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Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function

BACKGROUND: Retinal ganglion cells (RGCs) are the nervous retinal elements which connect the visual receptors to the brain forming the nervous visual system. Functional and/or morphological involvement of RGCs occurs in several ocular and neurological disorders and therefore these cells are targeted...

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Autores principales: Parisi, Vincenzo, Oddone, Francesco, Ziccardi, Lucia, Roberti, Gloria, Coppola, Gianluca, Manni, Gianluca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120106/
https://www.ncbi.nlm.nih.gov/pubmed/28676014
http://dx.doi.org/10.2174/1570159X15666170703111729
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author Parisi, Vincenzo
Oddone, Francesco
Ziccardi, Lucia
Roberti, Gloria
Coppola, Gianluca
Manni, Gianluca
author_facet Parisi, Vincenzo
Oddone, Francesco
Ziccardi, Lucia
Roberti, Gloria
Coppola, Gianluca
Manni, Gianluca
author_sort Parisi, Vincenzo
collection PubMed
description BACKGROUND: Retinal ganglion cells (RGCs) are the nervous retinal elements which connect the visual receptors to the brain forming the nervous visual system. Functional and/or morphological involvement of RGCs occurs in several ocular and neurological disorders and therefore these cells are targeted in neuroprotective strategies. Cytidine 5-diphosphocholine or Citicoline is an endogenous compound that acts in the biosynthesis of phospholipids of cell membranes and increases neurotransmitters’ levels in the Central Nervous System. Experimental studies suggested the neuromodulator effect and the protective role of Citicoline on RGCs. This review aims to present evidence of the effects of Citicoline in experimental models of RGCs degeneration and in human neurodegenerative disorders involving RGCs. METHODS: All published papers containing experimental or clinical studies about the effects of Citicoline on RGCs morphology and function were reviewed. RESULTS: In rodent retinal cultures and animal models, Citicoline induces antiapoptotic effects, increases the dopamine retinal level, and counteracts retinal nerve fibers layer thinning. Human studies in neurodegenerative visual pathologies such as glaucoma or non-arteritic ischemic neuropathy showed a reduction of the RGCs impairment after Citicoline administration. By reducing the RGCs’ dysfunction, a better neural conduction along the post-retinal visual pathways with an improvement of the visual field defects was observed. CONCLUSION: Citicoline, with a solid history of experimental and clinical studies, could be considered a very promising molecule for neuroprotective strategies in those pathologies (i.e. Glaucoma) in which morpho-functional changes of RGCc occurs.
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spelling pubmed-61201062019-02-01 Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function Parisi, Vincenzo Oddone, Francesco Ziccardi, Lucia Roberti, Gloria Coppola, Gianluca Manni, Gianluca Curr Neuropharmacol Article BACKGROUND: Retinal ganglion cells (RGCs) are the nervous retinal elements which connect the visual receptors to the brain forming the nervous visual system. Functional and/or morphological involvement of RGCs occurs in several ocular and neurological disorders and therefore these cells are targeted in neuroprotective strategies. Cytidine 5-diphosphocholine or Citicoline is an endogenous compound that acts in the biosynthesis of phospholipids of cell membranes and increases neurotransmitters’ levels in the Central Nervous System. Experimental studies suggested the neuromodulator effect and the protective role of Citicoline on RGCs. This review aims to present evidence of the effects of Citicoline in experimental models of RGCs degeneration and in human neurodegenerative disorders involving RGCs. METHODS: All published papers containing experimental or clinical studies about the effects of Citicoline on RGCs morphology and function were reviewed. RESULTS: In rodent retinal cultures and animal models, Citicoline induces antiapoptotic effects, increases the dopamine retinal level, and counteracts retinal nerve fibers layer thinning. Human studies in neurodegenerative visual pathologies such as glaucoma or non-arteritic ischemic neuropathy showed a reduction of the RGCs impairment after Citicoline administration. By reducing the RGCs’ dysfunction, a better neural conduction along the post-retinal visual pathways with an improvement of the visual field defects was observed. CONCLUSION: Citicoline, with a solid history of experimental and clinical studies, could be considered a very promising molecule for neuroprotective strategies in those pathologies (i.e. Glaucoma) in which morpho-functional changes of RGCc occurs. Bentham Science Publishers 2018-08 2018-08 /pmc/articles/PMC6120106/ /pubmed/28676014 http://dx.doi.org/10.2174/1570159X15666170703111729 Text en © 2018 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Parisi, Vincenzo
Oddone, Francesco
Ziccardi, Lucia
Roberti, Gloria
Coppola, Gianluca
Manni, Gianluca
Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function
title Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function
title_full Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function
title_fullStr Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function
title_full_unstemmed Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function
title_short Citicoline and Retinal Ganglion Cells: Effects on Morphology and Function
title_sort citicoline and retinal ganglion cells: effects on morphology and function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120106/
https://www.ncbi.nlm.nih.gov/pubmed/28676014
http://dx.doi.org/10.2174/1570159X15666170703111729
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