Literature DB >> 24264024

Dietary antioxidants and the biochemical response to oxidant inhalation : III. Selenium influence on mouse lung response and tolerance to ozone.

N M Elsayed1, M G Mustafa, A D Hacker, K Kuehn, G N Schrauzer.   

Abstract

We fed female strain A/St mice selenium (Se) test diets containing either no Se (-Se) or 1 ppm Se (+Se) for 11 wk. Both diets contained 55 ppm vitamin E. We then exposed three groups of mice from each dietary regimen to either 0.8 ppm (1568 μg/m(3)) O3 (low-level) continuously for 5 d, 10.0 ppm (19,600 μg/m(3)) O3 (high-level) for 12 h, or filtered room air, where the latter served as a control for both O3 exposures. After O3 exposures we analyzed the lungs for various physical and biochemical parameters, and compared the results to those obtained from the air controls. The results showed that the difference in dietary Se intake produced an eightfold difference in Se content and a three-fold difference in glutathione peroxidase (GP) activity in the lung, but few changes in other lung parameters. With low-level O3 exposure, NADPH production increased significantly in +Se mice, but did not change in -Se mice. With high-level O3 exposure we observed comparable effects for both dietary regimens, including animal mortality, which was 24% for -Se and 14% for +Se mice. Thus, it seems that diminished GP activity resulting from Se deficiency and the ensuing lack of increase in NADPH production were poorly correlated with mouse tolerance to O3. The lung Se content increased in both dietary regimens after O3 exposure, but the increase was greater after high-level O3 exposure. This suggests a "mobilization" of Se to the lung under O3 stress. It is possible that such a mobilization contributes to the lung reserve of antioxidants, and hence the comparable mortality in both dietary Se regimens.

Entities:  

Year:  1984        PMID: 24264024     DOI: 10.1007/BF02917510

Source DB:  PubMed          Journal:  Biol Trace Elem Res        ISSN: 0163-4984            Impact factor:   3.738


  41 in total

1.  Effect of ambient levels of ozone on monkeys.

Authors:  D L Dungworth; W L Castleman; C K Chow; P W Mellick; M G Mustafa; B Tarkington; W S Tyler
Journal:  Fed Proc       Date:  1975-07

2.  The relevance of pentose phosphate pathway stimulation in rat lung to the mechanism of paraquat toxicity.

Authors:  M S Rose; L L Smith; I Wyatt
Journal:  Biochem Pharmacol       Date:  1976-08-01       Impact factor: 5.858

3.  Altered sensitivity to oxygen toxicity.

Authors:  D F Tierney; L Ayers; R S Kasuyama
Journal:  Am Rev Respir Dis       Date:  1977-06

4.  Ozone interaction with rodent lung: effect on sulfhydryls and sulfhydryl-containing enzyme activities.

Authors:  A J DeLucia; P M Hoque; M G Mustafa; C E Cross
Journal:  J Lab Clin Med       Date:  1972-10

5.  Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent.

Authors:  J Sedlak; R H Lindsay
Journal:  Anal Biochem       Date:  1968-10-24       Impact factor: 3.365

6.  Ozone interactions with lung tissue. Biochemical approaches.

Authors:  C E Cross; A J De Lucia; A K Reddy; M Z Hussain; C K Chow
Journal:  Am J Med       Date:  1976-06       Impact factor: 4.965

7.  Pulmonary biochemical alterations resulting from ozone exposure.

Authors:  M G Mustafa; S D Lee
Journal:  Ann Occup Hyg       Date:  1976-07

8.  Pulmonary oxygen toxicity: lack of tolerance of mice of various ages.

Authors:  A Lanir; D Kerem; D Gershon
Journal:  Biochem Biophys Res Commun       Date:  1981-08-31       Impact factor: 3.575

9.  Effect of butylated hydroxytoluene and other antioxidants on mouse lung metabolism.

Authors:  S T Omaye; K A Reddy; C E Cross
Journal:  J Toxicol Environ Health       Date:  1977-12

10.  Selenium: biochemical role as a component of glutathione peroxidase.

Authors:  J T Rotruck; A L Pope; H E Ganther; A B Swanson; D G Hafeman; W G Hoekstra
Journal:  Science       Date:  1973-02-09       Impact factor: 47.728

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