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Clinical utility of vilazodone for the treatment of adults with major depressive disorder and theoretical implications for future clinical use

机译:维拉唑酮在成人重度抑郁症治疗中的临床应用及其对未来临床应用的理论意义

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Background: Vilazodone is the latest approved antidepressant available in the United States. Its dual mechanism of action combines the inhibition of serotonin transporters while simultaneously partially agonizing serotonin-1a (5-HT1A) receptors. This combined activity results in serotonin facilitation across the brain's serotonergic pathways, which has been termed by the authors as that of a serotonin partial agonist and reuptake inhibitor, or SPARI.Objective: The authors to review laboratory, animal model data, and human trial data to synthesize a working theory regarding the mechanism of antidepressant action of this agent and regarding its potential for additional indications.Methods: A MEDLINE and Internet search was conducted and the resultant evidence reviewed.Results: Vilazodone has randomized, controlled empirical data which has garnered it an approval for treating major depressive disorder. It combines two well-known pharmacodynamic mechanisms of serotonergic action into a novel agent. Although no head-to-head studies against other antidepressants are published, the efficacy data for vilazodone appears comparable to other known antidepressants, with associated gastrointestinal side effects similar to serotonin selective reuptake inhibitor and serotonin norepinephrine reuptake inhibitor antidepressants, but potentially with a lower incidence of sexual side effects and weight gain.Discussion: As a new option for the treatment of major depressive disorder, vilazodone, due to its unique SPARI mechanism of action, may hold promise for patients who cannot tolerate or have not responded to previous antidepressant monotherapies. Additionally, its use may extend to the treatment of other mental health conditions similar to those treated by serotonin selective reuptake inhibitors.
机译:背景:Vilazodone是美国最新批准的抗抑郁药。它的双重作用机制结合了对5-羟色胺转运蛋白的抑制作用,同时部分激动了5-羟色胺-1a(5-HT1A)受体。这种结合的活性导致5-羟色胺促进大脑的5-羟色胺能通路,这被作者称为5-羟色胺部分激动剂和再摄取抑制剂或SPARI。目的:作者审查实验室,动物模型数据和人体试验数据方法:通过MEDLINE和互联网搜索并审查了所得证据。结果:Vilazodone随机获得了可控的经验数据,从而获得了该药物的抗抑郁作用机理及其潜在的其他适应症。批准用于治疗重度抑郁症。它将血清素能作用的两种众所周知的药效学机理结合到一种新型药物中。尽管尚未发表针对其他抗抑郁药的正面研究,但维拉唑酮的疗效数据似乎与其他已知抗抑郁药相当,相关的胃肠道副作用类似于5-羟色胺选择性再摄取抑制剂和5-羟色胺去甲肾上腺素再摄取抑制剂抗抑郁药,但潜在发生率较低讨论:维拉唑酮作为一种治疗重度抑郁症的新选择,由于其独特的SPARI作用机制,可能为无法耐受或对先前抗抑郁单一疗法无反应的患者带来希望。另外,它的用途可以扩展到其他精神健康状况的治疗,类似于通过血清素选择性再摄取抑制剂治疗的精神疾病。

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