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dc.creatorReyes Corral, Martaes
dc.creatorSola Idígora, Noeliaes
dc.creatorPuerta Vázquez, Rocío de laes
dc.creatorMontaner, Joanes
dc.creatorYbot González, Patriciaes
dc.date.accessioned2021-04-28T16:49:07Z
dc.date.available2021-04-28T16:49:07Z
dc.date.issued2021
dc.identifier.citationReyes Corral, M., Sola Idígora, N., Puerta Vázquez, R.d.l., Montaner, J. y Ybot González, P. (2021). Nutraceuticals in the prevention of neonatal hypoxia–ischemia: A comprehensive review of their neuroprotective properties, mechanisms of action and future directions. International Journal of Molecular Sciences, 22 (5), 1-37.
dc.identifier.issn1661-6596es
dc.identifier.issn1422-0067es
dc.identifier.urihttps://hdl.handle.net/11441/108091
dc.description.abstractNeonatal hypoxia–ischemia (HI) is a brain injury caused by oxygen deprivation to the brain due to birth asphyxia or reduced cerebral blood perfusion, and it often leads to lifelong limiting sequelae such as cerebral palsy, seizures, or mental retardation. HI remains one of the leading causes of neonatal mortality and morbidity worldwide, and current therapies are limited. Hypothermia has been successful in reducing mortality and some disabilities, but it is only applied to a subset of newborns that meet strict inclusion criteria. Given the unpredictable nature of the obstetric compli-cations that contribute to neonatal HI, prophylactic treatments that prevent, rather than rescue, HI brain injury are emerging as a therapeutic alternative. Nutraceuticals are natural compounds present in the diet or used as dietary supplements that have antioxidant, anti-inflammatory, or antiapoptotic properties. This review summarizes the preclinical in vivo studies, mostly conducted on rodent models, that have investigated the neuroprotective properties of nutraceuticals in preventing and reducing HI-induced brain damage and cognitive impairments. The natural products reviewed include polyphenols, omega-3 fatty acids, vitamins, plant-derived compounds (tanshinones, sulforaphane, and capsaicin), and endogenous compounds (melatonin, carnitine, creatine, and lactate). These nutraceuticals were administered before the damage occurred, either to the mothers as a dietary supplement during pregnancy and/or lactation or to the pups prior to HI induction. To date, very few of these nutritional interventions have been investigated in humans, but we refer to those that have been successful in reducing ischemic stroke in adults. Overall, there is a robust body of preclinical evidence that supports the neuroprotective properties of nutraceuticals, and these may represent a safe and inexpensive nutritional strategy for the prevention of neonatal HI encephalopathy.es
dc.description.sponsorshipJunta de Andalucía C-0025-2018es
dc.formatapplication/pdfes
dc.format.extent37 p.es
dc.language.isoenges
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)es
dc.relation.ispartofInternational Journal of Molecular Sciences, 22 (5), 1-37.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMaternal supplementationes
dc.subjectNatural productses
dc.subjectNeonatal hypoxia–ischemiaes
dc.subjectNeuroprotectiones
dc.subjectNutraceuticalses
dc.subjectOmega-3 fatty acidses
dc.subjectPlant-derived compoundses
dc.subjectPolyphenolses
dc.subjectPreventiones
dc.subjectVitaminses
dc.titleNutraceuticals in the prevention of neonatal hypoxia–ischemia: A comprehensive review of their neuroprotective properties, mechanisms of action and future directionses
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Farmacologíaes
dc.relation.projectIDC-0025-2018es
dc.relation.publisherversionhttps://doi.org/10.3390/ijms22052524es
dc.identifier.doi10.3390/ijms22052524es
dc.journaltitleInternational Journal of Molecular Scienceses
dc.publication.volumen22es
dc.publication.issue5es
dc.publication.initialPage1es
dc.publication.endPage37es

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