TY - JOUR
T1 - Critical role of neuropeptides B/W receptor 1 signaling in social behavior and fear memory
AU - Nagata-Kuroiwa, Ruby
AU - Furutani, Naoki
AU - Hara, Junko
AU - Hondo, Mari
AU - Ishii, Makoto
AU - Abe, Tomomi
AU - Mieda, Michihiro
AU - Tsujino, Natsuko
AU - Motoike, Toshiyuki
AU - Yanagawa, Yuchio
AU - Kuwaki, Tomoyuki
AU - Yamamoto, Miyuki
AU - Yanagisawa, Masashi
AU - Sakurai, Takeshi
PY - 2011
Y1 - 2011
N2 - Neuropeptide B/W receptor 1 (NPBWR1) is a G-protein coupled receptor, which was initially reported as an orphan receptor, and whose ligands were identified by this and other groups in 2002 and 2003. To examine the physiological roles of NPBWR1, we examined phenotype of Npbwr1-/- mice. When presented with an intruder mouse, Npbwr1-/- mice showed impulsive contact with the strange mice, produced more intense approaches toward them, and had longer contact and chasing time along with greater and sustained elevation of heart rate and blood pressure compared to wild type mice. Npbwr1-/- mice also showed increased autonomic and neuroendocrine responses to physical stress, suggesting that impairment of NPBWR1 leads to stress vulnerability. We also observed that these mice show abnormality in the contextual fear conditioning test. These data suggest that NPBWR1 plays a critical role in limbic system function and stress responses. Histological and electrophysiological studies showed that NPBWR1 acts as an inhibitory regulator on a subpopulation of GABAergic neurons in the lateral division of the CeA and terminates stress responses. These findings suggest important roles of NPBWR1 in regulating amygdala function during physical and social stress.
AB - Neuropeptide B/W receptor 1 (NPBWR1) is a G-protein coupled receptor, which was initially reported as an orphan receptor, and whose ligands were identified by this and other groups in 2002 and 2003. To examine the physiological roles of NPBWR1, we examined phenotype of Npbwr1-/- mice. When presented with an intruder mouse, Npbwr1-/- mice showed impulsive contact with the strange mice, produced more intense approaches toward them, and had longer contact and chasing time along with greater and sustained elevation of heart rate and blood pressure compared to wild type mice. Npbwr1-/- mice also showed increased autonomic and neuroendocrine responses to physical stress, suggesting that impairment of NPBWR1 leads to stress vulnerability. We also observed that these mice show abnormality in the contextual fear conditioning test. These data suggest that NPBWR1 plays a critical role in limbic system function and stress responses. Histological and electrophysiological studies showed that NPBWR1 acts as an inhibitory regulator on a subpopulation of GABAergic neurons in the lateral division of the CeA and terminates stress responses. These findings suggest important roles of NPBWR1 in regulating amygdala function during physical and social stress.
UR - http://www.scopus.com/inward/record.url?scp=79952092573&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79952092573&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0016972
DO - 10.1371/journal.pone.0016972
M3 - Article
C2 - 21390312
AN - SCOPUS:79952092573
SN - 1932-6203
VL - 6
JO - PLoS One
JF - PLoS One
IS - 2
M1 - e16972
ER -