On the Role of NADPH and Glutathione in the Catalytic Mechanism of Hepatic Thyroxine 5-deiodination

スポンサーリンク

概要

• 論文の詳細を見る

• A possible metabolic linkage between hepatic thyroxine (T4) 5-deiodination and the NADPH-glutathione (GSH) cycle was studied in rat liver. Supplementation of 1mM NADPH to stocked liver homogenates in vitro produced 4 fold increase in 3, 5, 3-triiodothyronine (T3) formation from T4, whereas the effect of 1mM FMN, FDN, NAD, NADH, or GSH was relatively small. An exponential dose-response relation was obtained between NADPH and T3 generated. The dose-dependent increase in T3 formation on GSH was eliminated in the presence of 1mM MADPH, and the additive effect of GSH to NADPH was not apparent in comparison with NADPH alone. Inhibition of T3 generation by graded doses of methylene blue was not affected by the presence of 5mM GSH. Furthermore, metabolic changes in the hexose-monophosphate shunt were produced in male Wistar rats aged 5w by treating them with fastingrefeeding (FF group), with the administration of insulin. and glucose (IG group), with propylthiouracil (PTU group) and with T4 (T4 group). All these reatments significantly reduced hepatic T4 5-deiodinase activity (P<0.01-0.001 vs control), while glucose-6-phosphate dehydrogenase (G6PD) and glutathione reductase (GSSG-R) activities were increased. Between generated T3 and G6PD or GSSG-R activity, an inverse correlation was noted (r=-0.802 and -0.933, P<0.001). No consistent relation was found between T4 5-deiodinase activity and GSH or non-protein SH contents. The addition of 1mM NADPH and GSH to the homogenates of FF, T4 and the control group stocked for 4w at -20°C, restored T4 5-deiodinase activity from a level of 10% to 60% of the initial value, whereas the activity remained depressed in PTU (19%) and the IG group (37%). These results indicate that both GSH and NADPH are important cofactors of the T3 generating system, but NADPH is more rate-limiting and its effect appears to be rather direct, not mediated by GSH formation. It is possible that T4 5-deiodinase may be one of the NADPH-dependent enzymes.

• 社団法人 日本内分泌学会の論文

著者

• Nomura Keiichi

  Department Of Applied Chemistry Faculty Of Engineering Kanagawa University

• SATO TAMOTU

  Department of Pediatrics, School of Medicine, Kanazawa University

• MARUYAMA SHIGERU

  Department of Pediatrics, School of Medicine, Kanazawa University

関連論文

• Molecular Cloning and Expression of the Mannose/Glucose Specific Lectin from Castanea crenata Cotyledons
• Construction of a Yeast Strain with Regulatable Phospholipid Synthesis for Analysis of the Uptake and Metabolism of Phosphatidylethanolamine with Short Acyl Chains
• Synthesis and Characterization of Water-Soluble, All-Inorganic Composition, Dawson-Type Trisubstituted Heteropolytungstates. Effect of Alkali Metal Countercations (Li, Na, K, and Cs) on the P_2W_Nb_3O_^ Polyoxoanion
• On the Role of NADPH and Glutathione in the Catalytic Mechanism of Hepatic Thyroxine 5-deiodination
• Na-K-dependent ATPase in red cells and thyroid status.
• Reaction of Tetrachloroxylenes with Fuming Nitric Acid. Side-chain Nitrooxylation and Quinol Nitrate Formation

スポンサーリンク