Inhibition of the high affinity myo-inositol transport system: A common mechanism of action of antibipolar drugs?

被引:58
作者
Lubrich, B [1 ]
van Calker, D [1 ]
机构
[1] Univ Freiburg, Dept Psychiat, D-79104 Freiburg, Germany
关键词
affective disorders; mood stabilizer; SMIT;
D O I
10.1016/S0893-133X(99)00037-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mechanism of action of antibipolar drugs like lithium, carbamazepine, and valproate that are used in the treatment of manic-depressive illness, is unknown. Lithium is believed to act through uncompetitive inhibition of inositolmonophosphatase, which results in a depletion of neural cells of inositol and a concomitant modulation of phosphoinositol signaling. Here, we show that lithium ions, carbamazepine, and valproate, but not the tricyclic antidepressant amitriptyline, inhibit at therapeutically relevant concentrations and with a time course similar to their clinical actions the high affinity myo-inositol transport in astrocyte-like cells and downregulate the level of the respective mRNA. Inhibition of inositol uptake could thus represent an additional pathway for inositol depletion, which might be relevant in the mechanism of action of all three antibipolar drugs. (C) 1999 American College of Neuropsychopharmacology. Published by Elsevier Science Inc.
引用
收藏
页码:519 / 529
页数:11
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