| Redox regulation of protein tyrosine phosphatase 1B by manipulation of dietary selenium affects the triglyceride concentration in rat liver. | |
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MedLine Citation:
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PMID: 19022953 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Protein tyrosine phosphatase 1B (PTP1B) is a key enzyme in the counter-regulation of insulin signaling and in the stimulation of fatty acid synthesis. Selenium (Se), via the activities of glutathione peroxidase (GPx) and thioredoxin reductase (TrxR), is involved in the removal of H(2)O(2) and organic peroxides, which are critical compounds in the modulation of PTP1B activity via glutathionylation. Our study with growing rats investigated how the manipulation of dietary Se concentration influences the regulation of PTP1B and lipogenic effects mediated by PTP1B. Weanling albino rats were divided into 3 groups of 10. The negative control group (NC) was fed a Se-deficient diet for 8 wk. Rats in groups Se75 and Se150 received diets supplemented with 75 or 150 microg Se/kg. Se supplementation of the rats strongly influenced expression and activity of the selenoenzymes cytosolic GPx, plasma GPx, phospholipidhydroperoxide GPx, and cytosolic TrxR, and liver PTP1B. Liver PTP1B activity was significantly higher in groups Se75 and Se150 than in the NC group and this was attributed to a lowered inhibition of the enzyme by glutathionylation. The increased liver PTP1B activity in groups Se75 and Se150 resulted in 1.1- and 1.4-fold higher liver triglyceride concentrations than in the NC rats. The upregulation of the sterol regulatory element binding protein-1c and of fatty acid synthase, 2 PTP1B targets, provided a possible explanation for the lipogenic effect of PTP1B due to the manipulation of dietary Se. We therefore conclude that redox-regulated proteins, such as PTP1B, represent important interfaces between dietary antioxidants such as Se and the regulation of metabolic processes. |
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Authors:
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Andreas S Mueller; Sandra D Klomann; Nicole M Wolf; Sandra Schneider; Rupert Schmidt; Julia Spielmann; Gabriele Stangl; Klaus Eder; Josef Pallauf |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: The Journal of nutrition Volume: 138 ISSN: 1541-6100 ISO Abbreviation: J. Nutr. Publication Date: 2008 Dec |
Date Detail:
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Created Date: 2008-11-21 Completed Date: 2009-01-06 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 0404243 Medline TA: J Nutr Country: United States |
Other Details:
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Languages: eng Pagination: 2328-36 Citation Subset: IM |
Affiliation:
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Institute of Agricultural and Nutritional Sciences, Preventive Nutrition Group, Martin Luther University Halle Wittenberg, Halle, Saale, Germany. andreas.mueller@landw.uni-halle.de |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Animals Base Sequence DNA Primers / genetics Diet Fatty Acid Synthetase Complex, Type I / genetics Glutathione Peroxidase / genetics, metabolism Lipid Peroxides / metabolism Liver / drug effects*, metabolism* Male Models, Biological Oxidation-Reduction Phospholipids / metabolism Protein Tyrosine Phosphatase, Non-Receptor Type 1 / metabolism* RNA, Messenger / genetics, metabolism Rats Selenium / administration & dosage*, metabolism Selenoproteins / genetics, metabolism Sterol Regulatory Element Binding Protein 1 / genetics Thioredoxin-Disulfide Reductase / genetics, metabolism Triglycerides / metabolism* |
| Chemical | |
Reg. No./Substance:
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0/DNA Primers; 0/Lipid Peroxides; 0/Phospholipids; 0/RNA, Messenger; 0/Selenoproteins; 0/Sterol Regulatory Element Binding Protein 1; 0/Triglycerides; 7782-49-2/Selenium; EC 1.11.1.9/Glutathione Peroxidase; EC 1.8.1.9/Thioredoxin-Disulfide Reductase; EC 3.1.3.48/Protein Tyrosine Phosphatase, Non-Receptor Type 1; EC 6.-/Fatty Acid Synthetase Complex, Type I |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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