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Purinergic Receptors in Ocular Inflammation

dc.contributor.authorGuzmán Aránguez, Ana Isabel
dc.contributor.authorGasull, Xavier
dc.contributor.authorDiebold Luque, Yolanda
dc.contributor.authorPintor, Jesús
dc.date.accessioned2023-06-19T15:09:13Z
dc.date.available2023-06-19T15:09:13Z
dc.date.issued2014-07-14
dc.descriptionCopyright © 2014 Ana Guzman-Aranguez et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.description.abstractInflammation is a complex process that implies the interaction between cells and molecular mediators, which, when not properly “tuned,” can lead to disease. When inflammation affects the eye, it can produce severe disorders affecting the superficial and internal parts of the visual organ. The nucleoside adenosine and nucleotides including adenine mononucleotides like ADP and ATP and dinucleotides such as P1,P4-diadenosine tetraphosphate (Ap4A), and P1,P5-diadenosine pentaphosphate (Ap5A) are present in different ocular locations and therefore they may contribute/modulate inflammatory processes. Adenosine receptors, in particular adenosine receptors, present anti-inflammatory action in acute and chronic retinal inflammation. Regarding the A3 receptor, selective agonists like N6-(3-iodobenzyl)-5′-N-methylcarboxamidoadenosine (CF101) have been used for the treatment of inflammatory ophthalmic diseases such as dry eye and uveoretinitis. Sideways, diverse stimuli (sensory stimulation, large intraocular pressure increases) can produce a release of ATP from ocular sensory innervation or after injury to ocular tissues. Then, ATP will activate purinergic P2 receptors present in sensory nerve endings, the iris, the ciliary body, or other tissues surrounding the anterior chamber of the eye to produce uveitis/endophthalmitis. In summary, adenosine and nucleotides can activate receptors in ocular structures susceptible to suffer from inflammatory processes. This involvement suggests the possible use of purinergic agonists and antagonists as therapeutic targets for ocular inflammation.
dc.description.departmentUnidad Docente de Bioquímica y Biología Molecular
dc.description.facultyFac. de Óptica y Optometría
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.sponsorshipInstituto de Salud Carlos III (España)
dc.description.sponsorshipGeneralitat de Cataluña (España)
dc.description.sponsorshipRETICS (Redes Temáticas de Investigación Cooperativa en Salud)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/42239
dc.identifier.doi10.1155/2014/320906
dc.identifier.issn0962-9351
dc.identifier.officialurlhttp://dx.doi.org/10.1155/2014/320906
dc.identifier.relatedurlhttps://www.hindawi.com/journals/mi/2014/320906/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/35442
dc.issue.number320906
dc.journal.titleMediators of Inflammation
dc.language.isoeng
dc.page.initial11 p.
dc.publisherHindawi publishing Corporation
dc.relation.projectIDSAF 2010/16024
dc.relation.projectIDSAF-2013-44416-R
dc.relation.projectIDRD12/0034/0003
dc.relation.projectIDFIS PI11/01601
dc.relation.projectID2009SGR869
dc.relation.projectIDFEDER-CICYT Grant MAT2010-20452-C03-01
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu617.7-004
dc.subject.cdu577.15
dc.subject.keywordAdenosine
dc.subject.keywordEye metabolism
dc.subject.keywordInflammation
dc.subject.keywordPurinergic receptors
dc.subject.ucmBioquímica (Medicina)
dc.subject.ucmOftalmología
dc.subject.unesco3201.09 Oftalmología
dc.titlePurinergic Receptors in Ocular Inflammation
dc.typejournal article
dc.volume.number2014
dspace.entity.typePublication
relation.isAuthorOfPublicationd1e44010-b3d9-4270-892d-a1f97a4db789
relation.isAuthorOfPublication.latestForDiscoveryd1e44010-b3d9-4270-892d-a1f97a4db789

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