VISUAL RECOGNITION MEMORY IN SQUIRREL-MONKEYS - EFFECTS OF SEROTONIN ANTAGONISTS ON BASE-LINE AND HYPOXIA-INDUCED PERFORMANCE DEFICITS

被引:17
作者
DENOBLE, VJ
SCHRACK, LM
REIGEL, AL
DENOBLE, KF
机构
[1] The Du Pont Merck Pharmaceutical Company, Experimental Station, Wilmington, DE 19880-0400
关键词
SEROTONIN; VISUAL RECOGNITION TASK; ALZHEIMER DISEASE; PRIMATE; HYPOXIA;
D O I
10.1016/0091-3057(91)90064-9
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Cognitive deficits resulting from neuropathological brain changes such as Alzheimer's Disease or normal aging are most likely due to alterations in multiple neurotransmitter systems. While the majority of preclinical studies have focused on the effects of acetylcholine (ACh), it has been shown that activation of the serotonergic (5-HT) pathways in the central nervous system interferes with passive avoidance retention in rats. In contrast, decreased 5-HT activity has been shown to improve learning and memory in rats using similar procedures. In the present experiment, 5-HT antagonists were evaluated for their effects on performance in a delayed match to sample task (DMTS) in two groups of squirrel monkeys: one in which the baseline level of performance was low (< 65% correct, N = 5; group 1) and another in which DMTS performance was high (> 80% correct, N = 3; group 2) but impaired by exposure to hypoxia. Initial parametric tests exposing group 2 to various levels of oxygen deprivation were conducted to determine optimal conditions for performance deficits. Each monkey in both normoxia (group 1) and hypoxia (group 2) served as his own control and received an individualized range of doses for each test compound. For both groups, ketanserin and mianserin, the 5-HT2-selective antagonists, produced dose-dependent increases in DMTS performance at 0.3-1.5 mg/kg PO and 0.05-1.5 mg/kg PO, respectively. Pirenperone, another 5-HT2-selective antagonist, was active in improving performance in group 1 at 0.001 to 0.2 mg/kg PO but was not effective against hypoxia-induced performance deficits. Cyproheptadine, a nonselective antagonist, also produced increases in performance in both groups; however, the effects could not be replicated in the group (1) with a low performance baseline. The results of this study show that alterations of 5-HT are effective in preventing hypoxia-induced performance deficits and in improving normoxic performance levels, suggesting a major role for 5-HT in cognitive performance.
引用
收藏
页码:991 / 996
页数:6
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