Alteration of antioxidants during the progression of heart disease in streptozotocin-induced diabetic rats

References

• Kannel W.B., Hjortland M., Castelli W.P. Role of Diabetes in Congestive Heart Failure: The Framingham Study. American Journal of Cardiology 1974; 34: 29–34
   PubMed Web of Science ®Google Scholar
• Wohaieb S.A., Godin D.V. Alterations in free radical tissue-defense mechanisms in STZ-induced diabetes in rat. Effects of insulin treatment. Diabetes 1987; 36: 1014–1018
   PubMed Web of Science ®Google Scholar
• Regan T.J., Lyons M.M., Ahmad S.S., Levinsin G.E., Oldewurtel H.A., Haider M.R. Evidence for cardiomyopathy in familial diabetes mellitus. Journal of Clinical Investigation 1977; 60: 885–899
   Web of Science ®Google Scholar
• Factor S.M., Minase T., Sonnenblick E.H. Clinical and morphological features of human hypertensive-diabetic cardiomyopathy. American Heart Journal 1980; 99: 446–458
   PubMed Web of Science ®Google Scholar
• Litwin S.E., Raya T.E., Anderson P.G., Daugherty S., Goldman S. Abnormal cardiac function in the STZ-Diabetic Rat. Journal of Clinical Investigation 1990; 86: 481–488
   PubMed Web of Science ®Google Scholar
• Halliwell B. Lipid peroxidation, oxygen radicals, cell damage, and antioxidant therapy. Lancet 1984; 23: 1396–1396
   Google Scholar
• Halliwell B., Gutteridge J.M.C. Free Radicals in Biology and Medicine4th edn. Clarendon Press, Oxford 1999
   Google Scholar
• Trocino R.A., Akazawa S., Ishibashi M., Matsumoto K., Matsuo H., Yamamoto H., Goto S., Urata Y., Kondo T., Nagataki S. Significance of glutathione depletion and oxidative stress in early embryogenesis in glucose-induced rat embryo culture. Diabetes 1995; 44: 992–998
   PubMed Web of Science ®Google Scholar
• Sakamaki H., Akazawa S., Ishibashi M., Izumino K., Takino H., Yamasaki H., Yamaguchi Y., Goto S., Urata Y., Kondo T., Nagataki S. Significance of glutathione-dependent antioxidant system in diabetes-induced embryonic malformations. Diabetes 1999; 48: 1138–1144
   PubMed Web of Science ®Google Scholar
• Kawaguchi T., Takeyasu A., Matsunobu K., Uda T., Ishizawa M., Suzuki K., Nishiura T., Ishikawa M., Taniguchi N. Stimulation of Mn-superoxide dismutase by tumor necrosis factor-α; quantitative determination of Mn-SOD protein levels in TNF-resistant and sensitive cells by ELISA. Biochem. Biophys. Res. Commun 1990; 171: 1378–1836
   PubMed Web of Science ®Google Scholar
• Wong J.H.W., Elwell J.M., Oberley L.W., Goeddel D.V. Manganous superoxide dismutase is essential for cellular resistance to cytotoxicity of tumor necrosis factor. Cell 1989; 58: 923–931
   PubMed Web of Science ®Google Scholar
• Richmann P.G., Meister A. Regulation of γ-glutamylcysteine synthetase by non-allosteric feedback inhibition by glutathione. Journal of Biological Chemistry 1975; 250: 1422–1426
   PubMedGoogle Scholar
• Murakami K., Kondo T., Otsuka Y., Fujiwara Y., Shimada M., Kawakami Y. Impairment of glutathione metabolism in erythrocytes from patients with diabetes mellitus. Metabolism 1989; 38: 735–758
   Google Scholar
• Tagami S., Kondo T., Yoshida K., Hirokawa J., Ohtsuka Y., Kawakami Y. Effect of insulin on impaired antioxidant activities in aortic endothelial cells from diabetic rabbits. Metabolism 1982; 41: 1053–1057
   Google Scholar
• Trocino R.A., Akazawa S., Ishibashi M., Matsumoto K., Matsuo H., Yamamoto H., Goto S., Urata Y., Kondo T., Nagataki S. Significance of glutathione depletion and oxidative stress in early embyogenesis in glucose-induced rat embryo culture. Diabetes 1995; 44: 992–998
   PubMed Web of Science ®Google Scholar
• Urata Y., Yamamoto H., Goto S., Tsushima H., Akazawa S., Yamashita S., Kondo T. Long exposure to high glucose concentration impairs the responsive expression of γ-glutamylcysteine synthetase by interleukin-1β and tumor necrosis factor-α in mouse endothelial cells. Journal of Biological Chemistry 1996; 271: 15146–15152
   PubMed Web of Science ®Google Scholar
• Zarich S.W., Arbuckle B.E., Cohen L.R., Roberts M., Nesto R.W. Diastolic abnormalities in young asymptomatic diabetic patients assessed by pulsed doppler echocardiography. Journal of American College Cardiology 1988; 12: 114–120
   PubMed Web of Science ®Google Scholar
• Beutler E. A manual of biochemical methods. Red Cell Metabolism3rd ed., E. Beutler. Grune and Stratton, Orlando, FL 1984; 77–78, In
   Google Scholar
• Suzuki K., Tatsumi H., Satoh S., Senda T., T., Nakata T., Fujii J., Taniguchi N. Manganese-superoxide dismutase in endothelial cells: localization and mechanism of induction. American Journal of Physiology 1993; 265: H1173–H1178
   PubMed Web of Science ®Google Scholar
• Sambrook J., Fritsch E.F., Maniatis T. Extraction, purification, and analysis of messenger RNA from eukaryotic cell. Molecular Cloning: A Laboratory Manual2nd edn. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 1989; 7–39, In
   Google Scholar
• Kondo T., Yoshida K., Urata Y., Goto S., Gasa S., Taniguchi N. γ-Glutamyl cysteine synthetase and active transport of glutathione S-conjugate are responsive to heat shock in K562 erythroid cells. Journal of Biological Chemistry 1993; 268: 20366–20372
   PubMed Web of Science ®Google Scholar
• Kamata K., Kobayashi T. Changes in superoxide dismutase mRNA expression by STZ-induced diabetes. British Journal of Pharmacology 1996; 119: 583–589
   PubMed Web of Science ®Google Scholar
• Redinbaugh M.G., Turley R.B. Adaptation of the bicinchoninic acid protein assay for use with microtiter plates. 1986
   Google Scholar
• Fujii J., Watanabe H., Koyama S., Kato K. Echocardiographic study on diastolic posterior wall movement and left ventricular filling by disease category. American Heart Journal 1979; 98: 144–152
   PubMedGoogle Scholar
• Penpargkul S., Schaibei T., Yipintsoi T., Scheuer J. The Effect of Diabetes on Performance and Metabolism of Rat Hearts. Circulation Research 1980; 47: 911–921
   PubMed Web of Science ®Google Scholar
• Taniguchi N., Arai K., Kinoshita N. Glycation of copper/zinc superoxide dismutase and its inactivation: identification of glycated sites. Methods in Enzymology 1989; 179: 570–581
   PubMedGoogle Scholar
• Takata I., Kawamura N., Myint T., Miyazawa N., Suzuki K., Maruyama N., Mino M., Taniguchi N. Glycated Cu,Zn-superoxide dismutase in rat lenses: evidence for the presence of fragmentation in vivo. Biochemical Biophysical Research Communication 1996; 219: 243–248
   PubMedGoogle Scholar
• Lebovitz R.M., Zhang H., Vogel H., Cartwright J., Jr, Dionne L., Lu N., Huang S., Matzuk M. Neurodegeneration, myocardial injury, and perimental death in mitochondrial superoxide dismutase-deficient mice. Proc. Natl. Acad. Sci. USA 1996; 93: 9782–9787
   PubMed Web of Science ®Google Scholar
• Iwanaga M., Mori K., Iida T., Urata Y., Matsuo T., Yasunaga A., Shibata S., Kondo T. Nuclear factor kappa B dependent induction of gamma glutamylcysteine synthetase by ionizing radiation in T98G human glioblastoma cells. Free Radical Biology and Medicine 1998; 24: 1256–1268
   PubMed Web of Science ®Google Scholar
• Cho S., Hazama M., Urata Y., Goto S., Horiuchi S., Sumikawa K., Kondo T. Protective role of glutathione synthesis in response to oxidized low density lipoprotein in human vascular endothelial cells. Free Radical Biology and Medicine 1999; 26: 589–602
   PubMed Web of Science ®Google Scholar
• Arsalane K., Dubois C.M., Muanza T., Begin R., Boudreau F., Asselin C., Cantin A.M. Transforming growth factor-beta1 is a potent inhibitor of glutathione synthesis in the lung epithelial cell line A549: transcriptional effect on the GSH rate-limiting enzyme gamma-glutamylcysteine synthetase. American Journal of Respiratory Cell and Molecular Biology 1997; 17: 599–607
   PubMed Web of Science ®Google Scholar
• Sharma K., Ziyadeh F.N., Alzahabi B., McGowan T.A., Kappoor S., Kurnik B.R., Kurnik P.B., Weisberg L.S. Increased renal production of transforming growth factor-beta1 in patients with type II diabetes. Diabetes 1997; 46: 854–859
   PubMed Web of Science ®Google Scholar
• Brooks W.W., Conrad C.H. Myocardial fibrosis in transforming growth factor beta(1) Heterozygous mice. J. Mol. Cell Cardiol. 2000; 32: 187–195
   PubMedGoogle Scholar
• Fukumoto H., Naito Z., Asano G., Aramaki T. Immunohistochemical and morphometric evaluations of coronary atherosclerotic plaques associated with myocardial infarction and diabetes mellitus. Journal of Atherosclerosis and Thrombosis 1998; 5: 29–35
   PubMedGoogle Scholar
• Kaul N., Siveski-Iliskovic N., Hill M., Khaper N., Seneviratne C., Singal P.K. Probucol treatment reverses antioxidant and functional deficit in diabetic cardiomyopathy. Molecular Cell Biochemistry 1996; 160/161: 283–288
   Web of Science ®Google Scholar