Distribution of neuropeptide W immunoreactivity and mRNA in adult rat brain

被引:37
作者
Kitamura, Yoji
Tanaka, Hirokazu
Motoike, Toshiyuki
Ishii, Makoto
Williams, S. Clay
Yanagisawa, Masashi
Sakurai, Takeshi [1 ]
机构
[1] Univ Tsukuba, Inst Basic Med Sci, Dept Pharmacol, Tsukuba, Ibaraki 3058575, Japan
[2] Japan Sci & Technol Corp, ERATO Yanagisawa Orphan Receptor Project, Tokyo 1350064, Japan
[3] Univ Texas, SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
[4] Univ Texas, SW Med Ctr Dallas, Dept Mol Genet, Dallas, TX 75390 USA
关键词
neuropeptide W; brainstem; central amygdaloid nucleus; bed nucleus of the stria terminalis;
D O I
10.1016/j.brainres.2006.03.041
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuropeptide W (NPW) is a recently identified neuropeptide that binds to G-protein-coupled receptor (GPR) 7, which is highly expressed in several discrete regions of the rodent brain including the central amygdaloid nucleus and bed nucleus of the stria terminalis. Although several reports suggested that NPW is implicated in the regulation of energy homeostasis and nociception, the precise physiological role of NPW has remained unclear. In this study, we examined distribution of NPW messenger RNA and NPW immunoreactivity in the adult rat brain. NPW-immunoreactive (ir) cells were detected in the ventral tegmental area, periaqueductal gray, and Edinger-Westphal nucleus. NPW-ir fibers were observed in several brain regions, including the lateral septum, bed nucleus of the stria. terminalis, dorsomedial and posterior hypothalamus, central amygdaloid nucleus, CA1 field of hippocampus, interpeduncular nucleus, inferior colliculus, lateral parabrachial nucleus, facial nucleus, and hypoglossal nucleus. NPW-ir fibers were most abundantly observed in the central amygdaloid nucleus and the bed nucleus of the stria. terminalis, which are regions implicated in fear and anxiety. These results suggest that NPW might be involved in the regulation of stress and emotive responses, especially in fear and anxiety-related physiological and behavioral functions. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 134
页数:12
相关论文
共 17 条
[1]   Identification of natural ligands for the orphan G protein-coupled receptors GPR7 and GPR8 [J].
Brezillon, S ;
Lannoy, V ;
Franssen, JD ;
Le Poul, E ;
Dupriez, V ;
Lucchetti, J ;
Detheux, M ;
Parmentier, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (02) :776-783
[2]   Neuropeptide W-immunoreactivity in the hypothalamus and pituitary of the rat [J].
Dun, SL ;
Brailoiu, GC ;
Yang, J ;
Chang, JK ;
Dun, NJ .
NEUROSCIENCE LETTERS, 2003, 349 (02) :71-74
[3]   Identification of a neuropeptide modified with bromine as an endogenous ligand for GPR7 [J].
Fujii, R ;
Yoshida, H ;
Fukusumi, S ;
Habata, Y ;
Hosoya, M ;
Kawamata, Y ;
Yano, T ;
Hinuma, S ;
Kitada, C ;
Asami, T ;
Mori, M ;
Fujisawa, Y ;
Fujino, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (37) :34010-34016
[4]   Targeted disruption of GPR7, the endogenous receptor for neuropeptides B and W, leads to metabolic defects and adult-onset obesity [J].
Ishii, M ;
Fei, H ;
Friedman, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (18) :10540-10545
[5]   Neuropeptide B-deficient mice demonstrate hyperalgesia in response to inflammatory pain [J].
Kelly, MA ;
Beuckmann, CT ;
Williams, SC ;
Sinton, CM ;
Motoike, T ;
Richardson, JA ;
Hammer, RE ;
Garry, MG ;
Yanagisawa, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (28) :9942-9947
[6]  
KUPFERMANN I, 2000, PRINCIPLES NEURAL SC, P998
[7]   Emotion circuits in the brain [J].
LeDoux, JE .
ANNUAL REVIEW OF NEUROSCIENCE, 2000, 23 :155-184
[8]  
LEDOUX JE, 1988, J NEUROSCI, V8, P2517
[9]   Two related G protein-coupled receptors: The distribution of GPR7 in rat brain and the absence of GPR8 in rodents [J].
Lee, DK ;
Nguyen, T ;
Porter, CA ;
Cheng, R ;
George, SR ;
O'Dowd, BF .
MOLECULAR BRAIN RESEARCH, 1999, 71 (01) :96-103
[10]   A role for neuropeptide W in the regulation of feeding behavior [J].
Mondal, MS ;
Yamaguchi, H ;
Date, Y ;
Shimbara, T ;
Toshinai, K ;
Shimomura, Y ;
Mori, M ;
Nakazato, M .
ENDOCRINOLOGY, 2003, 144 (11) :4729-4733