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Unsuspected Intrinsic Property of Melanin to Dissociate Water Can Be Used for the Treatment of CNS Diseases
Indexado
WoS WOS:000372107500003
Scopus SCOPUS_ID:84959930600
DOI 10.2174/1871527315666160202122943
Año 2016
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Retinal adhesion mechanisms in mammals are quite complex and multifactorial in nature. To date, these mechanisms are incompletely understood due to a variety of chemical, physical, and physiological forces impinging upon retinal tissue: retinal pigment epithelium, nearby tissues as sclera and vitreous, the subretinal space, and the highly complex interphotoreceptor matrix that fills subretinal space. The adhesion of the retina to the choroid, rather than anatomical, is a dynamic process, as the retina detaches a few minutes after life ceases. The adhesion mechanisms described in the literature, such as intraocular pressure and the oncotic pressure of the choroid that seems to push the retina towards the choroid, the delicate anatomical relationships between the rod and cone photoreceptors, the retinal pigment epithelium, the existence of a complex material called interphotoreceptor matrix, as well as other metabolic and structural factors, still cannot explain the remarkable features observed in the adhesion mechanisms between the photoreceptor layer and retinal pigment epithelium cells. The unexpected intrinsic property of melanin to absorb light energy and transform it into chemically based free energy can explain normal adhesion of the sensory retina to the pigment epithelium. In this article, we explore and highlight this explanation, which states that it is definitely able to provide a new treatment avenue against devastating neurodegenerative properties.

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Disciplinas de Investigación



WOS
Neurosciences
Pharmacology & Pharmacy
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Solis-Herrera, Arturo Solis Hombre Human Photosynth Study Ctr - México
Centro. - México
1 Herrera, Arturo Solís Hombre Centro. - México
Human Photosynth Study Ctr - México
2 Arias Esparza, Maria del Carmen Mujer Human Photosynth Study Ctr - México
Centro. - México
2 Esparza, María del Carmen Arias Mujer Centro. - México
Human Photosynth Study Ctr - México
3 Sols Arias, Paola Eugenia Mujer Human Photosynth Study Ctr - México
3 Arias, Paola Eugenia Solís Mujer Centro. - México
4 AVILA-RODRIGUEZ, MARCO FIDEL Hombre Pontificia Univ Javeriana - Colombia
Pontificia Universidad Javeriana - Colombia
5 Barreto, George Hombre Pontificia Univ Javeriana - Colombia
Universidad Autónoma de Chile - Chile
Pontificia Universidad Javeriana - Colombia
6 Emeliyanov, D. Hombre Texas A&M Univ - Estados Unidos
Texas A and M University-Kingsville - Estados Unidos
7 Bachurin, Sergey O. Hombre Russian Acad Sci - Rusia
Institute of Physiologically Active Compounds of the Russian Academy of Science - Rusia
8 Aliev, Gjumrakch - Russian Acad Sci - Rusia
GALLY Int Biomed Res Consulting LLC - Estados Unidos
Univ Atlanta - Estados Unidos
Institute of Physiologically Active Compounds of the Russian Academy of Science - Rusia
"GALLY" International Biomedical Research Consulting LLC - Estados Unidos
University of Atlanta - Estados Unidos

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Financiamiento



Fuente
Pontificia Universidad Javeriana
GALLY International Biomedical Research Consulting LLC, San Antonio, Texas, USA
Russian Science Foundation (Rossiysky Nauchny Fond)
Human Photosynthesis Study Center, Aguascalientes, Mexico

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
This work was partially supported by Human Photosynthesis Study Center, Aguascalientes, Mexico, GALLY International Biomedical Research Consulting LLC, San Antonio, Texas, USA, and by the Russian Science Foundation (www.rscf.ru, Rossiysky Nauchny Fond), grant number 14-23-00160 for 2014-2016 years, title "Directed design, synthesis, and study of biological activity of multi-target compounds as innovative drugs for treatment of neurodegenerative diseases. George E. Barreto's work is supported by the Pontificia Universidad Javeriana.

Muestra la fuente de financiamiento declarada en la publicación.