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Chitosan nanoparticles and quercetin modulate gene expression and prevent the genotoxicity of aflatoxin B1 in rat liver.
Abdel-Wahhab, Mosaad A; Aljawish, Abdulhadi; El-Nekeety, Aziza A; Abdel-Aiezm, Sekena H; Abdel-Kader, Heba A M; Rihn, Bertrand H; Joubert, Olivier.
Afiliación
  • Abdel-Wahhab MA; Food Toxicology & Contaminants Department, National Research Center, Dokki, Cairo, Egypt.
  • Aljawish A; Université de Lorraine, Laboratoire d'Ingénierie des Biomolécules (LIBio), 2 avenue de la Forêt de Haye, TSA40602-F-54518 Vandœuvre-lès-Nancy, France.
  • El-Nekeety AA; Food Toxicology & Contaminants Department, National Research Center, Dokki, Cairo, Egypt.
  • Abdel-Aiezm SH; Cell Biology Department, National Research Center, Dokki, Cairo, Egypt.
  • Abdel-Kader HAM; Cell Biology Department, National Research Center, Dokki, Cairo, Egypt.
  • Rihn BH; Faculty of Pharmacy, EA 3452 CITHEFOR, Lorraine University, 54001 Nancy Cedex, France.
  • Joubert O; Faculty of Pharmacy, EA 3452 CITHEFOR, Lorraine University, 54001 Nancy Cedex, France.
Toxicol Rep ; 2: 737-747, 2015.
Article en En | MEDLINE | ID: mdl-28962409
The aims of the current study were to prepare chitosan nanoparticles (CNPs) and to evaluate its protective role alone or in combination with quercetin (Q) against AFB1-induce cytotoxicity in rats. Male Sprague-Dawley rats were divided into 12 groups and treated orally for 4 weeks as follow: the control group, the group treated with AFB1 (80 µg/kg b.w.) in corn oil, the groups treated with low (140 mg/kg b.w.) or high (280 mg/kg b.w.) dose of CNPs, the group treated with Q (50 mg/kg b.w.), the groups treated with Q plus the low or the high dose of CNPs and the groups treated with AFB1 plus Q and/or CNPs at the two tested doses. The results also revealed that administration of AFB1 resulted in a significant increase in serum cytokines, Procollagen III, Nitric Oxide, lipid peroxidation and DNA fragmentation accompanied with a significant decrease in GPx I and Cu-Zn SOD-mRNA gene expression. Q and/or CNPs at the two tested doses overcome these effects especially in the group treated with the high dose of CNPs plus Q. It could be concluded that CNPs is a promise candidate as drug delivery enhances the protective effect of Q against the cytogenetic effects of AFB1 in high endemic areas.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Toxicol Rep Año: 2015 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Irlanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Toxicol Rep Año: 2015 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Irlanda