The TRβ-selective agonist, GC-1, stimulates mitochondrial oxidative processes to a lesser extent than triiodothyronine
العنوان: | The TRβ-selective agonist, GC-1, stimulates mitochondrial oxidative processes to a lesser extent than triiodothyronine |
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المؤلفون: | Riccardo Zucchi, Gaetana Napolitano, Amedeo Columbano, S. Di Meo, Grazia Chiellini, Ts Scanlan, L. Di Stefano, Paola Venditti |
المصدر: | Journal of Endocrinology. 205:279-289 |
بيانات النشر: | Bioscientifica, 2010. |
سنة النشر: | 2010 |
مصطلحات موضوعية: | Male, Agonist, medicine.medical_specialty, Cytoplasmic and Nuclear, medicine.drug_class, Endocrinology, Diabetes and Metabolism, Wistar, Respiratory chain, Receptors, Cytoplasmic and Nuclear, Oxidative phosphorylation, Acetates, Mitochondrion, Biology, Oxygen Consumption, Endocrinology, Phenols, Models, Internal medicine, Receptors, medicine, Animals, Rats, Wistar, Respiratory system, GA-Binding Protein Transcription Factor, Hydrogen Peroxide, Mitochondria, Models, Animal, Nuclear Respiratory Factor 1, Oxidation-Reduction, PPAR gamma, Rats, Reactive Oxygen Species, Triiodothyronine, Receptor, chemistry.chemical_classification, Reactive oxygen species, Animal, Diabetes and Metabolism, chemistry |
الوصف: | Specific tissue responses to thyroid hormone are mediated by the hormone binding to two subtypes of nuclear receptors, TRα and TRβ. We investigated the relationship between TRβ activation and liver oxidative metabolism in hypothyroid rats treated with equimolar doses of triiodothyronine (T3) and GC-1, a TRβ agonist. T3 treatment produces increases in O2 consumption and H2O2 production higher than those elicited by GC-1. The greater effects of T3 on oxidative processes are linked to the higher hormonal stimulation of the content of respiratory chain components including autoxidizable electron carriers as demonstrated by the measurement of activities of respiratory complexes and H2O2 generation in the presence of respiratory inhibitors. It is conceivable that these differential effects are dependent on the inability of GC-1 to stimulate TRα receptors that are likely involved in the expression of some components of the respiratory chain. The greater increases in reactive oxygen species production and susceptibility to oxidants exhibited by mitochondria from T3-treated rats are consistent with their higher lipid and protein oxidative damage and lower resistance to Ca2+ load. The T3 and GC-1 effects on the expression levels of nuclear respiratory factor-1 and -2 and peroxisome proliferator-activated receptor-γ coactivator-1α suggest the involvement of respiratory factors in the agonist-linked changes in mitochondrial respiratory capacities and H2O2 production. |
تدمد: | 1479-6805 0022-0795 |
الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c593521cb01dc6b6fce88a562b42d828Test https://doi.org/10.1677/joe-10-0036Test |
حقوق: | OPEN |
رقم الانضمام: | edsair.doi.dedup.....c593521cb01dc6b6fce88a562b42d828 |
قاعدة البيانات: | OpenAIRE |
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We investigated the relationship between TRβ activation and liver oxidative metabolism in hypothyroid rats treated with equimolar doses of triiodothyronine (T3) and GC-1, a TRβ agonist. T3 treatment produces increases in O2 consumption and H2O2 production higher than those elicited by GC-1. The greater effects of T3 on oxidative processes are linked to the higher hormonal stimulation of the content of respiratory chain components including autoxidizable electron carriers as demonstrated by the measurement of activities of respiratory complexes and H2O2 generation in the presence of respiratory inhibitors. It is conceivable that these differential effects are dependent on the inability of GC-1 to stimulate TRα receptors that are likely involved in the expression of some components of the respiratory chain. The greater increases in reactive oxygen species production and susceptibility to oxidants exhibited by mitochondria from T3-treated rats are consistent with their higher lipid and protein oxidative damage and lower resistance to Ca2+ load. 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