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基于知识的多靶点血清素受体靶向长链芳基哌嗪衍生物的设计:治疗自闭症谱系障碍的潜在候选药物。

Knowledge-Based Design of Long-Chain Arylpiperazine Derivatives Targeting Multiple Serotonin Receptors as Potential Candidates for Treatment of Autism Spectrum Disorder.

机构信息

Dipartimento di Farmacia-Scienze del Farmaco, Università degli Studi di Bari Aldo Moro, via Orabona, 4, 70125 Bari, Italy.

Center for Research in Molecular Medicine and Chronic Diseases (CIMUS). Universidade de Santiago de Compostela. Avda. de Barcelona, s/n, 15782 Santiago de Compostela, Spain.

出版信息

ACS Chem Neurosci. 2021 Apr 21;12(8):1313-1327. doi: 10.1021/acschemneuro.0c00647. Epub 2021 Apr 1.

DOI:10.1021/acschemneuro.0c00647
PMID:33792287
Abstract

Autism spectrum disorder (ASD) includes a group of neurodevelopmental disorders characterized by core symptoms such as impaired social interaction and communication, repetitive and stereotyped behaviors, and restricted interests. To date, there are no effective treatments for these core symptoms. Several studies have shown that the brain serotonin (5-HT) neurotransmission system is altered in both ASD patients and animal models of the disease. Multiple pieces of evidence suggest that targeting 5-HT receptors may treat the core symptoms of ASD and associated intellectual disabilities. In fact, stimulation of the 5-HT receptor reduces repetitive and restricted behaviors; blockade of the 5-HT receptor reduces both learning deficits and repetitive behavior, and activation of the 5-HT receptor improves cognitive performances and reduces repetitive behavior. On such a basis, we have designed novel arylpiperazine derivatives pursuing unprecedently reported activity profiles: dual 5-HT/5-HT receptor agonist properties and mixed 5-HT agonist/5-HT agonist/5-HT antagonist properties. Seventeen new compounds were synthesized and tested in radioligand binding assay at the target receptors. We have identified the dual 5-HTR/5-HTR agonists and and the mixed 5-HTR agonist/5-HTR agonist/5-HTR antagonist . These compounds are metabolically stable in vitro and have suitable central nervous system druglike properties.

摘要

自闭症谱系障碍(ASD)包括一组神经发育障碍,其特征是存在核心症状,如社交互动和沟通受损、重复和刻板行为以及兴趣受限。迄今为止,这些核心症状还没有有效的治疗方法。多项研究表明,自闭症患者和疾病动物模型的大脑 5-羟色胺(5-HT)神经递质系统都发生了改变。多项证据表明,靶向 5-HT 受体可能治疗 ASD 的核心症状和相关的智力障碍。事实上,5-HT 受体的刺激可减少重复和受限的行为;5-HT 受体的阻断可减少学习缺陷和重复行为,而 5-HT 受体的激活可改善认知表现并减少重复行为。在此基础上,我们设计了新型芳基哌嗪衍生物,追求前所未有的活性谱:双重 5-HT/5-HT 受体激动剂特性和混合 5-HT 激动剂/5-HT 激动剂/5-HT 拮抗剂特性。合成了十七种新化合物,并在目标受体的放射性配体结合测定中进行了测试。我们已经确定了双重 5-HTR/5-HTR 激动剂 和 以及混合 5-HTR 激动剂/5-HTR 激动剂/5-HTR 拮抗剂 。这些化合物在体外具有代谢稳定性和适当的中枢神经系统类药性。

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