Nociceptor

A nociceptor ("pain receptor") is a sensory neuron that responds to damaging or potentially damaging stimuli by sending “possible threat” signals[1][2][3][4] to the spinal cord and the brain. If the brain perceives the threat as credible, it creates the sensation of pain to direct attention to the body part, so the threat can hopefully be mitigated; this process is called nociception.

Nociceptor
Four types of sensory neurons and their receptor cells. Nociceptors shown as free nerve endings type A
Identifiers
MeSH	D009619
Anatomical terminology

History

Nociceptors were discovered by Charles Scott Sherrington in 1906. In earlier centuries, scientists believed that animals were like mechanical devices that transformed the energy of sensory stimuli into motor responses. Sherrington used many different experiments to demonstrate that different types of stimulation to an afferent nerve fiber's receptive field led to different responses. Some intense stimuli trigger reflex withdrawal, certain autonomic responses, and pain. The specific receptors for these intense stimuli were called nociceptors.[5]

Location

In mammals, nociceptors are found in any area of the body that can sense noxious stimuli. External nociceptors are found in tissue such as the skin (cutaneous nociceptors), the corneas, and the mucosa. Internal nociceptors are found in a variety of organs, such as the muscles, the joints, the bladder, the gut, and the digestive tract. The cell bodies of these neurons are located in either the dorsal root ganglia or the trigeminal ganglia.[6] The trigeminal ganglia are specialized nerves for the face, whereas the dorsal root ganglia are associated with the rest of the body. The axons extend into the peripheral nervous system and terminate in branches to form receptive fields.

Development

Nociceptors develop from neural-crest stem cells. The neural crest is responsible for a large part of early development in vertebrates. It is specifically responsible for development of the peripheral nervous system (PNS). The neural-crest stem cells split from the neural tube as it closes, and nociceptors grow from the dorsal part of this neural-crest tissue. They form late during neurogenesis. Earlier forming cells from this region can become non-pain sensing receptors, either proprioceptors or low-threshold mechanoreceptors. All neurons derived from the neural crest, including embryonic nociceptors, express the TrkA, which is a receptor to nerve-growth factor (NGF). However, transcription factors that determine the type of nociceptor remain unclear.[7]

Following sensory neurogenesis, differentiation occurs, and two types of nociceptors are formed. They are classified as either peptidergic or nonpeptidergic nociceptors, each of which express a distinct repertoire of ion channels and receptors. Their specializations allow the receptors to innervate different central and peripheral targets. This differentiation occurs in both perinatal and postnatal periods. The nonpeptidergic nociceptors switch off the TrkA and begin expressing Ret, which is a transmembrane signaling component that allows the expression of glial-cell-derived growth factor (GDNF). This transition is assisted by Runx1 which is vital in the development of nonpeptidergic nociceptors. On the contrary, the peptidergic nociceptors continue to use TrkA, and they express a completely different type of growth factor. There currently is a lot of research about the differences between nociceptors.[7]

Types and functions

The peripheral terminal of the mature nociceptor is where the noxious stimuli are detected and transduced into electrical energy.[8] When the electrical energy reaches a threshold value, an action potential is induced and driven towards the central nervous system (CNS). This leads to the train of events that allows for the conscious awareness of pain. The sensory specificity of nociceptors is established by the high threshold only to particular features of stimuli. Only when the high threshold has been reached by either chemical, thermal, or mechanical environments are the nociceptors triggered. The majority of nociceptors are classified by which of the environmental modalities they respond to. Some nociceptors respond to more than one of these modalities and are consequently designated polymodal. Other nociceptors respond to none of these modalities (although they may respond to stimulation under conditions of inflammation) and are referred to as sleeping or silent.

Nociceptors have two different types of axons. The first are the Aδ fiber axons. They are myelinated and can allow an action potential to travel at a rate of about 20 meters/second towards the CNS. The other type is the more slowly conducting C fiber axons. These only conduct at speeds of around 2 meters/second.[9] This is due to the light or non-myelination of the axon. As a result, pain comes in two phases. The first phase is mediated by the fast-conducting Aδ fibers and the second part due to (Polymodal) C fibers. The pain associated with the Aδ fibers can be associated to an initial extremely sharp pain. The second phase is a more prolonged and slightly less intense feeling of pain as a result of the acute damage. If there is massive or prolonged input to a C fiber, there is a progressive build up in the spinal cord dorsal horn; this phenomenon is similar to tetanus in muscles but is called wind-up. If wind-up occurs there is a probability of increased sensitivity to pain.[10]

Thermal

Thermal nociceptors are activated by noxious heat or cold at various temperatures. There are specific nociceptor transducers that are responsible for how and if the specific nerve ending responds to the thermal stimulus. The first to be discovered was TRPV1, and it has a threshold that coincides with the heat pain temperature of 43 °C. Other temperature in the warm–hot range is mediated by more than one TRP channel. Each of these channels express a particular C-terminal domain that corresponds to the warm–hot sensitivity. The interactions between all these channels and how the temperature level is determined to be above the pain threshold are unknown at this time. The cool stimuli are sensed by TRPM8 channels. Its C-terminal domain differs from the heat sensitive TRPs. Although this channel corresponds to cool stimuli, it is still unknown whether it also contributes in the detection of intense cold. An interesting finding related to cold stimuli is that tactile sensibility and motor function deteriorate while pain perception persists.

Mechanical

Mechanical nociceptors respond to excess pressure or mechanical deformation. They also respond to incisions that break the skin surface. The reaction to the stimulus is processed as pain by the cortex, just like chemical and thermal responses. These mechanical nociceptors frequently have polymodal characteristics. So it is possible that some of the transducers for thermal stimuli are the same for mechanical stimuli. The same is true for chemical stimuli, since TRPA1 appears to detect both mechanical and chemical changes.

Chemical

Chemical nociceptors have TRP channels that respond to a wide variety of spices. The one that sees the most response and is very widely tested is capsaicin. Other chemical stimulants are environmental irritants like acrolein, a World War I chemical weapon and a component of cigarette smoke. Apart from these external stimulants, chemical nociceptors have the capacity to detect endogenous ligands, and certain fatty acid amines that arise from changes in internal tissues. Like in thermal nociceptors, TRPV1 can detect chemicals like capsaicin and spider toxins.[7]

Sleeping/silent

Although each nociceptor can have a variety of possible threshold levels, some do not respond at all to chemical, thermal or mechanical stimuli unless injury actually has occurred. These are typically referred to as silent or sleeping nociceptors since their response comes only on the onset of inflammation to the surrounding tissue.[6]

Polymodal

Many neurons perform only a single function; therefore, neurons that perform these functions in combination are given the classification "polymodal."[11]

Pathway

Afferent nociceptive fibers (those that send information to, rather than from the brain) travel back to the spinal cord where they form synapses in its dorsal horn. This nociceptive fiber (located in the periphery) is a first order neuron. The cells in the dorsal horn are divided into physiologically distinct layers called laminae. Different fiber types form synapses in different layers, and use either glutamate or substance P as the neurotransmitter. Aδ fibers form synapses in laminae I and V, C fibers connect with neurons in lamina II, Aβ fibers connect with lamina I, III, & V.[6] After reaching the specific lamina within the spinal cord, the first order nociceptive project to second order neurons that cross the midline at the anterior white commissure. The second order neurons then send their information via two pathways to the thalamus: the dorsal column medial-lemniscal system and the anterolateral system. The first is reserved more for regular non-painful sensation, while the lateral is reserved for pain sensation. Upon reaching the thalamus, the information is processed in the ventral posterior nucleus and sent to the cerebral cortex in the brain via fibers in the posterior limb of the internal capsule. As there is an ascending pathway to the brain that initiates the conscious realization of pain, there also is a descending pathway which modulates pain sensation. The brain can request the release of specific hormones or chemicals that can have analgesic effects which can reduce or inhibit pain sensation. The area of the brain that stimulates the release of these hormones is the hypothalamus.[12]

This effect of descending inhibition can be shown by electrically stimulating the periaqueductal grey area of the midbrain. The periaqueductal grey in turn projects to other areas involved in pain regulation, such as the nucleus raphes magnus which also receives similar afferents from the nucleus reticularis paragigantocellularis (NPG). In turn the nucleus raphe magnus projects to the substantia gelatinosa region of the dorsal horn and mediates the sensation of spinothalamic inputs. The periaqueductal grey also contains opioid receptors which explains one of the mechanisms by which opioids such as morphine and diacetylmorphine exhibit an analgesic effect.

Sensitivity

Nociceptor neuron sensitivity is modulated by a large variety of mediators in the extracellular space.[13] Peripheral sensitization represents a form of functional plasticity of the nociceptor. The nociceptor can change from being simply a noxious stimulus detector to a detector of non-noxious stimuli. The result is that low intensity stimuli from regular activity, initiates a painful sensation. This is commonly known as hyperalgesia. Inflammation is one common cause that results in the sensitization of nociceptors. Normally hyperalgesia ceases when inflammation goes down, however, sometimes genetic defects and/or repeated injury can result in allodynia: a completely non-noxious stimulus like light touch causes extreme pain. Allodynia can also be caused when a nociceptor is damaged in the peripheral nerves. This can result in deafferentation, which means the development of different central processes from the surviving afferent nerve. With this situation, surviving dorsal root axons of the nociceptors can make contact with the spinal cord, thus changing the normal input.[10]

Other animals

Nociception has been documented in non-mammalian animals, including fish[14] and a wide range of invertebrates, including leeches,[15] nematode worms,[16] sea slugs,[17] and larval fruit flies.[18] Although these neurons may have different pathways and relationships to the central nervous system than mammalian nociceptors, nociceptive neurons in non-mammals often fire in response to similar stimuli as mammals, such as high temperature (40 degrees C or more), low pH, capsaicin, and tissue damage.

Terminology

Due to historical understandings of pain, nociceptors are also called pain receptors. Although pain is real, psychological factors can strongly influence subjective intensity.[19]

See also

• Capsaicin and its mechanism of action in nociceptors.
• Piperine from black pepper
• TRPC ion channel

References

1. http://www.bodyinmind.org/what-is-pain/
2. "NOI - Neuro Orthopaedic Institute". www.noigroup.com. Archived from the original on 2018-10-17. Retrieved 2017-10-13.
3. "Nociception and pain: What is the difference and why does it matter? - Massage St. Louis, St. Louis, MO". www.massage-stlouis.com.
4. Animals, National Research Council (US) Committee on Recognition and Alleviation of Pain in Laboratory (8 December 2017). "Mechanisms of Pain". National Academies Press (US) – via www.ncbi.nlm.nih.gov.
5. Sherrington C. The Integrative Action of the Nervous System. Oxford: Oxford University Press; 1906.
6. Jessell, Thomas M.; Kandel, Eric R.; Schwartz, James H. (1991). Principles of neural science. Norwalk, CT: Appleton & Lange. pp. 472–79. ISBN 978-0-8385-8034-9.
7. Woolf CJ, Ma Q (August 2007). "Nociceptors—noxious stimulus detectors". Neuron. 55 (3): 353–64. doi:10.1016/j.neuron.2007.07.016. PMID 17678850.
8. Fein, A Nociceptors: the cells that sense pain http://cell.uchc.edu/pdf/fein/nociceptors_fein_2012.pdf
9. Williams, S. J.; Purves, Dale (2001). Neuroscience. Sunderland, Mass: Sinauer Associates. ISBN 978-0-87893-742-4.
10. Fields HL, Rowbotham M, Baron R (October 1998). "Postherpetic neuralgia: irritable nociceptors and deafferentation". Neurobiol. Dis. 5 (4): 209–27. doi:10.1006/nbdi.1998.0204. PMID 9848092.
11. Fein, Alan. Nociceptors: the cells that sense pain.
12. "Pain Pathway". Retrieved 2008-06-02.
13. Hucho T, Levine JD (August 2007). "Signaling pathways in sensitization: toward a nociceptor cell biology". Neuron. 55 (3): 365–76. doi:10.1016/j.neuron.2007.07.008. PMID 17678851.
14. 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 of London B: Biological Sciences. 270 (1520): 1115–1121. doi:10.1098/rspb.2003.2349. PMC 1691351. PMID 12816648.
15. 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.
16. Wittenburg N.; Baumeister R. (1999). "Thermal avoidance in Caenorhabditis elegans: an approach to the study of nociception". Proceedings of the National Academy of Sciences of the United States of America. 96 (18): 10477–10482. doi:10.1073/pnas.96.18.10477. PMC 17914. PMID 10468634.
17. Illich P. A.; Walters E. T. (1997). "Mechanosensory neurons innervating Aplysia siphon encode noxious stimuli and display nociceptive sensitization". The Journal of Neuroscience. 17: 459–469. doi:10.1523/JNEUROSCI.17-01-00459.1997. PMC 6793714. PMID 8987770.
18. Tracey J.; Daniel W.; Wilson R. I.; Laurent G.; Benzer S. (2003). "painless, a Drosophila gene essential for nociception". Cell. 113 (2): 261–273. doi:10.1016/S0092-8674(03)00272-1. PMID 12705873.
19. https://www.painscience.com/articles/pain-is-weird.php