Interoception and Gut Feelings: Unconscious Body Signals’ Impact on Brain Function, Behavior and Belief Processes

Part of the New Approaches to the Scientific Study of Religion book series (NASR, volume 1)

Abstract

The term “gut feelings” is widely used in everyday language and has a number of connotations ranging from intuition, instinctive feeling, making decisions without rational underpinnings, to serendipity. While in a psychosomatic context the gastrointestinal tract has long been known to respond to emotions and stress, exactly how the gut itself could be a source of feelings/emotions has remained elusive. Neurobiological research in the past two decades has revealed that there is a continuous flow of information from the digestive tract and other internal organs to the brain. A large part of this information does not reach the level of consciousness, but is important for the autonomic control of body functions. In addition, brain imaging techniques have revealed that part of the subconscious information that flows from internal organs is also fed into the corticolimbic system where it is very likely to influence thinking, emotions, and mood. This process is embodied in the term “interoception,” and it is emerging that - via the process of interoception - signals from the gut and other internal organs exert an influence on our “feelings” (emotion, cognition, and mood), and that a disturbance in this interoception has an impact on neuropsychiatric diseases. In this relationship, interoception is also very likely to have an impact on the neurobiological basis of belief processes.

Keywords

Autism Spectrum Disorder Afferent Neuron Anterior Cingulate Cortex Chronic Fatigue Syndrome Anterior Insula 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Ahlman H, Nilsson O (2001) The gut as the largest endocrine organ in the body. Ann Oncol 12(2):63–68CrossRefGoogle Scholar
  2. Berntson GG, Sarter M, Cacioppo JT (2003) Ascending visceral regulation of cortical affective information processing. Eur J Neurosci 18:2103–2109. doi: 10.1046/j.1460-9568.2003.02967.x CrossRefGoogle Scholar
  3. Binkofski F, Schnitzler A, Enck P, Frieling T, Posse S, Seitz RJ, Freund HJ (1998) Somatic and limbic cortex activation in esophageal distention: a functional magnetic resonance imaging study. Ann Neurol 44:811–815CrossRefGoogle Scholar
  4. Collins SM, Surette M, Bercik P (2012) The interplay between the intestinal microbiota and the brain. Nat Rev Microbiol 10:735–742. doi: 10.1038/nrmicro2876 CrossRefGoogle Scholar
  5. Craig AD (2002) How do you feel? Interoception: the sense of the physiological condition of the body. Nat Rev Neurosci 3:655–666. doi: 10.1038/nrn894 CrossRefGoogle Scholar
  6. Craig AD (2009) How do you feel – now? The anterior insula and human awareness. Nat Rev Neurosci 10:59–70. doi: 10.1038/nrn2555 CrossRefGoogle Scholar
  7. Cryan JF, Dinan TG (2012) Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour. Nat Rev Neurosci 13:701–712. doi: 10.1038/nrn3346 CrossRefGoogle Scholar
  8. Farzi A, Reichmann F, Meinitzer A, Mayerhofer R, Jain P, Hassan AM, Fröhlich EE, Wagner K, Painsipp E, Rinner B, Holzer P (2015) Synergistic effects of NOD1 or NOD2 and TLR4 activation on mouse sickness behavior in relation to immune and brain activity markers. Brain Behav Immun 44:106–120. doi: 10.1016/j.bbi.2014.08.011 CrossRefGoogle Scholar
  9. Furman DJ, Waugh CE, Bhattacharjee K, Thompson RJ, Gotlib IH (2013) Interoceptive awareness, positive affect, and decision making in major depressive disorder. J Affect Disord 151:780–785. doi: 10.1016/j.jad.2013.06.044 CrossRefGoogle Scholar
  10. Harshaw C (2015) Interoceptive dysfunction: toward an integrated framework for understanding somatic and affective disturbance in depression. Psychol Bull 141:311–363. doi: 10.1037/a0038101 CrossRefGoogle Scholar
  11. Holzer P (2008) The role of the vagus nerve in afferent signaling and homeostasis during visceral inflammation. In: Jancsó G (ed) Neurogenic inflammation in health and disease, Neuroimmune biology, vol 8. Elsevier, Amsterdam, pp 321–338CrossRefGoogle Scholar
  12. Holzer P (2015) Das Gehirn unter dem Einfluss des Darmmikrobioms. Neurologisch 01/2015:45–49Google Scholar
  13. Holzer P, Farzi A (2014) Neuropeptides and the microbiota-gut-brain axis. Adv Exp Med Biol 817:195–219. doi: 10.1007/978-1-4939-0897-4_9 CrossRefGoogle Scholar
  14. Holzer P, Schicho R, Holzer-Petsche U, Lippe IT (2001) The gut as a neurological organ. Wien Klin Wochenschr 113:647–660Google Scholar
  15. Mayer EA (2011) Gut feelings: the emerging biology of gut–brain communication. Nat Rev Neurosci 12:453–466. doi: 10.1038/nrn3071 CrossRefGoogle Scholar
  16. Mayer EA, Tillisch K (2011) The brain-gut axis in abdominal pain syndromes. Annu Rev Med 62:381–396. doi: 10.1146/annurev-med-012309-103958 CrossRefGoogle Scholar
  17. Mayer EA, Tillisch K, Gupta A (2015) Gut/brain axis and the microbiota. J Clin Invest 125:926–038. doi: 10.1172/JCI76304 CrossRefGoogle Scholar
  18. Murphy KG, Bloom SR (2006) Gut hormones and the regulation of energy homeostasis. Nature 444:854–859. doi: 10.1038/nature05484 CrossRefGoogle Scholar
  19. Paulus MP, Stein MB (2006) An insular view of anxiety. Biol Psychiatry 60:383–387. doi: 10.1016/j.biopsych.2006.03.042 CrossRefGoogle Scholar
  20. Paulus MP, Stein MB (2010) Interoception in anxiety and depression. Brain Struct Funct 214:451–463. doi: 10.1007/s00429-010-0258-9 CrossRefGoogle Scholar
  21. Perez-Burgos A, Mao YK, Bienenstock J, Kunze WA (2014) The gut-brain axis rewired: adding a functional vagal nicotinic “sensory synapse”. FASEB J 28:3064–3074. doi: 10.1096/fj.13-245282 CrossRefGoogle Scholar
  22. Preuschoff K, Quartz SR, Bossaerts P (2008) Human insula activation reflects risk prediction errors as well as risk. J Neurosci 28:2745–2752. doi: 10.1523/JNEUROSCI.4286-07.2008 CrossRefGoogle Scholar
  23. Singer T, Critchley HD, Preuschoff K (2009) A common role of insula in feelings, empathy and uncertainty. Trends Cogn Sci 13:334–340. doi: 10.1016/j.tics.2009.05.001 CrossRefGoogle Scholar
  24. Wicker B, Keysers C, Plailly J, Royet JP, Gallese V, Rizzolatti G (2003) Both of us disgusted in My insula: the common neural basis of seeing and feeling disgust. Neuron 40:655–664. doi:http://dx.doi.org/10.1016/S0896-6273(03)00679-2
  25. Wiebking C, Duncan NW, Tiret B, Hayes DJ, Marjaǹska M, Doyon J, Bajbouj M, Northoff G (2014) GABA in the insula – a predictor of the neural response to interoceptive awareness. NeuroImage 86:10–18. doi: 10.1016/j.neuroimage.2013.04.042 CrossRefGoogle Scholar
  26. Wittig BM, Zeitz M (2003) The gut as an organ of immunology. Int J Color Dis 18:181–187. doi: 10.1007/s00384-002-0444-1 Google Scholar

Copyright information

© Springer International Publishing AG 2017

Authors and Affiliations

  1. 1.Institute of Experimental and Clinical PharmacologyMedical University of GrazGrazAustria

Personalised recommendations