Please use this identifier to cite or link to this item: http://hdl.handle.net/2067/46214
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dc.contributor.authorAmato, Rosarioit
dc.contributor.authorRossino, Maria Graziait
dc.contributor.authorCammalleri, Maurizioit
dc.contributor.authorTimperio, Anna Mariait
dc.contributor.authorFanelli, Giuseppinait
dc.contributor.authorDal Monte, Massimoit
dc.contributor.authorPucci, Laurait
dc.contributor.authorCasini, Giovanniit
dc.date.accessioned2021-11-12T12:32:52Z-
dc.date.available2021-11-12T12:32:52Z-
dc.date.issued2021it
dc.identifier.issn1663-9812it
dc.identifier.urihttp://hdl.handle.net/2067/46214-
dc.description.abstractLisosan G (LG), a fermented powder obtained from whole grains, is a nutritional supplement containing a variety of metabolites with documented antioxidant properties. We have recently demonstrated that orally administered LG protects diabetic rodent retinas from oxidative stress, inflammation, apoptosis, blood-retinal barrier disruption, and functional damage. Here, we investigated whether LG may exert protective effects in a model of glaucoma and measured the amounts of selected LG components that reach the retina after oral LG administration. Six-month-old DBA/2J mice were given an aqueous LG solution in place of drinking water for 2 mo. During the 2 mo of treatment with LG, the intraocular pressure (IOP) was monitored and the retinal ganglion cell (RGC) functional activity was recorded with pattern-electroretinography (PERG). At the end of the 2-mo period, the expression of oxidative stress and inflammatory markers was measured with qPCR, and RGC survival or macroglial activation were assessed with immunofluorescence. Alternatively, LG was administered by gavage and the concentrations of four of the main LG components (nicotinamide, gallic acid, 4-hydroxybenzoic acid, and quercetin) were measured in the retinas in the following 24 h using mass spectrometry. LG treatment in DBA/2J mice did not influence IOP, but it affected RGC function since PERG amplitude was increased and PERG latency was decreased with respect to untreated DBA/2J mice. This improvement of RGC function was concomitant with a significant decrease of both oxidative stress and inflammation marker expression, of RGC loss, and of macroglial activation. All four LG metabolites were found in the retina, although with different proportions with respect to the amount in the dose of administered LG, and with different temporal profiles in the 24 h following administration. These findings are consistent with neuroenhancing and neuroprotective effects of LG in glaucoma that are likely to derive from its powerful antioxidant properties. The co-occurrence of different metabolites in LG may provide an added value to their beneficial effects and indicate LG as a basis for the potential treatment of a variety of retinal pathologies.it
dc.language.isoengit
dc.rightsCC0 1.0 Universal*
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/*
dc.titleThe Potential of Lisosan G as a Possible Treatment for Glaucomait
dc.typearticle*
dc.identifier.doi10.3389/fphar.2021.719951it
dc.identifier.pmid34393798it
dc.identifier.scopus2-s2.0-85112266587it
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85112266587it
dc.relation.journalFRONTIERS IN PHARMACOLOGYit
dc.relation.firstpage719951it
dc.relation.volume12it
dc.type.miur262*
item.fulltextWith Fulltext-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextrestricted-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.journal.journalissn1663-9812-
crisitem.journal.anceE204053-
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