» Articles » PMID: 25894692

Molecular and Cellular Mechanisms That Initiate Pain and Itch

Overview
Publisher Springer
Specialty Biology
Date 2015 Apr 21
PMID 25894692
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

Somatosensory neurons mediate our sense of touch. They are critically involved in transducing pain and itch sensations under physiological and pathological conditions, along with other skin-resident cells. Tissue damage and inflammation can produce a localized or systemic sensitization of our senses of pain and itch, which can facilitate our detection of threats in the environment. Although acute pain and itch protect us from further damage, persistent pain and itch are debilitating. Recent exciting discoveries have significantly advanced our knowledge of the roles of membrane-bound G protein-coupled receptors and ion channels in the encoding of information leading to pain and itch sensations. This review focuses on molecular and cellular events that are important in early stages of the biological processing that culminates in our senses of pain and itch.

Citing Articles

The μ-opioid receptor differentiates two distinct human nociceptive populations relevant to clinical pain.

Staedtler E, Sapio M, King D, Maric D, Ghetti A, Mannes A Cell Rep Med. 2024; 5(10):101788.

PMID: 39413733 PMC: 11513826. DOI: 10.1016/j.xcrm.2024.101788.


Functional Role of Piezo1 in the Human Eosinophil Cell Line AML14.3D10: Implications for the Immune and Sensory Nervous Systems.

Hwang S, Song J, Choi J, Jung Y, Park C, Kim Y Biomolecules. 2024; 14(9).

PMID: 39334923 PMC: 11429562. DOI: 10.3390/biom14091157.


Relation Between Reactive Oxygen Species Production and Transient Receptor Potential Vanilloid1 Expression in Human Skin During Aging.

Favero G, Giano M, Franco C, Pinto D, van Noorden C, Rinaldi F J Histochem Cytochem. 2024; 72(3):157-171.

PMID: 38440794 PMC: 10956443. DOI: 10.1369/00221554241236537.


Site-Specific Transient Receptor Potential Channel Mechanisms and Their Characteristics for Targeted Chronic Itch Treatment.

Go E, Lee J, Kim Y, Park C Biomolecules. 2024; 14(1).

PMID: 38254707 PMC: 10813675. DOI: 10.3390/biom14010107.


The Role and Mechanism of Spinal NF-κB-CXCL1/CXCR2 in Rats with Nucleus Pulposus-induced Radicular Pain.

Gao F, Wei M, Wang M, Yang Y, Duan X, Yang L Spine (Phila Pa 1976). 2023; 49(7):E87-E99.

PMID: 38098294 PMC: 10927303. DOI: 10.1097/BRS.0000000000004899.


References
1.
Perkins N, Tracey D . Hyperalgesia due to nerve injury: role of neutrophils. Neuroscience. 2000; 101(3):745-57. DOI: 10.1016/s0306-4522(00)00396-1. View

2.
Qu L, Li Y, Pan X, Zhang P, LaMotte R, Ma C . Transient receptor potential canonical 3 (TRPC3) is required for IgG immune complex-induced excitation of the rat dorsal root ganglion neurons. J Neurosci. 2012; 32(28):9554-62. PMC: 3437229. DOI: 10.1523/JNEUROSCI.6355-11.2012. View

3.
Zhang X, Mosser D . Macrophage activation by endogenous danger signals. J Pathol. 2007; 214(2):161-78. PMC: 2724989. DOI: 10.1002/path.2284. View

4.
Mishra S, Hoon M . The cells and circuitry for itch responses in mice. Science. 2013; 340(6135):968-71. PMC: 3670709. DOI: 10.1126/science.1233765. View

5.
Dillon S, Sprecher C, Hammond A, Bilsborough J, Rosenfeld-Franklin M, Presnell S . Interleukin 31, a cytokine produced by activated T cells, induces dermatitis in mice. Nat Immunol. 2004; 5(7):752-60. DOI: 10.1038/ni1084. View