The effects of a novel
vasopressin (AVP) fragment analog
NC-1900 (pGlu-Asn-Ser-Pro-Arg-Gly-NH2 acetate) were studied on the performance of memory retention and retrieval in mice.
NC-1900 of one time application of 1 hr after the acquired trial (electric
shock) extended the latent period of passive avoidance task 21 days after the acquired trial. Though the extended response was also recognized with AVP4-9, the potency was approx. 1/1000 of
NC-1900. The potentiation wasn't recognized with
vasopressin.
NC-1900 showed a significantly high correct answer after 21 days after the last trial in the search task. While, V1 antagonist Pmp1-Tyr (Me)2-AVP shortened the latent period of passive avoidance task. On the other hand,
NC-1900 extended the reaction latency 21 days after the acquired trial by the application 1 hr before the retention trial. Though this improvement of memory retrieval was recognized with
vasopressin and AVP4-9, the potency was 1/100-1/1000.
NC-1900 improved the retrieval 24 h after the CO2 exposure. V1 antagonists Pmp1-Tyr-Me2-AVP or Deamino-Pen1, O-Me-Tyr2-AVP, and PMA had no effects on the retrieval 21 days after the acquired trial. These results suggest that
NC-1900 may have the memory retention and retrieval potentiating action, and that
phospholipase C-
protein kinase C system may be involved in the former action, and the latter action not be involved.