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Group A nerve fiber

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(Redirected fromAδ fiber)
One of three classes of nerve fiber

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Group A nerve fibers are one of the three classes ofnerve fiber asgenerally classified byErlanger andGasser. The other two classes are thegroup B nerve fibers, and thegroup C nerve fibers. Group A are heavilymyelinated, group B are moderatelymyelinated, and group C are unmyelinated.[1][2]

The other classification is asensory grouping that uses the termstype Ia and type Ib,type II,type III, andtype IV, sensory fibers.[1]

Types

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There are four subdivisions of group A nerve fibers: alpha (α) Aα; beta (β) Aβ; , gamma (γ) Aγ, and delta (δ) Aδ. These subdivisions have different amounts of myelination and axon thickness andtherefore transmit signals atdifferent speeds. Larger diameter axons and more myelin insulation lead to faster signal propagation.

Group A nerves are found in both motor and sensory pathways.[2]

Motor fiber types
TypeErlanger-Gasser
Classification
DiameterMyelinConduction velocityAssociatedmuscle fibers
α13–20μmYes80–120 m/sExtrafusal muscle fibers
γ5–8μmYes4–24 m/s[3][4]Intrafusal muscle fibers

Differentsensory receptors are innervated by different types of nerve fibers.Proprioceptors are innervated by type Ia, Ib and II sensory fibers,mechanoreceptors by type II and III sensory fibers, andnociceptors andthermoreceptors by type III and IV sensory fibers.

Sensory fiber types
TypeErlanger-Gasser
Classification
DiameterMyelinConduction velocityAssociatedsensory receptors
Ia13–20μmYes80–120 m/s[5]Muscle spindle fibres
Ib13–20μmYes80–120 m/sGolgi tendon organ
II6–12μmYes33–75 m/sAllcutaneous mechanoreceptors includingpacinian corpuscles
III1–5μmThin3–30 m/sFree nerve endings of touch and pressure
Nociceptors ofneospinothalamic tract
Coldthermoreceptors
IVC0.2–1.5μmNo0.5–2.0 m/sNociceptors ofpaleospinothalamic tract
Warmth receptors

Type Aα fibers include thetype Ia andtype Ib sensory fibers of the alternative classification system, and are the fibers frommuscle spindle endings and theGolgi tendon, respectively.[1]

Type Aβ fibres, and type Aγ, are thetype IIafferent fibers fromstretch receptors.[1] Type Aβ fibres from the skin are mostly dedicated to touch. However a small fraction of these fast fibres, termed "ultrafast nociceptors", also transmit pain.[6]

Type Aδ fibers are theafferent fibers ofnociceptors. Aδ fibers carry information from peripheral mechanoreceptors and thermoreceptors to the dorsal horn of the spinal cord. This pathway describes the first-order neuron. Aδ fibers serve to receive and transmit information primarily relating toacute pain (sharp, immediate, and relatively short-lasting). This type of pain can result from several classifications of stimulants: temperature-induced, mechanical, and chemical. This can be part of awithdrawal reflex—initiated by the Aδ fibers in thereflex arc of activating withdrawal responses.[7][8] These are thetype III group. Aδ fibers carry cold, pressure, and acute pain signals; because they are thin (2–5 μm in diameter) andmyelinated, they send impulses faster than unmyelinatedC fibers, but more slowly than other, more thickly myelinated group A nerve fibers. Theirconduction velocities are moderate.[9]

Theircell bodies are located in thedorsal root ganglia and axons are sent to the periphery to innervate target organs and are also sent through the dorsal roots to the spinal cord. Within the spinal cord the axons reach theposterior grey column and terminate in Rexed laminae I to V.[10]

References

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  1. ^abcdHall, John (2011).Guyton and Hall textbook of medical physiology (12th ed.). Philadelphia, Pa.: Saunders/Elsevier. pp. 563–564.ISBN 978-1-4160-4574-8.
  2. ^ab"Classification of Nerve Fibers".pharmacy180.com. RetrievedSeptember 6, 2023.
  3. ^Andrew, BL; Part, NJ (1972)."Properties of fast and slow motor units in hind limb and tail muscles of the rat".Quarterly Journal of Experimental Physiology and Cognate Medical Sciences.57 (2):213–225.doi:10.1113/expphysiol.1972.sp002151.PMID 4482075.
  4. ^Russell NJ (1980)."Axonal conduction velocity changes following muscle tenotomy or deafferentation during development in the rat".J Physiol.298:347–360.doi:10.1113/jphysiol.1980.sp013085.PMC 1279120.PMID 7359413.
  5. ^Siegel, Allan; Sapru, Hreday (2005).Essential Neuroscience. Lippincott Williams & Wilkins. p. 257.ISBN 978-0781750776.
  6. ^Nagi, Saad S.; Marshall, Andrew G.; Makdani, Adarsh; Jarocka, Ewa; Liljencrantz, Jaquette; Ridderström, Mikael; Shaikh, Sumaiya; O’Neill, Francis; Saade, Dimah; Donkervoort, Sandra; Foley, A. Reghan; Minde, Jan; Trulsson, Mats; Cole, Jonathan; Bönnemann, Carsten G.; Chesler, Alexander T.; Bushnell, M. Catherine; McGlone, Francis; Olausson, Håkan (2019)."An ultrafast system for signaling mechanical pain in human skin".Science Advances.5 (7): eaaw1297.Bibcode:2019SciA....5.1297N.doi:10.1126/sciadv.aaw1297.ISSN 2375-2548.PMC 6609212.PMID 31281886.
  7. ^Skljarevski, V.; Ramadan, N. M. (2002). "The nociceptive flexion reflex in humans – review article".Pain.96 (1):3–8.doi:10.1016/s0304-3959(02)00018-0.PMID 11932055.S2CID 23881420.
  8. ^Striedter, Georg F. (2016).Neurobiology : a functional approach (Instructor's ed.). New York.ISBN 9780195396157.OCLC 919041751.{{cite book}}: CS1 maint: location missing publisher (link)
  9. ^Neuroscience. Purves, Dale. (5th ed.). Sunderland, Mass.: Sinauer Associates. 2012.ISBN 9780878936953.OCLC 754389847.{{cite book}}: CS1 maint: others (link)
  10. ^Basbaum, Allan I.; Bautista, Diana M.; Scherrer, Grégory; Julius, David (October 2009)."Cellular and Molecular Mechanisms of Pain".Cell.139 (2):267–284.doi:10.1016/j.cell.2009.09.028.PMC 2852643.PMID 19837031.
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