Publication:
Protective Effect of Vitamin A on Ara-C Induced Intestinal Damage in Mice

dc.authorscopusid12139290200
dc.authorscopusid7005543042
dc.authorscopusid6701590971
dc.authorscopusid35561472800
dc.authorscopusid6602111071
dc.authorscopusid8876487000
dc.authorscopusid8876487000
dc.contributor.authorElli, M.
dc.contributor.authorAydín, O.
dc.contributor.authorBilge, S.S.
dc.contributor.authorBozkurt, A.
dc.contributor.authorDaǧdemir, A.
dc.contributor.authorPinarli, F.G.
dc.contributor.authorAcar, S.
dc.date.accessioned2020-06-21T15:12:37Z
dc.date.available2020-06-21T15:12:37Z
dc.date.issued2009
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Elli] Murat, , Department of Pediatric Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aydín] Oǧuz,; [Bilge] Süleyman Sirri,; [Bozkurt] Ayhan, Department of Physiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Daǧdemir] Ayhan,; [Pinarli] Faruk Guclu,; [Acar] Sabri,en_US
dc.description.abstractBackground. Cytarabine (ARA-C) has been used for many years in the treatment of patients with leukemia and lymphoma. Gastrointestinal ulceration and mucositis are two of the well-known side effects of ARA-C. We set out to investigate whether vitamin A (VA) can help prevent ARA-C-induced mucosal lesions in mice. Materials and methods. Mice were divided into 5 groups. Group I (control group) received only saline; group II received ARA-C plus saline; group III received ARA-C plus VA; group IV received ARA-C plus a lipid solution, and group V received VA alone. VA (5000 IU/kg) was administered orally to the mice once daily for 7 days. ARA-C (3.6 mg) was administered intraperitoneally for 5 days to groups II, III and IV, starting on the third day of VA treatment. Intestinal segments from the proximal end of the jejunum of treated mice were isolated. Results. There was improved mucosal integrity, less necrosis and increased villus length with advanced mucosal proliferation in crypts in the VA plus ARA-C group when compared to the ARA-C groups without VA. Conclusion. We conclude that VA has a protective effect against ARA-C-induced mucosal damage in mice.en_US
dc.identifier.doi10.1177/030089160909500114
dc.identifier.endpage90en_US
dc.identifier.issn0300-8916
dc.identifier.issn2038-2529
dc.identifier.issue1en_US
dc.identifier.pmid19366062
dc.identifier.scopus2-s2.0-63449094374
dc.identifier.scopusqualityQ3
dc.identifier.startpage87en_US
dc.identifier.urihttps://doi.org/10.1177/030089160909500114
dc.identifier.volume95en_US
dc.identifier.wosWOS:000264700100015
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherIl Pensiero Scientifico Editore s.r.l.en_US
dc.relation.ispartofTumori Journalen_US
dc.relation.journalTumori Jen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCytarabineen_US
dc.subjectMiceen_US
dc.subjectMucosal Damageen_US
dc.subjectProtectionen_US
dc.subjectVitamin Aen_US
dc.titleProtective Effect of Vitamin A on Ara-C Induced Intestinal Damage in Miceen_US
dc.typeArticleen_US
dspace.entity.typePublication

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