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Effects of Valproic Acid Derivatives on Inositol Trisphosphate Depletion Teratogenicity Glycogen Synthase Kinase-3β Inhibition and Viral Replication: A Screening Approach for New Bipolar Disorder Drugs Derived from the Valproic Acid Core Structure

机译:丙戊酸衍生物对肌醇三磷酸消耗致畸性糖原合酶激酶3β抑制和病毒复制的影响:一种从丙戊酸核心结构衍生的新型双相情感障碍药物的筛选方法

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摘要

Inositol-1,4,5-trisphosphate (InsP3) depletion has been implicated in the therapeutic action of bipolar disorder drugs, including valproic acid (VPA). It is not currently known whether the effect of VPA on InsP3 depletion is related to the deleterious effects of teratogenicity or elevated viral replication, or if it occurs via putative inhibitory effects on glycogen synthase kinase-3β(GSK-3β). In addition, the structural requirements of VPA-related compounds to cause InsP3 depletion are unknown. In the current study, we selected a set of 10 VPA congeners to examine their effects on InsP3 depletion, in vivo teratogenic potency, HIV replication, and GSK-3β activity in vitro. We found four compounds that function to deplete InsP3 in the model eukaryote Dictyostelium discoideum, and these drugs all cause growth-cone enlargement in mammalian primary neurons, consistent with the effect of InsP3 depletion. No relationship was found between InsP3 depletion and teratogenic or elevated viral replication effects, and none of the VPA congeners were found to affect GSK-3β activity. Structural requirements of VPA congers to maintain InsP3 depletion efficacy greater than that of lithium are a carboxylic-acid function without dependence on side-chain length, branching, or saturation. Noteworthy is the enantiomeric differentiation if a chiral center exists, suggesting that InsP3 depletion is mediated by a stereoselective mode of action. Thus, the effect of InsP3 depletion can be separated from that of teratogenic potency and elevated viral replication effect. We have used this to identify two VPA derivatives that share the common InsP3-depleting action of VPA, lithium and carbamazepine, but do not show the side effects of VPA, thus providing promising novel candidates for bipolar disorder treatment.
机译:肌醇1,4,5-三磷酸(InsP3)耗竭与双相情感障碍药物(包括丙戊酸(VPA))的治疗作用有关。目前尚不清楚VPA对InsP3耗竭的影响是否与致畸性或病毒复制增加的有害影响有关,或者是否通过对糖原合酶激酶3β(GSK-3β)的假定抑制作用而发生。此外,导致InsP3耗尽的VPA相关化合物的结构要求未知。在当前的研究中,我们选择了10个VPA同系物来检查它们对InsP3耗竭,体内致畸效力,HIV复制和体外GSK-3β活性的影响。我们在模型真核生物盘基网柄菌中发现了四种具有消耗InsP3的功能的化合物,这些药物都引起哺乳动物原代神经元的生长锥增大,与InsP3消耗的效果一致。在InsP3耗竭与致畸或病毒复制作用升高之间未发现任何关系,并且未发现任何VPA同系物影响GSK-3β活性。维持InsP3耗尽效率高于锂的VPA聚合器的结构要求是羧酸功能,不依赖于侧链长度,支链或饱和度。值得注意的是,如果存在手性中心,则是对映异构体的分化,这表明InsP3的消耗是由立体选择性作用模式介导的。因此,可以将InsP3消耗的影响与致畸效力和提高的病毒复制作用分开。我们已经使用它来鉴定两种具有VPA共同的InsP3耗尽作用的VPA衍生物,锂和卡马西平,但未显示VPA的副作用,因此为双相情感障碍治疗提供了有希望的新型候选药物。

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