Literature DB >> 9430614

Dietary selenium supplementation is required to support full expression of three selenium-dependent glutathione peroxidases in various tissues of weanling pigs.

X G Lei1, H M Dann, D A Ross, W H Cheng, G F Combs, K R Roneker.   

Abstract

The current dietary allowance for selenium (Se) for pigs does not consider Se requirements for expression of several newly discovered Se-dependent enzymes and has raised environmental concerns. Our objective was to determine dietary Se requirements of young pigs for the full expression of cellular (GPX1), plasma (GPX3) and phospholipid hydroperoxide (GPX4) glutathione peroxidases. In Experiment 1, 18 weanling male pigs (4 wk old) were fed a corn-soybean meal basal diet (BD, 0.03 mg Se/kg) with the addition of 0, 0.1 or 0.3 mg Se/kg (Na2SeO3). In Experiment 2, 24 weanling barrows (6 wk old) were fed a similar BD with the addition of 0, 0.2, 0.3 or 0.5 mg Se/kg. Both experiments lasted for 5 wk. Pigs fed the BD had lower (P < 0.05) tissue GPX1 and GPX4 activities, plasma GPX activity, and(or) plasma Se concentrations than those fed the Se-supplemented diets. In Experiment 1, GPX1 and GPX4 activities in liver, heart and lung were lower (P < 0.05) in pigs fed 0.1 mg Se/kg than in those fed 0.3 mg Se/kg, although no such differences existed in thyroid or pituitary. Pigs fed 0.1 mg Se/kg also had lower (P < 0.05) plasma GPX3 activity at wk 5 and higher (P < 0.05) hepatic glutathione S-transferase activity than pigs fed 0.3 mg Se/kg. In Experiment 2, GPX1 and GPX4 activities in liver and heart, GPX1 and GPX4 mRNA levels in liver and GPX3 activity in plasma exhibited plateaus at 0.2 mg Se/kg. Pigs fed the BD had greater concentrations of F2-isoprostanes (a marker of in vivo lipid peroxidation) than those fed 0.2 mg Se/kg in plasma (P < 0.03) and liver (P < 0.04). We conclude that supplemental Se at 0.2 mg Se/kg of diet is required to support the full expression of three Se-dependent glutathione peroxidases in young pigs.

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Year:  1998        PMID: 9430614     DOI: 10.1093/jn/128.1.130

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  6 in total

Review 1.  Insights for Setting of Nutrient Requirements, Gleaned by Comparison of Selenium Status Biomarkers in Turkeys and Chickens versus Rats, Mice, and Lambs.

Authors:  Roger A Sunde; Jin-Long Li; Rachel M Taylor
Journal:  Adv Nutr       Date:  2016-11-15       Impact factor: 8.701

2.  Selenoprotein gene expression in thyroid and pituitary of young pigs is not affected by dietary selenium deficiency or excess.

Authors:  Ji-Chang Zhou; Hua Zhao; Jun-Gang Li; Xin-Jie Xia; Kang-Ning Wang; Ya-Jun Zhang; Yan Liu; Ying Zhao; Xin Gen Lei
Journal:  J Nutr       Date:  2009-04-08       Impact factor: 4.798

3.  Selenium-enriched Cardamine violifolia improves growth performance with potential regulation of intestinal health and antioxidant function in weaned pigs.

Authors:  Dan Wang; Yue Zhang; Qinliang Chen; Yanling Kuang; Jiajun Fan; Xiao Xu; Huiling Zhu; Qingyu Gao; Shuiyuan Cheng; Xin Cong; Yulan Liu
Journal:  Front Vet Sci       Date:  2022-08-11

4.  Selenoprotein Transcript Level and Enzyme Activity as Biomarkers for Selenium Status and Selenium Requirements in the Turkey (Meleagris gallopavo).

Authors:  Rachel M Taylor; Roger A Sunde
Journal:  PLoS One       Date:  2016-03-23       Impact factor: 3.240

5.  The selenium content of SEPP1 versus selenium requirements in vertebrates.

Authors:  Sam Penglase; Kristin Hamre; Ståle Ellingsen
Journal:  PeerJ       Date:  2015-09-10       Impact factor: 2.984

6.  Effects of Dietary Selenium Deficiency or Excess on Selenoprotein Gene Expression in the Spleen Tissue of Pigs.

Authors:  Zhuang Lu; Pengzu Wang; Teng Teng; Baoming Shi; Anshan Shan; Xin Gen Lei
Journal:  Animals (Basel)       Date:  2019-12-11       Impact factor: 2.752

  6 in total

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