Nitric oxide synthase (NOS) inhibitors have been shown to affect the develo
pment of long-term potentiation and the acquisition of new learning. In the
present study, we investigated the effects of NOS inhibitors in two animal
models in which aspects of cognition are measured in well-learned operant
tasks - a delayed non-match-to-position (DNMTP) task and a multiple signall
ed-unsignalled differential reinforcement of low rates (DRL) 15 s schedule
- models of short-term memory and behavioral inhibition/timing, respectivel
y. Since an overlap in the behavioral effects of NOS inhibitors and phencyc
lidine (PCP)-like N-methyl-D-aspartate (NMDA) antagonists has been observed
previously, we compared our results with NOS inhibitors to those obtained
with PCP. Whereas PCP produced a delay-independent decrease in the DNMTP ta
sk and increased burst responding (consecutive responses with inter-respons
e intervals of <3 s) in both the signalled and unsignalled components of th
e DRL procedure, 7-nitroindazole did not affect accuracy in the DNMTP task
nor did it alter the pattern of responding in either component of the DRL s
chedule. Similarly, N-G-nitro-L-arginine (L-NOARG) and N-G-nitro-L-arginine
-methyl-ester (L-NAME) did not affect accuracy in the DNMTP task These resu
lts suggest that NOS inhibitors do not produce PCP-like disruption of behav
ioral inhibition or timing, nor do they decrease accuracy in a conditional
discrimination task, as has been observed with PCP. The present results len
d further support to the hypothesis that nitric oxide modulation does not a
ffect retention of well-learned tasks, although it may affect acquisition o
f novel behavior, (C) 2000 Lippincott Williams & Wilkins.