Thioredoxin and glutaredoxin systems of rat liver cytosol are not influenced by thyroid dysfunction

1989 ◽  
Vol 67 (7) ◽  
pp. 384-387
Author(s):  
Ganesh B. Bhat ◽  
Brian C. W. Hummel ◽  
Paul G. Walfish

The relation of thyroid hormone status to the function of hepatic cytosolic components activating microsomal reverse triiodothyronine (rT3) 5′-monodeiodination was studied in rats. Hyperthyroidism was induced by administration of thyroxine and hypothyroidism, by thyroidectomy. The DTT-stimulated microsomal rT3 5′-monodeiodination rate was increased by 125% in hyperthyroid rats and reduced to about 30% in hypothyroid rats (when compared with euthyroid animals). Thyroid status was unrelated to NADPH-dependent activation of microsomal 5′-deiodinase by cytosol components or to cytosolic concentrations of thioredoxin and glutaredoxin, which stimulate in vitro microsomal deiodination of thyroid hormone.Key words: hyperthyroidism, hypothyroidism, glutaredoxin, thioredoxin, 5′-deiodinase.

2003 ◽  
Vol 55 (1-2) ◽  
pp. 3-7 ◽  
Author(s):  
Jadranka Dundjerski ◽  
Jelena Predic ◽  
Aleksandra Cvoro ◽  
Gordana Matic

This study was focused on Cd effects on basal and dexamethasone-induced tyrosine aminotransferase (TAT) activity in the rat liver cytosol. Cadmium (Cd), applied in the dose of 2 mg/kg b.w., stimulated both TAT activity and its induction by dexamethasone, inducing the most prominent alterations 24 h after administration. Doses lower than 2 mg Cd/kg b.w. were ineffective while the higher ones (3 and 4 mg Cd/kg b.w) led to the changes similar to those reached by 2 mg Cd/kg. The in vitro application of different Cd concentrations to the liver cytosol rendered the enzyme activity unchanged suggesting that the metal acted at the level of TAT gene transcription.


1981 ◽  
Vol 362 (1) ◽  
pp. 47-58 ◽  
Author(s):  
Stéphanie MÖRIKOFER-ZWEZ ◽  
Franziska B. STOECKLIN ◽  
Paul WALTER

1996 ◽  
Vol 99 (1-3) ◽  
pp. 147-164 ◽  
Author(s):  
Miroslav Styblo ◽  
Marielle Delnomdedieu ◽  
David J. Thomas

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