TY - JOUR
T1 - Effects of reserpine on retention of escape reversal in mice
T2 - Absence of state-dependent learning
AU - Kurtz, Perry
AU - Palfai, Tibor
PY - 1977/4
Y1 - 1977/4
N2 - Used a discriminated escape training paradigm in 4 experiments to study the effects of reserpine (RE) on learning and memory in 465 male Swiss mice. Injection of RE (ip) before reversal training had no effect on acquisition but did produce a time- and dose-dependent impairment of retention 10 days later. These results suggest that RE may have interfered with some aspect of memory storage. Retention impairments observed when a 2.0 mg/kg RE injection was given 2 hrs before reversal training were not attenuated by readministering the drug before testing, a finding that provides no support for a state-dependency interpretation. Furthermore, Ss treated with RE exhibited inferior retention of previous training, regardless of the pharmacological state present during that learning. This was interpreted as a drug-induced impairment of memory retrieval. In addition, performance during the initial discriminated escape training session suggested that RE may also impair acquisition under some conditions. In the last experiment, it was found that when the catecholamine precursor l -dihydroxyphenylalanine (100 mg/kg) and the indole amine precursor d,l -5-hydroxytryptophan (125 mg/kg) were both given after RE treatment, subsequent retention performance was not significantly impaired. Results are discussed in terms of the possible roles of biogenic amines in arousal, learning, and memory. (38 ref) (PsycINFO Database Record (c) 2006 APA, all rights reserved).
AB - Used a discriminated escape training paradigm in 4 experiments to study the effects of reserpine (RE) on learning and memory in 465 male Swiss mice. Injection of RE (ip) before reversal training had no effect on acquisition but did produce a time- and dose-dependent impairment of retention 10 days later. These results suggest that RE may have interfered with some aspect of memory storage. Retention impairments observed when a 2.0 mg/kg RE injection was given 2 hrs before reversal training were not attenuated by readministering the drug before testing, a finding that provides no support for a state-dependency interpretation. Furthermore, Ss treated with RE exhibited inferior retention of previous training, regardless of the pharmacological state present during that learning. This was interpreted as a drug-induced impairment of memory retrieval. In addition, performance during the initial discriminated escape training session suggested that RE may also impair acquisition under some conditions. In the last experiment, it was found that when the catecholamine precursor l -dihydroxyphenylalanine (100 mg/kg) and the indole amine precursor d,l -5-hydroxytryptophan (125 mg/kg) were both given after RE treatment, subsequent retention performance was not significantly impaired. Results are discussed in terms of the possible roles of biogenic amines in arousal, learning, and memory. (38 ref) (PsycINFO Database Record (c) 2006 APA, all rights reserved).
KW - reserpine, acquisition &
KW - retention of discriminated escape training, male mice
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U2 - 10.1037/h0077332
DO - 10.1037/h0077332
M3 - Article
C2 - 300745
AN - SCOPUS:0017603216
SN - 0021-9940
VL - 91
SP - 393
EP - 406
JO - Journal of Comparative and Physiological Psychology
JF - Journal of Comparative and Physiological Psychology
IS - 2
ER -