Nociception

Nociception (also nocioception, from Latin nocere 'to harm or hurt') is the sensory nervous system's process of encoding noxious stimuli. It deals with a series of events and processes required for an organism to receive a painful stimulus, convert it to a molecular signal, and recognize and characterize the signal in order to trigger an appropriate defense response.

In nociception, intense chemical (e.g., capsaicin present in Chili pepper or Cayenne pepper), mechanical (e.g., cutting, crushing), or thermal (heat and cold) stimulation of sensory neurons called nociceptors produces a signal that travels along a chain of nerve fibers via the spinal cord to the brain.[1] Nociception triggers a variety of physiological and behavioral responses to protect the organism against an aggression and usually results in a subjective experience, or perception, of pain in sentient beings.[2]

Detection of noxious stimuli

Mechanism of nociception via sensory afferents

Potentially damaging mechanical, thermal, and chemical stimuli are detected by nerve endings called nociceptors, which are found in the skin, on internal surfaces such as the periosteum, joint surfaces, and in some internal organs. Some nociceptors are unspecialized free nerve endings that have their cell bodies outside the spinal column in the dorsal root ganglia.[3] Other nociceptors rely on specialised structures in the skin to transduce noxious information such as nociceptive schwann cells.[4] Nociceptors are categorized according to the axons which travel from the receptors to the spinal cord or brain. After nerve injury it is possible for touch fibres that normally carry non-noxious stimuli to be perceived as noxious.[5]

Nociceptive pain consists of an adaptive alarm system.[6] Nociceptors have a certain threshold; that is, they require a minimum intensity of stimulation before they trigger a signal. Once this threshold is reached a signal is passed along the axon of the neuron into the spinal cord.

Nociceptive threshold testing deliberately applies a noxious stimulus to a human or animal subject in order to study pain. In animals, the technique is often used to study the efficacy of analgesic drugs and to establish dosing levels and period of effect. After establishing a baseline, the drug under test is given and the elevation in threshold recorded at specified time points. When the drug wears off, the threshold should return to the baseline (pre-treatment) value.

In some conditions, excitation of pain fibers becomes greater as the pain stimulus continues, leading to a condition called hyperalgesia.

Theory

Consequences

Nociception can also cause generalized autonomic responses before or without reaching consciousness to cause pallor, sweating, tachycardia, hypertension, lightheadedness, nausea and fainting.[7]

System overview

This diagram linearly (unless otherwise mentioned) tracks the projections of all known structures that allow for pain, proprioception, thermoception, and chemoception to their relevant endpoints in the human brain. Click to enlarge.

This overview discusses proprioception, thermoception, chemoception and nociception as they are all integrally connected.

Mechanical

Proprioception is determined by using standard mechanoreceptors (especially ruffini corpuscles (stretch) and transient receptor potential (TRP) channels). Proprioception is completely covered within the somatosensory system as the brain processes them together.

Thermoception refers to stimuli of moderate temperatures 24–28 °C (75–82 °F), as anything beyond that range is considered pain and moderated by nociceptors. TRP and potassium channels [TRPM (1-8), TRPV (1-6), TRAAK, and TREK] each respond to different temperatures (among other stimuli) which create action potentials in nerves which join the mechano (touch) system in the posterolateral tract. Thermoception, like proprioception, is then covered by the somatosensory system.[8][9][10][11][12]

TRP channels that detect noxious stimuli (mechanical, thermal, and chemical pain) relay that info to nociceptors that generate an action potential. Mechanical TRP channels react to depression of their cells (like touch), thermal TRP change shape in different temperatures, and chemical TRP act like taste buds, signalling if their receptors bond to certain elements/chemicals.

Neural

In non-mammalian animals

Nociception has been documented in non-mammalian animals, including fish[24] and a wide range of invertebrates,[25] including leeches,[26] nematode worms,[27] sea slugs,[28] and fruit flies.[29] As in mammals, nociceptive neurons in these species are typically characterized by responding preferentially to high temperature (40° Celsius or more), low pH, capsaicin, and tissue damage.

History of term

The term "nociception" was coined by Charles Scott Sherrington to distinguish the physiological process (nervous activity) from pain (a subjective experience).[30] It is derived from the Latin verb "nocēre", which means "to harm".

See also

  • Electroreception – Detection of weak electric fields, via specialized sense organs and brain structures
  • Mechanoreceptor – Sensory receptor cell responding to mechanical pressure or strain
  • Thermoception – Temperature stimulus inferred from a heat flux and converted into a molecular signal
  • Proprioception – Sense of the relative position of one's own body parts and strength of effort employed in movement

References

  1. ↑ Portenoy, Russell K.; Brennan, Michael J. (1994). "Chronic Pain Management". In Good, David C.; Couch, James R. (eds.). Handbook of Neurorehabilitation. Informa Healthcare. ISBN 978-0-8247-8822-3.
  2. ↑ Bayne, Kathryn (2000). "Assessing Pain and Distress: A Veterinary Behaviorist's Perspective". Definition of Pain and Distress and Reporting Requirements for Laboratory Animals: Proceedings of the Workshop Held June 22, 2000. National Academies Press. pp. 13–21. ISBN 978-0-309-17128-1.
  3. ↑ Purves, D. (2001). "Nociceptors". In Sunderland, MA. (ed.). Neuroscience. Sinauer Associates.
  4. ↑ Doan, Ryan A.; Monk, Kelly R. (16 August 2019). "Glia in the skin activate pain responses". Science. 365 (6454): 641–642. Bibcode:2019Sci...365..641D. doi:10.1126/science.aay6144. ISSN 1095-9203. PMID 31416950. S2CID 201015745.
  5. ↑ Dhandapani, Rahul; Arokiaraj, Cynthia Mary; Taberner, Francisco J.; Pacifico, Paola; Raja, Sruthi; Nocchi, Linda; Portulano, Carla; Franciosa, Federica; Maffei, Mariano; Hussain, Ahmad Fawzi; de Castro Reis, Fernanda (2018-04-24). "Control of mechanical pain hypersensitivity in mice through ligand-targeted photoablation of TrkB-positive sensory neurons". Nature Communications. 9 (1): 1640. Bibcode:2018NatCo...9.1640D. doi:10.1038/s41467-018-04049-3. ISSN 2041-1723. PMC 5915601. PMID 29691410.
  6. ↑ Woolf, Clifford J.; Ma, Qiufu (2007-08-02). "Nociceptors--noxious stimulus detectors". Neuron. 55 (3): 353–364. doi:10.1016/j.neuron.2007.07.016. ISSN 0896-6273. PMID 17678850.
  7. ↑ Feinstein, B.; Langton, J. N. K.; Jameson, R. M.; Schiller, F. (October 1954). "Experiments on pain referred from deep somatic tissues". The Journal of Bone & Joint Surgery. 36 (5): 981–997. doi:10.2106/00004623-195436050-00007. PMID 13211692.
  8. ↑ McCann, Stephanie (2017). Kaplan Medical Anatomy Flashcards: Clearly Labeled, Full-Color Cards. KAPLAN. ISBN 978-1-5062-2353-7.
  9. ↑ Albertine, Kurt. Barron’s Anatomy Flash Cards
  10. ↑ Hofmann, Thomas; Schaefer, Michael; Schultz, Günter; Gudermann, Thomas (28 May 2002). "Subunit composition of mammalian transient receptor potential channels in living cells". Proceedings of the National Academy of Sciences. 99 (11): 7461–7466. Bibcode:2002PNAS...99.7461H. doi:10.1073/pnas.102596199. PMC 124253. PMID 12032305.
  11. ↑ Noël, Jacques; Zimmermann, Katharina; Busserolles, Jérome; Deval, Emanuel; Alloui, Abdelkrim; Diochot, Sylvie; Guy, Nicolas; Borsotto, Marc; Reeh, Peter; Eschalier, Alain; Lazdunski, Michel (12 March 2009). "The mechano-activated K+ channels TRAAK and TREK-1 control both warm and cold perception". The EMBO Journal. 28 (9): 1308–1318. doi:10.1038/emboj.2009.57. PMC 2683043. PMID 19279663.
  12. ↑ Scholz, Joachim; Woolf, Clifford J. (November 2002). "Can we conquer pain?". Nature Neuroscience. 5 (11): 1062–1067. doi:10.1038/nn942. PMID 12403987. S2CID 15781811.
  13. ↑ Braz, Joao M.; Nassar, Mohammed A.; Wood, John N.; Basbaum, Allan I. (September 2005). "Parallel 'Pain' Pathways Arise from Subpopulations of Primary Afferent Nociceptor". Neuron. 47 (6): 787–793. doi:10.1016/j.neuron.2005.08.015. PMID 16157274. S2CID 2402859.
  14. ↑ Brown, A. G. (2012). Organization in the Spinal Cord: The Anatomy and Physiology of Identified Neurones. Springer Science & Business Media. ISBN 978-1-4471-1305-8.
  15. ↑ van den Pol, Anthony N. (15 April 1999). "Hypothalamic Hypocretin (Orexin): Robust Innervation of the Spinal Cord". The Journal of Neuroscience. 19 (8): 3171–3182. doi:10.1523/JNEUROSCI.19-08-03171.1999. PMC 6782271. PMID 10191330.
  16. ↑ Bajo, Victoria M.; Merchán, Miguel A.; Malmierca, Manuel S.; Nodal, Fernando R.; Bjaalie, Jan G. (10 May 1999). "Topographic organization of the dorsal nucleus of the lateral lemniscus in the cat". The Journal of Comparative Neurology. 407 (3): 349–366. doi:10.1002/(SICI)1096-9861(19990510)407:3<349::AID-CNE4>3.0.CO;2-5. PMID 10320216.
  17. ↑ Oliver, Douglas L. (2005). "Neuronal Organization in the Inferior Colliculus". The Inferior Colliculus. pp. 69–114. doi:10.1007/0-387-27083-3_2. ISBN 0-387-22038-0.
  18. ↑ Corneil, Brian D.; Olivier, Etienne; Munoz, Douglas P. (1 October 2002). "Neck Muscle Responses to Stimulation of Monkey Superior Colliculus. I. Topography and Manipulation of Stimulation Parameters". Journal of Neurophysiology. 88 (4): 1980–1999. doi:10.1152/jn.2002.88.4.1980. PMID 12364523.
  19. ↑ May, Paul J. (2006). "The mammalian superior colliculus: Laminar structure and connections". Neuroanatomy of the Oculomotor System. Progress in Brain Research. Vol. 151. pp. 321–378. doi:10.1016/S0079-6123(05)51011-2. ISBN 9780444516961. PMID 16221594.
  20. ↑ Benevento, Louis A.; Standage, Gregg P. (1 July 1983). "The organization of projections of the retinorecipient and nonretinorecipient nuclei of the pretectal complex and layers of the superior colliculus to the lateral pulvinar and medial pulvinar in the macaque monkey". The Journal of Comparative Neurology. 217 (3): 307–336. doi:10.1002/cne.902170307. PMID 6886056. S2CID 44794002.
  21. ↑ Sawamoto, Nobukatsu; Honda, Manabu; Okada, Tomohisa; Hanakawa, Takashi; Kanda, Masutaro; Fukuyama, Hidenao; Konishi, Junji; Shibasaki, Hiroshi (1 October 2000). "Expectation of Pain Enhances Responses to Nonpainful Somatosensory Stimulation in the Anterior Cingulate Cortex and Parietal Operculum/Posterior Insula: an Event-Related Functional Magnetic Resonance Imaging Study". The Journal of Neuroscience. 20 (19): 7438–7445. doi:10.1523/JNEUROSCI.20-19-07438.2000. PMC 6772793. PMID 11007903.
  22. ↑ Menon, Vinod; Uddin, Lucina Q. (29 May 2010). "Saliency, switching, attention and control: a network model of insula function". Brain Structure and Function. 214 (5–6): 655–667. doi:10.1007/s00429-010-0262-0. PMC 2899886. PMID 20512370.
  23. ↑ Shackman, Alexander J.; Salomons, Tim V.; Slagter, Heleen A.; Fox, Andrew S.; Winter, Jameel J.; Davidson, Richard J. (March 2011). "The integration of negative affect, pain and cognitive control in the cingulate cortex". Nature Reviews Neuroscience. 12 (3): 154–167. doi:10.1038/nrn2994. PMC 3044650. PMID 21331082.
  24. ↑ Sneddon, L. U.; Braithwaite, V. A.; Gentle, M. J. (2003). "Do fishes have nociceptors? Evidence for the evolution of a vertebrate sensory system". Proceedings of the Royal Society B. 270 (1520): 1115–1121. doi:10.1098/rspb.2003.2349. PMC 1691351. PMID 12816648.
  25. ↑ Jane A. Smith (1991). "A Question of Pain in Invertebrates". Institute for Laboratory Animals Journal. 33 (1–2).
  26. ↑ Pastor, J.; Soria, B.; Belmonte, C. (1996). "Properties of the nociceptive neurons of the leech segmental ganglion". Journal of Neurophysiology. 75 (6): 2268–2279. doi:10.1152/jn.1996.75.6.2268. PMID 8793740.
  27. ↑ Wittenburg, N.; Baumeister, R. (1999). "Thermal avoidance in Caenorhabditis elegans: an approach to the study of nociception". PNAS. 96 (18): 10477–10482. Bibcode:1999PNAS...9610477W. doi:10.1073/pnas.96.18.10477. PMC 17914. PMID 10468634.
  28. ↑ Illich, P. A.; Walters, E. T. (1997). "Mechanosensory neurons innervating Aplysia siphon encode noxious stimuli and display nociceptive sensitization". Journal of Neuroscience. 17 (1): 459–469. doi:10.1523/JNEUROSCI.17-01-00459.1997. PMC 6793714. PMID 8987770.
  29. ↑ Tracey, W.Daniel; Wilson, Rachel I; Laurent, Gilles; Benzer, Seymour (April 2003). "painless, a Drosophila Gene Essential for Nociception". Cell. 113 (2): 261–273. doi:10.1016/s0092-8674(03)00272-1. PMID 12705873. S2CID 1424315.
  30. ↑ Sherrington, C. (1906). The Integrative Action of the Nervous System. Oxford: Oxford University Press.
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