Mechanoreceptor

(Redirected from Rapidly adapting)

A mechanoreceptor, also called mechanoceptor, is a sensory receptor that responds to mechanical pressure or distortion. Mechanoreceptors are located on sensory neurons that convert mechanical pressure into electrical signals that, in animals, are sent to the central nervous system.

Vertebrate mechanoreceptors

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Cutaneous mechanoreceptors

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Cutaneous mechanoreceptors respond to mechanical stimuli that result from physical interaction, including pressure and vibration. They are located in the skin, like other cutaneous receptors. They are all innervated by Aβ fibers, except the mechanorecepting free nerve endings, which are innervated by Aδ fibers. Cutaneous mechanoreceptors can be categorized by what kind of sensation they perceive, by the rate of adaptation, and by morphology. Furthermore, each has a different receptive field.

 
Tactile receptors.

By sensation

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  • The Slowly Adapting type 1 (SA1) mechanoreceptor, with the Merkel corpuscle end-organ (also known as Merkel discs) detect sustained pressure and underlies the perception of form and roughness on the skin.[1] They have small receptive fields and produce sustained responses to static stimulation.
  • The Slowly Adapting type 2 (SA2) mechanoreceptors, with the Ruffini corpuscle end-organ (also known as the bulbous corpuscles), detect tension deep in the skin and fascia and respond to skin stretch, but have not been closely linked to either proprioceptive or mechanoreceptive roles in perception.[2] They also produce sustained responses to static stimulation, but have large receptive fields.
  • The Rapidly Adapting (RA) or Meissner corpuscle end-organ mechanoreceptor (also known as the tactile corpuscles) underlies the perception of light touch such as flutter[3] and slip on the skin.[4] It adapts rapidly to changes in texture (vibrations around 50 Hz). They have small receptive fields and produce transient responses to the onset and offset of stimulation.
  • The Pacinian corpuscle or Vater-Pacinian corpuscles or Lamellar corpuscles[5] in the skin and fascia detect rapid vibrations of about 200–300 Hz.[3][6] They also produce transient responses, but have large receptive fields.
  • Free nerve endings detect touch, pressure, stretching, as well as the tickle and itch sensations. Itch sensations are caused by stimulation of free nerve ending from chemicals.[7]
  • Hair follicle receptors called hair root plexuses sense when a hair changes position. Indeed, the most sensitive mechanoreceptors in humans are the hair cells in the cochlea of the inner ear (no relation to the follicular receptors – they are named for the hair-like mechanosensory stereocilia they possess); these receptors transduce sound for the brain.[7]

By rate of adaptation

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Cutaneous mechanoreceptors can also be separated into categories based on their rates of adaptation. When a mechanoreceptor receives a stimulus, it begins to fire impulses or action potentials at an elevated frequency (the stronger the stimulus, the higher the frequency). The cell, however, will soon "adapt" to a constant or static stimulus, and the pulses will subside to a normal rate. Receptors that adapt quickly (i.e., quickly return to a normal pulse rate) are referred to as "phasic". Those receptors that are slow to return to their normal firing rate are called tonic. Phasic mechanoreceptors are useful in sensing such things as texture or vibrations, whereas tonic receptors are useful for temperature and proprioception among others.

By receptive field

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Cutaneous mechanoreceptors with small, accurate receptive fields are found in areas needing accurate taction (e.g. the fingertips). In the fingertips and lips, innervation density of slowly adapting type I and rapidly adapting type I mechanoreceptors are greatly increased. These two types of mechanoreceptors have small discrete receptive fields and are thought to underlie most low-threshold use of the fingers in assessing texture, surface slip, and flutter. Mechanoreceptors found in areas of the body with less tactile acuity tend to have larger receptive fields.

Lamellar corpuscles

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Lamellar corpuscles, or Pacinian corpuscles or Vater-Pacini corpuscle, are deformation or pressure receptors located in the skin and also in various internal organs.[8] Each is connected to a sensory neuron. Because of its relatively large size, a single lamellar corpuscle can be isolated and its properties studied. Mechanical pressure of varying strength and frequency can be applied to the corpuscle by stylus, and the resulting electrical activity detected by electrodes attached to the preparation.

Deforming the corpuscle creates a generator potential in the sensory neuron arising within it. This is a graded response: the greater the deformation, the greater the generator potential. If the generator potential reaches threshold, a volley of action potentials (nerve impulses) are triggered at the first node of Ranvier of the sensory neuron.

Once threshold is reached, the magnitude of the stimulus is encoded in the frequency of impulses generated in the neuron. So the more massive or rapid the deformation of a single corpuscle, the higher the frequency of nerve impulses generated in its neuron.

The optimal sensitivity of a lamellar corpuscle is 250 Hz, the frequency range generated upon finger tips by textures made of features smaller than 200 micrometres.[9]

Ligamentous mechanoreceptors

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There are four types of mechanoreceptors embedded in ligaments. As all these types of mechanoreceptors are myelinated, they can rapidly transmit sensory information regarding joint positions to the central nervous system.[10]

  • Type I: (small) Low threshold, slow adapting in both static and dynamic settings
  • Type II: (medium) Low threshold, rapidly adapting in dynamic settings
  • Type III: (large) High threshold, slowly adapting in dynamic settings
  • Type IV: (very small) High threshold pain receptors that communicate injury

Type II and Type III mechanoreceptors in particular are believed to be linked to one's sense of proprioception.

Other mechanoreceptors

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Other mechanoreceptors than cutaneous ones include the hair cells, which are sensory receptors in the vestibular system of the inner ear, where they contribute to the auditory system and equilibrioception. Baroreceptors are a type of mechanoreceptor sensory neuron that is excited by stretch of the blood vessel. There are also juxtacapillary (J) receptors, which respond to events such as pulmonary edema, pulmonary emboli, pneumonia, and barotrauma.

Muscle spindles and the stretch reflex

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The knee jerk is the popularly known stretch reflex (involuntary kick of the lower leg) induced by tapping the knee with a rubber-headed hammer. The hammer strikes a tendon that inserts an extensor muscle in the front of the thigh into the lower leg. Tapping the tendon stretches the thigh muscle, which activates stretch receptors within the muscle called muscle spindles. Each muscle spindle consists of sensory nerve endings wrapped around special muscle fibers called intrafusal muscle fibers. Stretching an intrafusal fiber initiates a volley of impulses in the sensory neuron (a I-a neuron) attached to it. The impulses travel along the sensory axon to the spinal cord where they form several kinds of synapses:

  1. Some of the branches of the I-a axons synapse directly with alpha motor neurons. These carry impulses back to the same muscle causing it to contract. The leg straightens.
  2. Some of the branches of the I-a axons synapse with inhibitory interneurons in the spinal cord. These, in turn, synapse with motor neurons leading back to the antagonistic muscle, a flexor in the back of the thigh. By inhibiting the flexor, these interneurons aid contraction of the extensor.
  3. Still other branches of the I-a axons synapse with interneurons leading to brain centers, e.g., the cerebellum, that coordinate body movements.[11]

Mechanism of sensation

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In somatosensory transduction, the afferent neurons transmit messages through synapses in the dorsal column nuclei, where second-order neurons send the signal to the thalamus and synapse with third-order neurons in the ventrobasal complex. The third-order neurons then send the signal to the somatosensory cortex.

More recent work has expanded the role of the cutaneous mechanoreceptors for feedback in fine motor control.[12] Single action potentials from Meissner's corpuscle, Pacinian corpuscle and Ruffini ending afferents are directly linked to muscle activation, whereas Merkel cell-neurite complex activation does not trigger muscle activity.[13]

Invertebrate mechanoreceptors

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Insect and arthropod mechanoreceptors include:[14]

  • Campaniform sensilla: Small domes in the exoskeleton that are distributed all along the insect's body. These cells are thought to detect mechanical load as resistance to muscle contraction, similar to the mammalian Golgi tendon organs.
  • Hair plates: Sensory neurons that innervate hairs that are found in the folds of insect joints. These hairs are deflected when one body segment moves relative to an adjoining segment, they have proprioceptive function, and are thought to act as limit detectors encoding the extreme ranges of motion for each joint.[15]
  • Chordotonal organs: Internal stretch receptors at the joints, can have both extero- and proprioceptive functions. The neurons in the chordotonal organ in Drosophila melanogaster can be organized into club, claw, and hook neurons. Club neurons are thought to encode vibrational signals while claw and hook neurons can be subdivided into extension and flexion populations that encode joint angle and movement respectively.[16]
  • Slit sensilla: Slits in the exoskeleton that detect physical deformation of the animal's exoskeleton, have proprioceptive function.
  • Bristle sensilla: Bristle neurons are mechanoreceptors that innervate hairs all along the body. Each neuron extends a dendritic process to innervate a single hair and projects its axon to the ventral nerve cord. These neurons are thought to mediate touch sensation by responding to physical deflections of the hair.[17] In line with the fact that many insects exhibit different sized hairs, commonly referred to as macrochaetes (thicker longer hairs) and microchaetes (thinner shorter hairs), previous studies suggest that bristle neurons to these different hairs may have different firing properties such as resting membrane potential and firing threshold.[18][19]

Plant mechanoreceptors

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Mechanoreceptors are also present in plant cells where they play an important role in normal growth, development and the sensing of their environment.[20] Mechanoreceptors aid the Venus flytrap (Dionaea muscipula Ellis) in capturing large[21] prey.[22]

Molecular biology

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Mechanoreceptor proteins are ion channels whose ion flow is induced by touch. Early research showed that touch transduction in the nematode Caenorhabditis elegans was found to require a two transmembrane, amiloride-sensitive ion channel protein related to epithelial sodium channels (ENaCs).[23] This protein, called MEC-4, forms a heteromeric Na+-selective channel together with MEC-10. Related genes in mammals are expressed in sensory neurons and were shown to be gated by low pH. The first of such receptor was ASIC1a, named so because it is an acid sensing ion channel (ASIC).[24]

See also

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References

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  1. ^ Johnson KO, Hsiao SS (1992). "Neural mechanisms of tactual form and texture perception". Annual Review of Neuroscience. 15: 227–50. doi:10.1146/annurev.ne.15.030192.001303. PMID 1575442.
  2. ^ Torebjörk HE, Ochoa JL (December 1980). "Specific sensations evoked by activity in single identified sensory units in man". Acta Physiologica Scandinavica. 110 (4): 445–7. doi:10.1111/j.1748-1716.1980.tb06695.x. PMID 7234450.
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  6. ^ Biswas A, Manivannan M, Srinivasan MA (2015). "Vibrotactile sensitivity threshold: nonlinear stochastic mechanotransduction model of the Pacinian Corpuscle". IEEE Transactions on Haptics. 8 (1): 102–13. doi:10.1109/TOH.2014.2369422. PMID 25398183. S2CID 15326972.
  7. ^ a b Tortora GJ (2019). Principles of anatomy and physiology. John Wiley & Sons Australia, Limited. ISBN 978-0-7303-5500-7. OCLC 1059417106.
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  9. ^ Scheibert J, Leurent S, Prevost A, Debrégeas G (March 2009). "The role of fingerprints in the coding of tactile information probed with a biomimetic sensor". Science. 323 (5920): 1503–6. arXiv:0911.4885. Bibcode:2009Sci...323.1503S. doi:10.1126/science.1166467. PMID 19179493. S2CID 14459552.
  10. ^ Michelson JD, Hutchins C (March 1995). "Mechanoreceptors in human ankle ligaments". The Journal of Bone and Joint Surgery. British Volume. 77 (2): 219–24. doi:10.1302/0301-620X.77B2.7706334. PMID 7706334.
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  13. ^ McNulty PA, Macefield VG (December 2001). "Modulation of ongoing EMG by different classes of low-threshold mechanoreceptors in the human hand". The Journal of Physiology. 537 (Pt 3): 1021–32. doi:10.1111/j.1469-7793.2001.01021.x. PMC 2278990. PMID 11744774.
  14. ^ Tuthill JC, Wilson RI (October 2016). "Mechanosensation and Adaptive Motor Control in Insects". Current Biology. 26 (20): R1022–R1038. Bibcode:2016CBio...26R1022T. doi:10.1016/j.cub.2016.06.070. PMC 5120761. PMID 27780045.
  15. ^ Bässler, U. (1977-06-01). "Sensory control of leg movement in the stick insect Carausius morosus". Biological Cybernetics. 25 (2): 61–72. doi:10.1007/BF00337264. ISSN 1432-0770. PMID 836915. S2CID 2634261.
  16. ^ Mamiya, Akira; Gurung, Pralaksha; Tuthill, John C. (2018-11-07). "Neural Coding of Leg Proprioception in Drosophila". Neuron. 100 (3): 636–650.e6. doi:10.1016/j.neuron.2018.09.009. ISSN 0896-6273. PMC 6481666. PMID 30293823. S2CID 52927792.
  17. ^ Tuthill, John C.; Wilson, Rachel I. (2016-02-25). "Parallel Transformation of Tactile Signals in Central Circuits of Drosophila". Cell. 164 (5): 1046–1059. doi:10.1016/j.cell.2016.01.014. ISSN 0092-8674. PMC 4879191. PMID 26919434.
  18. ^ Corfas, G; Dudai, Y (1990-02-01). "Adaptation and fatigue of a mechanosensory neuron in wild-type Drosophila and in memory mutants". The Journal of Neuroscience. 10 (2): 491–499. doi:10.1523/JNEUROSCI.10-02-00491.1990. ISSN 0270-6474. PMC 6570162. PMID 2154560.
  19. ^ Li, Jiefu; Zhang, Wei; Guo, Zhenhao; Wu, Sophia; Jan, Lily Yeh; Jan, Yuh-Nung (2016-11-02). "A Defensive Kicking Behavior in Response to Mechanical Stimuli Mediated by Drosophila Wing Margin Bristles". Journal of Neuroscience. 36 (44): 11275–11282. doi:10.1523/JNEUROSCI.1416-16.2016. ISSN 0270-6474. PMC 5148243. PMID 27807168. S2CID 2187830.
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  21. ^ Chamovitz D (2012). What a plant knows : a field guide to the senses (1st ed.). New York: Scientific American/Farrar, Straus and Giroux. ISBN 9780374533885. OCLC 755641050.
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