期刊文献+

新型抗抑郁药:左米那普仑 被引量:10

Levomilnacipran: a new drug for treatment of major depressive disorder
原文传递
导出
摘要 左米那普仑缓释胶囊在2013年7月被美国国家食品药物监督管理局批准上市,用于抑郁症的治疗。左米那普仑作为米那普仑的活性异构体,属于5-羟色胺-去甲肾上腺素再摄取抑制剂(SNRI)。与SNRI类其他药物相比,左米那普仑抑制去甲肾上腺素转运体的能力更强。一些临床研究已经表明左米那普仑安全性、耐受性较好且疗效优于安慰剂。因此,在对当前抗抑郁药治疗无效或不能耐受时,左米那普仑能为我们提供一个新的选择。本文就左米那普仑的药理作用、药动学、临床疗效、安全性、耐受性等方面进行综述。 In July 2013, the US Federal Drug Administration (FDA) approved levomilnacipran extended release for the treatment of major depressibve disorder (MDD) in adult patients. Levomilnacipran, the more active enantiomer of milnacipran, is a potent and selective serotonin norepinephrine reuptake inhibitor. In contrast with other selective serotonin norepinephrine reuptake inhibitors, it has greater selectivity for inhibiting norepinephrine reuptake than serotonin reuptake. In clinical trials, levomilnacipran was generally safe and well tolerated. In addition, it has been shown to be more effective than placebo. As a result, levomilnacipran is a new choice especially for the MDD patients who either don' t respond to or don' t tolerate current antidepressants. The aim of this review was to review the mechanism of action, pharmacodynamics, pharmacokinetics, clinical efficacy, and safety and tolerability of levomilnacipran in this paper.
出处 《中国新药与临床杂志》 CAS CSCD 北大核心 2015年第6期418-422,共5页 Chinese Journal of New Drugs and Clinical Remedies
关键词 左米那普仑 抑郁症 肾上腺素能摄取抑制剂 药物耐受性 levomilnacipran depressive disorder adrenergic uptake inhibitors drug tolerability
  • 相关文献

参考文献15

  • 1MATHERS CD, LONCAR D. Projections of global mortality and burden of disease from 2002 to 2030 [J]. PLoS Med, 2006, 3 (11): e442. 被引量:1
  • 2QASEEM A, SNOW V, DENBERG TD, et ol. Using second- generation antidepressants to treat depressive disorders: a clinical practice guideline from the American college of physicians[J]. Ann Intern Med, 2008, 149(10): 725-733. 被引量:1
  • 3STAHL SM, GRADY MM, MORET C, et al. SNRIs: their pharmacology, clinical efficacy, and tolerability in comparison with other classes of antidepressants[J]. CNS Spectr, 2005, 10(9) : 732-747. 被引量:1
  • 4PAPAKOSTAS GI, THASE ME, FAVA M, et ol. Are antidepressant drugs that combine serotonergic and noradrenergic mechanisms of action more effective than the selective serotonin reuptake inhibitors in treating major depressive disorder.'? A meta- analysis of studies of newer agents [J]. Biol Psychiatry, 2007, 62(11): 1217-1227. 被引量:1
  • 5HUTT AJ, VANETOVA J. The chiral switch: the development of single enantiomer drugs from racemates Acta Facult. Pharm[EB/ OL]. (2010-04-20) [2014-03-04]. https://www.fpharm.uniba. sk/fileadmirduser_upload/admin/Acta_facultatis/Tomus L/Pharm - 02 Hutt AJ-Valentov_i_J.pdf. 被引量:1
  • 6FDA. Guidance on the Development of New Stereoisomeric Drugs [EB/OL]. ( 1992-05-01 )[2014-05-01].http ://www.fda.gov/ DrugslGuidanceComplianceRegulatory 122883.htm. 被引量:1
  • 7AUCLAIR AL, MARTEL JC, ASSIE MB, et ol. Levomilnacipran (F2695), a norepinephrine-preferring SNRI: profile in vitro and in models of depression and anxiety[J]. Neuropharmacology, 2013, 70 : 338-347. 被引量:1
  • 8FDA. Levomilnaeiprar[EB/OLJ. (2013 -07 -25) 2014 -05 -01J. http ://www.accessdata.fda.gov/drugsatfdadoes/label/2013/204 168s000lbl.pdf. 被引量:1
  • 9MONTGOMERY SA, MANSUY L, RUTH A, et ol. Efficacy and safety of levomilnacipran sustained release in moderate to severe major depressive disorder: a randomized, double-blind, placebo- controlled, proof-of-concept study[J]. J Clin Psychiatry, 2013, 74(4) : 363-369. 被引量:1
  • 10BAKISH D, GOMMOLL C, CHEN C, et ol. Levomilnacipran ER 40 mg and 80 mg in patients with major depressive disorder: a phase , randomized, double-blind, fixed-dose, placebo- controlled study[J]. J Psychiatry Neurosci, 2014, 39(1 ): 40-49. 被引量:1

同被引文献74

引证文献10

二级引证文献37

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部