» Articles » PMID: 3556478

Sensitization of Nociceptive Cutaneous Nerve Fibers from the Rat's Tail by Noxious Mechanical Stimulation

Overview
Journal Exp Brain Res
Specialty Neurology
Date 1987 Jan 1
PMID 3556478
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

This single fiber study on rat tail nerve afferents attempts to establish a peripheral neural correlate for the hyperalgesia to mechanical stimulation which follows injury to the skin. Mechano-heat sensitive C fibers (MH-C or "polymodal" nociceptors) and high-threshold mechanoreceptive A delta fibers (HTM-A delta) were examined with a series of constant noxious pressure stimulations (4-6-8-4 N on 25 mm2, 120 s each, 5 min intervals). These injurious stimuli were either directed to the most sensitive spot of the receptive fields (central stimulation) or closely outside their borders (1-5 mm). With this protocol no clear sensitization was seen in MH-C fibers apart from a stronger dynamic response to central stimulation in some of them. In contrast, most HTM-A delta units, irrespective of the site of noxious stimulation, developed spontaneous activity, lowering of their von Frey thresholds and expansion of their receptive fields. All HTM-A delta units responded to outside stimulation: upon the first stimulus (4 N) there was a delayed discharge of continuously increasing frequency ("recruited response"), but the onset of the last stimulation (4 N repeated) evoked vigorous dynamic responses in many fibers. The recruitment of HTM-A delta nociceptor activity may contribute to post-injury hyperalgesia to mechanical stimulation and it may counteract adaptation of the single afferent fiber during prolonged noxious influence.

Citing Articles

Epidural methadone and morphine pharmacokinetics and clinical effects in healthy volunteers: A randomized, crossover-design trial.

Hincker A, Reschke M, Ginosar Y, Kagan L, Kharasch E, Siemiatkowska A Br J Clin Pharmacol. 2024; 90(11):2883-2896.

PMID: 39049497 PMC: 11906210. DOI: 10.1111/bcp.16178.


Exaptation and Evolutionary Adaptation in Nociceptor Mechanisms Driving Persistent Pain.

Walters E Brain Behav Evol. 2023; 98(6):314-330.

PMID: 38035556 PMC: 10922759. DOI: 10.1159/000535552.


Nobel somatosensations and pain.

Reeh P, Fischer M Pflugers Arch. 2022; 474(4):405-420.

PMID: 35157132 PMC: 8924131. DOI: 10.1007/s00424-022-02667-x.


Evaluation of pain scoring and free cortisol levels of postoperative analgesic methods in cardiac surgery: A new perspective.

Ozmen O, Ozcelik F, Kaygin M, Yilmaz H, Karakaya M Turk Gogus Kalp Damar Cerrahisi Derg. 2020; 27(3):294-303.

PMID: 32082876 PMC: 7021431. DOI: 10.5606/tgkdc.dergisi.2019.15143.


Mechanically sensitive Aδ nociceptors that innervate bone marrow respond to changes in intra-osseous pressure.

Nencini S, Ivanusic J J Physiol. 2017; 595(13):4399-4415.

PMID: 28295390 PMC: 5491870. DOI: 10.1113/JP273877.


References
1.
Adriaensen H, Gybels J, Handwerker H, van Hees J . Nociceptor discharges and sensations due to prolonged noxious mechanical stimulation--a paradox. Hum Neurobiol. 1984; 3(1):53-8. View

2.
Woolf C . Evidence for a central component of post-injury pain hypersensitivity. Nature. 1983; 306(5944):686-8. DOI: 10.1038/306686a0. View

3.
Fleischer E, Handwerker H, Joukhadar S . Unmyelinated nociceptive units in two skin areas of the rat. Brain Res. 1983; 267(1):81-92. DOI: 10.1016/0006-8993(83)91041-7. View

4.
Lynn B, Carpenter S . Primary afferent units from the hairy skin of the rat hind limb. Brain Res. 1982; 238(1):29-43. DOI: 10.1016/0006-8993(82)90768-5. View

5.
Kruger L, Perl E, Sedivec M . Fine structure of myelinated mechanical nociceptor endings in cat hairy skin. J Comp Neurol. 1981; 198(1):137-54. DOI: 10.1002/cne.901980112. View