Literature DB >> 23711480

The fundamental unit of pain is the cell.

David B Reichling1, Paul G Green, Jon D Levine.   

Abstract

The molecular/genetic era has seen the discovery of a staggering number of molecules implicated in pain mechanisms [18,35,61,69,96,133,150,202,224]. This has stimulated pharmaceutical and biotechnology companies to invest billions of dollars to develop drugs that enhance or inhibit the function of many these molecules. Unfortunately this effort has provided a remarkably small return on this investment. Inevitably, transformative progress in this field will require a better understanding of the functional links among the ever-growing ranks of "pain molecules," as well as their links with an even larger number of molecules with which they interact. Importantly, all of these molecules exist side-by-side, within a functional unit, the cell, and its adjacent matrix of extracellular molecules. To paraphrase a recent editorial in Science magazine [223], although we live in the Golden age of Genetics, the fundamental unit of biology is still arguably the cell, and the cell is the critical structural and functional setting in which the function of pain-related molecules must be understood. This review summarizes our current understanding of the nociceptor as a cell-biological unit that responds to a variety of extracellular inputs with a complex and highly organized interaction of signaling molecules. We also discuss the insights that this approach is providing into peripheral mechanisms of chronic pain and sex dependence in pain.
Copyright © 2013 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cell biology; Chronic pain; Extracellular matrix; Mitochondrion; Neuroplasticity

Mesh:

Year:  2013        PMID: 23711480     DOI: 10.1016/j.pain.2013.05.037

Source DB:  PubMed          Journal:  Pain        ISSN: 0304-3959            Impact factor:   6.961


  39 in total

1.  Spinal dopaminergic projections control the transition to pathological pain plasticity via a D1/D5-mediated mechanism.

Authors:  Ji-Young V Kim; Dipti V Tillu; Tammie L Quinn; Galo L Mejia; Adia Shy; Marina N K Asiedu; Elaine Murad; Alan P Schumann; Stacie K Totsch; Robert E Sorge; Patrick W Mantyh; Gregory Dussor; Theodore J Price
Journal:  J Neurosci       Date:  2015-04-22       Impact factor: 6.167

Review 2.  The pharmacology of nociceptor priming.

Authors:  Ram Kandasamy; Theodore J Price
Journal:  Handb Exp Pharmacol       Date:  2015

3.  Screening the role of pronociceptive molecules in a rodent model of endometriosis pain.

Authors:  Pedro Alvarez; Jon D Levine
Journal:  J Pain       Date:  2014-04-20       Impact factor: 5.820

Review 4.  Commonalities between pain and memory mechanisms and their meaning for understanding chronic pain.

Authors:  Theodore J Price; Kufreobong E Inyang
Journal:  Prog Mol Biol Transl Sci       Date:  2015-01-30       Impact factor: 3.622

5.  Anatomical and physiological factors contributing to chronic muscle pain.

Authors:  Nicholas S Gregory; Kathleen A Sluka
Journal:  Curr Top Behav Neurosci       Date:  2014

6.  Pain in cancer survivors.

Authors:  Matthew Rd Brown; Juan D Ramirez; Paul Farquhar-Smith
Journal:  Br J Pain       Date:  2014-11

7.  [1 + 1 = 0. Reprogramming of nociceptors].

Authors:  T Hucho
Journal:  Schmerz       Date:  2014-12       Impact factor: 1.107

Review 8.  Stress-induced pain: a target for the development of novel therapeutics.

Authors:  Anthony C Johnson; Beverley Greenwood-Van Meerveld
Journal:  J Pharmacol Exp Ther       Date:  2014-09-05       Impact factor: 4.030

9.  Pain in human and non-human animals caused by electricity.

Authors:  Terry L Whiting
Journal:  Can Vet J       Date:  2016-08       Impact factor: 1.008

10.  Opioid-Induced Hyperalgesic Priming in Single Nociceptors.

Authors:  Eugen V Khomula; Dionéia Araldi; Ivan J M Bonet; Jon D Levine
Journal:  J Neurosci       Date:  2020-11-17       Impact factor: 6.167

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