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壳聚糖纳米颗粒和槲皮素调节基因表达并预防黄曲霉毒素B对大鼠肝脏的遗传毒性。

Chitosan nanoparticles and quercetin modulate gene expression and prevent the genotoxicity of aflatoxin B in rat liver.

作者信息

Abdel-Wahhab Mosaad A, Aljawish Abdulhadi, El-Nekeety Aziza A, Abdel-Aiezm Sekena H, Abdel-Kader Heba A M, Rihn Bertrand H, Joubert Olivier

机构信息

Food Toxicology & Contaminants Department, National Research Center, Dokki, Cairo, Egypt.

Université de Lorraine, Laboratoire d'Ingénierie des Biomolécules (LIBio), 2 avenue de la Forêt de Haye, TSA40602-F-54518 Vandœuvre-lès-Nancy, France.

出版信息

Toxicol Rep. 2015 May 12;2:737-747. doi: 10.1016/j.toxrep.2015.05.007. eCollection 2015.

Abstract

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 AFB-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 AFB (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 AFB plus Q and/or CNPs at the two tested doses. The results also revealed that administration of AFB 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 AFB in high endemic areas.

摘要

本研究的目的是制备壳聚糖纳米颗粒(CNPs),并评估其单独或与槲皮素(Q)联合使用对黄曲霉毒素诱导的大鼠细胞毒性的保护作用。将雄性Sprague-Dawley大鼠分为12组,并按以下方式口服给药4周:对照组、用玉米油中的黄曲霉毒素(80μg/kg体重)处理的组、用低剂量(140mg/kg体重)或高剂量(280mg/kg体重)CNPs处理的组、用Q(50mg/kg体重)处理的组、用Q加低剂量或高剂量CNPs处理的组,以及用两种测试剂量的黄曲霉毒素加Q和/或CNPs处理的组。结果还显示,给予黄曲霉毒素导致血清细胞因子、前胶原III、一氧化氮、脂质过氧化和DNA片段化显著增加,同时伴随谷胱甘肽过氧化物酶I(GPx I)和铜锌超氧化物歧化酶(Cu-Zn SOD)-mRNA基因表达显著降低。两种测试剂量的Q和/或CNPs克服了这些影响,尤其是在高剂量CNPs加Q处理的组中。可以得出结论,CNPs作为药物递送载体是一个有前景的候选物,可增强Q在高流行地区对黄曲霉毒素细胞遗传学效应的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b847/5598511/02e2872e805a/gr1.jpg

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