TY - JOUR
T1 - N-methyl-D-aspartate receptors are indispensable for the formation of long-term potentiation in the rat suprachiasmatic nucleus in vitro
AU - Nisikawa, Yukiko
AU - Shimazoe, Takao
AU - Shibata, Shigenobu
AU - Watanabe, Shigenori
PY - 1998/1/26
Y1 - 1998/1/26
N2 - Optic nerve (ON) stimulation caused a postsynaptic field potential in the suprachiasmatic nucleus (SCN) of rat hypothalamic slices. The postsynaptic field potential was suppressed by 6-cyano-7-nitroquinoxaline- 2,3-dione (CNQX), a non-NMDA receptor antagonist, in a concentration- dependent manner, but not affected by D-amino-5-phosphonovaleric acid (APV), a competitive NMDA receptor antagonist. Tetanic stimulation to the ON induced long-term potentiation (LTP) in the SCN. Application of APV at 50 μM inhibited the induction of LTP by tetanic stimulation but CNQX at lower dose (5 μM) didn't inhibit it. These results suggest that NMDA receptors are indispensable for the induction of LTP after tetanic stimulation.
AB - Optic nerve (ON) stimulation caused a postsynaptic field potential in the suprachiasmatic nucleus (SCN) of rat hypothalamic slices. The postsynaptic field potential was suppressed by 6-cyano-7-nitroquinoxaline- 2,3-dione (CNQX), a non-NMDA receptor antagonist, in a concentration- dependent manner, but not affected by D-amino-5-phosphonovaleric acid (APV), a competitive NMDA receptor antagonist. Tetanic stimulation to the ON induced long-term potentiation (LTP) in the SCN. Application of APV at 50 μM inhibited the induction of LTP by tetanic stimulation but CNQX at lower dose (5 μM) didn't inhibit it. These results suggest that NMDA receptors are indispensable for the induction of LTP after tetanic stimulation.
KW - Long-term potentiation
KW - N-Methyl-D-aspartate receptor
KW - NMDA receptor
KW - Suprachiasmatic nucleus
KW - Synaptic potential
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U2 - 10.1016/S0006-8993(97)01177-3
DO - 10.1016/S0006-8993(97)01177-3
M3 - Article
C2 - 9519277
AN - SCOPUS:0032567701
SN - 0006-8993
VL - 782
SP - 303
EP - 305
JO - Brain Research
JF - Brain Research
IS - 1-2
ER -