TY - JOUR
T1 - Scopolamine- and Morphine-Induced Impairments of Spontaneous Alternation Performance in Mice
T2 - Reversal With Glucose and With Cholinergic and Adrenergic Agonists
AU - Stone, William S.
AU - Walser, Bryan
AU - Gold, Scott D.
AU - Gold, Paul E.
PY - 1991/4
Y1 - 1991/4
N2 - Administration of epinephrine and glucose, as well as drugs that influence cholinergic and opiate systems, can enhance or impair memory. The present experiments examined the possibility that peripheral glucose administration might reverse scopolamine- and morphine-induced impairments in a spontaneous alternation task. Mice received all drug administrations 30 min before testing. Scopolamine-induced (3 mg/kg), deficits in alternation performance were reversed by glucose (100 and 250 mg/kg) amphetamine (1 mg/kg), epinephrine, physostigmine, and oxotremorine (each 0.1 mg/kg). Morphine (10 mg/kg) also impaired spontaneous alternation performance, and glucose (100 and 300 mg/kg) reversed this impairment as well. These findings are consistent with the view that central cholinergic systems, possibly under inhibitory opiate regulation, may contribute to glucose and epinephrine effects on memory storage.
AB - Administration of epinephrine and glucose, as well as drugs that influence cholinergic and opiate systems, can enhance or impair memory. The present experiments examined the possibility that peripheral glucose administration might reverse scopolamine- and morphine-induced impairments in a spontaneous alternation task. Mice received all drug administrations 30 min before testing. Scopolamine-induced (3 mg/kg), deficits in alternation performance were reversed by glucose (100 and 250 mg/kg) amphetamine (1 mg/kg), epinephrine, physostigmine, and oxotremorine (each 0.1 mg/kg). Morphine (10 mg/kg) also impaired spontaneous alternation performance, and glucose (100 and 300 mg/kg) reversed this impairment as well. These findings are consistent with the view that central cholinergic systems, possibly under inhibitory opiate regulation, may contribute to glucose and epinephrine effects on memory storage.
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U2 - 10.1037/0735-7044.105.2.264
DO - 10.1037/0735-7044.105.2.264
M3 - Article
C2 - 2043273
AN - SCOPUS:0025854291
SN - 0735-7044
VL - 105
SP - 264
EP - 271
JO - Behavioral Neuroscience
JF - Behavioral Neuroscience
IS - 2
ER -