TY - JOUR T1 - Methimazole As an Antioxidant and Immunomodulator in Thyroid Cells: Mechanisms Involving Interferon-γ Signaling and H<sub>2</sub>O<sub>2</sub> Scavenging JF - Molecular Pharmacology JO - Mol Pharmacol SP - 972 LP - 980 DO - 10.1124/mol.60.5.972 VL - 60 IS - 5 AU - Ho Kim AU - Tae-Hoon Lee AU - Young Sun Hwang AU - Mi Ae Bang AU - Kang Hwa Kim AU - Jae Mi Suh AU - Hyo Kyun Chung AU - Dae-Yeul Yu AU - Kyung-Kwang Lee AU - O-Yu Kwon AU - Heung Kyu Ro AU - Minho Shong Y1 - 2001/11/01 UR - http://molpharm.aspetjournals.org/content/60/5/972.abstract N2 - The antithyroid drug, methimazole (MMI) is used to treat patients with Graves' hyperthyroidism. The major action of MMI is to inhibit synthesis of thyroid hormone in the thyroid gland. However, MMI also has antioxidant and immunomodulatory effects on thyrocytes and/or immune cells. This study identifies novel antioxidant and immunomodulatory effects of MMI involving the interferon-γ (IFN-γ) signaling pathway in thyroid cells. MMI inhibits transcription of the intercellular adhesion molecule-1 (ICAM-1) gene by modulating the function of transcription factor STAT1 (signal transducer and activator of transcription 1), which binds to the IFN-γ activated site of the ICAM-1 promoter. Furthermore, MMI rapidly eliminates H2O2 produced by IFN-γ treatment in thyroid cells and thus inhibits the H2O2-mediated phosphorylation of tyrosine 701 in STAT1. MMI also eliminates H2O2in vitro. MMI facilitates electron transfer from NADPH to H2O2 using thioredoxin or glutathione, fulfilling a role similar to peroxiredoxin or glutathione peroxidase, respectively. MMI prevents the IFN-γ and H2O2-mediated reversible inactivation of phosphatases. These effects inhibit full activation of the IFN-γ-induced Janus kinase(JAK)/STAT signaling pathway in FRTL-5 thyroid cells. These results may in part explain the antioxidant and immunomodulatory effects of MMI in thyroid cells of Graves' disease patients. ER -