Department of Neuroscience, Faculty of Science, Carleton University, 3414 Herzberg, 1125 Colonel By Drive, Ottawa, K1S 5B6, ON, Canada.
Curr Neuropharmacol. 2017 Nov 14;15(8):1192-1207. doi: 10.2174/1570159X15666170413115754.
The treatment of schizophrenia is challenging due to the wide range of symptoms (positive, negative, cognitive) associated with the disease. Typical antipsychotics that antagonize D2 receptors are effective in treating positive symptoms, but extrapyramidal side-effects (EPS) are a common occurrence. Atypical antipsychotics targeting 5-HT2A and D2 receptors are more effective at treating cognitive and negative symptoms compared to typical antipsychotics, but these drugs also result in side-effects such as metabolic syndromes.
To identify evidence in the literature that elucidates the pharmacological profile of aripiprazole.s.
We searched PubMed for peer reviewed articles on aripiprazole and its clinical efficacy, side-effects, pharmacology, and effects in animal models of schizophrenia symptoms.
Aripiprazole is a newer atypical antipsychotic that displays a unique pharmacological profile, including partial D2 agonism and functionally selective properties. Aripiprazole is effective at treating the positive symptoms of schizophrenia and has the potential to treat negative and cognitive symptoms at least as well as other atypical antipsychotics. The drug has a favorable side-effect profile and has a low propensity to result in EPS or metabolic syndromes. Animal models of schizophrenia have been used to determine the efficacy of aripiprazole in symptom management. In these instances, aripiprazole resulted in the reversal of deficits in extinction, pre-pulse inhibition, and social withdrawal. Because aripiprazole requires a greater than 90% occupancy rate at D2 receptors to be clinically active and does not produce EPS, this suggests a functionally selective effect on intracellular signaling pathways.
A combination of factors such as dopamine system stabilization via partial agonism, functional selectivity at D2 receptors, and serotonin-dopamine system interaction may contribute to the ability of aripiprazole to successfully manage schizophrenia symptoms. This review examines these mechanisms of action to further clarify the pharmacological actions of aripiprazole.
由于与该疾病相关的广泛症状(阳性、阴性、认知),精神分裂症的治疗具有挑战性。拮抗 D2 受体的典型抗精神病药在治疗阳性症状方面有效,但锥体外系副作用(EPS)很常见。与典型抗精神病药相比,针对 5-HT2A 和 D2 受体的非典型抗精神病药在治疗认知和阴性症状方面更有效,但这些药物也会导致代谢综合征等副作用。
确定文献中阐明阿立哌唑药理学特征的证据。
我们在 PubMed 上搜索了关于阿立哌唑及其临床疗效、副作用、药理学和在精神分裂症症状动物模型中的作用的同行评议文章。
阿立哌唑是一种新型非典型抗精神病药,具有独特的药理学特征,包括部分 D2 激动作用和功能选择性。阿立哌唑在治疗精神分裂症的阳性症状方面有效,并且至少与其他非典型抗精神病药一样有潜力治疗阴性和认知症状。该药物具有良好的副作用谱,并且不易导致 EPS 或代谢综合征。精神分裂症动物模型已被用于确定阿立哌唑在症状管理中的疗效。在这些情况下,阿立哌唑导致消退、前脉冲抑制和社交回避的缺陷得到逆转。由于阿立哌唑在临床上需要达到 D2 受体 90%以上的占有率才能发挥作用,并且不会产生 EPS,这表明它对细胞内信号通路具有功能选择性作用。
通过部分激动作用稳定多巴胺系统、D2 受体的功能选择性以及 5-HT 与多巴胺系统相互作用等因素的结合,可能有助于阿立哌唑成功管理精神分裂症症状。本综述检查了这些作用机制,以进一步阐明阿立哌唑的药理学作用。