iBet uBet web content aggregator. Adding the entire web to your favor.
iBet uBet web content aggregator. Adding the entire web to your favor.



Link to original content: https://en.wikipedia.org/wiki/Sensory_neuron
Sensory neuron - Wikipedia Jump to content

Sensory neuron

From Wikipedia, the free encyclopedia
Four types of sensory neuron

Sensory neurons, also known as afferent neurons, are neurons in the nervous system, that convert a specific type of stimulus, via their receptors, into action potentials or graded receptor potentials.[1] This process is called sensory transduction. The cell bodies of the sensory neurons are located in the dorsal root ganglia of the spinal cord.[2]

The sensory information travels on the afferent nerve fibers in a sensory nerve, to the brain via the spinal cord. Spinal nerves transmit external sensations via sensory nerves to the brain through the spinal cord.[3] The stimulus can come from exteroreceptors outside the body, for example those that detect light and sound, or from interoreceptors inside the body, for example those that are responsive to blood pressure or the sense of body position.

Types and function

[edit]

Sensory neurons in vertebrates are predominantly pseudounipolar or bipolar, and different types of sensory neurons have different sensory receptors that respond to different kinds of stimuli. There are at least six external and two internal sensory receptors:

External receptors

[edit]
See also: Perception § Types of perception

External receptors that respond to stimuli from outside the body are called exteroreceptors.[4] Exteroreceptors include chemoreceptors such as olfactory receptors (smell) and taste receptors, photoreceptors (vision), thermoreceptors (temperature), nociceptors (pain), hair cells (hearing and balance), and a number of other different mechanoreceptors for touch and proprioception (stretch, distortion and stress).

Smell

[edit]

The sensory neurons involved in smell are called olfactory sensory neurons. These neurons contain receptors, called olfactory receptors, that are activated by odor molecules in the air. The molecules in the air are detected by enlarged cilia and microvilli.[5] These sensory neurons produce action potentials. Their axons form the olfactory nerve, and they synapse directly onto neurons in the cerebral cortex (olfactory bulb). They do not use the same route as other sensory systems, bypassing the brain stem and the thalamus. The neurons in the olfactory bulb that receive direct sensory nerve input, have connections to other parts of the olfactory system and many parts of the limbic system. 9.

Taste

[edit]

Taste sensation is facilitated by specialized sensory neurons located in the taste buds of the tongue and other parts of the mouth and throat. These sensory neurons are responsible for detecting different taste qualities, such as sweet, sour, salty, bitter, and savory. When you eat or drink something, chemicals in the food or liquid interact with receptors on these sensory neurons, triggering signals that are sent to the brain. The brain then processes these signals and interprets them as specific taste sensations, allowing you to perceive and enjoy the flavors of the foods you consume. [6] When taste receptor cells are stimulated by the binding of these chemical compounds (tastants), it can lead to changes in the flow of ions, such as sodium (Na+), calcium (Ca2+), and potassium (K+), across the cell membrane. [7] In response to tastant binding, ion channels on the taste receptor cell membrane can open or close. This can lead to depolarization of the cell membrane, creating an electrical signal.

Similar to olfactory receptors, taste receptors (gustatory receptors) in taste buds interact with chemicals in food to produce an action potential.

Vision

[edit]

Photoreceptor cells are capable of phototransduction, a process which converts light (electromagnetic radiation) into electrical signals. These signals are refined and controlled by the interactions with other types of neurons in the retina. The five basic classes of neurons within the retina are photoreceptor cells, bipolar cells, ganglion cells, horizontal cells, and amacrine cells. The basic circuitry of the retina incorporates a three-neuron chain consisting of the photoreceptor (either a rod or cone), bipolar cell, and the ganglion cell. The first action potential occurs in the retinal ganglion cell. This pathway is the most direct way for transmitting visual information to the brain. There are three primary types of photoreceptors: Cones are photoreceptors that respond significantly to color. In humans the three different types of cones correspond with a primary response to short wavelength (blue), medium wavelength (green), and long wavelength (yellow/red).[8] Rods are photoreceptors that are very sensitive to the intensity of light, allowing for vision in dim lighting. The concentrations and ratio of rods to cones is strongly correlated with whether an animal is diurnal or nocturnal. In humans, rods outnumber cones by approximately 20:1, while in nocturnal animals, such as the tawny owl, the ratio is closer to 1000:1.[8] Retinal ganglion cells are involved in the sympathetic response. Of the ~1.3 million ganglion cells present in the retina, 1-2% are believed to be photosensitive.[9]

Issues and decay of sensory neurons associated with vision lead to disorders such as:

  1. Macular degeneration – degeneration of the central visual field due to either cellular debris or blood vessels accumulating between the retina and the choroid, thereby disturbing and/or destroying the complex interplay of neurons that are present there.[10]
  2. Glaucoma – loss of retinal ganglion cells which causes some loss of vision to blindness.[11]
  3. Diabetic retinopathy – poor blood sugar control due to diabetes damages the tiny blood vessels in the retina.[12]

Auditory

[edit]

The auditory system is responsible for converting pressure waves generated by vibrating air molecules or sound into signals that can be interpreted by the brain.

This mechanoelectrical transduction is mediated with hair cells within the ear. Depending on the movement, the hair cell can either hyperpolarize or depolarize. When the movement is towards the tallest stereocilia, the Na+ cation channels open allowing Na+ to flow into cell and the resulting depolarization causes the Ca++ channels to open, thus releasing its neurotransmitter into the afferent auditory nerve. There are two types of hair cells: inner and outer. The inner hair cells are the sensory receptors .[13]

Problems with sensory neurons associated with the auditory system leads to disorders such as:

  1. Auditory processing disorder – Auditory information in the brain is processed in an abnormal way. Patients with auditory processing disorder can usually gain the information normally, but their brain cannot process it properly, leading to hearing disability.[14]
  2. Auditory verbal agnosia – Comprehension of speech is lost but hearing, speaking, reading, and writing ability is retained. This is caused by damage to the posterior superior temporal lobes, again not allowing the brain to process auditory input correctly.[15]

Temperature

[edit]

Thermoreceptors are sensory receptors, which respond to varying temperatures. While the mechanisms through which these receptors operate is unclear, recent discoveries have shown that mammals have at least two distinct types of thermoreceptors.[16] The bulboid corpuscle, is a cutaneous receptor a cold-sensitive receptor, that detects cold temperatures. The other type is a warmth-sensitive receptor.

Mechanoreceptors

[edit]
Main article: Mechanoreceptor
Further information: Mechanosensation

Mechanoreceptors are sensory receptors which respond to mechanical forces, such as pressure or distortion.[17]

Specialized sensory receptor cells called mechanoreceptors often encapsulate afferent fibers to help tune the afferent fibers to the different types of somatic stimulation. Mechanoreceptors also help lower thresholds for action potential generation in afferent fibers and thus make them more likely to fire in the presence of sensory stimulation.[18]

Some types of mechanoreceptors fire action potentials when their membranes are physically stretched.

Proprioceptors are another type of mechanoreceptors which literally means "receptors for self". These receptors provide spatial information about limbs and other body parts.[19]

Nociceptors are responsible for processing pain and temperature changes. The burning pain and irritation experienced after eating a chili pepper (due to its main ingredient, capsaicin), the cold sensation experienced after ingesting a chemical such as menthol or icillin, as well as the common sensation of pain are all a result of neurons with these receptors.[20]

Problems with mechanoreceptors lead to disorders such as:

  1. Neuropathic pain - a severe pain condition resulting from a damaged sensory nerve [20]
  2. Hyperalgesia - an increased sensitivity to pain caused by sensory ion channel, TRPM8, which is typically responds to temperatures between 23 and 26 degrees, and provides the cooling sensation associated with menthol and icillin [20]
  3. Phantom limb syndrome - a sensory system disorder where pain or movement is experienced in a limb that does not exist [21]

Internal receptors

[edit]

Internal receptors that respond to changes inside the body are known as interoceptors.[4]

Blood

[edit]

The aortic bodies and carotid bodies contain clusters of glomus cells – peripheral chemoreceptors that detect changes in chemical properties in the blood such as oxygen concentration.[22] These receptors are polymodal responding to a number of different stimuli.

Nociceptors

[edit]

Nociceptors respond to potentially damaging stimuli by sending signals to the spinal cord and brain. This process, called nociception, usually causes the perception of pain.[23][24] They are found in internal organs as well as on the surface of the body to "detect and protect".[24] Nociceptors detect different kinds of noxious stimuli indicating potential for damage, then initiate neural responses to withdraw from the stimulus.[24]

  1. Thermal nociceptors are activated by noxious heat or cold at various temperatures.[24]
  2. Mechanical nociceptors respond to excess pressure or mechanical deformation, such as a pinch.[24]
  3. Chemical nociceptors respond to a wide variety of chemicals, some of which signal a response. They are involved in the detection of some spices in food, such as the pungent ingredients in Brassica and Allium plants, which target the sensory neural receptor to produce acute pain and subsequent pain hypersensitivity.[25]

Connection with the central nervous system

[edit]

Information coming from the sensory neurons in the head enters the central nervous system (CNS) through cranial nerves. Information from the sensory neurons below the head enters the spinal cord and passes towards the brain through the 31 spinal nerves.[26] The sensory information traveling through the spinal cord follows well-defined pathways. The nervous system codes the differences among the sensations in terms of which cells are active.

Classification

[edit]

Adequate stimulus

[edit]

A sensory receptor's adequate stimulus is the stimulus modality for which it possesses the adequate sensory transduction apparatus. Adequate stimulus can be used to classify sensory receptors:

  1. Baroreceptors respond to pressure in blood vessels
  2. Chemoreceptors respond to chemical stimuli
  3. Electromagnetic radiation receptors respond to electromagnetic radiation[27]
    1. Infrared receptors respond to infrared radiation
    2. Photoreceptors respond to visible light
    3. Ultraviolet receptors respond to ultraviolet radiation [citation needed]
  4. Electroreceptors respond to electric fields
    1. Ampullae of Lorenzini respond to electric fields, salinity, and to temperature, but function primarily as electroreceptors
  5. Hydroreceptors respond to changes in humidity
  6. Magnetoreceptors respond to magnetic fields
  7. Mechanoreceptors respond to mechanical stress or mechanical strain
  8. Nociceptors respond to damage, or threat of damage, to body tissues, leading (often but not always) to pain perception
  9. Osmoreceptors respond to the osmolarity of fluids (such as in the hypothalamus)
  10. Proprioceptors provide the sense of position
  11. Thermoreceptors respond to temperature, either heat, cold or both

Location

[edit]

Sensory receptors can be classified by location:

  1. Cutaneous receptors are sensory receptors found in the dermis or epidermis.[28]
  2. Muscle spindles contain mechanoreceptors that detect stretch in muscles.

Morphology

[edit]

Somatic sensory receptors near the surface of the skin can usually be divided into two groups based on morphology:

  1. Free nerve endings characterize the nociceptors and thermoreceptors and are called thus because the terminal branches of the neuron are unmyelinated and spread throughout the dermis and epidermis.
  2. Encapsulated receptors consist of the remaining types of cutaneous receptors. Encapsulation exists for specialized functioning.

Rate of adaptation

[edit]
  1. A tonic receptor is is a sensory receptor that adapts slowly to a stimulus[29] and continues to produce action potentials over the duration of the stimulus.[30] In this way it conveys information about the duration of the stimulus. Some tonic receptors are permanently active and indicate a background level. Examples of such tonic receptors are pain receptors, joint capsule, and muscle spindle.[31]
  2. A phasic receptor is a sensory receptor that adapts rapidly to a stimulus. The response of the cell diminishes very quickly and then stops.[32] It does not provide information on the duration of the stimulus;[30] instead some of them convey information on rapid changes in stimulus intensity and rate.[31] An example of a phasic receptor is the Pacinian corpuscle.

Drugs

[edit]

There are many drugs currently on the market that are used to manipulate or treat sensory system disorders. For instance, gabapentin is a drug that is used to treat neuropathic pain by interacting with one of the voltage-dependent calcium channels present on non-receptive neurons.[20] Some drugs may be used to combat other health problems, but can have unintended side effects on the sensory system. Dysfunction in the hair cell mechanotransduction complex, along with the potential loss of specialized ribbon synapses, can lead to hair cell death, often caused by ototoxic drugs like aminoglycoside antibiotics poisoning the cochlea.[33] Through the use of these toxins, the K+ pumping hair cells cease their function. Thus, the energy generated by the endocochlear potential which drives the auditory signal transduction process is lost, leading to hearing loss.[34]

Neuroplasticity

[edit]

Ever since scientists observed cortical remapping in the brain of Taub's Silver Spring monkeys, there has been a large amount of research into sensory system plasticity. Huge strides have been made in treating disorders of the sensory system. Techniques such as constraint-induced movement therapy developed by Taub have helped patients with paralyzed limbs regain use of their limbs by forcing the sensory system to grow new neural pathways.[35] Phantom limb syndrome is a sensory system disorder in which amputees perceive that their amputated limb still exists and they may still be experiencing pain in it. The mirror box developed by V.S. Ramachandran, has enabled patients with phantom limb syndrome to relieve the perception of paralyzed or painful phantom limbs. It is a simple device which uses a mirror in a box to create an illusion in which the sensory system perceives that it is seeing two hands instead of one, therefore allowing the sensory system to control the "phantom limb". By doing this, the sensory system can gradually get acclimated to the amputated limb, and thus alleviate this syndrome.[36]

Other animals

[edit]

Hydrodynamic reception is a form of mechanoreception used in a range of animal species.

Additional images

[edit]
  • Illustration of tactile receptors in the skin
    Illustration of tactile receptors in the skin
  • Illustration of lamellated corpuscle
    Illustration of lamellated corpuscle
  • Illustration of Ruffini corpuscle
    Illustration of Ruffini corpuscle
  • Illustration of skin Merkel cell
    Illustration of skin Merkel cell
  • Illustration of tactile corpuscle
    Illustration of tactile corpuscle
  • Illustration of root hair plexus
    Illustration of root hair plexus
  • Illustration of free nerve endings
    Illustration of free nerve endings

See also

[edit]

References

[edit]
  1. ^ Parsons, Richard (2018). CGP: A-Level Biology Complete Revision & Practice. Newcastle Upon Thynde: Coordination Group Publishing Ltd. p. 138. ISBN 9781789080261.
  2. ^ Purves, Dale; Augustine, George; Fitzpatrick, David; Hall, William; LaMantia, Anthony-Samuel; McNamara, James; White, Leonard (2008). Neuroscience (4th ed.). Sinauer Associates, Inc. pp. 207. ISBN 978-0878936977.
  3. ^ Koop LK, Tadi P (July 25, 2022). Neuroanatomy, Sensory Nerves. StatPearls [Internet]. Treasure Island FL: StatPearls. PMID 30969668. NBK539846.
  4. ^ a b Campbell, Neil (1996). Biology (4th ed.). Benjamin/Cummings Pub. Co. p. 1028. ISBN 0805319409.
  5. ^ Breed, Michael D., and Moore, Janice. Encyclopedia of Animal Behavior . London: Elsevier, 2010. Print.
  6. ^ Vincis R, Fontanini A (2019). "Central taste anatomy and physiology". Smell and Taste. Handbook of Clinical Neurology. Vol. 164. pp. 187–204. doi:10.1016/B978-0-444-63855-7.00012-5. ISBN 978-0-444-63855-7. PMC 6989094. PMID 31604547. {{cite book}}: |journal= ignored (help)
  7. ^ Taruno A, Nomura K, Kusakizako T, Ma Z, Nureki O, Foskett JK (January 2021). "Taste transduction and channel synapses in taste buds". Pflugers Arch. 473 (1): 3–13. doi:10.1007/s00424-020-02464-4. PMC 9386877. PMID 32936320.
  8. ^ a b "eye, human." Encyclopædia Britannica. Encyclopædia Britannica Ultimate Reference Suite. Chicago: Encyclopædia Britannica, 2010.
  9. ^ Foster RG, Provencio I, Hudson D, Fiske S, De Grip W, Menaker M (July 1991). "Circadian photoreception in the retinally degenerate mouse (rd/rd)". J Comp Physiol A. 169 (1): 39–50. doi:10.1007/BF00198171. PMID 1941717.
  10. ^ de Jong, Paulus T.V.M. (2006-10-05). "Age-Related Macular Degeneration". New England Journal of Medicine. 355 (14): 1474–1485. doi:10.1056/NEJMra062326. ISSN 0028-4793. PMID 17021323.
  11. ^ Alguire, Patrick; Dallas, Wilbur; Willis, John; Kenneth, Henry (1990). "Ch. 118 Tonometry". Clinical methods : the history, physical, and laboratory examinations (3rd ed.). Butterworths. ISBN 978-0409900774. OCLC 15695765.
  12. ^ "NIHSeniorHealth: Diabetic Retinopathy - Causes and Risk Factors". nihseniorhealth.gov. Archived from the original on 2017-01-14. Retrieved 2016-12-19.
  13. ^ Purves, Dale; Augustine, George; Fitzpatrick, David; Hall, William; LaMantia, Anthony-Samuel; McNamara, James; White, Leonard (2008). Neuroscience (4th ed.). Sinauer Associates, Inc. pp. 327–330. ISBN 978-0878936977.
  14. ^ "Auditory Processing Disorder (APD)" (PDF). British Society of Audiology APD Special Interest Group MRC Institute of Hearing Research. Archived from the original (PDF) on 2016-04-02. Retrieved 2016-12-19.
  15. ^ Stefanatos, Gerry A.; Gershkoff, Arthur; Madigan, Sean (2005-07-01). "On pure word deafness, temporal processing, and the left hemisphere". Journal of the International Neuropsychological Society. 11 (4): 456–470, discussion 455. doi:10.1017/S1355617705050538. ISSN 1355-6177. PMID 16209426. S2CID 25584363.
  16. ^ Krantz, John. Experiencing Sensation and Perception Archived 2017-11-17 at the Wayback Machine. Pearson Education, Limited, 2009. p. 12.3
  17. ^ Winter R, Harrar V, Gozdzik M, Harris LR (November 2008). "The relative timing of active and passive touch". Brain Res. 1242: 54–8. doi:10.1016/j.brainres.2008.06.090. PMID 18634764.
  18. ^ Purves, Dale; Augustine, George; Fitzpatrick, David; Hall, William; LaMantia, Anthony-Samuel; McNamara, James; White, Leonard (2008). Neuroscience (4th ed.). Sinauer Associates, Inc. pp. 209. ISBN 978-0878936977.
  19. ^ Purves, Dale; Augustine, George; Fitzpatrick, David; Hall, William; LaMantia, Anthony-Samuel; McNamara, James; White, Leonard (2008). Neuroscience (4th ed.). Sinauer Associates. pp. 215–216. ISBN 978-0878936977.
  20. ^ a b c d Lee, Y; Lee, C; Oh, U (2005). "Painful channels in sensory neurons". Molecules and Cells. 20 (3): 315–324. doi:10.1016/S1016-8478(23)25242-5. PMID 16404144.
  21. ^ Halligan, Peter W; Zeman, Adam; Berger, Abi (1999-09-04). "Phantoms in the brain". BMJ: British Medical Journal. 319 (7210): 587–588. doi:10.1136/bmj.319.7210.587. ISSN 0959-8138. PMC 1116476. PMID 10473458.
  22. ^ Satir P, Christensen ST (June 2008). "Structure and function of mammalian cilia". Histochem Cell Biol. 129 (6): 687–93. doi:10.1007/s00418-008-0416-9. PMC 2386530. PMID 18365235.
  23. ^ Sherrington C. The Integrative Action of the Nervous System. Oxford: Oxford University Press; 1906.
  24. ^ a b c d e St. John Smith, Ewan (2017-10-14). "Advances in understanding nociception and neuropathic pain". Journal of Neurology. 265 (2): 231–238. doi:10.1007/s00415-017-8641-6. ISSN 0340-5354. PMC 5808094. PMID 29032407.
  25. ^ Zhao, Jianhua; Lin King, John V.; Paulsen, Candice E.; Cheng, Yifan; Julius, David (2020-07-08). "Irritant-evoked activation and calcium modulation of the TRPA1 receptor". Nature. 585 (7823): 141–145. Bibcode:2020Natur.585..141Z. doi:10.1038/s41586-020-2480-9. ISSN 1476-4687. PMC 7483980. PMID 32641835.
  26. ^ Kalat, James W. (2013). Biological Psychology (11th ed.). Wadsworth. ISBN 978-1-111-83100-4.
  27. ^ Michael J. Gregory. "Sensory Systems". Clinton Community College. Archived from the original on 2013-06-25. Retrieved 2013-06-06.
  28. ^ "Cutaneous receptor".
  29. ^ Binder, Marc D.; Hirokawa, Nobutaka; Windhorst, Uwe (2009). Encyclopedia of Neuroscience. Springer. ISBN 978-3-540-29678-2.
  30. ^ a b mentor.lscf.ucsb.edu/course/fall/eemb157/lecture/Lectures%2016,%2017%2018.ppt [dead link‍]
  31. ^ a b "Sensory Receptor Function". frank.mtsu.edu. Archived from the original on August 3, 2008.
  32. ^ Sherwood, Lauralee; Klandorf, Hillar; Yancey, Paul (2012). Animal Physiology: From Genes to Organisms. Cengage Learning. ISBN 978-0-8400-6865-1. Retrieved 13 December 2017.
  33. ^ Wagner EL, Shin JB (June 2019). "Mechanisms of Hair Cell Damage and Repair". Trends Neurosci. 42 (6): 414–424. doi:10.1016/j.tins.2019.03.006. PMC 6556399. PMID 30992136.
  34. ^ Priuska, E.M.; Schacht, J. (1997). "Mechanism and prevention of aminoglycoside ototoxicity: Outer hair cells as targets and tools". Ear, Nose, & Throat Journal. 76 (3): 164–171. doi:10.1177/014556139707600310. PMID 9086645. S2CID 8216716.
  35. ^ Schwartz and Begley 2002, p. 160; "Constraint-Induced Movement Therapy", excerpted from "A Rehab Revolution," Stroke Connection Magazine, September/October 2004. Print.
  36. ^ Blakeslee, Sandra; Ramachandran, V. S. (1998). Phantoms in the brain : probing the mysteries of the human mind. William Morrow & Company. ISBN 978-0-688-15247-5. OCLC 43344396.
[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Sensory_neuron&oldid=1250042476"