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通过大鼠海马膜中[35S]GTPγS结合测定抗精神病药物的5-HT1A受体激动剂特性。

5-HT1A receptor agonist properties of antipsychotics determined by [35S]GTPgammaS binding in rat hippocampal membranes.

作者信息

Odagaki Yuji, Toyoshima Ryoichi

机构信息

Department of Psychiatry, Faculty of Medicine, Saitama Medical University, Saitama, Japan.

出版信息

Clin Exp Pharmacol Physiol. 2007 May-Jun;34(5-6):462-6. doi: 10.1111/j.1440-1681.2007.04595.x.

Abstract
  1. 5-Hydroxytryptamine 1A (5-HT1A) receptors have attracted increasing attention as a promising target for antipsychotic therapy. Although many atypical antipsychotic drugs, including the prototype clozapine, have been reported to be partial agonists at 5-HT1A receptors, these results are often fragmental and derived mainly from experiments that used cultured cells. 2. In the present study, [35S]guanosine 5'-O-(3-thiotriphosphate) ([35S]GTPgammaS) binding assay in rat hippocampal membranes was applied to a series of antipsychotic drugs, especially atypical antipsychotics. 3. Most, but not all, of atypical antipsychotic drugs and the classical antipsychotic drug nemonapride behaved as partial agonists at 5-HT1A receptors with varied potencies and relative efficacies. The most potent compound was perospirone with a mean EC50 of 27 nmol/L, followed by aripiprazole (45 nmol/L) > ziprasidone (480 nmol/L) > nemonapride (790 nmol/L) > clozapine (3900 nmol/L) > quetiapine (26,000 nmol/L). The maximal percentage increases over the basal binding (%Emax) for these antipsychotic drugs were 30-50%, with the exception of perospirone (approximately 15%), whereas 5-HT stimulated the binding to a mean %Emax of 105%. 4. Increasing concentrations of the selective and neutral 5-HT1A antagonist WAY100635 shifted the concentration-response curve of nemonapride-stimulated [35S]GTPgammaS binding to the right and in parallel. 5. The relative efficacy or intrinsic activity of a compound was affected differently by the differing concentrations of guanosine diphosphate (GDP) in the assay buffer, which should be taken into consideration when determining the relative efficacies of these antipsychotics as 5-HT1A receptor agonists. 6. These results provide important information concerning the relevance of 5-HT1A receptor partial agonist properties in the treatment for schizophrenic patients with most, if not all, of atypical antipsychotic drugs.
摘要
  1. 5-羟色胺1A(5-HT1A)受体作为抗精神病治疗的一个有前景的靶点已引起越来越多的关注。尽管许多非典型抗精神病药物,包括原型氯氮平,已被报道为5-HT1A受体的部分激动剂,但这些结果往往是零散的,且主要来自使用培养细胞的实验。2. 在本研究中,大鼠海马膜中的[35S]鸟苷5'-O-(3-硫代三磷酸)([35S]GTPγS)结合试验应用于一系列抗精神病药物,尤其是非典型抗精神病药物。3. 大多数(但不是全部)非典型抗精神病药物和经典抗精神病药物奈莫必利在5-HT1A受体上表现为部分激动剂,其效力和相对效能各不相同。最有效的化合物是哌罗匹隆,平均EC50为27 nmol/L,其次是阿立哌唑(45 nmol/L)>齐拉西酮(480 nmol/L)>奈莫必利(790 nmol/L)>氯氮平(3900 nmol/L)>喹硫平(26,000 nmol/L)。这些抗精神病药物相对于基础结合率的最大百分比增加(%Emax)为30-50%,哌罗匹隆除外(约15%),而5-羟色胺刺激结合的平均%Emax为105%。4. 选择性和中性5-HT1A拮抗剂WAY100635浓度的增加使奈莫必利刺激的[35S]GTPγS结合的浓度-反应曲线向右平行移动。5. 测定缓冲液中不同浓度的二磷酸鸟苷(GDP)对化合物的相对效能或内在活性有不同影响,在确定这些抗精神病药物作为5-HT1A受体激动剂的相对效能时应予以考虑。6. 这些结果提供了重要信息,涉及大多数(如果不是全部)非典型抗精神病药物在治疗精神分裂症患者时5-HT1A受体部分激动剂特性的相关性。

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