TY - JOUR
T1 - Conditioned Suppression of Motility
T2 - Possibility for Evaluation of Learning and Memory in Mice
AU - Nabeshima, Toshitaka
AU - Kozawa, Teruo
AU - Kameyama, Tsutomu
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1988/2/1
Y1 - 1988/2/1
N2 - Mice showed a marked suppression of motility when placed in the same environment where they had been given electric shocks (ES) 24 h before. This conditioned suppression of motility (CS) was attenuated by the administration of cycloheximide (CXM, 25 - 150 mg/kg) immediately after ES treatment in a dose-dependent manner. CXM (50 mg/kg) administered 1 h after ES failed to attenuate the CS. These effects seem to be caused by retrograde amnesia. Furthermore the amnesic action of CXM was antagonized by naloxone (10 mg/kg), which did not affect CS. Physostigmine (0.2 mg/kg), propranolol (1 mg/kg) and cyproheptadine (2 mg/kg) did not antagonize CXM-induced amnesia significantly. In the same way the arnnssia inducing actions of phencyclidine and scopolamine were detected. The CS method seems to be useful to examine learning and memory performances in animals and has the advantage that evaluation is extremely easy.
AB - Mice showed a marked suppression of motility when placed in the same environment where they had been given electric shocks (ES) 24 h before. This conditioned suppression of motility (CS) was attenuated by the administration of cycloheximide (CXM, 25 - 150 mg/kg) immediately after ES treatment in a dose-dependent manner. CXM (50 mg/kg) administered 1 h after ES failed to attenuate the CS. These effects seem to be caused by retrograde amnesia. Furthermore the amnesic action of CXM was antagonized by naloxone (10 mg/kg), which did not affect CS. Physostigmine (0.2 mg/kg), propranolol (1 mg/kg) and cyproheptadine (2 mg/kg) did not antagonize CXM-induced amnesia significantly. In the same way the arnnssia inducing actions of phencyclidine and scopolamine were detected. The CS method seems to be useful to examine learning and memory performances in animals and has the advantage that evaluation is extremely easy.
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U2 - 10.1248/bpb1978.11.779
DO - 10.1248/bpb1978.11.779
M3 - Article
C2 - 3254975
AN - SCOPUS:0024267335
SN - 0386-846X
VL - 11
SP - 779
EP - 784
JO - Journal of Pharmacobio-Dynamics
JF - Journal of Pharmacobio-Dynamics
IS - 12
ER -