Ameliorative effect of NC-1900, a new AVP4-9 analog, through vasopressin V1A receptor on scopolamine-induced impairments of spatial memory in the eight-arm radial maze

K. Mishima, H. Tsukikawa, I. Miura, K. Inada, K. Abe, Y. Matsumoto, N. Egashira, K. Iwasaki, M. Fujiwara

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The mechanism by which NC-1900, a new pGlu-Asn-Cys(Cys)-Pro-Arg-Gly-NH2 (AVP4-9) analog, improves spatial memory in rats using an eight-arm radial maze was examined. Even at very low doses (0.2 ng/kg for s.c., 1 μg/kg for p.o., 1 fg for i.c.v.) NC-1900 improved scopolamine-induced impairment of spatial memory. NC-1900 (1 ng/kg, s.c.) also improved impairment of spatial memory induced by pirenzepine, a muscarinic1 (M1) receptor antagonist, and by KN-62, a Ca2+/calmodulin (CaM)-dependent protein kinase II inhibitor. [Pmp1, Tyr(Me)2]-Arg8-vasopressin, a vasopressin1A (V1A) receptor antagonist, and nicardipine, L-type Ca2+ blocker, but not OPC-31260, a V2 antagonist, suppressed the effect of NC-1900 on scopolamine-induced impairment of spatial memory. A microdialysis study showed that NC-1900 did not affect acetylcholine release in the ventral hippocampus (VH) of intact rats or of scopolamine-treated rats. NC-1900 (1 μM) increased [Ca2+]i in the VH than in the dorsal hippocampus (DH). Pretreatment with nicardipine (1 μM) and Ca2+-free conditions inhibited the NC-1900-induced [Ca2+]i response in the VH. Whereas co-administration of NC-1900 (1 μM) and carbachol (500 μM) increased [Ca2+]i in the VH. Moreover, nicardipine concentration-dependently inhibited the increase in [Ca2+]i induced by the co-administration of NC-1900 and carbachol in the VH. These results suggest that NC-1900 activates the V1A receptor at the postsynaptic cholinergic nerve, and causes a transient influx of intracellular Ca2+ through L-type Ca2+ channels, to interact with the M1 receptor. The activation of these Ca2+-dependent processes induced by NC-1900 may be involved in the positive effect of NC-1900 on scopolamine-induced impairment of spatial memory.

Original languageEnglish
Pages (from-to)541-552
Number of pages12
Issue number4
Publication statusPublished - Mar 2003
Externally publishedYes


All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Cellular and Molecular Neuroscience

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