion or loss are generally considered to be some of the most 'painful' experiences that we endure. Indeed, many of us go to great lengths to avoid situations that may engender these experiences (such as public speaking). Why is it that these negative social experiences have such a profound effect on our emotional well-being? Emerging evidence suggests that experiences of social pain — the painful feelings associated with social disconnection — rely on some of the same neurobiological substrates that underlie experiences of physical pain. Understanding the ways in which physical and social pain overlap may provide new insights into the surprising relationship between these two types of experiences.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Effects of an open-label placebo intervention on reactions to social exclusion in healthy adults: a randomized controlled trial
Scientific Reports Open Access 16 September 2023
-
A Systematic Review and Meta-analysis of Electrophysiological Studies of Online Social Exclusion: Evidence for the Neurobiological Impacts of Cyberbullying
Adolescent Research Review Open Access 22 May 2023
-
The unseen epidemic: trauma and loneliness in urban midlife women
Women's Midlife Health Open Access 27 October 2022
Access options
Subscribe to this journal
Receive 12 print issues and online access
$189.00 per year
only $15.75 per issue
Rent or buy this article
Prices vary by article type
from$1.95
to$39.95
Prices may be subject to local taxes which are calculated during checkout



References
MacLean, P. D. in Neurobiology of Cingulate Cortex and Limbic Thalamus: A Comprehensive Handbook (eds Vogt, B. A. & Gabriel, M.) 1–15 (Birkhauser, 1993).
Jaremka, L. M., Gabriel, S. & Carvallo, M. What makes us the best also makes us feel the worst: the emotional impact of independent and interdependent experiences. Self Identity 10, 44–63 (2011).
Baumeister, R. F. & Leary, M. R. The need to belong: desire for interpersonal attachments as a fundamental human motivation. Psych. Bull. 117, 497–529 (1995). This paper discusses the importance of social connection for survival and evaluates the hypothesis that humans have a fundamental 'need to belong'.
Harlow, H. F. & Zimmerman, R. R. Affectional responses in the infant monkey. Science 102, 501–509 (1959).
Bowlby, J. Attachment and Loss, Vol. I: Attachment (Basic Books, 1969).
Panksepp, J. Affective Neuroscience (Oxford Univ. Press, 1998).
Eisenberger, N. I., Lieberman, M. D. & Williams, K. D. Does rejection hurt? An fMRI study of social exclusion. Science 302, 290–292 (2003). This was the first study to examine the neural correlates of social pain in humans and the first to show activation of affective pain-related neural regions in response to social exclusion.
Eisenberger, N. I. & Lieberman, M. D. Why rejection hurts: the neurocognitive overlap between physical and social pain. Trends Cogn. Sci. 8, 294–300 (2004).
Eisenberger, N. I. in The Handbook of Social Neuroscience (eds Decety, J. & Cacioppo, J.) 586–598 (Oxford Univ. Press, 2011).
MacDonald, G. & Leary, M. R. Why does social exclusion hurt? The relationship between social and physical pain. Psych. Rev. 131, 202–223 (2005). This paper provides an in-depth review of the psychological overlap between physical and social pain.
International Association for the Study of Pain (IASP) Task Force on Taxonomy. in Classification of Chronic Pain, 2nd edn (eds Merskey H. & Bogduk, N.) 209–214 (IASP Press, 1994).
Freud, S. Beyond the Pleasure Principle and Other Writings 239 (Penguin Books, 1926).
Leary, M. R. & Springer, C. in Behaving Badly: Aversive Behaviors in Interpersonal Relationships (ed. Kowalski, R. M.) 151–175 (American Psychological Association, 2001).
Tang, N. K. Y. & Crane, C. Suicidality in chronic pain: a review of prevalence risk factors and psychological links. Psychol. Med. 36, 575–586 (2006).
Darbonne, A. R. Study of psychological content in the communications of suicidal individuals. J. Consult. Clin. Psych. 33, 46–50 (1969).
Mee, S., Bunney, B. G., Reist, C., Potkin, S. G. & Bunney, W. E. Psychological pain: a review of evidence. J. Psychiatr. Res. 40, 680–690 (2006).
Beck, A. T., Laude, R. & Bohnert, M. Ideational components of anxiety neurosis. Arch. Gen. Psychiatry 31, 319–325 (1974).
Chen, Z., Williams, K. D., Fitness, J. & Newton, N. When hurt will not heal: exploring the capacity to relive social and physical pain. Psychol. Sci. 19, 789–795 (2008).
Riva, P., Wirth, J. H. & Williams, K. D. The consequences of pain: the social and physical pain overlap on psychological responses. Eur. J. Soc. Psychol. 41, 681–687 (2011).
Gudmundsdottir, M. Embodied grief: bereaved parents' narratives of their suffering body. Omega (Westport) 59, 253–269 (2009).
Zisook, S., Devaul, R. A. & Click, M. A. Measuring symptoms of grief and bereavement. Am. J. Psychiatry 139, 1590–1593 (1982).
Eccleston, C. & Combez, G. Pain demands attention: a cognitive-affective of the interruptive function of pain. Psychol. Bull. 125, 356–366 (1999).
Nagasako, E. M., Oaklander, A. L. & Dworkin, R. H. Congenital insensitivity to pain: an update. Pain 101, 213–219 (2003).
Price, D. D., von der Gruen, A., Miller, Raffi, A. & Price, C. A psychophysical analysis of morphine analgesia. Pain 22, 261–269 (1985).
Kieffer, B. L. & Gavériaux-Ruff, C. Exploring the opioid system by gene knockout. Prog. Neurobiol. 66, 285–306 (2002).
Panksepp, J., Herman, B., Conner, R., Bichop, P. & Scott, J. P. The biology of social attachments: opiates alleviate separation distress. Biol. Psychiatry 13, 607–618 (1978). This paper provides a review of the research showing that opioids can reduce social pain (separation distress) in addition to physical pain.
Herman, B. H. & Panksepp, J. Effects of morphine and naxolone on separation distress and approach and approach attachment: evidence for opiate mediation of social affect. Pharmacol. Biochem. Behav. 9, 213–220 (1978).
Kalin, N. H., Shelton, S. E. & Barksdale, C. M. Opiate modulation of separation-induced distress in non-human primates. Brain Res. 440, 285–292 (1988).
Warnick, J. E., McCurdy, C. R. & Sufka, K. J. Opioid receptor function in social attachment in young domestic fowl. Behav. Brain Res. 160, 277–285 (2005).
Moles, A., Kieffer, B. L. & D'Amato, F. R. Deficit in attachment behavior in mice lacking the mu-opioid receptor gene. Science 304, 1983–1986 (2004).
Panksepp, J., Najam, N. & Soares, F. Morphine reduces social cohesion in rats. Pharmacol. Biochem. Behav. 11, 131–134 (1979).
Fabre-Nys, C., Meller, R. E. & Keverne, E. B. Opiate antagonists stimulate affiliative behaviour in monkeys. Pharmacol. Biochem. Behav. 16, 653–659 (1992).
Treede, R.-D., Kenshalo, D. R., Gracely, R. H. & Jones, A. K. P. The cortical representation of pain. Pain 79, 105–111 (1999).
Price, D. D. Psychological and neural mechanisms of the affective dimension of pain. Science 288, 1769–1772 (2000).
Danziger, N. & Willer, J.C. Tension-type headache as the unique pain experience of a patient with congenital insensitivity to pain. Pain 117, 478–483 (2005).
Ballantine, H. T., Bouckoms, A. J., Thomas, E. K. & Giriunas, I. E. Treatment of psychiatric illness by stereotactic cingulotomy. Biol. Psychiatry 22, 807–819 (1987).
Foltz, E. L. & White, L. E. Pain “relief” by frontal cingulumotomy. J. Neurosurg. 19, 89–100 (1962). This neurosurgical report demonstrates that, among patients with chronic pain, lesions to the dACC can reduce the 'distress' or 'suffering' associated with a physically painful experience.
Johansen, J. P., Fields, H. L. & Manning, B. H. The affective component of pain in rodents: direct evidence for a contribution of the anterior cingulate cortex. Proc. Natl Acad. Sci. USA 98, 8077–8082 (2001).
Gabriel, M., Kubota, Y., Sparenborg, S., Straube, K. & Vogt, B. A. Effects of cingulate cortical lesions on avoidance learning and training-induced unit activity in rabbits. Exp. Brain Res. 86, 585–600 (1991).
Berthier, M., Starkstein, M. D. & Leiguarda, R. Asymbolia for pain: a sensory-limbic disconnection syndrome. Ann. Neurol. 24, 41–49 (1988).
Greenspan, J. D., Lee, R. L. & Lenz, F. A. Pain sensitivity alterations as a function of lesion location in the parasylvian. Pain 81, 273–282 (1999).
Rainville, P., Duncan, G. H., Price, D. D., Carrier, B. & Bushnell, M. D. Pain affect encoded in human anterior cingulate but not somatosensory cortex. Science 277, 968–971 (1997). This study creatively highlights the role of the dACC in the affective component of pain.
Craig, A. D., Reiman, E. M., Evans, A. & Bushnell, M. C. Functional imaging of an illusion of pain. Nature 384, 258–260 (1996).
Craig, A. D. How do you feel? Interoception: the sense of the physiological condition of the body. Nature Rev. Neurosci. 3, 655–666 (2002).
Kulkarni, B. et al. Attention to pain localization and unpleasantness discriminates the functions of the medial and lateral pain systems. Eur. J. Neurosci 21, 3133–3142 (2005).
Shreckenberger, M. et al. The unpleasantness of toxic pain is encoded by the insular cortex. Neurology 64, 1175–1183 (2005).
Tölle, T. R. et al. Region specific encoding of sensory pain and affective components of pain in the human brain:a positron emission tomography correlation analysis. Ann. Neurol. 45, 40–47 (1999).
Baumgartner, U. et al. High opiate receptor binding potential in the human lateral pain system. Neuroimage 30, 692–699 (2006).
Jones, A. K. P. et al. In vivo distribution of opioid receptors in man in relation to the cortical projections of the medial and lateral pain systems measured with positron emission tomography. Neurosci. Lett. 126, 25–28 (1991).
Schnitzler, A. & Ploner, M. Neurophysiology and functional neuroanatomy of pain perception. J. Clin. Neurophysiol. 17, 592–603 (2000).
Apkarian, A. V., Bushnell, M. C., Treede, R.-D. & Zubieta, J. K. Human brain mechanisms of pain perception and regulation in health and disease. Eur. J. Pain 9, 463–484 (2005).
Bushnell, M. C. et al. Pain perception: is there a role for primary somatesensory cortex? Proc. Natl Acad. Sci. USA 96, 7705–7709 (1999).
Greenspan, J. D. & Winifield, J. A. Reversible and tactile deficits associated with a cerebral tumor compressing the posterior insula and parietal operculum. Pain 50, 29–39 (1992).
Ploner, M., Freund, H. J. & Schnitzler, A. Pain affect without pain sensation in a patient with a postcentral lesion. Pain 81, 211–214 (1999).
Hofbauer, R. K., Rainville, P., Duncan, G. H. & Bushnell, M. C. Cortical representations of the sensory dimension of pain. J. Neurophysiol. 86, 402–411 (2001).
MacLean, P. D. The Triune Brain in Evolution: Role in Paleocerebral Functions (First Plenum Printing, 1990).
MacLean, P. D. & Newman, J. D. Role of midline frontolimbic cortex in production of the isolation call squirrel monkeys. Brain Res. 450, 111–123 (1988).
Hadland, K. A., Rushworth, M. F. S., Gaffan, D. & Passingham, R. E. The effect of cingulate lesions on social behaviour and emotion. Neuropsychologia 41, 919–931 (2003).
Smith, W. The functional significance of the rostral cingular cortex as revealed by its responses to electrical excitation. J. Neurophysiol. 8, 241–255 (1945).
Robinson, B. W. in Social Communication Among Primates (ed. Altmann, S. A.) 135–147 (Univ. of Chicago Press, 1967).
Murphy, M. R., MacLean, P. D. & Hamilton, S. C. Species-typical behavior of hamsters deprived from birth of the neocortex. Science 213, 459–461 (1981).
Slotnick, B. M. & Nigrosh, B. J. Maternal behavior of mice with cingulated cortical, amygdala, or septal lesions. J. Comp. Physiol. Psychol. 88, 118–127 (1975).
Stamm, J. The function of the medial cortex in maternal behavior of rats. J. Comp. Physiol. Psychol. 48, 347–356 (1955).
Le Beau, J. Anterior cingulectomy in man. J.Neurosurg. 11, 268–276 (1954).
Tow, P. M. & Whitty, C. W. M. Personality changes after operations on the cingulate gyrus in man. J. Neuorol. Neurosurg. Psychiatry 16, 186–193 (1953).
DeWall, C. N. et al. Tylenol reduces social pain: behavioral and neural evidence. Psychol. Sci 21, 931–937 (2010). This study demonstrated that Tylenol, a physical pain reliever, could reduce social pain as well.
Masten, C. L., Telzer, E. H., Fuligni, A. J., Lieberman, M. D. & Eisenberger, N. I. Time spent with friends in adolescence relates to less neural sensitivity to later peer rejection. Soc. Cogn. Affect. Neurosci. 7, 106–114 (2012).
Bolling, D. Z. et al. Dissociable brain mechanisms for processing social exclusion and rule violation. Neuroimage 54, 2462–2471 (2011).
Krill, A. & Platek, S. M. In-group and out-group membership mediates anterior cingulate activation to social activation to social exclusion. Front. Evol. Neurosci. 1, 1 (2009).
Masten, C. L., Telzer, E. H. & Eisenberger, N. I. An fMRI investigation of attributing negative social treatment to racial discrimination. J. Cogn. Neurosci. 23, 1042–1051 (2011).
Bolling, D. Z., Pelphrey, K. A. & Vander Wyk, B. C. Differential brain responses to social exclusion by one's own versus opposite-gender peers. Soc. Neurosci. 7 Oct 2011 (doi:10.1080/17470919.2011.623181).
Moor, B. G. et al. Social exclusion and punishment of excluders: neural correlates and developmental trajectories. Neuroimage 59, 708–717 (2012).
Masten, C. L. et al. Neural correlates of social exclusion during adolescence: understanding the distress of peer rejection. Soc. Cogn. Affect. Neurosci. 4, 143–157 (2009).
Masten, C. L. et al. An fMRI investigation of responses to peer rejection in adolescents with autism spectrum disorders. Dev. Cogn. Neurosci. 1, 260–270 (2011).
Bolling, D. Z. et al. Enhanced neural responses to rule violation in children with autism: a comparison to social exclusion. Dev. Cogn. Neurosci. 1, 280–294 (2011).
Onoda, K. et al. Decreased ventral anterior cingulate cortex activity is associated with reduced social pain during emotional support. Soc. Neurosci. 4, 443–454 (2009).
DeWall, C. N., Masten, C. L., Powell, D., Schurtz, D. R. & Eisenberger, N. I. Do neural responses to rejection depend on attachment style? An fMRI study. Soc. Cogn. Affect. Neurosci. 7, 184–192 (2012).
Eisenberger, N. I., Taylor, S. E., Gable, S. L., Hilmert, C. J. & Lieberman, M. D. Neural pathways link social support to attenuated neuroendocrine stress responses. Neuroimage 35, 1601–1612 (2007).
Onoda, K. et al. Does low self-esteem enhance social pain? The relationships between trait self-esteem and anterior cingulate cortex activation induced by ostracism. Soc. Cogn. Affect. Neurosci. 5, 383–391 (2010).
Eisenberger, N. I., Way, B., Taylor, S. E., Welch, W. T. & Lieberman, M. D. Understanding genetic risk for aggression: clues from the brain's response to social exclusion. Biol. Psychiatry 61, 1100–1108 (2007).
Eisenberger, N. I., Gable, S. L. & Lieberman, M. D. Functional magnetic resonance imaging responses relate to differences in real-world social experience. Emotion 7, 745–754 (2007).
Sebastian, C. L. et al. Developmental influences on the neural bases of responses to social rejection: implications of social neuroscience for education. Neuroimage 57, 686–694 (2011).
Devinsky, O., Morrell, M. J. & Vogt, B. A. Contributions of anterior cingulate cortex to behavior. Brain 118, 279–306 (1995).
Somerville, L. H., Heatherton, T. F. & Kelley, W. M. Anterior congulate cortex responds differentially to expectancy violation and social rejection. Nature Neurosci. 9, 1007–1008 (2006).
Hung., Y, Smith, M. L. & Taylor, M. J. Development of ACC-amygdala activations in processing unattended fear. Neuroimage 60, 545–552 (2012).
Wager, T. D. et al. Brain mediators of cardiovascular responses to social threat, part II: prefrontal-subcortical pathways and relationship with anxiety. Neuroimage 47, 836–851 (2009).
Eisenberger, N. I., Inagaki, T. K., Muscatell, K. A., Haltom, K. E. B. & Leary, M. R. The neural sociometer: brain mechanisms underlying state self-esteem. J. Cogn. Neurosci. 23, 3448–3455 (2011).
Takahashi, H. et al. When your gain is my pain and your pain is my gain: neural correlates of envy and schadenfreude. Science 323, 937–939 (2009).
Kross, E., Egner, T., Ochsner, K., Hirsch, J. & Downey, G. Neural dynamics of rejection sensitivity. J. Cogn. Neurosci. 19, 945–956 (2007).
Burklund, L. J., Eisenberger, N. I. & Lieberman, M. D. Rejection sensitivity moderates dorsal anterior cingulate activity to disapproving facial expressions. Soc. Neurosci. 2, 238–253 (2007).
Fisher, H. E., Brown, L. L., Aron, A., Strong, G. & Mashek, D. Reward, addiction, and emotion regulation systems associated with rejection in love. J. Neurophysiol. 104, 51–60 (2010).
Kross, E., Berman, M. G., Mischel, W., Smith, E. E. & Wager, T. D. Social rejection shares somatosensory representations with physical pain. Proc. Natl Acad. Sci. USA 108, 6270–6275 (2011). This study included both a physical and social pain task, and highlighted overlapping neural activity in response to both tasks.
Gündel, H., O'Connor, M.F., Littrell, L., Fort, C. & Lane, R. D. Functional neuroanatomy of grief: an fMRI study. J. Psychiatry 160, 1946–1953 (2003).
O'Connor, M. F. et al. Craving love? Enduing grief activates brain's reward center. Neuroimage 42, 969–972 (2008).
Kersting, A. et al. Neural activation underlying acute grief in women after their loss of an unborn child. Am. J. Psychiatry 166, 1402–1410 (2009).
Asmundson, G. J. G., Norton, G. R. & Jackobson, S. J. Social, blood/injury, and agrophobic fears in patients with physically unexplained chronic pain: are they clinically significant? Anxiety 2, 28–33 (1996).
MacDonald, G. & Kingsbury, R. Does physical pain augment anxious attachment? J. Soc. Pers. Relat. 23, 291–304 (2006).
Ciechanowski, P. S., Walker, E. A., Katon, W. J. & Russo, J. E. Attachment theory: a model for health care utilization and somatization. Psychosom. Med. 64, 660–667 (2002).
Ehnvall, A., Mitchell, P. B., Hadzi-Palovic, D., Malhi, G. S. & Parker, G. Pain during depression and relationship to rejection sensitivity. Acta Psychiatri. Scand. 119, 375–382 (2009).
Waldinger, R. J., Schulz, M. S., Barsky, A. J. & Ahern, D. K. Mapping the road from childhood trauma to adult somatization: the role of attachment. Psychosom. Med. 68, 129–135 (2006).
Eisenberger, N. I., Jarcho, J. M., Lieberman, M. D. & Naliboff, B. D. An experimental study of shared sensitivity to physical pain and social rejection. Pain 126, 132–138 (2006).
Chou, W. Y. et al. Human opioid receptor A118G polymorphism affects intravenous patient-controlled analgesia morphine consumption after total abdominal hysterectomy. Anesthesiology 105, 334–337 (2006).
Way, B. M., Taylor, S. E. & Eisenberger, N. I. Variation in the mu-opioid receptor gene (OPRM1) is associated with dispositional and neural sensitivity to social rejection. Proc. Natl Acad. Sci. USA 106, 15079–15084 (2009). This study demonstrated that a gene linked with physical pain sensitivity ( OPRM1 ) is also associated with rejection sensitivity.
Brown, R. J., Schrag, A. & Trimble, M. R. Dissociation, childhood interpersonal trauma, and family functioning in patients with somatization disorder. Am. J. Psychiatry 162, 899–905 (2005).
van den Hout, J. H. C., Vlaeyen, J. W. S., Peters, M. L., Engelhard, I. M. & van den Hout, M. A. Does failure hurt? The effects of failure feedback on pain report, tolerence and pain avoidance. Eur. J. Pain 4, 335–346 (2000).
Levine, F. M., Krass, S. M. & Padawer, W. J. Failure hurts: the effects of stress due to difficult tasks and failure feedback on pain report. Pain 54, 335–340 (1993).
Bernstein, M. J. & Claypool, H. M. Social exclusion and pain sensitivity: why exclusion sometimes hurts and sometimes numbs. Pers. Soc. Psychol. Bull. 38, 185–196 (2012).
Watkins, L. R. & Mayer, D. J. Organization of endogenous opiate and nonopiate pain control systems. Science 11, 1185–1192 (1982).
Fields, H. Stress dependent opioid control of pain. Nature Rev. Neurosci. 5, 565–575 (2004).
DeWall, C. N. & Baumeister, R. F. Alone but feeling no pain: effects of social exclusion on physical pain tolerance and pain threshold, affective forecasting, and interpersonal empathy. J. Pers. Soc. Psychol. 91, 1–15 (2006).
King, T. E., Joynes, R. L., Meagher, M. W. & Grau, J. W. Impact of shock on pain reactivity: II. Evidence for enhanced pain. J. Exp. Psychol. 22, 265–278 (1996).
Rhudy, J. L. & Meagher, M. W. Fear and anxiety: divergent effects on human pain thresholds. Pain 84, 65–75 (2000).
Watkins, L. R. & Maier, S. F. The pain of being sick: implications of immune-to-brain communication for understanding pain. Annu. Rev. Psychol. 51, 29–57 (2000).
Eisenberger, N. I., Inagaki, T. K., Mashal, N. M. & Irwin, M. R. Inflammation and social experience: an inflammatory challenge induces feelings of social disconnection in addition to depressed mood. Brain Behav. Immun. 24, 558–563 (2010).
Eisenberger, N. I., Inagaki, T. K., Rameson, L., Mashal, N. M. & Irwin, M. R. An fMRI study of cytokine-induced depressed mood and social pain: the role of sex differences. Neuroimage 47, 881–890 (2009).
Zaza, C. & Baine, N. Cancer pain and psychosocial factors: a critical review of the literature. J. Pain Symptom Manage. 24, 526–542 (2002).
Kulik, J. A. & Mahler, H. I. Social support and recovery from surgery. Health Psychol. 8, 221–238 (1989).
Master, S. L. et al. A picture's worth: partner photographs reduce experimentally induced pain. Psychol. Sci. 20, 1316–1318 (2009). This study demonstrated that minimal social support cues (holding hands with one's partner or viewing a picture of them) could reduce physical pain experience.
Eisenberger, N. I. et al. Attachment figures activate a safety signal-related neural region and reduce pain experience. Proc. Natl Acad. Sci. USA 108, 11721–11726 (2011).
Younger, J., Aron, A., Parke, S., Chatterjee, N. & Mackey, S. Viewing pictures of a romantic partner reduces experimental pain: involvement of neural reward systems. PLoS ONE 5, e13309 (2010).
Seeman, T. E. Social ties and health: the benefits of social integration. Ann. Epidemiol. 6, 442–451 (1996).
Hawkley, L. C. & Cacioppo, J. T. Loneliness matters: a theoretical and empirical review of consequences and mechanisms. Ann. Behav. Med. 40, 218–227 (2010).
Cole, S. W. et al. Social regulation of gene expression in human leukocytes. Genome Biol. 8, R189 (2007).
Dickerson, S. S., Gable, S. L., Irwin, M. R., Aziz, N. & Kemeny, M. E. Social-evaluative threat and proinflammatory cytokine regulation: An experimental laboratory investigation. Psychol. Sci. 20, 1237–1244 (2009).
Hennessy, M. B., Deak, T. & Schiml-Webb, P. A. Early attachment figure separation and increased risk for later depression: potential mediation by proinflammatory processes. Neurosci. Biobehav. Rev. 34, 782–790 (2010).
Irwin, M. R. & Cole, S. W. Reciprocal regulation of the neural and innate immune systems. Nature Rev. Immunol. 11, 625–632 (2011).
Grebe, K. M. et al. Cutting edge: sympathetic nervous systems increases proinflammatory cytokines and exacerbates influenza a virus pathogenesis. J. Immunol. 184, 540–544 (2009).
Critchley H. D. Neural mechanisms of autonomic, affective, and cognitive integration. J. Comp. Neurol. 493, 154–166 (2005).
Critchley, H. D. et al. Human cingulate cortex and autonomic control: converging neuroimaging and clinical evidence. Brain 126, 2139–2152 (2003).
Slavich, G. M., Way, B. M., Eisenberger, N. I. & Taylor, S. E. Neural sensitivity to social rejection is associated with inflammatory responses to social stress. Proc. Natl Acad. Sci. USA 107, 14817–14822 (2010).
Gruenewald, T. L., Seeman, T. E., Ryff, C. D., Karlamangla, A. S. & Singer, B. H. Combination of biomarkers predictive of later life mortality. Proc. Natl Acad. Sci. USA 103, 14158–14163 (2006).
Howren, M. B., Lamkin, D. & Suls, J. Associations of depression with c-reactive protein, IL-1, and IL-6: a meta-analysis. Psychosom. Med. 71, 171–186 (2009).
Reichenberg, A. et al. Cytokine-associated emotional and cognitive disturbances in humans. Arch. Gen. Psychiatry 58, 445–452 (2001).
Slavich, G. M., O'Donovan, A., Epel, E. S. & Kemeny, M. E. Black sheep get the blues: a psychobiological model of social rejection and depression. Neurosci. Biobehav. Rev. 35, 39–45 (2010).
Lamm, C., Decety, J. & Singer, T. Meta-analytic evidence for common and distinct neural networks associated with directly experienced pain and empathy for pain. Neuroimage 54, 2492–2502 (2011).
Keysers, C., Kaas, J. H. & Gazzola, V. Somatosensation in social perception. Nature Rev. Neurosci. 11, 417–428 (2010).
Moll, J. et al. Human fronto-mesolimbic networks guide decisions about charitable donation. Proc. Natl Acad. Sci. USA 103, 15623–15628 (2006).
Inagaki, T. K. & Eisenberger, N. I. Neural correlates of giving support to a loved one. Psychosom. Med. 74, 3–7 (2012).
Wager, T. D. et al. Brain mediators of cardiovascular response to social threat: part I: reciprocal dorsal and ventral sub-regions of the medial prefrontal cortex and heart-rate reactivity. Neuroimage 47, 821–835 (2009).
Botvinick, M. M., Cohen, J. D. & Carter, C. S. Conflict monitoring and anterior cingulate cortex: an update. Trends Cogn. Sci. 8, 539–546 (2004).
Bush, G. Luu, P. & Posner, M. I. Cognitive and emotional influences in anterior cingulated cortex. Trends Cogn. Sci. 4, 215–222 (2000).
Shackman, A. J. et al. The integration of negative affect, pain and cognitive control in the cingulate cortex. Nature Rev. Neurosci. 12, 154–167 (2011). This article reviews the literature showing that the dACC activates in response to various types of inputs, including negative affect, pain and cognitive control.
Etkin, A., Egner, T. & Kalisch, R. Emotional processing in anterior cingulate and medial prefrontal cortex. Trends Cogn. Sci. 15, 85–93 (2011).
Jackson, P. L., Meltzoff, A. N. & Decety, J. How do we perceive the pain of others? A window into the neural processes involved in empathy. Neuroimage 24, 771–779 (2005).
Masten, C. L., Morelli, S. A. & Eisenberger, N. I. An fMRI investigation of empathy for 'social pain' and subsequent prosocial behavior. Neuroimage 55, 381–388 (2011).
Meyer, M. L. et al. Empathy for the social suffering of friends and strangers recruits distinct patterns of brain activation. Soc. Cogn. Affect. Neurosci. 20 Mar 2012 (doi:10.1093/scan/nss019).
Beeney, J. E., Franklin, R. G. Jr, Levy, K. N. & Adams, R. B. Jr. I feel your pain: emotional closeness modulates neural responses to empathically experienced rejection. Soc. Neurosci. 6, 369–376 (2011).
Eisenberger, N. I. The neural bases of social pain: evidence for shared representations with physical pain. Psychosom. Med. 74, 126–135 (2012).
Spunt, R. P., Lieberman, M. D., Cohen, J. R. & Eisenberger, N. I. The phenomenology of error processing: the dorsal anterior cingulate response to stop-signal errors tracks reports of negative affect. J. Cogn. Neurosci. (in the press).
Acknowledgements
I am grateful to M. Lieberman, S. Taylor, M. Irwin and the members of the Social and Affective Neuroscience Laboratory for their helpful comments on earlier versions of this review.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Competing interests
The author declares no competing financial interests.
Related links
Glossary
- Isolation calls
-
A type of distress vocalization produced by infant mammals in response to separation from a caregiver. These vocalizations function to facilitate reunion with the caregiver.
- Cyberball
-
A virtual ball-tossing game that can be used to induce social inclusion or exclusion, depending on the behaviour of the other virtual players (whether they toss the ball to the participant).
- Anxious attachment
-
A style of relating to close others characterized by a heightened concern about being abandoned by close others and therefore an exaggerated sensitivity to signs of acceptance or rejection by others.
- Avoidant attachment
-
A style of relating to close others characterized by an avoidance of seeking out support or closeness from others.
- Rejection sensitivity
-
The tendency to anxiously expect, readily perceive and intensely react to experiences of social rejection.
Rights and permissions
About this article
Cite this article
Eisenberger, N. The pain of social disconnection: examining the shared neural underpinnings of physical and social pain. Nat Rev Neurosci 13, 421–434 (2012). https://doi.org/10.1038/nrn3231
Published:
Issue Date:
DOI: https://doi.org/10.1038/nrn3231
This article is cited by
-
Effects of an open-label placebo intervention on reactions to social exclusion in healthy adults: a randomized controlled trial
Scientific Reports (2023)
-
Young adults’ empathic responses to others in psychological pain as compared to physical pain: does prior experience of pain matter?
Current Psychology (2023)
-
A Systematic Review and Meta-analysis of Electrophysiological Studies of Online Social Exclusion: Evidence for the Neurobiological Impacts of Cyberbullying
Adolescent Research Review (2023)
-
The bright side of dispositional greed: empathy for pain
Current Psychology (2023)
-
Childhood maltreatment is associated with cortical thinning in people with eating disorders
European Archives of Psychiatry and Clinical Neuroscience (2023)