SEROTONERGIC MECHANISMS IN ANXIETY

被引:69
作者
EISON, AS [1 ]
EISON, MS [1 ]
机构
[1] BRISTOL MYERS SQUIBB CO, CNS DRUG DISCOVERY, WALLINGFORD, CT 06492 USA
关键词
ANXIETY; AZAPIRONE BENZODIAZEPINE; 5HT(1A) RECEPTOR; 5HT(2) RECEPTOR; 5-HT3; RECEPTOR; SEROTONIN;
D O I
10.1016/0278-5846(94)90023-X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Eison, Arlene, S. and Michael S. Eison: Serotonergic Mechanisms in Anxiety. Frog. Neuro-Psychopharmacol. and Biol. Psychiat. 1994, 18(1): 47-62. 1. Anatomical, behavioral, neurochemical and electrophysiological evidence collectively support a role for central 5-HT in the modulation of anxiety and the anti-anxiety action of the benzodiazepines. 2. The advent of selective agonists and antagonists for 5-HT receptor subtypes (5-HT1, 5-HT2, 5-HT3) has rekindled investigation of the role of 5-HT in anxiety mechanisms. 3. The azapirones represent a new class of agent: which possesses affinity for 5-HT1A receptors (partial agonists) and is active in anxiolytic animal models as well as in the clinic (buspirone) 4. While preclinical data supporting the anxiolytic potential of 5-HT2 antagonists remains controversial, a recent clinical study supports ritanserin's anxiolytic effects. 5. Several animal models support the anxiolytic potential of the 5-HT3 antagonist odansetron (GR38032F). Confirmation of it's therapeutic utility awaits clinical results.
引用
收藏
页码:47 / 62
页数:16
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