Neuroprotective effects of quercetin on the cerebellum of zinc oxide nanoparticles (ZnoNps)-exposed rats

被引:6
|
作者
Abdelrahman, Shaimaa A. [1 ]
El-Shal, Amal S. [2 ,3 ]
Abdelrahman, Abeer A. [2 ]
Saleh, Ebtehal Zaid Hassen [1 ]
Mahmoud, Abeer A. [1 ]
机构
[1] Zagazig Univ, Fac Med, Med Histol & Cell Biol Dept, Zagazig, Egypt
[2] Zagazig Univ, Fac Med, Med Biochem & Mol Biol Dept, Zagazig, Egypt
[3] Armed Forces Coll Med AFCM, Med Biochem & Mol Biol Dept, Cairo, Egypt
来源
TISSUE BARRIERS | 2023年 / 11卷 / 03期
关键词
Quercetin; zinc oxide nanoparticles; miRNA; cerebellum; neurotoxicity; ZNO NANOPARTICLES; BRAIN; ANTIOXIDANT; FLAVONOIDS; TOXICITY; BLOOD; CELLS; CALBINDIN-D-28K; NEUROTOXICITY; HIPPOCAMPUS;
D O I
10.1080/21688370.2022.2115273
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Engineered nanomaterials induce hazardous effects at the cellular and molecular levels. We investigated different mechanisms underlying the neurotoxic potential of zinc oxide nanoparticles (ZnONPs) on cerebellar tissue and clarified the ameliorative role of Quercetin supplementation. Forty adult male albino rats were divided into control group (I), ZnONPs-exposed group (II), and ZnONPs and Quercetin group (III). Oxidative stress biomarkers (MDA & TOS), antioxidant biomarkers (SOD, GSH, GR, and TAC), serum interleukins (IL-1 beta, IL-6, IL-8), and tumor necrosis factor alpha (TNF-alpha) were measured. Serum micro-RNA (miRNA): miRNA-21-5p, miRNA-122-5p, miRNA-125b-5p, and miRNA-155-3p expression levels were quantified by real-time quantitative polymerase-chain reaction (RT-QPCR). Cerebellar tissue sections were stained with Hematoxylin & Eosin and Silver stains and examined microscopically. Expression levels of Calbindin D28k, GFAP, and BAX proteins in cerebellar tissue were detected by immunohistochemistry. Quercetin supplementation lowered oxidative stress biomarkers levels and ameliorated the antioxidant parameters that were decreased by ZnONPs. No significant differences in GR activity were detected between the study groups. ZnONPs significantly increased serum IL-1 beta, IL-6, IL-8, and TNF-alpha which were improved with Quercetin. Serum miRNA-21-5p, miRNA-122-5p, miRNA-125b-5p, and miRNA-155-p expression levels showed significant increase in ZnONPs group, while no significant difference was observed between Quercetin-treated group and control group. ZnONPs markedly impaired cerebellar tissue structure with decreased levels of calbindin D28k, increased BAX and GFAP expression. Quercetin supplementation ameliorated cerebellar tissue apoptosis, gliosis and improved calbindin levels. In conclusion: Quercetin supplementation ameliorated cerebellar neurotoxicity induced by ZnONPs at cellular and molecular basis by different studied mechanisms.
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页数:16
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