4.7 Review

Review of Pharmacological Treatment in Mood Disorders and Future Directions for Drug Development

期刊

NEUROPSYCHOPHARMACOLOGY
卷 37, 期 1, 页码 77-101

出版社

SPRINGERNATURE
DOI: 10.1038/npp.2011.198

关键词

mood disorders; clinical pharmacology; clinical trials; neurotransmission; circadian; signal transduction

资金

  1. NIMH
  2. American Foundation for Suicide Prevention (AFSP)
  3. Corcept
  4. Ortho-McNeil-Janssen
  5. Otsuka
  6. Novartis
  7. NIAAA
  8. National Alliance for Schizophrenia and Depression (NARSAD)
  9. Mayo Foundation
  10. Pfizer
  11. AHRQ
  12. NARSAD
  13. Bristol-Myers Squibb
  14. Eli Lilly and Company
  15. Euthymics Bioscience
  16. Forest Pharmaceuticals
  17. Janssen Pharmaceutica
  18. Novartis Pharmaceuticals
  19. Otsuka Pharmaceuticals
  20. Pamlab
  21. Pfizer Inc.
  22. Repligen Corp.
  23. St Jude Medical

向作者/读者索取更多资源

After a series of serendipitous discoveries of pharmacological treatments for mania and depression several decades ago, relatively little progress has been made for novel hypothesis-driven drug development in mood disorders. Multifactorial etiologies of, and lack of a full understanding of, the core neurobiology of these conditions clearly have contributed to these development challenges. There are, however, relatively novel targets that have raised opportunities for progress in the field, such as glutamate and cholinergic receptor modulators, circadian regulators, and enzyme inhibitors, for alternative treatment. This review will discuss these promising new treatments in mood disorders, the underlying mechanisms of action, and critical issues of their clinical application. For these new treatments to be successful in clinical practice, it is also important to design innovative clinical trials that identify the specific actions of new drugs, and, ideally, to develop biomarkers for monitoring individualized treatment response. It is predicted that future drug development will identify new agents targeting the molecular mechanisms involved in the pathophysiology of mood disorders. Neuropsychopharmacology Reviews (2012) 37, 77-101; doi: 10.1038/npp.2011.198; published online 7 September 2011

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