DESETHYLAMIODARONE IS A COMPETITIVE INHIBITOR OF THE BINDING OF THYROID-HORMONE TO THE THYROID-HORMONE ALPHA-1-RECEPTOR PROTEIN

被引:51
作者
VANBEEREN, HC
BAKKER, O
WIERSINGA, WM
机构
[1] Department of Endocrinology, Academic Medical Centre F5-171, University of Amsterdam, 1105 AZ Amsterdam
关键词
DESETHYLAMIODARONE (DEA); ALPHA-1-THYROID HORMONE RECEPTOR (T(3)R); TRIIODOTHYRONINE (T-3);
D O I
10.1016/0303-7207(95)03578-U
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Desethylamiodarone (DEA), the major metabolite of the potent antiarrythmic drug amiodarone, is a non-competitive inhibitor of the binding of thyroid hormone (T-3) to the beta 1-thyroid hormone receptor (T(3)R). In the present study, we investigated whether DEA acts in a similar way with respect to the alpha 1-T(3)R. The chicken alpha 1-T(3)R, expressed in an E. coli system, was incubated in the presence or absence of DEA with [I-125]T-3 in buffer containing 0.05% Triton X-100, 0.05% BSA and 1% ethanol (v/v) in order to solubilise DEA. DEA, but not amiodarone, inhibited T-3 binding in a dose-dependent manner; the IC50 value was 3.5 x 10(-5) M. Scatchard analyses in the presence of DEA demonstrated a dose-dependent decrease in K-a values, but no change in MBC. Lineweaver-Burk plots clearly indicated competitive inhibition by DEA. Pre-incubation of the alpha 1-receptor with DEA decreased maximal [I-125]T-3 binding, which was independent of the duration of pre-incubation. In conclusion, in contrast to the beta 1-T(3)R, where DEA acts as a non-competitive inhibitor, we now report as a new finding the competitive action of DEA to the alpha 1-T(3)R.
引用
收藏
页码:15 / 19
页数:5
相关论文
共 50 条
[31]   MECHANISMS BY WHICH THYROID-HORMONE RECEPTOR MUTATIONS CAUSE CLINICAL SYNDROMES OF RESISTANCE TO THYROID-HORMONE [J].
JAMESON, JL .
THYROID, 1994, 4 (04) :485-492
[32]   COLCHICINE-BINDING PROTEIN AND SECRETION OF THYROID-HORMONE [J].
WILLIAMS, JA ;
WOLFF, J .
JOURNAL OF CELL BIOLOGY, 1972, 54 (01) :157-&
[33]   THE BINDING OF THYROID-HORMONE RECEPTORS TO DNA [J].
WILSON, BD ;
WIUM, CA ;
GENT, WL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 124 (01) :29-36
[34]   THYROID-HORMONE BINDING IN DOG PLASMA [J].
DAVIS, PJ ;
HANDWERGER, BS .
ENDOCRINOLOGY, 1973, 93 (06) :1445-1448
[35]   MITOCHONDRIAL THYROID-HORMONE BINDING AND ACTIVATION [J].
LAZARUS, JH ;
MILCH, PO ;
STERLING, R .
CLINICAL RESEARCH, 1976, 24 (03) :A428-A428
[36]   DNA BINDING OF THYROID-HORMONE RECEPTORS [J].
MACLEOD, KM ;
BAXTER, JD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1975, 62 (03) :577-583
[37]   3 NEW MUTATIONS OF THYROID-HORMONE RECEPTOR-BETA ASSOCIATED WITH RESISTANCE TO THYROID-HORMONE [J].
BARTOLONE, L ;
REGALBUTO, C ;
BENVENGA, S ;
FILETTI, S ;
TRIMARCHI, F ;
PONTECORVI, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (01) :323-326
[38]   2 THYROID-HORMONE RESPONSE ELEMENTS ARE PRESENT IN THE PROMOTER OF HUMAN THYROID-HORMONE RECEPTOR BETA-1 [J].
SUZUKI, S ;
MIYAMOTO, T ;
OPSAHL, A ;
SAKURAI, A ;
DEGROOT, LJ .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (03) :305-314
[39]   HOMOZYGOSITY FOR A DOMINANT NEGATIVE THYROID-HORMONE RECEPTOR GENE RESPONSIBLE FOR GENERALIZED RESISTANCE TO THYROID-HORMONE [J].
ONO, S ;
SCHWARTZ, ID ;
MUELLER, OT ;
ROOT, AW ;
USALA, SJ ;
BERCU, BB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (05) :990-994
[40]   MITOCHONDRIAL THYROID-HORMONE BINDING AND ACTIVATION [J].
MILCH, PO ;
LAZARUS, JH ;
STERLING, K .
CLINICAL RESEARCH, 1975, 23 (05) :A574-A574