Journal
CZECH JOURNAL OF ANIMAL SCIENCE
Volume 62, Issue 1, Pages 32-41Publisher
CZECH ACADEMY AGRICULTURAL SCIENCES
DOI: 10.17221/15/2016-CJAS
Keywords
nano-ZnO; bulk ZnO; zinc transportation; TPEN; IEC-6 cells
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Funding
- Sichuan Agricultural University (Shuangzhi Project)
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Zinc plays an important role in functional and structural integrity of cells. The aim of the current study was to compare cell viability, zinc uptake efficiency, and gene expression of metallothionein (MT), divalent metal transporter (DMT-1), and other important zinc transporters (ZnTs) under experimental treatment of TPEN (N, N, N', N'-Tetrakis (2-pyridylmethyl) ethylenediamine) (2 mu M), and three zinc sources (zinc oxide nanoparticle (nano-ZnO), bulk zinc oxide (ZnO), and zinc sulfate (ZnSO4)) at different levels (25, 50, and 100 mu M) in rat intestinal epithelial cell line IEC-6. Cells were classified into TPEN group and TPEN + zinc sources groups. In the present study, significantly decreased cell viability was observed in TPEN group, while supplementations with nano-ZnO at all levels and ZnO (50 and 100 mu M) significantly increased the cell viability. ZnSO4 at a high concentration (100 mu M) inhibited cell viability. Furthermore, cells of nano-ZnO group showed the highest viability at a 25 mu M concentration. The uptake efficiency of nano-ZnO is higher than that of ZnSO4 and ZnO. Additionally, a significant down-regulation for ZnT-1, ZnT-4, MT, DMT-1 mRNA with TPEN treatment was detected. Compared with the unchanged ZnT-4, all zinc treatments up-regulated the gene expressions of ZnT-1, ZnT-5, ZnT-7, MT, and DMT-1. Our results indicate that nano-ZnO is more effective than ZnO and ZnSO4 in enhancing cell viability, and its lower cytotoxicity, higher uptake efficiency, and comparative transportation at low concentration also favour its potential use as a new zinc source in feed additives.
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