Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease

Dry eye disease (DED) is a multifactorial disorder in which the eyes respond to minor stimuli with abnormal sensations, such as dryness, blurring, foreign body sensation, discomfort, irritation, and pain. Corneal pain, as one of DED’s main symptoms, has gained recognition due to its increasing preva...

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Main Authors: Darine Fakih, Tiffany Migeon, Nathan Moreau, Christophe Baudouin, Annabelle Réaux-Le Goazigo, Stéphane Mélik Parsadaniantz
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/9/1859
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author Darine Fakih
Tiffany Migeon
Nathan Moreau
Christophe Baudouin
Annabelle Réaux-Le Goazigo
Stéphane Mélik Parsadaniantz
author_facet Darine Fakih
Tiffany Migeon
Nathan Moreau
Christophe Baudouin
Annabelle Réaux-Le Goazigo
Stéphane Mélik Parsadaniantz
author_sort Darine Fakih
collection DOAJ
description Dry eye disease (DED) is a multifactorial disorder in which the eyes respond to minor stimuli with abnormal sensations, such as dryness, blurring, foreign body sensation, discomfort, irritation, and pain. Corneal pain, as one of DED’s main symptoms, has gained recognition due to its increasing prevalence, morbidity, and the resulting social burden. The cornea is the most innervated tissue in the body, and the maintenance of corneal integrity relies on a rich density of nociceptors, such as polymodal nociceptor neurons, cold thermoreceptor neurons, and mechano-nociceptor neurons. Their sensory responses to different stimulating forces are linked to the specific expression of transient receptor potential (TRP) channels. TRP channels are a group of unique ion channels that play important roles as cellular sensors for various stimuli. These channels are nonselective cation channels with variable Ca<sup>2+</sup> selectivity. TRP homologs are a superfamily of 28 different members that are subdivided into 7 different subfamilies based on differences in sequence homology. Many of these subtypes are expressed in the eye on both neuronal and non-neuronal cells, where they affect various stress-induced regulatory responses essential for normal vision maintenance. This article reviews the current knowledge about the expression, function, and regulation of TRPs in ocular surface tissues. We also describe their implication in DED and ocular pain. These findings contribute to evidence suggesting that drug-targeting TRP channels may be of therapeutic benefit in the clinical setting of ocular pain.
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spelling doaj.art-3d528ed4aea14f6fbb703778e1335f7f2023-11-23T18:21:54ZengMDPI AGPharmaceutics1999-49232022-09-01149185910.3390/pharmaceutics14091859Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye DiseaseDarine Fakih0Tiffany Migeon1Nathan Moreau2Christophe Baudouin3Annabelle Réaux-Le Goazigo4Stéphane Mélik Parsadaniantz5Laboratoires Théa, 12 Rue Louis Blériot, CEDEX 2, 63017 Clermont-Ferrand, FranceCNRS, INSERM, Institut de la Vision, Sorbonne Université, 17 Rue Moreau, 75012 Paris, FranceCNRS, INSERM, Institut de la Vision, Sorbonne Université, 17 Rue Moreau, 75012 Paris, FranceCNRS, INSERM, Institut de la Vision, Sorbonne Université, 17 Rue Moreau, 75012 Paris, FranceCNRS, INSERM, Institut de la Vision, Sorbonne Université, 17 Rue Moreau, 75012 Paris, FranceCNRS, INSERM, Institut de la Vision, Sorbonne Université, 17 Rue Moreau, 75012 Paris, FranceDry eye disease (DED) is a multifactorial disorder in which the eyes respond to minor stimuli with abnormal sensations, such as dryness, blurring, foreign body sensation, discomfort, irritation, and pain. Corneal pain, as one of DED’s main symptoms, has gained recognition due to its increasing prevalence, morbidity, and the resulting social burden. The cornea is the most innervated tissue in the body, and the maintenance of corneal integrity relies on a rich density of nociceptors, such as polymodal nociceptor neurons, cold thermoreceptor neurons, and mechano-nociceptor neurons. Their sensory responses to different stimulating forces are linked to the specific expression of transient receptor potential (TRP) channels. TRP channels are a group of unique ion channels that play important roles as cellular sensors for various stimuli. These channels are nonselective cation channels with variable Ca<sup>2+</sup> selectivity. TRP homologs are a superfamily of 28 different members that are subdivided into 7 different subfamilies based on differences in sequence homology. Many of these subtypes are expressed in the eye on both neuronal and non-neuronal cells, where they affect various stress-induced regulatory responses essential for normal vision maintenance. This article reviews the current knowledge about the expression, function, and regulation of TRPs in ocular surface tissues. We also describe their implication in DED and ocular pain. These findings contribute to evidence suggesting that drug-targeting TRP channels may be of therapeutic benefit in the clinical setting of ocular pain.https://www.mdpi.com/1999-4923/14/9/1859ocular paindry eyeTRPV1TRPM8topical treatment
spellingShingle Darine Fakih
Tiffany Migeon
Nathan Moreau
Christophe Baudouin
Annabelle Réaux-Le Goazigo
Stéphane Mélik Parsadaniantz
Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease
Pharmaceutics
ocular pain
dry eye
TRPV1
TRPM8
topical treatment
title Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease
title_full Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease
title_fullStr Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease
title_full_unstemmed Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease
title_short Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease
title_sort transient receptor potential channels important players in ocular pain and dry eye disease
topic ocular pain
dry eye
TRPV1
TRPM8
topical treatment
url https://www.mdpi.com/1999-4923/14/9/1859
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