Effects of Lithium and Carbamazepine on Thyroid Hormone Metabolism in Rat Brain
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作者:
Andreas Baumgartner
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Andreas Baumgartner
Graziano Pinna
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Graziano Pinna
Luis Hiedra
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Luis Hiedra
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机构:
Ursula Gaio
Carsten Hessenius
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Carsten Hessenius
Angel Campos-Barros
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Angel Campos-Barros
Murat Eravci
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Murat Eravci
Hans Prengel
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Hans Prengel
Rudy Thoma
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Rudy Thoma
Harald Meinhold
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机构:Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
Harald Meinhold
机构:
[1] Universitätsklinikum Benjamin Franklin,From the Department of Nuclear Medicine (Radiochemistry)
[2] Free University of Berlin and Formula Berlin GmbH,undefined
来源:
Neuropsychopharmacology
|
1997年
/
16卷
关键词:
Lithium;
Carbamazepine;
Thyroid hormones;
Deiodinases;
Rat brain;
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暂无
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学科分类号:
摘要:
The effects of lithium (LI) and carbamazepine (CBM) on thyroid hormone metabolism were investigated in 11 regions of the brain and three peripheral tissues in rats decapitated at three different times of day (4:00 a.m., 1:00 p.m., and 8:00 p.m.). Interest was focused on the changes in the two enzymes that catalyze: (1) the 5′deiodination of T4 to the biologically active T3, i.e., type II 5′deiodinase (5′D-II) and (2) the 5 (or inner-ring) deiodination of T3 to the biologically inactive 3′3-T2, i.e., type III 5 deiodinase (5D-III). A 14-day treatment with both LI and CBM induced significant reductions in 5D-III activity. However, 5′D-II activity was elevated by CBM and reduced by LI, both administered in concentrations leading to serum levels comparable with those seen in the prophylactic treatment of affective disorders. The effects were dose dependent, varied according to the region of the brain under investigation, and strongly depended on the time of death within the 24-hour rhythm. The consequences of these complex effects of LI and CBM on deiodinase activities for thyroid hormone function in the CNS and also their possible involvement in the mechanisms underlying the mood-stabilizing effects of both LI and CBM remain to be investigated.
机构:
Univ Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, CanadaUniv Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, Canada
Martel, J
Cayrou, C
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Univ Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, CanadaUniv Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, Canada
Cayrou, C
Puymirat, J
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机构:
Univ Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, CanadaUniv Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, Canada
机构:
Univ Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, CanadaUniv Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, Canada
Martel, J
Cayrou, C
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Univ Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, CanadaUniv Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, Canada
Cayrou, C
Puymirat, J
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机构:
Univ Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, CanadaUniv Laval, Med Res Ctr, Lab Human Genet, CHUQ, Ste Foy, PQ G1V 4G2, Canada