Infusion of neurosteroids into the rat nucleus basalis affects paradoxical sleep in accordance with their memory modulating properties

被引:32
作者
Darnaudéry, M
Pallarés, M
Bouyer, JJ
Le Moal, M
Mayo, W
机构
[1] Univ Bordeaux 2, INSERM, U259, Lab Psychobiol Comportements Adaptatifs, F-33077 Bordeaux, France
[2] Univ Autonoma Barcelona, Fac Psicol, Dept Psicobiol & Metodol Ciencies Salut, Bellaterra 08193, Spain
关键词
neurosteroids; sleep-wakefulness cycle; REM sleep; pregnenolone sulfate; allopregnanolone; nucleus basalis magnocellularis;
D O I
10.1016/S0306-4522(99)00019-6
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The neurosteroids pregnenolone sulfate and allopregnanolone affect memory processes in an opposite manner, pregnenolone sulfate acts as a potent memory-enhancer whereas allopregnanolone impairs memory performance. The mechanisms underlying these memory modulating properties have yet to be elucidated. We have previously reported that infusions of either neurosteroid into the nucleus basalis magnocellularis, one of the main forebrain cholinergic nuclei, differentially affect spatial memory in rats. The relationships between memory performance and paradoxical sleep are well documented, therefore we investigated whether neurosteroids infused into the nucleus basalis magnocellularis affected the sleep-wakefulness cycle in rats, measured by electroencephalographic recordings. Results show that pregnenolone sulfate (5 ng) increased by 12%, whereas allopregnanolone (2 ng) decreased by 24%, the duration of paradoxical sleep in the 24 h interval following injection compared to control recordings. Pregnenolone sulfate inhibits GABA(A) receptors whereas allopregnanolone stimulates them. Since cholinergic neurons of the nucleus basalis magnocellularis are GABA-modulated, it may be postulated that these neurosteroids modify paradoxical sleep by acting on the cholinergic transmission. This may account, at least in part, for the memory modulating properties of these compounds. (C) 1999 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:583 / 588
页数:6
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