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WS-50030 [7-{4-[3-(1H-茚满-3-基)丙基]哌嗪-1-基}-1,3-苯并恶唑-2(3H)-酮]:一种新型多巴胺 D2 受体部分激动剂/5-羟色胺再摄取抑制剂,具有抗精神病样和抗抑郁样的临床前活性。

WS-50030 [7-{4-[3-(1H-inden-3-yl)propyl]piperazin-1-yl}-1,3-benzoxazol-2(3H)-one]: a novel dopamine D2 receptor partial agonist/serotonin reuptake inhibitor with preclinical antipsychotic-like and antidepressant-like activity.

机构信息

Discovery Neuroscience, Wyeth Research, CN8000, Princeton, NJ 08543, USA.

出版信息

J Pharmacol Exp Ther. 2010 Jan;332(1):190-201. doi: 10.1124/jpet.109.157388. Epub 2009 Oct 14.

Abstract

The preclinical characterization of WS-50030 [7-{4-[3-(1H-inden-3-yl)propyl]piperazin-1-yl}-1,3-benzoxazol-2(3H)-one] is described. In vitro binding and functional studies revealed highest affinity to the D(2) receptor (D(2L) K(i), 4.0 nM) and serotonin transporter (K(i), 7.1 nM), potent D(2) partial agonist activity (EC(50), 0.38 nM; E(max), 30%), and complete block of the serotonin transporter (IC(50), 56.4 nM). Consistent with this in vitro profile, WS-50030 (10 mg/kg/day, 21 days) significantly increased extracellular 5-HT in the rat medial prefrontal cortex, short-term WS-50030 treatment blocked apomorphine-induced climbing (ID(50), 0.51 mg/kg) in a dose range that produced minimal catalepsy in mice and induced low levels of contralateral rotation in rats with unilateral substantia nigra 6-hydroxydopamine lesions (10 mg/kg i.p.), a behavioral profile similar to that of the D(2) partial agonist aripiprazole. In a rat model predictive of antipsychotic-like activity, WS-50030 and aripiprazole reduced conditioned avoidance responding by 42 and 55% at 10 mg/kg, respectively. Despite aripiprazole's reported lack of effect on serotonin transporters, long-term treatment with aripiprazole or WS-50030 reversed olfactory bulbectomy-induced hyperactivity at doses that did not reduce activity in sham-operated rats, indicating antidepressant-like activity for both compounds. Despite possessing serotonin reuptake inhibitory activity in addition to D(2) receptor partial agonism, WS-50030 displays activity in preclinical models predictive of antipsychotic- and antidepressant efficacy similar to aripiprazole, suggesting potential efficacy of WS-50030 versus positive and negative symptoms of schizophrenia, comorbid mood symptoms, bipolar disorder, major depressive disorder, and treatment-resistant depression. Furthermore, WS-50030 provides a tool to further explore how combining these mechanisms might differentiate from other antipsychotics or antidepressants.

摘要

WS-50030 [7-{4-[3-(1H-茚-3-基)丙基]哌嗪-1-基}-1,3-苯并恶唑-2(3H)-酮]的临床前特征描述如下。体外结合和功能研究显示其对 D(2)受体(D(2L) K(i),4.0 nM)和血清素转运体(K(i),7.1 nM)具有最高亲和力,具有强效 D(2)部分激动剂活性(EC(50),0.38 nM;E(max),30%),并完全阻断血清素转运体(IC(50),56.4 nM)。与这种体外特征一致,WS-50030(10 mg/kg/天,21 天)显著增加了大鼠内侧前额叶皮层的细胞外 5-HT,短期 WS-50030 治疗可阻断阿扑吗啡诱导的攀爬(ID(50),0.51 mg/kg),在产生最小的刻板行为的剂量范围内,在小鼠中,并且在单侧黑质 6-羟多巴胺损伤的大鼠中诱导低水平的对侧旋转(10 mg/kg i.p.),这一行为特征类似于 D(2)部分激动剂阿立哌唑。在一种预测抗精神病样活性的大鼠模型中,WS-50030 和阿立哌唑分别在 10 mg/kg 时将条件回避反应降低了 42%和 55%。尽管阿立哌唑据报道对血清素转运体没有影响,但长期治疗阿立哌唑或 WS-50030 可逆转嗅球切除术诱导的过度活跃,而在未减少假手术大鼠活动的剂量下,这表明这两种化合物均具有抗抑郁样活性。尽管 WS-50030 除了具有 D(2)受体部分激动剂作用外还具有血清素再摄取抑制活性,但它在预测抗精神病和抗抑郁疗效的临床前模型中表现出与阿立哌唑相似的活性,表明 WS-50030 可能对精神分裂症的阳性和阴性症状、共病情绪症状、双相情感障碍、重性抑郁障碍和治疗抵抗性抑郁症有效。此外,WS-50030 提供了一种工具,可进一步探索结合这些机制如何与其他抗精神病药或抗抑郁药区分开来。

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