The neuropeptide Y (NPY) Y1 receptor subtype mediates NPY-induced antidepressant-like activity in the mouse forced swimming test

被引:171
作者
Redrobe, JP
Dumont, Y
Fournier, A
Quirion, R
机构
[1] McGill Univ, Douglas Hosp, Res Ctr, Dept Psychiat, Verdun, PQ H4H 1R3, Canada
[2] Univ Quebec, INRS Sante, Pointe Claire, PQ H9R 1G6, Canada
关键词
neuropeptide Y; NPYY1; receptors; NPYY2; antidepressant; forced swimming test; mouse;
D O I
10.1016/S0893-133X(01)00403-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The present study was undertaken to investigate the possible antidepressant-like effects of neuropeptide Y (NPY) in the mouse forced swimming test, an animal model widely used for the screening of potential antidepressant drugs. In addition, experiments were performed, using agonists and selective antagonists, to assess the potential role of NPY Y-1 and Y-2 receptor subtypes in this model. Complementary studies were performed in an open field apparatus to rule out any changes in locomotor activity that might have interfered with the interpretation of data from the mouse forced swimming test. Intracerebroventricular injections (0.03 nmole-3 nmole) of NPY, [Leu(31)Pro(34)]PYY (Y-1 agonist), NPY13-36 (Y-2 agonist), BIBP3226, BIBO3304 (Y-1 antagonists) and BIIE0246 (Y-2 antagonist) were performed 30 min prior to testing in the mouse forced swimming test and open field. NPY administration significantly reduced immobility time in a dose dependent manner (p <.01 vs. control group), as did [Leu(31)Pro(34)]PYY (p <.01 vs. control group) and BIIE0246 (p <.05 vs. control group). In contrast, BIBO3304, BIBP3226 and NPY13-36 did not display any activity at the doses tested. However, pretreatment with BIBO3304 or BTBP3226 significantly blocked the anti-immobility effects of NPY. Data from the open field demonstrated that BIIE0246 increased horizontal ambulation of the dose found to be active in the forced swimming test. Taken together, our results demonstrate that NPY displays antidepressant-like activity in the mouse forced swimming test, and suggest that this activity is mediated by the NPY Y-1 receptor subtype. (C) 2002 American College of Neuropsychopharmacology. Published by Elsevier Science Inc.
引用
收藏
页码:615 / 624
页数:10
相关论文
共 52 条
[31]   NEUROPEPTIDE-Y - A POTENT INDUCER OF CONSUMMATORY BEHAVIOR IN RATS [J].
LEVINE, AS ;
MORLEY, JE .
PEPTIDES, 1984, 5 (06) :1025-1029
[32]   REGION-SPECIFIC INHIBITION OF POTASSIUM-EVOKED [H-3] NORADRENALINE RELEASE FROM RAT-BRAIN SYNAPTOSOMES BY NEUROPEPTIDE Y-(13-36) - INVOLVEMENT OF NPY-RECEPTORS OF THE Y2-TYPE [J].
MARTIRE, M ;
PISTRITTO, G ;
MORES, N ;
AGNATI, LF ;
FUXE, K .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 230 (02) :231-234
[33]  
Michel MC, 1998, PHARMACOL REV, V50, P143
[34]   ELECTROCONVULSIVE SHOCKS INCREASE THE EXPRESSION OF NEUROPEPTIDE-Y (NPY) MESSENGER-RNA IN THE PIRIFORM CORTEX AND THE DENTATE GYRUS [J].
MIKKELSEN, JD ;
WOLDBYE, D ;
KRAGH, J ;
LARSEN, PJ ;
BOLWIG, TG .
MOLECULAR BRAIN RESEARCH, 1994, 23 (04) :317-322
[35]   Differences in the neuropeptide Y-like immunoreactivity of the plasma and platelets of human volunteers and depressed patients [J].
Nilsson, C ;
Karlsson, G ;
Blennow, K ;
Heilig, M ;
Ekman, R .
PEPTIDES, 1996, 17 (03) :359-362
[36]   THE FLINDERS SENSITIVE LINE RATS - A GENETIC ANIMAL-MODEL OF DEPRESSION [J].
OVERSTREET, DH .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1993, 17 (01) :51-68
[37]   ADMINISTRATION OF ANTIDEPRESSANTS, DIAZEPAM AND PSYCHOMOTOR STIMULANTS FURTHER CONFIRMS THE UTILITY OF FLINDERS SENSITIVE LINE RATS AS AN ANIMAL-MODEL OF DEPRESSION [J].
OVERSTREET, DH ;
PUCILOWSKI, O ;
REZVANI, AH ;
JANOWSKY, DS .
PSYCHOPHARMACOLOGY, 1995, 121 (01) :27-37
[38]  
PORSOLT RD, 1977, ARCH INT PHARMACOD T, V229, P327
[39]   The role of 5-HT1A and 5-HT1B receptors in antidepressant drug actions in the mouse forced swimming test [J].
Redrobe, JP ;
MacSweeney, CP ;
Bourin, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 318 (2-3) :213-220
[40]   Multiple receptors for neuropeptide Y in the hippocampus: putative roles in seizures and cognition [J].
Redrobe, JP ;
Dumont, Y ;
St-Pierre, JA ;
Quirion, R .
BRAIN RESEARCH, 1999, 848 (1-2) :153-166