Anxiolytic actions of the substance P (NK1) receptor antagonist L-760735 and the 5-HT1A agonist 8-OH-DPAT in the social interaction test in gerbils
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作者:
Cheeta, S
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机构:Kings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Cheeta, S
Tucci, S
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机构:Kings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Tucci, S
Sandhu, J
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机构:Kings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Sandhu, J
Williams, AR
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机构:Kings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Williams, AR
Rupniak, NMJ
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机构:Kings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Rupniak, NMJ
File, SE
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Kings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, EnglandKings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
File, SE
[1
]
机构:
[1] Kings Coll London, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
[2] Merck Sharp & Dohme Ltd, Neurosci Res Ctr, Dept Pharmacol, Harlow CM20 2QR, Essex, England
anxiety;
benzodiazepine;
fluoxetine;
(+/-)-8-OH-DPAT;
social interaction test;
substance P (NK1) receptor antagonist;
D O I:
10.1016/S0006-8993(01)02846-3
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The gerbil social interaction test has previously detected anxiolytic effects of nicotine and diazepam. In the present study, the high affinity substance P (NK1) receptor antagonist L-760735 (3 mg/kg) significantly increased the time spent in social interaction, whereas its low affinity analogue L-781773 (3 mg/kg) was without effect. Diazepam (0.1 mg/kg) and the 5-HT1A receptor agonist 8-OH-DPAT (0.003 and 0.01 mg/kg) also increased social interaction, whereas an acute dose of the selective serotonin re-uptake inhibitor fluoxetine (10 mg/kg) decreased the time spent in social interaction. Diazepam (0.1 mg/kg) significantly increased locomotor activity, but this effect was independent of the increase in social interaction. The other drugs tested were without effect on locomotor activity. The present findings suggest that the gerbil social interaction may well provide a useful assay for detecting both anxiolytic and anxiogenic compounds, and suggests that the high affinity NK1 receptor antagonist L-760735 may prove to be useful as an anxiolytic therapy. (C) 2001 Elsevier Science BY. All rights reserved.
机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England
Cheeta, S
Irvine, EE
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Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England
Irvine, EE
Kenny, PJ
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Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England
Kenny, PJ
File, SE
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Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England
机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England
Cheeta, S
Irvine, EE
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机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England
Irvine, EE
Kenny, PJ
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Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England
Kenny, PJ
File, SE
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Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 UL, England