TY - JOUR
T1 - The role of nociceptin in cognition
AU - Nabeshima, Toshitaka
AU - Noda, Yukihiro
AU - Mamiya, Takayoshi
N1 - Funding Information:
Above studies were performed in collaboration with Drs. H. Takeshima, M. Nishi, T. Manabe, T. Takahashi, H. Katagiri (Tokyo University) and T. Houtani, T. Noda, T. Sugimoto (Kansai University). This study was supported, in part, by Grants-in-Aid for Center of Excellence (COE), Science Research (#10044260 and #10897005) for the Ministry of Education, Science and Culture and by an SRF Grant for Biomedical Research.
PY - 1999/11/27
Y1 - 1999/11/27
N2 - The physiological role of the modulation via the nociceptin receptor is still unclear. Here we report the role of the nociceptin system in learning and memory. Nociceptin-knockout mice possess greater learning ability in the water maze task, show an enhanced latent learning in the water finding task, have better memory in the passive avoidance task, and further, show larger long-term potentiation in the hippocampal CA1 region than wild-type mice. Nociceptin itself induces an impairment of the passive avoidance task in wild-type mice. This impairment is reversed by naloxone benzoylhydrazone (NalBzoH), but not by other opioids in wild-type mice. Further, experiments on cultured cells transfected with nociceptin receptor cDNA show that NalBzoH competes [3H]-nociceptin binding and attenuates the nociceptin-induced inhibition of cAMP accumulation induced by forskolin. These results demonstrate that the nociceptin system seems to play a negative role in learning and memory and that NalBzoH acts as a potent antagonist for the nociceptin receptor. In addition, the antagonists for the nociceptin receptor may be worth testing for alleviating memory disorders. Copyright (C) 1999 Elsevier Science B.V.
AB - The physiological role of the modulation via the nociceptin receptor is still unclear. Here we report the role of the nociceptin system in learning and memory. Nociceptin-knockout mice possess greater learning ability in the water maze task, show an enhanced latent learning in the water finding task, have better memory in the passive avoidance task, and further, show larger long-term potentiation in the hippocampal CA1 region than wild-type mice. Nociceptin itself induces an impairment of the passive avoidance task in wild-type mice. This impairment is reversed by naloxone benzoylhydrazone (NalBzoH), but not by other opioids in wild-type mice. Further, experiments on cultured cells transfected with nociceptin receptor cDNA show that NalBzoH competes [3H]-nociceptin binding and attenuates the nociceptin-induced inhibition of cAMP accumulation induced by forskolin. These results demonstrate that the nociceptin system seems to play a negative role in learning and memory and that NalBzoH acts as a potent antagonist for the nociceptin receptor. In addition, the antagonists for the nociceptin receptor may be worth testing for alleviating memory disorders. Copyright (C) 1999 Elsevier Science B.V.
UR - http://www.scopus.com/inward/record.url?scp=0033433983&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033433983&partnerID=8YFLogxK
U2 - 10.1016/S0006-8993(99)01906-X
DO - 10.1016/S0006-8993(99)01906-X
M3 - Article
C2 - 10612708
AN - SCOPUS:0033433983
SN - 0006-8993
VL - 848
SP - 167
EP - 173
JO - Brain Research
JF - Brain Research
IS - 1-2
ER -