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Analyses of selenotranscriptomes and selenium concentrations in response to dietary selenium deficiency and age reveal common and distinct patterns by tissue and sex in telomere-dysfunctional mice

Author:
Lei Cao, Li Zhang, Huawei Zeng, Ryan TY Wu, Tung-Lung Wu
Source:
Journal of nutrition 2017 v.47 no.10 pp. 1858-1866
ISSN:
0022-3166
Subject:
Torula, analysis of variance, data analysis, diet, females, glutathione peroxidase, heart, iodide peroxidase, kidneys, liver, longevity, males, messenger RNA, mice, nutrient deficiencies, selenium, selenoproteins, sodium selenate, telomerase, testes, thioredoxins, tissues, weanlings
Abstract:
Background: The hierarchies of tissue selenium distribution and selenotranscriptomes are thought to critically affect healthspan and longevity. Objective: We determined selenium status and selenotranscriptomes in response to long-term dietary selenium deficiency and age in tissues of male and female mice. Methods: Weanling telomerase RNA component knockout C57BL/6 mice were fed a selenium-deficient (0.03 mg Se/kg) Torula yeast-based AIN-93G diet or a diet supplemented with sodium selenate (0.15 mg Se/kg) until age 18 or 24 mo. Plasma, hearts, kidneys, livers, and testes were collected to assay for selenotranscriptomes, selected selenoproteins, and tissue selenium concentrations. Data were analyzed with the use of 2-factor ANOVA (diet 3 age) in both sexes. Results: Dietary selenium deficiency decreased (P # 0.05) selenium concentrations (65–72%) and glutathione peroxidase (GPX) 3 (82–94%) and selenoprotein P (SELENOP) (17–41%) levels in the plasma of both sexes of mice and mRNA levels (9–68%) of 4, 4, and 12 selenoproteins in the heart, kidney, and liver ofmales, respectively, and 5, 16, and 14 selenoproteins, respectively, in females. Age increased seleniumconcentrations and SELENOP levels (27%and 30%, respectively; P#0.05) in the plasma of males only but decreased (12–46%; P < 0.05) mRNA levels of 1, 5, and 13 selenoproteins in the heart, kidney, and liver of males, respectively, and 6, 5, and 0 selenoproteins, respectively, in females. Among these mRNAs, selenoprotein H (Selenoh), selenoprotein M (Selenom), selenoprotein W (Selenow), methionine-R-sulfoxide reductase 1 (MsrB1), Gpx1, Gpx3, thioredoxin reductase 1 (Txnrd1), Txnrd2, selenoprotein S (Selenos), selenoprotein F (Selenof), and selenoprotein O (Selenoo) responded in parallel to dietary selenium deficiency and age in $1 tissue or sex, or both. Dietary selenium deficiency upregulated (40–160%; P# 0.05) iodothyronine deiodinase 2 (Dio2) and selenoprotein N (Selenon) in the kidneys of males. Age upregulated (11–44%; P < 0.05) Selenon in the kidneys of males, selenoprotein K (Selenok) and selenoprotein I (Selenoi) in the kidneys of females, and Selenof and Selenok in the testes. Conclusions: These results illustrate tissue-specific sexual dimorphisms of selenium status and selenotranscriptomes because of dietary selenium deficiency and age.
Agid:
6472286
Handle:
10113/6472286