阿戈美拉汀治疗广泛性焦虑障碍:关注其独特的作用机制。

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Psychopharmacology Pub Date : 2022-06-30 eCollection Date: 2022-01-01 DOI:10.1177/20451253221105128
Mark J Millan
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引用次数: 9

摘要

广泛性焦虑症(GAD)是焦虑症最常见的诊断形式,通常通过认知行为方法或药物治疗;特别是苯二氮卓类药物(急性)和5 -羟色胺或5 -羟色胺/去甲肾上腺素再摄取抑制剂(长期)。然而,有效性、依从性和可接受性远非理想,这增强了人们对替代方案的兴趣。临床上用于治疗重度抑郁症的阿戈美拉汀在啮齿动物中表现出抗焦虑特性,并在几项双盲、短期(12周)和预防复发(6个月)研究中有效治疗广泛性焦虑症(包括重症患者)。在有效剂量下,不良反应的发生率并不高于安慰剂。阿戈美拉汀具有独特的结合谱,作为褪黑激素(MT1/MT2)受体激动剂和5-HT2C受体拮抗剂,但既不识别单胺转运体,也不识别GABAA受体。大量证据支持5-HT2C受体在诱导焦虑状态中的作用,它们的阻断可能在介导阿戈美拉汀的抗焦虑作用中起主要作用,包括杏仁核和终纹床核以及海马体中的种群。MT受体在视交叉上核、丘脑网状核和海马中的募集似乎发挥了互补作用。在5-HT2C和MT受体的下游,调节应激敏感的谷氨酸能回路,改变促焦虑神经肽、促肾上腺皮质激素释放因子和抗利尿激素的释放,可能与阿戈美拉汀的作用有关。总之,阿戈美拉汀发挥其抗焦虑作用的机制与目前用于治疗广泛性焦虑症的其他药物明显不同。简明扼要:阿戈美拉汀如何帮助治疗焦虑症。•焦虑症对生活质量有显著的负面影响。•最常见的焦虑症类型,被称为广泛性焦虑症(GAD),与紧张和过度担忧有关。•这些症状可能导致其他症状,如疲劳、失眠、易怒和注意力不集中。广泛性焦虑症通常通过认知行为疗法或药物治疗。然而,广泛使用的药物如苯二氮卓类药物和血清素再摄取抑制剂有副作用。•阿戈美拉汀是一种公认的抗抑郁药物,在大鼠身上显示出降低焦虑(“抗焦虑”)的特性,并被证明能有效治疗广泛性焦虑症,副作用最小。然而,它究竟是如何作用于大脑来控制广泛性焦虑症的尚不清楚。因此,本综述旨在阐明阿戈美拉汀治疗广泛性焦虑症的作用机制。方法:•作者回顾了阿戈美拉汀治疗动物焦虑的研究。•他们还研究了阿戈美拉汀对广泛性焦虑症患者的影响。结果:•研究表明阿戈美拉汀“阻断”神经细胞中的一种受体,这种受体在引起焦虑中起作用,称为5-HT2C受体。•阻断这种受体,特别是在特定的大脑区域,如杏仁核的神经细胞、末纹床核和海马体,产生阿戈美拉汀治疗期间所见的焦虑减少。•阿戈美拉汀还能激活褪黑激素(MT)受体,这种受体被认为能控制焦虑,促进睡眠,维持睡眠周期。因此阿戈美拉汀可以解决广泛性焦虑症患者常见的睡眠障碍。•除了5-HT2C和MT受体外,已知与焦虑症有关的神经细胞中的信号分子(称为“神经递质”和“神经肽”)也受到阿戈美拉汀的影响。结论:阿戈美拉汀的抗焦虑作用是由不同于目前用于治疗广泛性焦虑症的其他药物的机制引起的。•这解释了其治疗成功和最小的不良副作用。
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Agomelatine for the treatment of generalized anxiety disorder: focus on its distinctive mechanism of action.

Generalized anxiety disorder (GAD), the most frequently diagnosed form of anxiety, is usually treated by cognitive-behavioural approaches or medication; in particular, benzodiazepines (acutely) and serotonin or serotonin/noradrenaline reuptake inhibitors (long term). Efficacy, compliance, and acceptability are, however, far from ideal, reinforcing interest in alternative options. Agomelatine, clinically employed in the treatment of major depression, expresses anxiolytic properties in rodents and was effective in the treatment of GAD (including severely ill patients) in several double-blind, short-term (12 weeks) and relapse-prevention (6 months) studies. At active doses, the incidence of adverse effects was no higher than for placebo. Agomelatine possesses a unique binding profile, behaving as a melatonin (MT1/MT2) receptor agonist and 5-HT2C receptor antagonist, yet recognizing neither monoamine transporters nor GABAA receptors. Extensive evidence supports a role for 5-HT2C receptors in the induction of anxious states, and their blockade likely plays a primary role in mediating the anxiolytic actions of agomelatine, including populations in the amygdala and bed nucleus of stria terminalis, as well as the hippocampus. Recruitment of MT receptors in the suprachiasmatic nucleus, thalamic reticular nucleus, and hippocampus appears to fulfil a complimentary role. Downstream of 5-HT2C and MT receptors, modulation of stress-sensitive glutamatergic circuits and altered release of the anxiogenic neuropeptides, corticotrophin-releasing factor, and vasopressin, may be implicated in the actions of agomelatine. To summarize, agomelatine exerts its anxiolytic actions by mechanisms clearly distinct from those of other agents currently employed for the management of GAD.

Plain language summary: How agomelatine helps in the treatment of anxiety disorders.

Introduction: • Anxiety disorders have a significant negative impact on quality of life.• The most common type of anxiety disorder, called generalized anxiety disorder (GAD), is associated with nervousness and excessive worry.• These symptoms can lead to additional symptoms like tiredness, sleeplessness, irritability, and poor attention.• GAD is generally treated through either cognitive-behavioural therapy or medication. However, widely used drugs like benzodiazepines and serotonin reuptake inhibitors have adverse effects.• Agomelatine, a well-established antidepressant drug, has shown anxiety-lowering ('anxiolytic') properties in rats and has been shown to effectively treat GAD with minimal side effects.• However, exactly how it acts on the brain to manage GAD is not yet clear.• Thus, this review aims to shed light on agomelatine's mechanism of action in treating GAD.

Methods: • The authors reviewed studies on how agomelatine treats anxiety in animals.• They also looked at clinical studies on the effects of agomelatine in people with GAD.

Results: • The study showed that agomelatine 'blocks' a receptor in nerve cells, which plays a role in causing anxiety, called the 5-HT2C receptor.• Blocking this receptor, especially in specific brain regions such as nerve cells of the amygdala, bed nucleus of stria terminalis, and hippocampus, produced the anxiety reduction seen during agomelatine treatment.• Agomelatine also activates the melatonin (MT) receptor, which is known to keep anxiety in check, promote sleep, and maintain the sleep cycle.• Agomelatine should thus tackle sleep disturbances commonly seen in patients with GAD.• Beyond 5-HT2C and MT receptors, signalling molecules in nerve cells that are known to be involved in anxiety disorders (called 'neurotransmitters' and 'neuropeptides') are also affected by agomelatine.

Conclusion: • Agomelatine's anxiolytic effects are caused by mechanisms that are distinct from those of other medications currently used to treat GAD.• This explains its therapeutic success and minimal adverse side effects.

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来源期刊
CiteScore
7.90
自引率
2.40%
发文量
35
审稿时长
10 weeks
期刊介绍: Therapeutic Advances in Psychopharmacology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of psychopharmacology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in psychopharmacology, providing a forum in print and online for publishing the highest quality articles in this area.
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