Effect of propylthiouracil on the level of Schiff's bases in tissues of rats on diet with different doses of potassium iodide

Neuroendocrinology Letters

Volumn 27, Issue 5, 2006, Pages 595-599

  Sewerynek, Ewa ^a   Świerczyńska Machura, Dominika ^b   Lewiński, Andrzej ^a  

^a MEDICAL UNIVERSITY OF LODZ   (Poland)

^b NOFER INSTITUTE OF OCCUPATIONAL MEDICINE   (Poland)

Author keywords

Kidney; Liver; Lung; Potassium iodide; Propylthiouracil; Schiff's bases

Indexed keywords

POTASSIUM IODIDE; PROPYLTHIOURACIL; SCHIFF BASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARTICLE; CONTROLLED STUDY; KIDNEY HOMOGENATE; KIDNEY INJURY; LIVER HOMOGENATE; LIVER INJURY; LUNG HOMOGENATE; LUNG INJURY; MALE; NONHUMAN; OXIDATIVE STRESS; PRIMARY PREVENTION; PROTECTION; RAT; RAT STRAIN;

EID: 33846014327     PISSN: 0172780X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (24)

1. Bagchi N, Brown T R, Sundick R S. Thyroid cell injury is an initial event in the induction of autoimmune thyroiditis by iodine in obese strain chickens. Endocrinology 1995; 136: 5054-5060.
2. Bruck R, Oren R, Shirin H et al. Hypothyroidism minimalizes liver damage and improves survival in rats with thioacetamide induced fulminant hepatic failure. Hepatology 1998; 27: 1013-1020.
3. Burge JA, Aust SD. Microsomal lipid peroxidation. Methods Enzymol. 1978; 52:302-310
4. Comporti M. Lipid peroxidation and cellular damage in toxic liver injury. Lab Invest 1985; 53: 599-623.
5. Denef JF, Many MC, van den Hove MF. Iodine-induced thyroid inhibition and cell necrosis: two consequences of the same free-radical mediated mechanism? Mol Cell Endocrinol 1996; 121: 101-103.
6. Fernandez V, Barrientos X, Kipreos K et al. Superoxide radical generation, NADPH oxidase activity, and cytochrome P-450 content of rat liver microsomal fractions in an experimental hyperthyroid state: relation to lipid peroxidation. Endocrinology 1985; 117: 496-501.
7. Folis RH. Thyroiditis resulting from administration of excess iodine to hamsters with hyperplastic goitres. Proc Soc Exp Biol Med 1959; 102: 425-429.
8. Gonzalez-Reimers CE, Santolaria-Fernandez FJ, Gonzalez-Hernandez T et al. Effect of propylthiouracil on liver cell development in the male albino mouse: protective effect against ethanol-induced alterations. Drug Alcohol Depend 1988; 21: 11-18.
9. Hicks M, Wong LS, Day RO. Antioxidant activity of propylthiouracil. Biochem Pharmacol 1992; 43: 439-444.
10. Israel Y, Kalant H, Orrego H et al. Experimental alcohol-induced hepatic necrosis: suppression by propylthiouracil. Proc Natl Acad Sci USA 1975; 72: 1137-1141.
11. Lòpez-Torres M, Pérez-Campo R, Cadenas S et al. A comparative study of free radicals in vertebrates - II. Non-enzymatic antioxidants and oxidative stress. Comp Biochem Physiol 1993; 105B: 757-763.
12. Mahmoud I, Colin I, Many MC et al. Direct toxic effect of iodide in excess of iodine-deficient thyroid glands: epithelial necrosis and inflammation associated with lipofuscin accumulation. Exp Mol Pathol 1986; 44: 259-271.
13. Many MC, Mestdagh C, Van den Hove MF et al. In vitro study of acute toxic effects of high iodide doses in human thyroid follicles. Endocrinology 1992; 131: 621-630.
14. Many MC, Papadopoulos J, Martin C et al. Iodine induced cell damage in mouse hyperplastic thyroid is associated to lipid peroxidation. Progress in Thyroid Research Balkema, Rotterdam 1991; 635-638.
15. Orego H, Blake JE, Blendis LM et al. Long-term treatment of alcoholic liver disease with propylthiouracil. N Engl J Med 1987; 317: 1421-1427.
16. Orgiazzi J and Mornex R. Hyperthyroidism. In: Greer MA: The thyroid gland. Raven Press, New York 1990; 405-495.
17. Pérez-Campo R, Lòpez-Torres M, Rojas C et al. A comparative study of free radicals in vertebrates - I. Antioxidant enzymes. Comp Biochem Physiol 1993; 105B: 749-755.
18. Poli G, Albano E, Diazanni MU. The role of lipid peroxidation in liver damage. Chem Phys Lipids 1987; 45: 117-142.
19. Rodriguez-Pierce M, Sosenko IRS, Whitney P et al. Propylthiouracil treatment decreases the susceptibility to oxygen radical-induced lung damage in newborn rats exposed to prolonged hyperoxia. Pediatr Res 1994; 34: 530-535.
20. Sewerynek E, Wiktorska J, Nowak D et al. Methimazole protection against oxidative stress induced by hyperthyroidism in Graves' disease. Endocrine Reg 2000; 34: 83-89.
21. Świerczyńska-Machura D, Sewerynek E, Lewiński A. Effect of iodine on oxidative stress in selected rat organs. Polish J Endocrinol 2002; 53: 181-191.
22. Świerczyńska-Machura D, Lewiński, E. Sewerynek. Melatonin effects on Schiff's base levels induced by iodide administration in rats. Neuroendocrinol Lett 2004; 25: 70-74.
23. Wiktorska JA, Lewiński A, Sewerynek E. Effects of different antioxidants on lipid peroxidation in brain homogenates induced by thyrotoxicosis in rats. Neuroendocrinol Lett 2005; 26: 704-708.
24. Videla LA, Sir T, Wolff C. Increased lipid peroxidation in hyperthyroid patients: suppression by propylthiouracil treatment. Free Rad Res Commun 1988; 5: 1-10.