Agomelatine: An Astounding Sui-generis Antidepressant?

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Muhammad Naveed, Lian-Di Li, Gang Sheng, Zi-Wei Du, Ya-Ping Zhou, Sun Nan, Ming-Yi Zhu, Jing Zhang, Qi-Gang Zhou
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引用次数: 4

Abstract

Major depressive disorder (MDD) is one of the foremost causes of disability and premature death worldwide. Although the available antidepressants are effective and well tolerated, they also have many limitations. Therapeutic advances in developing a new drug's ultimate relation between MDD and chronobiology, which targets the circadian rhythm, led to a renewed focus on psychiatric disorders. In order to provide a critical analysis about antidepressant properties of agomelatine, a detailed PubMed (Medline), Scopus (Embase), Web of Science (Web of Knowledge), Cochrane Library, Google Scholar, and PsycInfo search was performed using the following keywords: melatonin analog, agomelatine, safety, efficacy, adverse effects, pharmacokinetics, pharmacodynamics, circadian rhythm, sleep disorders, neuroplasticity, MDD, bipolar disorder, anhedonia, anxiety, generalized anxiety disorder (GAD), and mood disorders. Agomelatine is a unique melatonin analog with antidepressant properties and a large therapeutic index that improves clinical safety. Published articles revealed that agomelatine is a melatonin receptors (MT1 and MT2) agonist and 5HT2C receptor antagonist. The effects receptors' on melatonin receptors enable the resynchronization of irregular circadian rhythms with beneficial effects on sleep architectures. In this way, agomelatine is accredited for its unique mode of action, which helps to exert antidepressant effects and resynchronize the sleep-wake cycle. To sum up, an agomelatine has not only antidepressant properties but also has anxiolytic effects.

阿戈美拉汀:令人震惊的瑞士抗抑郁药?
重度抑郁症(MDD)是世界范围内导致残疾和过早死亡的主要原因之一。尽管现有的抗抑郁药有效且耐受性良好,但它们也有许多局限性。在开发一种新的药物的治疗进展之间的重度抑郁症和时间生物学的最终关系,目标是昼夜节律,导致重新关注精神疾病。为了提供关于阿戈美拉汀抗抑郁特性的批判性分析,使用以下关键词进行了详细的PubMed (Medline), Scopus (Embase), Web of Science (Web of Knowledge), Cochrane Library, Google Scholar和PsycInfo搜索:褪黑素类似物、阿戈美拉汀、安全性、有效性、不良反应、药代动力学、药效学、昼夜节律、睡眠障碍、神经可塑性、重度抑郁症、双相情感障碍、快感缺乏、焦虑、广泛性焦虑症(GAD)和情绪障碍。阿戈美拉汀是一种独特的褪黑素类似物,具有抗抑郁特性和大的治疗指数,可提高临床安全性。已发表的文章显示阿戈美拉汀是褪黑激素受体(MT1和MT2)激动剂和5HT2C受体拮抗剂。受体对褪黑激素受体的影响使不规则的昼夜节律重新同步,对睡眠结构有有益的影响。通过这种方式,阿戈美拉汀以其独特的作用方式获得认可,有助于发挥抗抑郁作用并重新同步睡眠-觉醒周期。综上所述,阿戈美拉汀不仅具有抗抑郁的特性,而且具有抗焦虑的作用。
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来源期刊
Current molecular pharmacology
Current molecular pharmacology Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
4.90
自引率
3.70%
发文量
112
期刊介绍: Current Molecular Pharmacology aims to publish the latest developments in cellular and molecular pharmacology with a major emphasis on the mechanism of action of novel drugs under development, innovative pharmacological technologies, cell signaling, transduction pathway analysis, genomics, proteomics, and metabonomics applications to drug action. An additional focus will be the way in which normal biological function is illuminated by knowledge of the action of drugs at the cellular and molecular level. The journal publishes full-length/mini reviews, original research articles and thematic issues on molecular pharmacology. Current Molecular Pharmacology is an essential journal for every scientist who is involved in drug design and discovery, target identification, target validation, preclinical and clinical development of drugs therapeutically useful in human disease.
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