Key Points
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The mirror mechanism is a basic brain mechanism that transforms sensory representations of others' behaviour into one's own motor or visceromotor representations concerning that behaviour. According to its location, it may fulfil a range of cognitive functions, including action and emotion understanding.
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A large number of studies in monkeys demonstrate that premotor and parietal mirror neurons encode action goals rather than mere bodily movements. Similar results have been found in humans.
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Different lines of evidence support the claim that the mirror mechanism might contribute to understanding others' actions, facilitating the identification of the outcome to which those actions are directed.
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The mirror mechanism is also involved in others' emotion processing. Brain-imaging and lesion studies indicate that identifying others' emotions may depend on one's own visceromotor processes and representations concerning those emotions.
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Recent studies suggest that the mirror mechanism may contribute to understanding the vitality forms that characterize others' actions by transforming the sensory information concerning others' vitality forms into motor representations of those forms.
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Mirror-based understanding has been defined as an 'understanding from the inside' because it provides a route to knowledge of others, which can be taken by capitalizing on one's own motor or visceromotor representations. This also suggests that how people experience their own actions, emotions and vitality forms may share a core phenomenal aspect with how people experience the same actions, emotions and vitality forms when observing others displaying them.
Abstract
The mirror mechanism is a basic brain mechanism that transforms sensory representations of others' behaviour into one's own motor or visceromotor representations concerning that behaviour. According to its location in the brain, it may fulfil a range of cognitive functions, including action and emotion understanding. In each case, it may enable a route to knowledge of others' behaviour, which mainly depends on one's own motor or visceromotor representations.
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References
di Pellegrino, G., Fadiga, L., Fogassi, L., Gallese, V. & Rizzolatti, G. Understanding motor events: a neurophysiological study. Exp. Brain Res. 91, 176–180 (1992).
Gallese, V., Fadiga, L., Fogassi, L. & Rizzolatti, G. Action recognition in the premotor cortex. Brain 119, 593–609 (1996).
Rizzolatti, G., Fadiga, L., Gallese, V. & Fogassi, L. Premotor cortex and the recognition of motor actions. Cogn. Brain Res. 3, 131–141 (1996).
Rizzolatti, G., Cattaneo, L., Fabbri-Destro, M. & Rozzi, S. Cortical mechanisms underlying the organization of goal-directed actions and mirror neuron-based action understanding. Physiol. Rev. 94, 655–706 (2014). This rich, exhaustive review describes the functional organization of the cortical motor system and the goal-directed mirror mechanism in monkeys and humans.
Keysers, C. & Gazzola, V. Expanding the mirror: vicarious activity for action, emotion and sensation. Curr. Opin. Neurobiol. 19, 666–671 (2009).
Nelissen, K., Luppino, G., Vanduffel, W., Rizzolatti, G. & Orban, G. A. Observing others: multiple action representation in the frontal lobe. Science 310, 332–336 (2005).
Nelissen, K. et al. Action observation circuits in the macaque monkey cortex. J. Neurosci. 31, 3743–3756 (2011). This detailed connectional study combines fMRI and neural tracer techniques, and defines the functional paths by which visual information concerning others' actions reaches the premotor cortex.
Rizzolatti, G. & Sinigaglia, C. The functional role of parieto-frontal mirror circuit: interpretations and misinterpretations. Nat. Rev. Neurosci. 11, 264–274 (2010).
Kraskov, A., Dancause, N., Quallo, M. M., Shepherd, S. & Lemon, R. N. Corticospinal neurons in macaque ventral premotor cortex with mirror properties: a potential mechanism for action suppression? Neuron 64, 922–930 (2009).
Vigneswaran, G., Philipp, R., Lemon, R. N. & Kraskov, A. M1 corticospinal mirror neurons and their role in movement suppression during action observation. Curr. Biol. 23, 236–243 (2013). This single-neuron study provides the first demonstration that corticospinal neurons of the monkey primary motor cortex are endowed with mirror properties and suggests a mechanism for suppressing involuntary movements during action observation.
Cisek, P. & Kalaska, J. F. Neural correlates of mental rehearsal in dorsal premotor cortex. Nature 431, 993–996 (2004).
Tkach, D., Reimer, J. & Hatsopoulos, N. G. Congruent activity during action and action observation in motor cortex. J. Neurosci. 27, 13241–13250 (2007).
Dushanova, J. & Donoghue, J. Neurons in primary motor cortex engaged during action observation. Eur. J. Neurosci. 31, 386–398 (2010).
Falcone, R., Brunamonti, E., Ferraina, S. & Genovesio, A. Neural encoding of self and another agent's goal in the primate prefrontal cortex: human–monkey interactions. Cereb Cortex http://dx.doi.org./10.1093/cercor/bhv224 (2015).
Caspers, S., Zilles, K., Laird, A. R. & Eickhoff, S. B. ALE meta-analysis of action observation and imitation in the human brain. Neuroimage 50, 1148–1167 (2010). This review summarizes a large number of experiments on action observation and imitation, and individuates a basic circuit that is involved in goal ascription in humans.
Grosbras, M. H., Beaton, S. & Eickhoff, S. B. Brain regions involved in human movement perception: a quantitative voxel-based meta-analysis. Hum. Brain Mapp. 33, 431–454 (2012).
Molenberghs, P., Cunnington, R. & Mattingley, J. B. Brain regions with mirror properties: a meta-analysis of 125 human fMRI studies. Neurosci. Biobehav. Rev. 36, 341–349 (2012).
Gazzola, V. & Keysers, C. The observation and execution of actions share motor and somatosensory voxels in all tested subjects: single-subject analyses of unsmoothed fMRI data. Cereb. Cortex 19, 1239–1255 (2009).
Keysers, C., Kaas, J. H. & Gazzola, V. Somatosensation in social perception. Nat. Rev. Neurosci. 11, 417–428 (2010).
Mukamel, R., Ekstrom, A. D., Kaplan, J., Iacoboni, M. & Fried, I. Single-neuron responses in humans during execution and observation of actions. Curr. Biol. 20, 750–756 (2010).
Rizzolatti, G., Fogassi, L. & Gallese, V. Neurophysiological mechanisms underlying the understanding and imitation of action. Nat. Rev. Neurosci. 2, 661–670 (2001).
Kilner, J. M. More than one pathway to action understanding. Trends Cogn. Sci. 15, 352–357 (2011).
Cook, R. & Bird, G. Do mirror neurons really mirror and do they really code for action goals? Cortex 49, 2944–2945 (2013).
Ferrari, P. F., Rozzi, S. & Fogassi, L. Mirror neurons responding to observation of actions made with tools in monkey ventral premotor cortex. J. Cogn. Neurosci. 17, 212–226 (2005).
Rochat, M. J. et al. Responses of mirror neurons in area F5 to hand and tool grasping observation. Exp. Brain Res. 204, 605–616 (2010).
Fogassi, L. et al. Parietal lobe: from action organization to intention understanding. Science 302, 662–667 (2005).
Kohler, E. et al. Hearing sounds, understanding actions: action representation in mirror neurons. Science 297, 846–848 (2002).
Gazzola, V., Aziz-Zadeh, L. & Keysers, C. Empathy and the somatotopic auditory mirror system in humans. Curr. Biol. 16, 1824–1829 (2006).
Lewis, J. W., Brefczynski, J. A., Phinney, R. E., Janik, J. J. & De Yoe, E. A. Distinct cortical pathways for processing tool versus animal sounds. J. Neurosci. 25, 5148–5158 (2005).
Rizzolatti, G. et al. Functional organization of inferior area 6 in the macaque monkey. II. area F5 and the control of distal movements. Exp. Brain Res. 71, 491–507 (1988).
Bonini, L. et al. Selectivity for grip type and action goal in macaque inferior parietal and ventral premotor grasping neurons. J. Neurophysiol. 108, 1607–1619 (2012).
Bonini, L., Maranesi, M., Livi, A., Fogassi, L. & Rizzolatti, G. Ventral premotor neurons encoding representations of action during self and others' inaction. Curr. Biol. 24, 1611–1614 (2014). This single-neuron study shows that the monkey PMv encodes action goals not only when performing and observing actions to be performed but also when refraining from acting and observing actions to be refrained from.
Abdollahi, R. O., Jastorff, J. & Orban, G. A. Common and segregated processing of observed actions in human SPL. Cereb. Cortex 11, 2734–2753 (2012).
Cattaneo, L., Sandrini, M. & Schwarzbach, J. State-dependent TMS reveals a hierarchical representation of observed acts in the temporal, parietal, and premotor cortices. Cereb. Cortex 20, 2252–2258 (2010).
Silvanto, J., Muggleton, N. & Walsh, V. State dependency in brain stimulation studies of perception and cognition. Trends Cogn. Sci. 12, 447–454 (2008).
Jastorff, J., Begliomini, C., Fabbri-Destro, M., Rizzolatti, G. & Orban, G. A. Coding observed motor acts: different organizational principles in the parietal and premotor cortex of humans. J. Neurophysiol. 104, 128–140 (2010).
Brass, M., Bekkering, H., Wohlschläger, A. & Prinz, W. Compatibility between observed and executed finger movements: comparing symbolic, spatial, and imitative cues. Brain Cogn. 44, 124–143 (2000).
Craighero, L., Bello, A., Fadiga, L. & Rizzolatti, G. Hand action preparation influences the responses to hand pictures. Neuropsychologia 40, 492–502 (2002).
Kilner, J. M., Paulignan, Y. & Blakemore, S. J. An interference effect of observed biological movement on action. Curr. Biol. 13, 522–525 (2003).
Cattaneo, L. et al. One's motor performance predictably modulates the understanding of others' actions through adaptation of premotor visuo-motor neurons. Soc. Cogn. Affect. Neurosci. 6, 301–310 (2011).
Calvo-Merino, B., Glaser, D. E., Grezes, J., Passingham, R. E. & Haggard, P. Action observation and acquired motor skills: an fMRI study with expert dancers. Cereb. Cortex 15, 1243–1249 (2005). This article provides the most elegant demonstration that acquired motor skills change the responsiveness of the mirror cortical areas during the observation of actions exploiting those skills.
Calvo-Merino, B., Grezes, J., Glaser, D. E., Passingham, R. E. & Haggard, P. Seeing or doing? Influence of visual and motor familiarity in action observation. Curr. Biol. 16, 1905–1910 (2006).
Cross, E. S., Hamilton, A. F. & Grafton, S. T. Building a motor simulation de novo: observation of dance by dancers. Neuroimage 31, 1257–1267 (2006).
Casile, A. & Giese, M. A. Non visual motor training influences biological motion perception. Curr. Biol. 16, 69–74 (2006).
Costantini, M., Ambrosini, E., Cardellicchio, P. & Sinigaglia, C. How your hand drives my eyes. Soc. Cogn. Affect. Neurosci. 9, 705–711 (2014).
Michael, J. et al. Continuous theta-burst stimulation demonstrates a causal role of premotor homunculus in action understanding. Psychol. Sci. 25, 963–972 (2014).
Heilman, K. M., Rothi, L. J. & Valenstein, E. Two forms of ideomotor apraxia. Neurology 32, 342–346 (1982).
Rothi, L. J., Heilman, K. M. & Watson, R. T. Pantomime comprehension and ideomotor apraxia. J. Neurol. Neurosurg. Psychiatry 48, 207–210 (1985).
Pazzaglia, M., Pizzamiglio, L., Pes, E. & Aglioti, S. M. The sound of actions in apraxia. Curr. Biol. 18, 1766–1772 (2008). This neuropsychological study convincingly demonstrates a causative link between execution of actions and their recognition.
De Renzi, E. & Faglioni, P. in Handbook of Clinical and Experimental Neuropsychology (eds Denes, G. & Pizzamiglio, L.) 421–440 (Psychology Press, 1999).
Gothard, K. & Hoffman, K. in Primate Neuroethology (eds Platt, M. & Ghazanfar, A.) 292–315 (Oxford Univ. Press, 2010).
Caruana, F., Jezzini, A., Sbriscia-Fioretti, B., Rizzolatti, G. & Gallese, V. Emotional and social behaviors elicited by electrical stimulation of the insula in the macaque monkey. Curr. Biol. 21, 195–199 (2011).
Jezzini, A., Caruana, F., Stoianov, I., Gallese, V. & Rizzolatti, G. Functional organization of the insula and inner perisylvian regions. Proc. Natl Acad. Sci. USA 109, 10077–10082 (2012). This detailed study of the physiological organization of the monkey insula shows the profound functional heterogeneity of different sectors of the insula.
Kurth, F., Zilles, K., Fox, P. T., Laird, A. R. & Eickhoff, S. B. A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis. Brain Struct. Funct. 214, 519–534 (2010). This detailed meta-analysis of fMRI studies of the human insula highlights its functional heterogeneity.
Ojemann, G. A. & Whitaker, H. A. Language localization and variability. Brain Lang. 6, 239–260 (1978).
Vignolo, L. A., Boccardi, E. & Caverni, L. Unexpected CT-scan findings in global aphasia. Cortex 22, 55–69 (1986).
Penfield, W. & Faulk, M. E. The insula: further observations on its function. Brain 78, 445–470 (1955).
Isnard, J., Guenot, M., Sindou, M. & Mauguiére, F. Clinical manifestation of insular lobe seizures: a stereo-electroencephalo-graphic study. Epilepsia 45, 1079–1090 (2004).
Catenoix, H. et al. The role of the anterior insular cortex in ictal vomiting: a stereotactic electroencephalography study. Epilepsy Behav. 13, 560–563 (2008).
Yaxley, S., Rolls, E. T. & Sienkiewicz, Z. J. Gustatory responses of single neurons in the insula of the macaque monkey. J. Neurophysiol. 63, 689–700 (1990).
Scott, T. R., Plata-Salaman, C. R., Smith, V. L. & Giza, B. K. Gustatory neural coding in the monkey cortex: stimulus intensity. J. Neurophysiol. 65, 76–86 (1991).
Phillips, M. L. et al. A specific neural substrate for perceiving facial expressions of disgust. Nature 389, 495–498 (1997).
Phillips, M. L. et al. Neural responses to facial and vocal expressions of fear and disgust. Proc. Biol. Sci. 265, 1809–1817 (1998).
Hennenlotter, A. & Schroeder, U. Partly dissociable neural substrates for recognizing basic emotions: a critical review. Prog. Brain Res. 156, 443–456 (2006).
Krolak-Salmon, P. et al. An attention modulated response to disgust in human ventral anterior insula. Ann. Neurol. 53, 446–453 (2003).
Wicker, B. et al. Both of us disgusted in my insula: the common neural basis of seeing and feeling disgust. Neuron 40, 655–664 (2003). This study was the first to demonstrate that feeling an emotion and observing an emotion in another individual activate the same voxels in the AI.
Jabbi, M., Bastiaansen, J. & Keysers, C. A common anterior insula representation of disgust observation, experience and imagination shows divergent functional connectivity pathways. PLoS ONE 3, e2939 (2008). This paper is an important extension of the previous study (reference 61) showing that not only feeling one's own disgust and observing others' disgust but also the internal imagery of disgust have a common representation in the AI.
Sprengelmeyer, R., Rausch, M., Eysel, U. T. & Przuntek, H. Neural structures associated with recognition of facial expressions of basic emotions. Proc. Biol. Sci. 265, 1927–1931 (1998).
Hennenlotter, A. et al. A common neural basis for receptive and expressive communication of pleasant facial affect. Neuroimage 26, 581–591 (2005).
Jabbi, M., Swart, M. & Keysers, C. Empathy for positive and negative emotions in the gustatory cortex. Neuroimage 34, 1744–1753 (2007).
Singer, T. et al. Empathy for pain involves the affective but not sensory components of pain. Science 303, 1157–1162 (2004).
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).
Iannetti, G. D., Salomons, T. V., Moayedi, M., Mouraux, A. & Davis, K. D. Beyond metaphor: contrasting mechanisms of social and physical pain. Trends Cogn. Sci. 17, 371–378 (2013).
Zaki, J., Wager, T. D., Singer, T., Keysers, C. & Gazzola, V. The anatomy of suffering: understanding the relationship between nociceptive and empathic pain. Trends Cogn. Sci. 20, 249–259 (2016).
Caruana, F. et al. Mirth and laughter elicited by electrical stimulation of the human anterior cingulate cortex. Cortex 71, 323–331 (2015).
Caruana, F. et al. A mirror mechanism for laughter in the anterior cingulate cortex. Emotion (in the press).
Gallese, V., Keysers, C. & Rizzolatti, G. A unifying view of the basis of social cognition. Trends Cogn. Sci. 8, 396–403 (2004).
Goldman, A. & Sripada, C. S. Simulationist models of face-based emotion recognition. Cognition 94, 193–213 (2005).
Niedenthal, P. M. Embodying emotion. Science 316, 1002–1005 (2007).
Calder, A. J., Keane, J., Manes, F., Antoun, N. & Young, A. W. Impaired recognition and experience of disgust following brain injury. Nat. Neurosci. 3, 1077–1078 (2000).
Adolphs, R., Tranel, D. & Damasio, A. R. Dissociable neural systems for recognizing emotions. Brain Cogn. 52, 61–69 (2003).
Kipps, M., Duggins, A. J., McCusker, E. A. & Calder, A. J. Disgust and happiness recognition correlate with anteroventral insula and amygdala volume respectively in preclinical Huntington's disease. J. Cogn. Neurosci. 19, 1206–1217 (2007).
Canessa, N. et al. Understanding others' regret: a fMRI study. PLoS ONE 4, e7402 (2009).
Trevarthen, C. in Intersubjective Communication and Emotion in Early Ontogeny (ed. Bråten, S.) 15–46 (Cambridge Univ. Press, 1998).
Stern, D. N. The Interpersonal World of the Infant (Basic Books, 1985).
Stern, D. N. Forms of Vitality: Exploring Dynamic Experience in Psychology, Arts, Psychotherapy, and Development (Oxford Univ. Press, 2010).
Di Cesare, G., Di Dio, C., Marchi, M. & Rizzolatti, G. Expressing our internal states and understanding those of others. Proc. Natl Acad. Sci. USA 112, 10331–10335 (2015). This fMRI study was the first to provide evidence for the presence ofthe mirror mechanism for vitality forms in the dorsocentral insula.
Borra, E. et al. Cortical connections of the macaque anterior intraparietal (AIP) area. Cereb. Cortex 18, 1094–1111 (2008).
Gerbella, M., Belmalih, A., Borra, E., Rozzi, S. & Luppino, G. Cortical connections of the anterior (F5a) subdivision of the macaque ventral premotor area F5. Brain Struct. Funct. 216, 43–65 (2011).
Borra, E., Gerbella, M., Rozzi, S. & Luppino, G. Anatomical evidence for the involvement of the macaque ventrolateral prefrontal area 12r in controlling goal-directed actions. J. Neurosci. 31, 12351–12363 (2011).
Almashaikhi, T. et al. Functional connectivity of insular efferences. Hum. Brain Mapp. 35, 5279–5294 (2014).
Di Cesare, G. et al. The neural correlates of 'vitality form' recognition: an fMRI study. Soc. Cogn. Affect. Neurosci. 9, 951–960 (2014).
Di Cesare, G. et al. Vitality forms processing in the insula during action observation: a multivoxel pattern analysis. Front. Hum. Neurosci. http://dx.doi.org/10.3389/fnhum.2016.00267 (2016).
Rochat, M. J. et al. Impaired vitality form recognition in autism. Neuropsychologia 51, 1918–1924 (2013).
Boria, S. et al. Intention understanding in autism. PLoS ONE 4, e5596 (2009).
Hamilton, A. F., Brindley, R. M. & Frith, U. Imitation and action understanding in autistic spectrum disorders: how valid is the hypothesis of a deficit in the mirror neuron system? Neuropsychologia 45, 1859–1868 (2007).
Hobson, R. P. & Lee, A. Imitation and identification in autism. J. Child Psychol. Psychiatry 40, 649–659 (1999).
Hobson, R. P. & Hobson, J. A. Dissociable aspects of imitation: a study in autism. J. Exp. Child Psychol. 101, 170–185 (2008).
Gizzonio, V. et al. Failure in pantomime execution correlates with the severity of social behavior deficits in children with autism: a praxis study. J. Autism Dev. Disord. 45, 3085–3097 (2015).
MacNeil, L. K. & Mostofsky, S. H. Specificity of dyspraxia in children with autism. Neuropsychology 26, 165–171 (2012).
Rizzolatti, G. & Sinigaglia, C. in Action Science: Foundations of an Emerging Discipline (eds Prinz, W., Beisert, M. & Herwig, A.) 201–227 (MIT Press, 2013).
Sinigaglia, C. & Rizzolatti, G. Through the looking glass: self and others. Consci. Cogn. 20, 64–74 (2011).
Sinigaglia, C. & Butterfill, S. A puzzle about the relations between thought, experience, and the motoric. Synthese 192, 1923–1936 (2015).
Jeannerod, M. The representing brain: neural correlates of motor intention and imagery. Behav. Brain Sci. 17, 187–202 (1994).
de Lange, F. P., Spronk, M., Willems, R. M., Toni, I. & Bekkering, H. Complementary systems for understanding action intentions. Curr. Biol. 18, 454–457 (2008).
Brass, M., Schmitt, R. M., Spengler, S. & Gergely, G. Investigating action understanding: inferential processes versus action simulation. Curr. Biol. 17, 2117–2121 (2007).
Liepelt, R., Von Cramon, D. Y. & Brass, M. How do we infer other's goals from non stereotypic actions? The outcome of context-sensitive inferential processing in right inferior parietal and posterior temporal cortex. Neuroimage 43, 784–792 (2008).
Corradi-Dell'Acqua, C., Hofstetter, C. & Vuilleumier, P. Cognitive and affective theory of mind share the same local patterns of activity in posterior temporal but not medial prefrontal cortex. Soc. Cogn. Affect. Neurosci. 9, 1175–1184 (2014).
Kilner, J. M. & Frith, C. Action observation: inferring intentions without mirror neurons. Curr. Biol. 18, R32–R33 (2008).
Keysers, C. & Gazzola, V. Integration simulation and theory of mind: from self to social cognition. Trends Cogn. Sci. 11, 194–196 (2007).
Engen, H. G. & Singer, T. Empathy circuits. Curr. Opin. Neurobiol. 23, 275–282 (2012).
Southgate, V., Johnson, M. H., El Karoui, I. & Csibra, G. Motor system activation reveals infants' on-line prediction of others' goals. Psychol. Sci. 21, 355–359 (2010).
Gerson, S. A. & Woodward, A. L. The joint role of trained, untrained, and observed actions at the origins of goal recognition. Infant Behav. Dev. 37, 94–104 (2014).
Woodward, A. L. & Gerson, S. A. Mirroring and the development of action understanding. Phil. Trans. R. Soc. B 369, 20130181 (2014).
Acknowledgements
The authors thank S. Butterfill for his helpful comments on the manuscript. This works was supported by a grant from Fondazione Cariparma, by Inter University Attraction Program (IUAP) and an European Research Council (ERC) Advanced Grant to G.R.
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Glossary
- Mirror neurons
-
Neurons that discharge both when an individual performs a given behaviour and when an individual observes another person performing the same or a similar behaviour; these neurons are found in many brain cortical areas of monkeys and other species, including humans, marmosets and birds.
- Mirror mechanism
-
A basic brain mechanism that transforms sensory representations of others' behaviour into one's own motor or visceromotor representations concerning that behaviour and, depending on the location, can fulfil a range of cognitive functions, including action and emotion understanding.
- Action goals
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The outcomes to which actions are directed. In non-technical contexts, the term is also used when people talk about the goal of their struggles or assert that their goal is to work at their best.
- Vitality form
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Agents' affective states, moods and attitudes that characterize how their actions and emotions are displayed and experienced; it has been hypothesized that the identification of others' vitality forms, which is crucial for social interaction, could involve the mirror mechanism.
- Understanding from the inside
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A notion that describes how the mirror mechanism might provide a route to knowledge of others by capitalizing on one's own motor or visceromotor representations. It also reflects the idea that there are phenomenal aspects common to experiences of one's own and other's actions, emotions and vitality forms.
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Rizzolatti, G., Sinigaglia, C. The mirror mechanism: a basic principle of brain function. Nat Rev Neurosci 17, 757–765 (2016). https://doi.org/10.1038/nrn.2016.135
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DOI: https://doi.org/10.1038/nrn.2016.135
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