Toxicity of DON on GPx1-Overexpressed or Knockdown Porcine Splenic Lymphocytes In Vitro and Protective Effects of Sodium Selenite

Joint Authors

Deng, J. L.
Xu, Zhiwen
Chen, Changhao
Fan, Yu
Chen, Chaoxi
He, Hongyi
Wang, Xuemei
Zhang, Zhuo
Peng, Guangneng
Hu, Yanchun
Tao, Siyi
Mao, Xinru
Zuo, Z. C.
Ren, Z. H.

Source

Oxidative Medicine and Cellular Longevity

Issue

Vol. 2019, Issue 2019 (31 Dec. 2019), pp.1-24, 24 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2019-02-28

Country of Publication

Egypt

No. of Pages

24

Main Subjects

Biology

Abstract EN

Deoxynivalenol (DON) is a common contaminant of grain worldwide and is often detected in the human diet and animal feed.

Selenium is an essential trace element in animals.

It has many biological functions.

The role of selenium in the body is mainly orchestrated by selenoprotein.

Glutathione peroxidase (GPx) also exists widely in the body and has attracted much attention due to its high antioxidant capacity.

In order to explore the effect of the GPx1 gene on toxicity of DON, in this study, we overexpressed or knockdown GPx1 in porcine splenic lymphocytes, then added different concentrations of DON (0.1025, 0.205, 0.41, and 0.82 μg/mL) and sodium selenite (2 μmol/L) to the culture system.

Using various techniques, we detected antioxidant function, free radical content, cell apoptosis, and methylation-related gene expression to explore the effect of GPx1 expression on DON-induced cell damage.

We also explored whether selenium can antagonize the toxicity of DON in these two cell models and revealed the protective effect of sodium selenite on DON-induced cell damage in GPx1-overexpressing or knockdown splenic lymphocytes.

Finally, our findings revealed the following: (1) GPx1 can regulate the antioxidant capacity, apoptosis rate, and expression of DNA methylation-related genes in pig splenic lymphocytes.

(2) Na2SeO3 (2 μmol/L) can regulate the antioxidant capacity, apoptosis rate, and expression of DNA methylation-related genes in pig splenic lymphocytes, and this effect is more significant in GPx1-overexpressing cells than in GPx1-knockdown cells.

(3) DON can cause oxidative damage, apoptosis, and methylation injury in GPx1-overexpressing or knockdown pig splenic lymphocytes in a concentration-dependent manner.

(4) Na2SeO3 (2 μmol/L) can antagonize the toxic effect of DON on GPx1-overexpressing or knockdown pig splenic lymphocytes.

Our findings may have important implications for food/feed safety, human health, and environmental protection.

American Psychological Association (APA)

Ren, Z. H.& Chen, Changhao& Fan, Yu& Chen, Chaoxi& He, Hongyi& Wang, Xuemei…[et al.]. 2019. Toxicity of DON on GPx1-Overexpressed or Knockdown Porcine Splenic Lymphocytes In Vitro and Protective Effects of Sodium Selenite. Oxidative Medicine and Cellular Longevity،Vol. 2019, no. 2019, pp.1-24.
https://search.emarefa.net/detail/BIM-1204279

Modern Language Association (MLA)

Ren, Z. H.…[et al.]. Toxicity of DON on GPx1-Overexpressed or Knockdown Porcine Splenic Lymphocytes In Vitro and Protective Effects of Sodium Selenite. Oxidative Medicine and Cellular Longevity No. 2019 (2019), pp.1-24.
https://search.emarefa.net/detail/BIM-1204279

American Medical Association (AMA)

Ren, Z. H.& Chen, Changhao& Fan, Yu& Chen, Chaoxi& He, Hongyi& Wang, Xuemei…[et al.]. Toxicity of DON on GPx1-Overexpressed or Knockdown Porcine Splenic Lymphocytes In Vitro and Protective Effects of Sodium Selenite. Oxidative Medicine and Cellular Longevity. 2019. Vol. 2019, no. 2019, pp.1-24.
https://search.emarefa.net/detail/BIM-1204279

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1204279