Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/48403
Campo DC Valoridioma
dc.contributor.authorSahagún, Ana M.en_US
dc.contributor.authorVaquera, Joséen_US
dc.contributor.authorGarcía, Juan J.en_US
dc.contributor.authorCalle, Ángela P.en_US
dc.contributor.authorDiez, María Joséen_US
dc.contributor.authorFernández, Nélidaen_US
dc.contributor.authorLoro, Juan F.en_US
dc.contributor.authorPortilla, Hugo O.en_US
dc.contributor.authorSierra, Matildeen_US
dc.contributor.otherloro, juan-
dc.contributor.otherSierra, Matilde-
dc.contributor.otherFernandez, Nelida-
dc.contributor.otherGarcia, Juan Jose-
dc.contributor.otherDiez, M Jose-
dc.contributor.otherSahagun Prieto, Ana M-
dc.date.accessioned2018-11-23T21:26:45Z-
dc.date.available2018-11-23T21:26:45Z-
dc.date.issued2015en_US
dc.identifier.issn1472-6882en_US
dc.identifier.urihttp://hdl.handle.net/10553/48403-
dc.description.abstractBackground: Several studies have indicated that dietary fiber may have a protective effect on gastrointestinal mucosa. The aim of this study was to evaluate the protective action of the soluble fiber Plantago ovata husk against intestinal damage.Methods: To evaluate the anti-ulcerogenic effect on duodenal mucosa of the soluble fiber Plantago ovata husk, low-dose acetylsalicylic acid (10 mg/kg) was given orally to animals once daily for 14 or 28 days with and without Plantago ovata husk (100 mg/kg). 24 h after final dosing duodenal samples were removed for anatomopathological evaluation. Villi were examined by both light and scanning electron microscopy.Results: Acetylsalicylic acid induced severe lesions in duodenal mucosa of rabbits, including erosions, epithelium disorganization, and cell vacuolization, increasing as well the amount of mononuclear and caliciform cells. Damage was much more severe in animals treated for 28 days. In groups receiving Plantago ovata husk, a significant attenuation of acetylsalicylic acid-induced lesions was already observed in group treated for 14 days, becoming more evident in those treated for 28 days, all of them with duodenal cytoarchitecture normal and similar to control animals.Conclusions: These findings suggest that Plantago ovata husk may protect intestinal mucosa probably by limiting acetylsalicylic acid penetration into epithelial cells, although further studies are needed to confirm the same effect in other experimental models of induced mucosal damage and to elucidate the mechanisms of fiber protection.en_US
dc.languagespaen_US
dc.relation.ispartofBMC Complementary and Alternative Medicineen_US
dc.sourceBMC Complementary and Alternative Medicine,v. 15 (298)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3201 Ciencias clínicasen_US
dc.subject.otherPeptic-Ulcer Diseaseen_US
dc.subject.otherSoluble Dietary Fiberen_US
dc.subject.otherAcetylsalicylic-Aciden_US
dc.subject.otherDuodenal-Ulceren_US
dc.subject.otherGastric-Mucosaen_US
dc.subject.otherPsylliumen_US
dc.subject.otherDamageen_US
dc.subject.otherSeedsen_US
dc.subject.otherRisken_US
dc.subject.otherRatsen_US
dc.titleStudy of the protective effect on intestinal mucosa of the hydrosoluble fiber Plantago ovata husken_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s12906-015-0827-9en_US
dc.identifier.scopus84940046848-
dc.identifier.isi000360264200001-
dcterms.isPartOfBmc Complementary And Alternative Medicine
dcterms.sourceBmc Complementary And Alternative Medicine[ISSN 1472-6882],v. 15
dc.contributor.authorscopusid6603354979-
dc.contributor.authorscopusid6507754786-
dc.contributor.authorscopusid6507213834-
dc.contributor.authorscopusid7004543407-
dc.contributor.authorscopusid35492627100-
dc.contributor.authorscopusid7102523615-
dc.contributor.authorscopusid6507389169-
dc.contributor.authorscopusid56800803100-
dc.contributor.authorscopusid7101602192-
dc.identifier.issue298-
dc.relation.volume15en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000360264200001-
dc.contributor.daisngid2821213-
dc.contributor.daisngid1401979-
dc.contributor.daisngid3899072-
dc.contributor.daisngid1015964-
dc.contributor.daisngid3184124-
dc.contributor.daisngid341909-
dc.contributor.daisngid1235180-
dc.contributor.daisngid3210878-
dc.contributor.daisngid18340770-
dc.contributor.daisngid984880-
dc.identifier.investigatorRIDL-9319-2014-
dc.identifier.investigatorRIDF-8990-2016-
dc.identifier.investigatorRIDF-9573-2016-
dc.identifier.investigatorRIDF-8979-2016-
dc.identifier.investigatorRIDF-8956-2016-
dc.identifier.investigatorRIDF-8928-2016-
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Sahagun, AM-
dc.contributor.wosstandardWOS:Vaquera, J-
dc.contributor.wosstandardWOS:Garcia, JJ-
dc.contributor.wosstandardWOS:Calle, AP-
dc.contributor.wosstandardWOS:Diez, MJ-
dc.contributor.wosstandardWOS:Fernandez, N-
dc.contributor.wosstandardWOS:Loro, JF-
dc.contributor.wosstandardWOS:Portilla, HO-
dc.contributor.wosstandardWOS:Sierra, M-
dc.date.coverdateAgosto 2015en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,829
dc.description.jcr1,987
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Bioquímica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0002-0517-8209-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameLoro Ferrer, Juan Francisco-
Colección:Artículos
Vista resumida

Google ScholarTM

Verifica

Altmetric


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.