摘要
多年来,无论是第一代(FGAs)和第二代抗精神病药物(SGAs),持续获得有效治疗精神病症状的增长证据。目前,虽然他们被广泛应用于精神病性抑郁症和其他临床条件,如搅拌和/或行为障碍,但是他们代表的第一线治疗精神分裂症和双相情感障碍。尽管是代表治疗严重的精神病性疾病一个不可缺少的工具,但是他们被广泛知道有一些不必要的副作用,临床医生必须意识到并仔细处理,为病人提供最好的短期和长期治疗。然而,尽管考虑到一些最有效的第二代抗精神病药物长期使用,临床医生一定不要忽视风险与发病的潜在的严重的代谢副作用,如体重增加,血脂异常,胰岛素抵抗和II型糖尿病。 Asenapine是欧洲许可的一个最新的第二代抗精神病药物,用于治疗精神分裂症和美国精神分裂症的治疗。它属于氯氮平,奥氮平和喹硫平同一类,与他们分享一个相当复杂的药理结合剖面。事实上,Asenapine显示高亲和力的5-羟色胺(5-HT)2A型受体 (5HT2A) 和在较小程度上的2型多巴胺受体(D2),类似于其他第二代抗精神病药物。Asenapine的行为也在5-羟色胺(5-HT)2C型受体,H1和α2 -受体拮抗剂水平。Asenapine被报道有效单独用药或与情绪稳定剂(锂、丙戊酸钠)组合使用在躁狂或混合发作的治疗,相比第二代抗精神病药物具有较低的倾向,诱导,或遵循,抑郁症状。这些独特的属性可能解释了对使用这种药物在混合状态越来越大的兴趣,除了精神分裂症和急性狂热。 本文的目的是检讨现行的药理性质和Asenapine临床使用数据,以及对未来可能的这种第二代抗精神病药物的指示。
关键词: 抗精神病药物,双相情感障碍,精神病,精神分裂症,第二代抗精神病药。
Current Medicinal Chemistry
Title:Current Trends on Antipsychotics: Focus on Asenapine
Volume: 23 Issue: 21
Author(s): Donatella Marazziti, Armando Piccinni, Stefano Baroni, Francesco Mungai, Silvio Presta, Federico Mucci and Liliana Dell'Osso
Affiliation:
关键词: 抗精神病药物,双相情感障碍,精神病,精神分裂症,第二代抗精神病药。
摘要: Over the years, both first- (FGAs) and second-generation antipsychotics (SGAs), continue to gain increasing evidence of being effective in the treatment of psychotic symptoms. Currently, they represent the first-line treatment of schizophrenia and bipolar disorder, although they are widely used in psychotic depression and other clinical conditions, such as agitation and/or behavioural disturbances. Despite representing an indispensable tool for the treatment of severe psychotic disorders, they are widely known to have a number of unwanted side effects that the clinician must be aware of, and handle carefully to provide the patient the best available treatment in the short and long-term. However, even with respect to the long-term use of some of the most effective SGAs, it is imperative for clinicians not to overlook the risk linked to the onset of potentially severe metabolic side effects such as weight gain, dyslipidaemia, insulinresistance and type II diabetes.
Asenapine is one of the newest SGAs licenced in Europe for the treatment of manic episodes and in the US for schizophrenia. It belongs to the same class of clozapine, olanzapine and quetiapine, sharing with them a rather complex pharmacological binding profile. In fact, asenapine shows a high affinity for the serotonin (5HT) receptor of the type 2A (5HT2A) and to a lesser extent for the dopamine receptor of the type 2 (D2), similar to other SGAs. Asenapine behaves also as an antagonist at the level of 5HT2C, H1 and α2-receptors. Asenapine has been reported to be effective either in monotherapy or in combination with mood stabilers (lithium and valproate) in the treatment of manic or mixed episodes, with a lower propensity to induce, or being followed by, depressive symptoms, when compared to other SGAs. These unique properties may explain the increasing interest towards the use of this drug in mixed states, besides schizophrenia and acute mania.
The aim of this paper was at reviewing current data on pharmacological properties and clinical use of asenapine, as well as on possible future indication of this SGA.
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Cite this article as:
Donatella Marazziti, Armando Piccinni, Stefano Baroni, Francesco Mungai, Silvio Presta, Federico Mucci and Liliana Dell'Osso , Current Trends on Antipsychotics: Focus on Asenapine, Current Medicinal Chemistry 2016; 23 (21) . https://dx.doi.org/10.2174/0929867323666160525115014
DOI https://dx.doi.org/10.2174/0929867323666160525115014 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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