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Neuropeptide systems as novel therapeutic targets for depression and anxiety disorders
被引:327
作者:

Holmes, A
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机构:
NIAAA, Sect Behav Sci & Genet, Bethesda, MD 20892 USA NIAAA, Sect Behav Sci & Genet, Bethesda, MD 20892 USA

Heilig, M
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h-index: 0
机构: NIAAA, Sect Behav Sci & Genet, Bethesda, MD 20892 USA

Rupniak, NMJ
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h-index: 0
机构: NIAAA, Sect Behav Sci & Genet, Bethesda, MD 20892 USA

Steckler, T
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机构: NIAAA, Sect Behav Sci & Genet, Bethesda, MD 20892 USA

Griebel, G
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机构: NIAAA, Sect Behav Sci & Genet, Bethesda, MD 20892 USA
机构:
[1] NIAAA, Sect Behav Sci & Genet, Bethesda, MD 20892 USA
[2] Karolinska Inst, Div Psychiat, NEUROTEC Dept, Stockholm, Sweden
[3] Merck Res Labs, West Point, PA 19456 USA
[4] Janssen Pharmaceut NV, Johnson & Johnson Pharmaceut Res & Dev, Beerse, Belgium
[5] Dept Psychopharmacol, Bagneux, France
关键词:
D O I:
10.1016/j.tips.2003.09.011
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The health burden of stress-related diseases, including depression and anxiety disorders, is rapidly increasing, whereas the range of available pharmacotherapies to treat these disorders is limited and suboptimal with regard to efficacy and tolerability. Recent findings support a major role for neuropeptides in mediating the response to stress and thereby identify neuropeptide systems as potential novel therapeutic targets for the treatment of depression and anxiety disorders. In preclinical models, pharmacological and/or genetic manipulation of substance P, corticotropin-releasing factor (CRF), vasopressin, neuropeptide Y and galanin function alters anxiety- and depression-related responses. Recently, specific and highly potent small-molecule neuropeptide receptor agonists and antagonists have been developed that can readily cross the blood-brain barrier. Clinical assessment of several compounds is currently underway, with antidepressant efficacy confirmed in double-blind, placebo-controlled trials of tachykinin NK1 (substance P) receptor antagonists, and preliminary evidence of antidepressant activity in an open-label trial of a CRF1 receptor antagonist.
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页码:580 / 588
页数:9
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