Anxiolytic-like effects of PNU-101017, a partial agonist at the benzodiazepine receptor

被引:0
|
作者
A. H. Tang
S. R. Franklin
D. B. Carter
V. H. Sethy
L. M. Needham
E. J. Jacobsen
P. F. Von Voigtlander
机构
[1] CNS Diseases Research 7251-209-406,
[2] Pharmacia & Upjohn Inc.,undefined
[3] 301 Henrietta Street,undefined
[4] Kalamazoo,undefined
[5] MI 49001,undefined
[6] USA Fax (+1) 616/833-2525,undefined
[7] Structural,undefined
[8] Analytical and Medicinal Chemistry,undefined
[9] Pharmacia & Upjohn Inc.,undefined
[10] 301 Henrietta Street,undefined
[11] Kalamazoo,undefined
[12] MI 49001,undefined
[13] USA,undefined
来源
Psychopharmacology | 1997年 / 131卷
关键词
Key words GABAA receptor; Benzodiazepine; Partial agonist; Anxiolytic;
D O I
暂无
中图分类号
学科分类号
摘要
PNU-101017 is a chemically novel ligand at the benzodiazepine recognition site of cloned GABAA receptors. It was reported to potentiate GABA-mediated chloride current in cultured cells with a moderate intrinsic activity and a biphasic dose-response relationship. In this study, we confirmed that PNU-101017 has a partial agonist-like effect in the antagonism of metrazole-induced seizures in mice. It produced no sedation or ataxia, but did antagonize diazepam-induced motor deficit of mice in the rotarod test. PNU-101017 was weakly active in anti-conflict anxiolytic tests, but attenuated the plasma corticosteroid response to mild stress in rats. It also antagonized stress-induced elevation of cerebellar cGMP levels in mice. Like chlordiazepoxide, it increased drinking of saline solution in thirsty rats. PNU-101017 did not potentiate the CNS-depressant effects of ethanol, and produced no evidence of physical dependence when administered repeatedly. Agonists with low intrinsic activity at the benzodiazepine receptor, such as PNU-101017, should be further explored for therapeutic uses.
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页码:255 / 263
页数:8
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