Behavioral insensitivity to restraint stress, absent fear suppression of behavior and impaired spatial learning in transgenic rats with hippocampal neuropeptide Y overexpression

被引:257
作者
Thorsell, A
Michalkiewicz, M
Dumont, Y
Quirion, R
Caberlotto, L
Rimondini, R
Mathé, AA
Heilig, M
机构
[1] Huddinge Hosp, Karolinska Inst, Addict Ctr S, SE-14186 Huddinge, Sweden
[2] W Virginia Univ, Hlth Sci Ctr N, Dept Physiol, Morgantown, WV 26506 USA
[3] McGill Univ, Dept Psychiat, Verdun, PQ H4H 1R3, Canada
[4] McGill Univ, Douglas Hosp Res Ctr, Verdun, PQ H4H 1R3, Canada
[5] St Gorans Univ Hosp, Karolinska Inst, Dept Psychiat, SE-11281 Stockholm, Sweden
基金
英国惠康基金;
关键词
anxiety; amygdala;
D O I
10.1073/pnas.220232997
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exogenous neuropeptide Y (NPY) reduces experimental anxiety in a wide range of animal models. The generation of an NPY-transgenic rat has provided a unique model to examine the role of endogenous NPY in control of stress and anxiety-related behaviors using paradigms previously used by pharmacological studies. Locomotor activity and baseline behavior on the elevated plus maze were normal in transgenic subjects. Two robust phenotypic traits were observed. (i) Transgenic subjects showed a markedly attenuated sensitivity to behavioral consequences of stress, in that they were insensitive to the normal anxiogenic-like effect of restraint stress on the elevated plus maze and displayed absent fear suppression of behavior in a punished drinking test. (ii) A selective impairment of spatial memory acquisition was found in the Morris water maze. Control experiments suggest these traits to be independent. These phenotypic traits were accompanied by an over-expression of prepro-NPY mRNA and NPY peptide and decreased NPY-Y1 binding within the hippocampus, a brain structure implicated both in memory processing and stress responses. Data obtained using this unique model support and extend a previously postulated anti-stress action of NPY and provide novel evidence for a role of NPY in learning and memory.
引用
收藏
页码:12852 / 12857
页数:6
相关论文
共 50 条
[1]   Evidence that the median raphe nucleus - Dorsal hippocampal pathway mediates diazepam withdrawal induced anxiety [J].
Andrews, N ;
File, SE ;
Fernandes, C ;
Gonzalez, LE ;
Barnes, NM .
PSYCHOPHARMACOLOGY, 1997, 130 (03) :228-234
[2]  
BROQUA P, 1995, BEHAV PHARMACOL, V6, P215
[3]   Alterations in neuropeptide Y and Y1 receptor mRNA expression in brains from an animal model of depression: region specific adaptation after fluoxetine treatment [J].
Caberlotto, L ;
Fuxe, K ;
Overstreet, DH ;
Gerrard, P ;
Hurd, YL .
MOLECULAR BRAIN RESEARCH, 1998, 59 (01) :58-65
[4]   The anxiolytic-like effect of metabotropic glutamate receptor antagonists after intrahippocampal injection in rats [J].
ChojnackaWojcik, E ;
Tatarczynska, E ;
Pilc, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 319 (2-3) :153-156
[5]  
COLMERS WF, 1988, J NEUROSCI, V8, P3827
[6]  
Crawley J. N., 2007, WHATS WRONG MY MOUSE
[7]   [125I]-GR231118:: a high affinity radioligand to investigate neuropeptide YY1 and Y4 receptors [J].
Dumont, Y ;
Quirion, R .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (01) :37-46
[8]   BIIE0246, a potent and highly selective non-peptide neuropeptide YY2 receptor antagonist [J].
Dumont, Y ;
Cadieux, A ;
Doods, H ;
Pheng, LH ;
Abounader, R ;
Hamel, E ;
Jacques, D ;
Regoli, D ;
Quirion, R .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (06) :1075-1088
[9]   MOLECULAR-CLONING OF A NOVEL-G PROTEIN-COUPLED RECEPTOR THAT MAY BELONG TO THE NEUROPEPTIDE RECEPTOR FAMILY [J].
EVA, C ;
KEINANEN, K ;
MONYER, H ;
SEEBURG, P ;
SPRENGEL, R .
FEBS LETTERS, 1990, 271 (1-2) :81-84
[10]   THE INTERPLAY OF LEARNING AND ANXIETY IN THE ELEVATED PLUS-MAZE [J].
FILE, SE .
BEHAVIOURAL BRAIN RESEARCH, 1993, 58 (1-2) :199-202