Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Gut feelings: the emerging biology of gut–brain communication

Key Points

  • Recent neurobiological insights into this gut–brain crosstalk have revealed a complex, bidirectional communication system that not only assures proper maintenance of gastrointestinal homeostasis and digestion but is likely to have multiple effects on affect, motivation and higher cognitive functions.

  • Sympathetic and parasympathetic innervations modulate intestinal function and are likely to mediate the reported emotion-related patterns of regional changes in motor, secretory and possibly immune activity in the gastrointestinal tract.

  • There are three basic mechanisms by which sensory information is encoded in the gut: by primary afferent neurons, by immune cells and by enteroendocrine cells.

  • Both extrinsic and intrinsic primary afferents provide input to multiple reflex loops that are aimed at optimizing gut function and maintaining gastrointestinal homeostasis during internal perturbations.

  • The output of enteroendocrine cells is involved both in the regulation of digestive functions through enteric nervous system circuits, as well as in the regulation of CNS processes through endocrine and paracrine signalling to vagal afferents.

  • Immune cells in the gut remain immunologically hyporesponsive to commensal bacteria, while maintaining their responsiveness to pathogenic organisms, and their products indirectly influence the functional properties of enteroendocrine cells.

  • Recent evidence suggests that various forms of subliminal interoceptive inputs from the gut, including those generated by intestinal microbes, may influence memory formation, emotional arousal and affective behaviours. The human insula, and related brain networks (including the anterior cingulate cortex, orbitofrontal cortex and amygdala), has emerged as the most plausible brain region to support this integration.

  • It remains to be determined whether intuitive decision making is based on an interoceptive map of gut responses that enables the brain to make rapid gut-based decisions based on interoceptive memories of such responses.

  • There is extensive evidence of alterations in brain–gut signalling systems during perturbation to gut homeostasis, in several chronic gastrointestinal disorders and in eating disorders. Further understanding of the bidirectional crosstalk between the brain and the digestive system may aid the development of effective therapies for these conditions.

Abstract

The concept that the gut and the brain are closely connected, and that this interaction plays an important part not only in gastrointestinal function but also in certain feeling states and in intuitive decision making, is deeply rooted in our language. Recent neurobiological insights into this gut–brain crosstalk have revealed a complex, bidirectional communication system that not only ensures the proper maintenance of gastrointestinal homeostasis and digestion but is likely to have multiple effects on affect, motivation and higher cognitive functions, including intuitive decision making. Moreover, disturbances of this system have been implicated in a wide range of disorders, including functional and inflammatory gastrointestinal disorders, obesity and eating disorders.

Access options

Rent or Buy article

Get time limited or full article access on ReadCube.

from$8.99

All prices are NET prices.

Access all Nature Journals

Immediate access to more than 50 journals, including Nature

$49.99/month

Learn more
Figure 1: Gut to brain communication.
Figure 2: Gut–brain signalling related to food intake.
Figure 3: Gut signalling systems, gut sensations and meta-representations of such sensations.
Figure 4: Interoceptive memory and prediction error in chronic disease.

References

  1. 1

    Furness, J. B. The Enteric Nervous System (Blackwell, Oxford, 2006). A comprehensive overview of all aspects of the enteric nervous system.

    Google Scholar 

  2. 2

    Furness, J. B., Kunze, W. A., Bertrand, P. P., Clerc, N. & Bornstein, J. C. Intrinsic primary afferent neurons of the intestine. Prog. Neurobiol. 54, 1–18 (1998).

    CAS  Article  PubMed  Google Scholar 

  3. 3

    Costa, M., Furness, J. B., Llewellyn-Smith, I. J. & Johnson, L. R. in Physiology of the Gastrointestinal Tract (eds Johnson, L. R. et al.) 1–40 (Raven, New York, 1987).

    Google Scholar 

  4. 4

    Gershon, M. D. et al. in Physiology of the Gastrointestinal Tract (eds Johnson, L. R. et al.) 381–422 (Raven Press, New York, 1994).

    Google Scholar 

  5. 5

    Gershon, M. D. The Second Brain (Harper Collins, New York, 1998).

    Google Scholar 

  6. 6

    Mayer, E. A. & Brunnhuber, S. in Handbook of Clinical Neurology 3rd edn (in the press).

  7. 7

    Cannon, W. B. Organization for physiological homeostasis. Physiol. Rev. 9, 399–431 (1929).

    Article  Google Scholar 

  8. 8

    James, W. What is an emotion? Mind 9, 188–205 (1884).

    Article  Google Scholar 

  9. 9

    Mayer, E. A. et al. Brain imaging approaches to the study of functional GI disorders: a Rome working team report. Neurogastroenterol. Motil. 21, 579–596 (2009).

    CAS  Article  PubMed  Google Scholar 

  10. 10

    Round, J. L. & Mazmanian, S. K. The gut microbiota shapes intestinal immune responses during health and disease. Nature Rev. Immunol. 9, 313–323 (2009).

    CAS  Article  Google Scholar 

  11. 11

    Artis, D. & Grencis, R. K. The intestinal epithelium: sensors to effectors in nematode infection. Mucosal Immunol. 1, 252–264 (2008).

    CAS  Article  PubMed  Google Scholar 

  12. 12

    Rhee, S. H., Pothoulakis, C. & Mayer, E. A. Principles and clinical implications of the brain-gut-enteric microbiota axis. Nature Rev. Gastroenterol. Hepatol. 6, 306–314 (2009). A review of emerging concepts and preclinical evidence that support the idea of intestinal microbiota to brain signalling.

    CAS  Article  Google Scholar 

  13. 13

    Collins, S. M. & Bercik, P. The relationship between intestinal microbiota and the central nervous system in normal gastrointestinal function and disease. Gastroenterology 136, 2003–2014 (2009).

    Article  PubMed  Google Scholar 

  14. 14

    Forsythe, P., Sudo, N., Dinan, T., Taylor, V. H. & Bienenstock, J. Mood and gut feelings. Brain Behav. Immun. 24, 9–16 (2010).

    Article  PubMed  Google Scholar 

  15. 15

    Price, J. L., Carmichael, S. T. & Drevets, W. C. Networks related to the orbital and medial prefrontal cortex: a substrate for emotional behavior? Prog. Brain Res. 107, 523–536 (1996).

    CAS  Article  PubMed  Google Scholar 

  16. 16

    Ongur, D. & Price, J. L. The organization of networks within the orbital and medical prefrontal cortex of rats, monkeys and humans. Cereb. Cortex 10, 206–219 (2000).

    CAS  Article  PubMed  Google Scholar 

  17. 17

    Vogt, B. A. in The Cerebral Cortex (eds Jones, E. G. & Peters, A.) 89–149 (Plenum Press, New York, 1985).

    Google Scholar 

  18. 18

    Bandler, R., Keay, K. A. in The Emotional Motor System. Progress in Brain Research (eds Holstege, G., Bandler, R. & Saper, C. B.) 285–300 (Elsevier, Amsterdam, 1996).

    Book  Google Scholar 

  19. 19

    Holstege, G. et al. in The Emotional Motor System (eds Jones, E. G. & Peters, A.) 3–6 (Elsevier, Amsterdam, 1996).

    Book  Google Scholar 

  20. 20

    Mayer, E. A. The neurobiology of stress and gastrointestinal disease. Gut 47, 861–869 (2000).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  21. 21

    Mason, P. From descending pain modulation to obesity via the medullary raphe. Pain 152, S20–S24 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  22. 22

    Fields, H. State-dependent opioid control of pain. Nature Rev. Neurosci. 5, 565–575 (2004).

    CAS  Article  Google Scholar 

  23. 23

    Martinez, V. & Taché, Y. CRF1 receptors as a therapeutic target for irritable bowel syndrome. Curr. Pharm. Des. 12, 4071–4088 (2006).

    CAS  Article  PubMed  Google Scholar 

  24. 24

    Almy, T. P., Kern, F. & Tulin, M. Alterations in colonic function in man under stress. I: experimental production of sigmoid spasm in healthy persons. Gastroenterology 8, 616–626 (1947).

    CAS  PubMed  PubMed Central  Google Scholar 

  25. 25

    Welgan, P., Meshkinpour, H. & Ma, L. Role of anger in antral motor activity in irritable bowel syndrome. Dig. Dis. Sci. 45, 248–251 (2000).

    CAS  Article  PubMed  Google Scholar 

  26. 26

    Valentino, R. J., Miselis, R. R. & Pavcovich, L. A. Pontine regulation of pelvic viscera: pharmacological target for pelvic visceral dysfunction. Trends in Pharmacol. Sci. 20, 253–260 (1999).

    CAS  Article  Google Scholar 

  27. 27

    Browning, K. N. & Travagli, R. A. Plasticity of vagal brainstem circuits in the control of gastrointestinal function. Auton. Neurosci. 161, 6–13 (2011).

    CAS  Article  PubMed  Google Scholar 

  28. 28

    Jaenig, W. in The Integrative Action of the Autonomic Nervous System (ed. Jaenig, W.) 317–318 (Cambridge Univ. Press, New York, 2006).

    Book  Google Scholar 

  29. 29

    Furness, J. B. & Costa, M. The adrenergic innervation of the gastrointestinal tract. Ergeb. Physiol. 69, 1–51 (1974).

    CAS  Google Scholar 

  30. 30

    Elenkov, I. J., Wilder, R. L., Chrousos, G. P. & Vizi, E. S. The sympathetic nerve - an integrative interface between two supersystems: the brain and the immune system. Pharmacol. Rev. 52, 585–638 (2000).

    Google Scholar 

  31. 31

    Lyte, M., Vulchanova, L. & Brown, D. R. Stress at the intestinal surface: catecholamines and mucosa-bacteria interactions. Cell Tissue Res. 343, 23–32 (2010). A comprehensive overview of evidence for interactions between peripheral stress mediators and bidirectional interactions of the mucosa and intestinal microbiota.

    Article  CAS  PubMed  Google Scholar 

  32. 32

    Hori, T., Katafuchi, T., Take, S., Shimizu, N. & Niijima, A. The autonomic nervous system as a communication channel between the brain and the immune system. Neuroimmunomodulation 2, 203–215 (1995).

    CAS  Article  PubMed  Google Scholar 

  33. 33

    Gopal, R., Birdsell, D. & Monroy, F. P. Regulation of toll-like receptors in intestinal epithelial cells by stress and Toxoplasma gondii infection. Parasite Immunol. 30, 563–576 (2008).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  34. 34

    Powley, T. L. et al. in Brain–Gut Interactions (eds Tache, Y. & Wingate, D.) 73–82 (CRC Press, Boston, 1991).

    Google Scholar 

  35. 35

    Stephens, R. L. & Tache, Y. Intracisternal injection of a TRH analogue stimulates gastric luminal serotonin release in rats. Am. J. Physiol. 256, G377–G383 (1989).

    CAS  PubMed  PubMed Central  Google Scholar 

  36. 36

    Pavlov, V. A. & Tracey, K. J. The cholinergic anti-inflammatory pathway. Brain Behav. Immun. 19, 493–499 (2005).

    CAS  Article  PubMed  Google Scholar 

  37. 37

    Almy, T. P., Kern, F. & Tulin, M. Alterations in colonic function in man under stress. II: experimental production of sigmoid spasm in healthy persons. Gastroenterology 12, 425–436 (1949).

    CAS  Article  PubMed  Google Scholar 

  38. 38

    Welgan, P., Meshkinpour, H. & Beeler, M. Effect of anger on colon motor and myoelectric activity in irritable bowel syndrome. Gastroenterology 94, 1150–1156 (1988).

    CAS  Article  PubMed  Google Scholar 

  39. 39

    Elenkov, I. J. & Chrousos, G. P. Stress hormones, proinflammatory and antiinflammatory cytokines, and autoimmunity. Ann. NY Acad. Sci. 966, 290–303 (2002).

    CAS  Article  PubMed  Google Scholar 

  40. 40

    Khasar, S. G. et al. Stress induces a switch of intracellular signaling in sensory neurons in a model of generalized pain. J. Neurosci. 28, 5721–5730 (2008). The first evidence that psychosocial stressors can modulate the phenotype of afferent neurons, providing the possible mechanisms for stress induced hyperalgesia.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  41. 41

    Seminowicz, D. A. et al. Regional gray matter density changes in brains of patients with irritable bowel syndrome. Gastroenterology 139, 48–57 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  42. 42

    Wood, J. D. in Physiology of the Gastrointestinal Tract (ed. Johnson, L. R.) 67–110 (Raven, New York, 1987).

    Google Scholar 

  43. 43

    Kurokawa, K. et al. Comparative metagenomics revealed commonly enriched gene sets in human gut microbiomes. DNA Res. 14, 169–181 (2007).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  44. 44

    Clerc, N. & Furness, J. B. Intrinsic primary afferent neurones of the digestive tract. Neurogastroenterol. Motil. 16, 24–27 (2004).

    Article  PubMed  Google Scholar 

  45. 45

    Sengupta, J. N. & Gebhart, G. F. in Physiology of the Gastrointestinal Tract (ed. Johnson, L. R.) 483–519 (Raven, New York, 1994).

    Google Scholar 

  46. 46

    Keita, A. V. & Soderholm, J. D. The intestinal barrier and its regulation by neuroimmune factors. Neurogastroenterol. Motil. 22, 718–733 (2010).

    CAS  Article  PubMed  Google Scholar 

  47. 47

    Kunze, W. A. & Furness, J. B. The enteric nervous system and regulation of intestinal motility. Annu. |Rev. Physiol. 61, 117–142 (1999).

    CAS  Article  PubMed  Google Scholar 

  48. 48

    Grundy, D. et al. Fundamentals of neurogastroenterology: basic science. Gastroenterology 130, 1391–1411 (2006).

    CAS  Article  PubMed  Google Scholar 

  49. 49

    Phillips, R. J. & Powley, T. L. Tension and stretch receptors in gastrointestinal smooth muscle: re-evaluating vagal mechanoreceptor electrophysiology. Brain Res. Brain Res. Rev. 34, 1–26 (2000).

    CAS  Article  PubMed  Google Scholar 

  50. 50

    Lynn, P., Zagorodnyuk, V., Hennig, G., Costa, M. & Brookes, S. Mechanical activation of rectal intraganglionic laminar endings in the guinea pig distal gut. J. Physiol. 564, 589–601 (2005).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  51. 51

    Sanders, K. M. Interstitial cells in smooth muscles. Review series. J. Cell. Mol. Med. 14, 1197–1198 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  52. 52

    Brierley, S. M. Molecular basis of mechanosensitivity. Auton. Neurosci. 153, 58–68 (2009).

    Article  CAS  PubMed  Google Scholar 

  53. 53

    Kyloh, M. Nicholas, S., Zagorodnyuk, V. P., Brookes, S. J. & Spencer, N. J. Identification of the visceral pain pathway activated by noxious colorectal distension in mice. Front. Neurosci. 5, 16 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  54. 54

    Grundy, D. Signalling the state of the digestive tract. Auton. Neurosci. 125, 76–80 (2006).

    Article  PubMed  Google Scholar 

  55. 55

    Brierley, S. M., Jones, R. C., Gebhart, G. F. & Blackshaw, L. A. Splanchnic and pelvic mechanosensory afferents signal different qualities of colonic stimuli in mice. Gastroenterology 127, 166–178 (2004).

    Article  PubMed  Google Scholar 

  56. 56

    Gold, M. S. & Gebhart, G. F. Nociceptor sensitization in pain pathogenesis. Nature Med. 16, 1248–1257 (2010).

    CAS  Article  PubMed  Google Scholar 

  57. 57

    Feng, B. & Gebhart, G. F. Characterization of silent afferents in the pelvic and splanchnic innervations of the mouse colorectum. Am. J. Physiol. Gastrointest. Liver Physiol. 300, G170–G180 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. 58

    Gershon, M. D. Nerves, reflexes, and the enteric nervous system: pathogenesis of the irritable bowel syndrome. J. Clin. Gastroenterol. 39, S184–S193 (2005).

    Article  PubMed  Google Scholar 

  59. 59

    de Lartigue, G., de La Serre, C. B. & Raybould, H. E. Vagal afferent neurons in high fat diet-induced obesity; intestinal microflora, gut inflammation and cholecystokinin. Physiol. Behav. 2 Mar 2011 (doi:10.1016/j.physbeh.2011.02.040). A review of interactions between intestinal microflora, mucosal inflammation and altered cholecystokinin–vagal interactions in high fat induced obesity.

    CAS  Article  Google Scholar 

  60. 60

    Dockray, G. J. Cholecystokinin and gut-brain signalling. Regul. Pept. 155, 6–10 (2009).

    CAS  Article  PubMed  Google Scholar 

  61. 61

    de Lartigue, G. et al. Cocaine- and amphetamine-regulated transcript mediates the actions of cholecystokinin on rat vagal afferent neurons. Gastroenterology 138, 1479–1490 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. 62

    Barbara, G. et al. Mast cell-dependent excitation of visceral-nociceptive sensory neurons in irritable bowel syndrome. Gastroenterology 132, 26–37 (2007).

    CAS  Article  PubMed  Google Scholar 

  63. 63

    Raybould, H. E. Gut chemosensing: interactions between gut endocrine cells and visceral afferents. Auton. Neurosci. 153, 41–46 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. 64

    Gershon, M. D. & Tack, J. The serotonin signaling system: from basic understanding to drug development for functional GI disorders. Gastroenterology 132, 397–414 (2007). A comprehensive review of the role of the gut-based serotonin signalling system in health and its possible role in gastrointestinal disease.

    CAS  Article  Google Scholar 

  65. 65

    McLaughlin, J. T. et al. Fatty acids stimulate cholecystokinin secretion via an acyl chain length-specific, Ca2+-dependent mechanism in the enteroendocrine cell line STC-1. J. Physiol. 513, 11–18 (1998).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  66. 66

    Liou, A. P. et al. The G-protein-coupled receptor GPR40 directly mediates long-chain fatty acid-induced secretion of cholecystokinin. Gastroenterology 140, 903–912 (2011).

    CAS  Article  PubMed  Google Scholar 

  67. 67

    Rozengurt, E. & Sternini, C. Taste receptor signaling in the mammalian gut. Curr. Opin. Pharmacol. 7, 557–562 (2007).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  68. 68

    Hughes, D. T. & Sperandio, V. Inter-kingdom signalling: communication between bacteria and their hosts. Nature Rev. Microbiol. 6, 111–120 (2008).

    CAS  Article  Google Scholar 

  69. 69

    Leslie, F. C. et al. Plasma cholecystokinin concentrations are elevated in acute upper gastrointestinal infections. QJM 96, 870–871 (2003).

    CAS  Article  PubMed  Google Scholar 

  70. 70

    McDermott, J. R. et al. Immune control of food intake: enteroendocrine cells are regulated by CD4+ T lymphocytes during small intestinal inflammation. Gut 55, 492–497 (2006).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  71. 71

    Rozengurt, E. Taste receptors in the gastrointestinal tract. I. Bitter taste receptors and α-gustducin in the mammalian gut. Am. J. Physiol. Gastrointest. Liver Physiol. 291, G171–G177 (2006).

    CAS  Article  PubMed  Google Scholar 

  72. 72

    Artis, D. Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut. Nature Rev. Immunol. 8, 411–420 (2008).

    CAS  Article  Google Scholar 

  73. 73

    Medzhitov, R. Recognition of microorganisms and activation of the immune response. Nature 449, 819–826 (2007).

    CAS  Article  PubMed  Google Scholar 

  74. 74

    Mawe, G. M., Strong, D. S. & Sharkey, K. A. Plasticity of enteric nerve functions in the inflamed and postinflamed gut. Neurogastroenterol. Motil. 21, 481–491 (2009).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  75. 75

    Berntson, G. G., Sarter, M. & Cacioppo, J. T. Ascending visceral regulation of cortical affective information processing. Eur. J. Neurosci. 18, 2103–2109 (2003).

    Article  PubMed  Google Scholar 

  76. 76

    Craig, A. D. An ascending general homeostatic afferent pathway originating in lamina I. Prog. Brain Res. 107, 225–242 (1996).

    CAS  Article  PubMed  Google Scholar 

  77. 77

    Craig, A. D. Interoception: the sense of the physiological condition of the body. Curr. Opin. Neurobiol. 13, 500–505 (2003).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  78. 78

    Craig, A. D. How do you feel? Interoception: the sense of the physiological condition of the body. Nature Rev. Neurosci. 3, 655–666 (2002).

    CAS  Article  Google Scholar 

  79. 79

    Craig, A. in Handbook of Emotions 3rd edn (eds Lewis, M. & Haviland-Jones, J. M.) 272–288 (Guilford Publications, New York, 2008).

    Google Scholar 

  80. 80

    Craig, A. D. How do you feel-now? The anterior insula and human awareness. Nature Rev. Neurosci. 10, 59–70 (2009).

    CAS  Article  Google Scholar 

  81. 81

    Damasio, A. R. The Feeling of What Happens: Body and Emotion in the Making of Consciousness (Harcourt Brace, New York, New York, 1999).

    Google Scholar 

  82. 82

    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). A comprehensive quantitative meta-analysis of published neuroimaging studies involving insula activation, providing the best evidence to date for function-specific subregions of the human insula.

    Article  PubMed  PubMed Central  Google Scholar 

  83. 83

    Mutschler, I. et al. Functional organization of the human anterior insular cortex. Neurosci. Lett. 457, 66–70 (2009).

    CAS  Article  PubMed  Google Scholar 

  84. 84

    Penfield, W. & Faulk, M. E. Jr. The insula; further observations on its function. Brain 78, 445–470 (1955).

    CAS  Article  PubMed  Google Scholar 

  85. 85

    Augustine, J. R. Circuitry and functional aspects of the insular lobe in primates including humans. Brain Res. Rev. 22, 229–244 (1996).

    CAS  Article  PubMed  Google Scholar 

  86. 86

    Cauda, F. et al. Functional connectivity of the insula in the resting brain. Neuroimage 55, 8–23 (2011). A detailed characterization of resting state connectivity of insula subregions, supporting the concept of function-specific networks related to ventral and dorsal subregions of the anterior insular cortex.

    Article  PubMed  Google Scholar 

  87. 87

    Small, D. M. & Prescott, J. Odor/taste integration and the perception of flavor. Exp. Brain Res. 166, 345–357 (2005).

    Article  PubMed  Google Scholar 

  88. 88

    Small, D. M. Central gustatory processing in humans. Adv. Otorhinolaryngol. 63, 191–220 (2006).

    PubMed  PubMed Central  Google Scholar 

  89. 89

    Kaye, W. H., Fudge, J. L. & Paulus, M. New insights into symptoms and neurocircuit function of anorexia nervosa. Nature Rev. Neurosci. 10, 573–584 (2009). A comprehensive review of current biological concepts related to eating disorders, with an emphasis on altered processing and modulation of intereoceptive signals.

    CAS  Article  Google Scholar 

  90. 90

    Bercik, P. The microbiota-gut-brain axis: learning from intestinal bacteria? Gut 60, 288–289 (2011).

    Article  PubMed  Google Scholar 

  91. 91

    Bercik, P. et al. Chronic gastrointestinal inflammation induces anxiety-like behavior and alters central nervous system biochemistry in mice. Gastroenterology 139, 2102–2112.e1 (2010). The first demonstration of an important role of intestinal inflammation in brain signalling systems and associated behavioural changes in rodents.

    CAS  Article  PubMed  Google Scholar 

  92. 92

    Heijtz, R. D. et al. Normal gut microbiota modulates brain development and behavior. Proc. Natl Acad. Sci. USA 108, 3047–3052 (2011). The first demonstration of an important role of intestinal microbiota early in life in brain development and adult anxiety-like behaviour.

    CAS  Article  Google Scholar 

  93. 93

    Sclafani, A. Oral and postoral determinants of food reward. Physiol. Behav. 81, 773–779 (2004).

    CAS  Article  PubMed  Google Scholar 

  94. 94

    Van Oudenhove, L. et al. Emotional modulation of fatty acid induced gut-brain signalling in brainstem, subcortical and cortical regions: an fMRI study. Gastroenterology 138, S-45 (2010). The first demonstration in humans of an interaction between subliminal gut stimuli and experimentally induced emotional states.

    Article  Google Scholar 

  95. 95

    Berman, S. M. et al. Abnormal CNS response to anticipation of visceral distension in female patients with irritable bowel syndrome (IBS) an FMRI study. Gastroenterology 130, A-78 (2006).

    Article  CAS  Google Scholar 

  96. 96

    Ploghaus, A., Becerra, L., Borras, C. & Borsook, D. Neural circuitry underlying pain modulation: expectation, hypnosis, placebo. Trends Cogn. Sci. 7, 197–200 (2003).

    Article  PubMed  Google Scholar 

  97. 97

    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).

    CAS  Article  PubMed  Google Scholar 

  98. 98

    Grill, H. J. & Norgren, R. The taste reactivity test. I. Mimetic responses to gustatory stimuli in neurologically normal rats. Brain Res. 143, 263–279 (1978).

    CAS  Article  PubMed  Google Scholar 

  99. 99

    Steiner, J. E. The gustofacial response: observation on normal and anencephalic newborn infants. Symp. Oral Sens. Percept. 254–278 (1973).

  100. 100

    Foo, H. & Mason, P. Analgesia accompanying food consumption requires ingestion of hedonic foods. J. Neurosci. 29, 13053–13062 (2009).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  101. 101

    Pepino, M. Y. & Mennella, J. A. Sucrose-induced analgesia is related to sweet preferences in children but not adults. Pain 119, 210–218 (2005).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  102. 102

    Jiang, H., Betancourt, L. & Smith, R. G. Ghrelin amplifies dopamine signaling by cross talk involving formation of growth hormone secretagogue receptor/dopamine receptor subtype 1 heterodimers. Mol. Endocrinol. 20, 1772–1785 (2006).

    CAS  Article  PubMed  Google Scholar 

  103. 103

    Preuschoff, K., Quartz, S. R. & Bossaerts, P. Human insula activation reflects risk prediction errors as well as risk. J. Neurosci. 28, 2745–2752 (2008). An elegant demonstration of the involvement of ventral and dorsal anterior insula subregions in risk prediction and error correction, supporting the concept of function-specific insula subregions.

    CAS  Article  Google Scholar 

  104. 104

    Ploghaus, A. et al. Learning about pain: the neural substrate of the prediction error for aversive events. Proc. Natl Acad. Sci. USA 97, 9281–9286 (2000).

    CAS  Article  PubMed  Google Scholar 

  105. 105

    Bechara, A., Damasio, A. R., Damasio, H. & Anderson, S. W. Insensitivity to future consequences following damage to human prefrontal cortex. Cognition 50, 7–15 (1994).

    CAS  Article  Google Scholar 

  106. 106

    Allman, J. M. et al. The von Economo neurons in frontoinsular and anterior cingulate cortex in great apes and humans. Brain Struct. Funct. 214, 495–517 (2010).

    Article  PubMed  Google Scholar 

  107. 107

    Gershon, M. D. Review article: serotonin receptors and transporters - roles in normal and abnormal gastrointestinal motility. Aliment. Pharmacol. Ther. 20, 3–14 (2004).

    CAS  Article  PubMed  Google Scholar 

  108. 108

    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).

    CAS  Article  PubMed  Google Scholar 

  109. 109

    la Fleur, S. E., Wick, E. C., Idumalla, P. S., Grady, E. F. & Bhargava, A. Role of peripheral corticotropin-releasing factor and urocortin II in intestinal inflammation and motility in terminal ileum. Proc. Natl Acad. Sci. USA 102, 7647–7652 (2005).

    CAS  Article  PubMed  Google Scholar 

  110. 110

    Maier, S. F. & Watkins, L. R. Cytokines for psychologists: implications and bidirectional immune-to-brain communication for understanding behavior, mood, and cognition. Psychol. Rev. 105, 83–107 (1998).

    CAS  Article  PubMed  Google Scholar 

  111. 111

    Singer, T., Critchley, H. D. & Preuschoff, K. A common role of insula in feelings, empathy and uncertainty. Trends Cogn. Sci. 13, 334–340 (2009).

    Article  PubMed  Google Scholar 

  112. 112

    Vergnolle, N. Postinflammatory visceral sensitivity and pain mechanisms. Neurogastroenterol. Motil. 20, 73–80 (2008).

    Article  PubMed  Google Scholar 

  113. 113

    Watkins, L. R. & Maier, S. F. Immune regulation of central nervous system functions: from sickness responses to pathological pain. J. Intern. Med. 257, 139–155 (2005).

    CAS  Article  PubMed  Google Scholar 

  114. 114

    Dunn, A. J. Mechanisms by which cytokines signal the brain. Int. Rev. Neurobiol. 52, 43–65 (2002).

    CAS  Article  PubMed  Google Scholar 

  115. 115

    D'Mello, C., Le, T. & Swain, M. G. Cerebral microglia recruit monocytes into the brain in response to tumor necrosis factorα signaling during peripheral organ inflammation. J. Neurosci. 29, 2089–2102 (2009).

    CAS  Article  PubMed  Google Scholar 

  116. 116

    Holzer, P. Efferent-like roles of afferent neurons in the gut: blood flow regulation and tissue protection. Auton. Neurosci. 125, 70–75 (2006).

    Article  PubMed  PubMed Central  Google Scholar 

  117. 117

    Berthoud, H. R. & Morrison, C. The brain, appetite, and obesity. Annu. Rev. Psychol. 59, 55–92 (2008).

    Article  PubMed  Google Scholar 

  118. 118

    Drossman, D. A. et al. (eds) ROME III: The Functional Gastrointestinal Disorders (Degnon Associates, McLean, Virginia 2006).

    Google Scholar 

  119. 119

    Longstreth, G. F. et al. in ROME III: The Functional Gastrointestinal Disorders (eds Drossman, D. A. et al.) 487–556 (Degnon Associates, McLean, Virginia, 2006).

    Google Scholar 

  120. 120

    Mayer, E. A. Clinical practice. Irritable bowel syndrome. N. Engl. J. Med. 358, 1692–1699 (2008).

    CAS  Article  PubMed  Google Scholar 

  121. 121

    Mayer, E. A. & Tillisch, K. The brain-gut axis in abdominal pain syndromes. Annu. Rev. Med. 62, 381–396 (2011).

    CAS  Article  PubMed  Google Scholar 

  122. 122

    Tillisch, K. & Labus, J. S. Advances in imaging the brain-gut axis: functional gastrointestinal disorders. Gastroenterology 140, 407–411e1 (2011).

    Article  PubMed  Google Scholar 

  123. 123

    Mayer, E. A. et al. Functional GI disorders: from animal models to drug development. Gut 57, 384–404 (2008).

    CAS  Article  PubMed  Google Scholar 

  124. 124

    Blankstein, U., Chen, J., Diamant, N. E. & Davis, K. D. Altered brain structure in irritable bowel syndrome: potential contributions of pre-existing and disease-driven factors. Gastroenterology 138, 1783–1789 (2010).

    Article  PubMed  Google Scholar 

  125. 125

    Mayer, E. A. & Bushnell, M. C. in Functional Pain Syndromes: Presentation and Pathophysiology (eds Mayer, E. A. & Bushnell, M. C.) 531–565 (IASP Press, Seattle, 2009).

    Google Scholar 

  126. 126

    Sengupta, J. N. Visceral pain: the neurophysiological mechanism. Handb. Exp. Pharmacol. 194, 31–74 (2009).

    CAS  Article  Google Scholar 

  127. 127

    Spiller, R. C. Postinfectious irritable bowel syndrome. Gastroenterology 124, 1662–1671 (2003).

    Article  PubMed  Google Scholar 

  128. 128

    Verma-Gandhu, M. et al. Visceral pain perception is determined by the duration of colitis and associated neuropeptide expression in the mouse. Gut 56, 358–364 (2007).

    CAS  Article  PubMed  Google Scholar 

  129. 129

    Chang, L. et al. Differences in brain responses to rectal distension between patients with inflammatory and functional GI disorders. Gastroenterology 126, A-106 (2004).

    Article  Google Scholar 

  130. 130

    Graff, L. A., Walker, J. R. & Bernstein, C. N. Depression and anxiety in inflammatory bowel disease: a review of comorbidity and management. Inflamm. Bowel Dis. 15, 1105–1118 (2009).

    Article  PubMed  Google Scholar 

  131. 131

    Tache, Y. & Bernstein, C. N. Evidence for the role of the brain-gut axis in inflammatory bowel disease: depression as cause and effect? Gastroenterology 136, 2058–2061 (2009).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  132. 132

    Ghia, J. E. et al. Reactivation of inflammatory bowel disease in a mouse model of depression. Gastroenterology 136, 2280–2288.e1–4 (2009). An interesting study demonstrating the interaction of stress, emotional states and gut inflammation.

    CAS  Article  PubMed  Google Scholar 

  133. 133

    Fairburn, C. G. & Harrison, P. J. Eating disorders. Lancet 361, 407–416 (2003).

    Article  PubMed  Google Scholar 

  134. 134

    Finucane, M. M. et al. National, regional, and global trends in body-mass index since 1980: systematic analysis of health examination surveys and epidemiological studies with 960 country-years and 9.1 million participants. Lancet 377, 557–567 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  135. 135

    Volkow, N. D., Wang, G. J. & Baler, R. D. Reward, dopamine and the control of food intake: implications for obesity. Trends Cogn. Sci. 15, 37–46 (2011). An excellent review of data and concepts related to food addiction and obesity.

    CAS  Article  PubMed  Google Scholar 

  136. 136

    Padwal, R. et al. Bariatric surgery: a systematic review and network meta-analysis of randomized trials. Obes. Rev. 28 Mar 2011 (doi:10.1111/j.1467-789X.2011.00866.x).

    CAS  Article  PubMed  Google Scholar 

  137. 137

    Paulino, G. et al. Increased expression of receptors for orexigenic factors in nodose ganglion of diet-induced obese rats. Am. J. Physiol. Endocrinol. Metab. 296, e898–e903 (2009). An interesting study that demonstrates the molecular mechanisms underlying fat induced phenotypic changes in vagal afferents, which may play a part in the decreased influences of interoceptive mechanisms in diet-induced obesity.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  138. 138

    Paulus, M. P. & Stein, M. B. An insular view of anxiety. Biol. Psychiatry 60, 383–387 (2006).

    Article  PubMed  Google Scholar 

  139. 139

    Grupe, D. W. & Nitschke, J. B. Uncertainty is associated with biased expectancies and heightened responses to aversion. Emotion 11, 413–424 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  140. 140

    Sarinopoulos, I. et al. Uncertainty during anticipation modulates neural responses to aversion in human insula and amygdala. Cereb. Cortex 20, 929–940 (2010).

    CAS  Article  PubMed  Google Scholar 

  141. 141

    Sutton, R. S. & Barton, A. G. Reinforcement Learning: An Introduction (MIT press, Cambridge, USA, 1998).

    Google Scholar 

  142. 142

    Behrens, T. E., Woolrich, M. W., Walton, M. E. & Rushworth, M. F. Learning the value of information in an uncertain world. Nature Neurosci. 10, 1214–1221 (2007). An elegant study demonstrating how human subjects assess uncertainty and adjust their decision making accordingly. The study indentifies a key role of brain responses of the anterior cingulate cortex in this process.

    CAS  Article  PubMed  Google Scholar 

  143. 143

    Ganfornina, M. D., Sanchez, D. & Bastiani, M. J. Embryonic development of the enteric nervous system of the grasshopper Schistocerca americana. J. Comp. Neurol. 372, 581–596 (1996).

    CAS  Article  PubMed  Google Scholar 

  144. 144

    Campbell, G. & Burnstock, G. in Handbook of Physiology: the Gastrointestinal System (ed. Code, C. F.) 2213–2266 (American Physiological Society, Washington D. C., 1968).

    Google Scholar 

  145. 145

    Shimizu, H., Koizumi, O. & Fujisawa, T. Three digestive movements in Hydra regulated by the diffuse nerve net in the body column. J. Comp. Physiol. A Neuroethol. Sens. Neural Behav. Physiol. 190, 623–630 (2004).

    Article  PubMed  Google Scholar 

  146. 146

    Bullock, T. H. & Horridge, G. A. Structure and function in the nervous system of invertebrates (W. H. Freeman & Co., San Francisco and London, 1965).

  147. 147

    Gershon, M. D., Chalazonitis, A. & Rothman, T. P. From neural crest to bowel: development of the enteric nervous system. J. Neurobiol. 24, 199–214 (1993).

    CAS  Article  PubMed  Google Scholar 

  148. 148

    MacLean, P. D., Vogt, B. A. & Gabriel, M. in Neurobiology of Cingulate Cortex and Limbic Thalamus: A Comprehensive Handbook 1–15 (Birkhäuser, Boston, 1993).

    Book  Google Scholar 

  149. 149

    Damasio, A. R. The somatic marker hypothesis and the possible functions of the prefrontal cortex. Phil. Trans. R. Soc. Lond. B 351, 1413–1420 (1996).

    CAS  Article  Google Scholar 

Download references

Acknowledgements

Supported by grants DK048351, DK064539, DK082370 and AT002681 from the National Institutes of Health.

Author information

Affiliations

Authors

Ethics declarations

Competing interests

The author declares no competing financial interests.

Related links

Related links

FURTHER INFORMATION

Emeran A. Mayer's homepage

Glossary

Enteric nervous system

Ganglionated plexus of neurons that is located between the layers of the gut. These neurons, which are equal in number to those in the spinal cord, are able to regulate basic gut functions, such as the peristaltic reflex.

Emotional motor system

System of parallel outflows from cortico–limbic–pontine networks that is engaged during distinct homeostatic states. A medial component provides tonic modulation of spinal reflexes and a lateral component plays a part in executing distinct regional motor patterns of the viscera through autonomic pathways

Enteroendocrine cell

Specialized epithelial cell that releases secretory granules, containing one or several gut peptides, on the basolateral side (and possibly luminal side) in response to luminal chemical, mechanical and possibly neural stimuli.

Enterochromaffin cell

Specialized epithelial cell that releases secretory granules, containing primarily serotonin, on the basolateral side (and possibly luminal side) in response to luminal chemical, mechanical and possibly neural stimuli.

Intrinsic reflex

Also known as an intramural reflex. A reflex of the enteric nervous system in which the afferents, interneuron and efferent neurons that are involved are all contained within the gut wall.

Intrinsic, primary afferent

Afferent neuron with its cell body contained within the enteric nervous system, that encodes mechanical and paracrine signals.

Commensal bacteria

Refers to the 100 trillion bacteria that live in symbiosis with the gut and make up the intestinal microflora.

Myenteric

Subplexus of the enteric nervous system, which is localized between the circular and longitudinal muscle layer.

Ego-syntonic

Psychological term referring to behaviours, values and feelings that are in harmony with, or acceptable to, the needs and goal of a person or that are consistent with a person's ideal self image. This trait is typically seen in patients with anorexia nervosa.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Mayer, E. Gut feelings: the emerging biology of gut–brain communication. Nat Rev Neurosci 12, 453–466 (2011). https://doi.org/10.1038/nrn3071

Download citation

Further reading

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing