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首页> 外文期刊>Frontiers in Psychiatry >Therapeutic Potential of Selectively Targeting the α 2C-Adrenoceptor in Cognition, Depression, and Schizophrenia—New Developments and Future Perspective
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Therapeutic Potential of Selectively Targeting the α 2C-Adrenoceptor in Cognition, Depression, and Schizophrenia—New Developments and Future Perspective

机译:在认知,抑郁和精神分裂症中选择性靶向α 2C -肾上腺素受体的治疗潜力—新进展和未来展望

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α_(2A)- and α_(2C)-adrenoceptors (ARs) are the primary α_(2)-AR subtypes involved in central nervous system (CNS) function. These receptors are implicated in the pathophysiology of psychiatric illness, particularly those associated with affective, psychotic, and cognitive symptoms. Indeed, non-selective α_(2)-AR blockade is proposed to contribute toward antidepressant (e.g., mirtazapine) and atypical antipsychotic (e.g., clozapine) drug action. Both α_(2C)- and α_(2A)-AR share autoreceptor functions to exert negative feedback control on noradrenaline (NA) release, with α_(2C)-AR heteroreceptors regulating non-noradrenergic transmission (e.g., serotonin, dopamine). While the α_(2A)-AR is widely distributed throughout the CNS, α_(2C)-AR expression is more restricted, suggesting the possibility of significant differences in how these two receptor subtypes modulate regional neurotransmission. However, the α_(2C)-AR plays a more prominent role during states of low endogenous NA activity, while the α_(2A)-AR is relatively more engaged during states of high noradrenergic tone. Although augmentation of conventional antidepressant and antipsychotic therapy with non-selective α_(2)-AR antagonists may improve therapeutic outcome, animal studies report distinct yet often opposing roles for the α_(2A)- and α_(2C)-ARs on behavioral markers of mood and cognition, implying that non-selective α_(2)-AR antagonism may compromise therapeutic utility both in terms of efficacy and side-effect liability. Recently, several highly selective α_(2C)-AR antagonists have been identified that have allowed deeper investigation into the function and utility of the α_(2C)-AR. ORM-13070 is a useful positron emission tomography ligand, ORM-10921 has demonstrated antipsychotic, antidepressant, and pro-cognitive actions in animals, while ORM-12741 is in clinical development for the treatment of cognitive dysfunction and neuropsychiatric symptoms in Alzheimer’s disease. This review will emphasize the importance and relevance of the α_(2C)-AR as a neuropsychiatric drug target in major depression, schizophrenia, and associated cognitive deficits. In addition, we will present new prospects and future directions of investigation.
机译:α_(2A)-和α_(2C)-肾上腺素能受体(ARs)是参与中枢神经系统(CNS)功能的主要α_(2)-AR亚型。这些受体与精神病的病理生理有关,特别是与情感,精神病和认知症状有关的那些。确实,提出了非选择性的α_(2)-AR阻断有助于抗抑郁药(例如米氮平)和非典型抗精神病药(例如氯氮平)的药物作用。 α_(2C)-和α_(2A)-AR均具有自体受体功能,可对去甲肾上腺素(NA)释放施加负反馈控制,而α_(2C)-AR异体受体可调节非去甲肾上腺素能传递(例如5-羟色胺,多巴胺)。尽管α_(2A)-AR在整个中枢神经系统中分布广泛,但α_(2C)-AR的表达受到更多限制,这表明这两种受体亚型调节区域神经传递的方式可能存在重大差异。然而,α_(2C)-AR在低内源性NA活性状态下起着更为突出的作用,而α_(2A)-AR在高去甲肾上腺素能状态下的参与度相对较高。尽管使用非选择性α_(2)-AR拮抗剂增强常规抗抑郁药和抗精神病药物的治疗效果可能会有所改善,但动物研究报告称,α_(2A)-和α_(2C)-ARs在行为标志物上具有截然不同但往往相反的作用情绪和认知,这意味着非选择性α_(2)-AR拮抗作用可能会在功效和副作用责任方面损害治疗效用。最近,已鉴定出几种高度选择性的α_(2C)-AR拮抗剂,可以更深入地研究α_(2C)-AR的功能和用途。 ORM-13070是一种有用的正电子发射断层扫描配体,ORM-10921在动物中具有抗精神病,抗抑郁和促认知作用,而ORM-12741正在临床开发中,用于治疗阿尔茨海默氏病的认知功能障碍和神经精神症状。这篇综述将强调α_(2C)-AR作为严重抑郁症,精神分裂症和相关的认知缺陷的神经精神药物靶标的重要性和相关性。此外,我们将介绍新的前景和未来的研究方向。

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