Thyroid hormone-induced oxidative damage on lipids, glutathione and DNA in the mouse heart

References

• Harman D. Aging: prospects for further increases in the functional life span. Age 1994; 17: 119–146
   Google Scholar
• Asayama K., Dobashi K., Hayashibe H., Megata Y., Kato K. Lipid peroxidation and free radical scavengers in thyroid dysfunction in the rat: a possible mechanism of injury to heart and skeletal muscle in hyperthyroidism. Endocrinology 1987; 121: 2112–2118
   PubMed Web of Science ®Google Scholar
• Moreno M., Lann A., Lombardi A., Goglia F. How the thyroid controls metabolism in the rat: different roles for triiodothyronine and diiodothyronines. Journal of Physiology 1997; 505: 529–538
   PubMed Web of Science ®Google Scholar
• Stevens R.J., Nishio M.L., Hood D.A. Effect of hypothyroidism on the expression of cytochrome c and cytochrome c oxidase in heart and muscle during development. Molecular and Cellular Biochemistry 1995; 143: 119–127
   PubMed Web of Science ®Google Scholar
• Mano T., Sinohara R., Sawai Y., Oda N., Nishida Y., Mokuno T., Kotake M., Hamada M., Masunaga R., Nakai A., Nagasaka A. Effects of thyroid hormone on coenzyme Q and other free radical scavengers in rat heart muscle. Journal of Endocrinology 1995; 145: 131–136
   PubMed Web of Science ®Google Scholar
• Venditti P., Balestrieri M., Di Meo S., De Leo T. Effect of thyroid state on lipid peroxidation, antioxidant defenses, and susceptibility to oxidative stress in rat tissues. Journal of Endocrinology 1997; 155: 151–157
   PubMed Web of Science ®Google Scholar
• Fernández V., Simizu K., Barros S.B.M., Azzalis L.A., Pimentel R., Junqueira V.B.C., Videla L.A. Effects of hyperthyroidism on rat liver glutathione metabolism: related enzymes activities, efflux, and turnover. Endocrinology 1991; 129: 85–91
   PubMed Web of Science ®Google Scholar
• Loft S., Poulsen H.E. Markers of oxidative damage to DNA: antioxidants and molecular damage. Methods in Enzymology 1999; 300: 166–184
   PubMed Web of Science ®Google Scholar
• Barja de Quiroga G., Pérez-Campo R., López-Torres M. Antioxidant defenses and peroxidation in liver and brain of aged rats. Biochemical Journal 1990; 272: 247–250
   PubMed Web of Science ®Google Scholar
• Smith L. Spectrophotometric assay of cytochrome oxidase. Methods of biochemical analysis, D. Gick. Wiley-Interscience, New York 1955; 427–434, In
   Google Scholar
• Uchiyama M., Mihara M. Determination of malonaldehyde precursor in tissues by thiobarbituric acid test. Analitical Biochemistry 1978; 86: 271–278
   PubMed Web of Science ®Google Scholar
• Nohl H., Gille L., Schönheit K., Liu Y. Conditions allowing redox-cycling ubisemiquinone in mitochondria to establish a direct redox couple with molecular oxygen. Free Radical Biology and Medicine 1996; 20: 207–213
   PubMed Web of Science ®Google Scholar
• Tietze F. Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione; applications to mammalian blood and other tissues. Analitical Biochemistry 1969; 27: 502–522
   PubMed Web of Science ®Google Scholar
• Sacchetta P., Di Cola D., Federici G. Alkaline hydrolysis of N-ethylmaleimide allows a rapid assay of glutathione disulfide in biological samples. Analitical Biochemistry 1986; 154: 205–208
   PubMed Web of Science ®Google Scholar
• Latorre A., Moya A., Ayala A. Evolution of mitochondrial DNA in Drosophila Suboscura. Proceedings of the National Academy of Sciences of USA 1986; 83: 8649–8653
   PubMed Web of Science ®Google Scholar
• Asunción J.G., Millan A., Pla R., Bruseghini L., Esteras A., Pallardo F.V., Sastrê J., Viña J. Mitochondrial glutathione oxidation correlates with age-associated oxidative damage to mitochondrial DNA. FASEB Journal 1996; 10: 333–338
   PubMed Web of Science ®Google Scholar
• Barja G., Herrero A. Oxidative damage to mitochondrial DNA is inversely related to maximum life span in the heart and brain of mammals. FASEB Journal 2000; 15: 312–318
   Google Scholar
• Beckman K.B., Ames B.N. Detection and quantification of oxidative adducts of mitochondrial DNA. Methods in Enzymology 1996; 264: 442–453
   PubMedGoogle Scholar
• Connors J.M., Hedge G.A. Feedback effectiveness of periodic vs Constant triiodothyronine replacement. Endocrinology 1980; 106: 911–917
   PubMed Web of Science ®Google Scholar
• Gross J., Pitt-Rivers R. 3,5,3′- Triiodothyronine. 2. Physiological activity. Biochemical Journal 1953; 53: 652–656
   PubMed Web of Science ®Google Scholar
• Desphande N., Hulbert A.J. Dietary w6 fatty acids and the effects of hyperthyroidism in mice. Journal of Endocrinology 1995; 144: 431–439
   PubMed Web of Science ®Google Scholar
• Schmehl I., Luvisetto S., Canton M., Gennari F., Azzone G.F. Nature of respiratory stimulation in hyperthyroidism: the redox behaviour of cytochrome c. FEBS Letters 1995; 375: 206–210
   PubMed Web of Science ®Google Scholar
• Guerrero A., Pamplona R., Portero-Otín M., Barja G., López-Torres M. Effect of thyroid status on lipid composition and peroxidation in the mouse liver. Free Radical Biology and Medicine 1999; 26: 73–80
   PubMed Web of Science ®Google Scholar
• Nishio M.L., Ornatsky O.I., Hood D.A. Effects of hypothyroidism and aortic constriction on mitochondria during cardiac hypertrophy. Medicine and Science in Sports and Exercise 1995; 27: 1500–1508
   PubMed Web of Science ®Google Scholar
• Asayama K., Dobashi K., Hayashibe H., Kato K. Vitamin E protects against thyroxine-induced acceleration of lipid peroxidation in cardiac and skeletal muscles in rats. Journal of Nutrition Science and Vitaminology 1989; 35: 407–418
   PubMed Web of Science ®Google Scholar
• Venditti P., De Leo T., Di Meo S. Antioxidant-sensitive shortening of ventricular action potential in hyperthyroid rats is independent of lipid peroxidation. Molecular and Cellular Endocrinology 1998; 142: 15–23
   PubMed Web of Science ®Google Scholar
• Faas F.H., Carter W.J. Fatty-acid desaturation and microsomal lipid fatty-acid composition in experimental hyperthyroidism. Biochemical Journal 1981; 193: 845–852
   PubMed Web of Science ®Google Scholar
• Raederstorff D., Meler C.A., Moser U., Walter P. Hypothyroidism and thyroxin substitution affect the n-3 fatty acid composition of rat liver mitochondria. Lipids 1991; 26: 781–787
   PubMed Web of Science ®Google Scholar
• Hoch F.L. Lipids and thyroid hormones. Progress in Lipid Research 1988; 27: 199–270
   PubMed Web of Science ®Google Scholar
• Brand M.D., Steverding D., Kadenbach B., Stevenson P.M., Hafner R.P. The mechanism of the increase in mitochondrial proton permeability induced by thyroid hormones. European Journal of Biochemistry 1992; 206: 775–781
   PubMedGoogle Scholar
• Huh K., Kwon T.-H., Kim J.-S., Park J.M. Role of the hepatic xanthine oxidase in thyroid dysfunction: effect of thyroid hormones in oxidative stress in rat liver. Archives in Pharmacology Research 1998; 21: 236–240
   PubMed Web of Science ®Google Scholar
• Richter C., Park J.W., Ames B.N. Normal oxidative damage to mitochondrial and nuclear DNA is extensive. Proceedings of the National Academy of Sciences of USA 1988; 85: 6465–66467
   PubMed Web of Science ®Google Scholar
• Chung M.H., Kasai H., Nishimura S., Yu B.P. Protection of DNA damage by dietary restriction. Free Radical Biology and Medicine 1992; 12: 523–525
   PubMed Web of Science ®Google Scholar
• Suter M., Richter C. Fragmented mitochondrial DNA is the predominant carrier of oxidized DNA bases. Biochemistry 1999; 38: 459–464
   PubMed Web of Science ®Google Scholar
• Herrero A., Barja G. 8-oxo-deoxyguanosine levels in heart and brain mitochondrial and nuclear DNA of two mammals and three birds in relation to their different rates of aging. Aging Clinical and Experimental Research 1999; 11: 294–300
   Web of Science ®Google Scholar
• Mecocci P., MacGarvey U., Kaufman A.E., Koontz D., Shoffner J.M., Wallace D.C., Beal M.F. Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain. Annuals in Neurology 1993; 34: 609–616
   PubMed Web of Science ®Google Scholar
• Beckman K.B., Ames B.N. The free radical theory of aging matures. Physiological Reviews 1998; 78: 547–581
   PubMed Web of Science ®Google Scholar
• Anson R.M., Croteau D.L., Stierum R.H., Filburn C., Parsell R., Bohr V.A. Homogenous repair of singlet oxygen-induced DNA damage in differentially transcribed regions and strands of human mitochondrial DNA. Nucleic Acids Research 1998; 26: 662–668
   PubMed Web of Science ®Google Scholar
• Bohr V.A., Dianov G.L. Oxidative DNA damage processing in nuclear and mitochondrial DNA. Biochimie 1999; 81: 155–160
   PubMed Web of Science ®Google Scholar
• Souza-Pinto N.C., Croteau D.L., Hudson E.K., Hansford R.G., Bohr V.A. Age-associated increase in 8-oxo-deoxyguanosine glycosylase/AP lyase activity in rat mitochondria. Nucleic Acids Research 1999; 27: 1935–1942
   PubMed Web of Science ®Google Scholar
• López-Torres M., Romero M., Barja G. Effect of thyroid hormones on mitochondrial oxygen free radical production and DNA oxidative damage in the rat heart. Molecular and Cellular Endocrinology 2000, in press
   PubMed Web of Science ®Google Scholar
• Yamaguchi R., Hirano T., Asami S., Sugita A., Kasai H. Increase in the 8-hydroxyguanine repair activity in the rat kidney after the administration of a renal carcinogen, ferric nitriloacetate. Environmental Health Perspectives 1996; 104: 651–653
   PubMed Web of Science ®Google Scholar
• Grishko V.I., Driggers W.J., LeDoux S.P., Wilson G.L. Repair of oxidative damage in nuclear DNA sequences with different transcriptional activities. Mutation Research 1997; 384: 73–80
   PubMedGoogle Scholar
• Antipenko A.Y., Antipenko Y.N. Thyroid hormones and regulation of cell reliability system. Advances in Enzyme Regulation 1994; 34: 173–198
   PubMedGoogle Scholar
• Asami S., Hirano T., Yamaguchi R., Tsurudome Y., Itoh H., Kasai H. Effects of forced and spontaneous exercise on 8-hydroxydeoxyguanosine levels in rat organs. Biochemistry Biophysics Research Communications 1998; 243: 678–682
   PubMed Web of Science ®Google Scholar