Plihal W, Pietrowsky R, Born J
University of Bamberg, Germany.
Psychoneuroendocrinology. 1999 Apr;24(3):313-31. doi: 10.1016/s0306-4530(98)00080-8.
To investigate the role of glucocorticoids for effects of early and late nocturnal sleep on declarative and procedural memory, 2 mg dexamethasone (versus placebo) were administered to healthy men 7 h prior to retention sleep. The retention sleep interval covered either the early or late half of nocturnal sleep. Following placebo, recall of a paired associate list (declarative memory) benefitted more from early than late sleep and recall of mirror tracing skills (procedural memory) benefitted more from late than early sleep. Dexamethasone did not affect slow wave sleep dominating early sleep, but blocked the beneficial effect of early sleep on recall of paired associates. Conversely, dexamethasone reduced rapid eye movement sleep dominating late sleep, but did not affect late sleeps beneficial effect on mirror tracing skills. The natural inhibition of endogenous glucocorticoid secretion during early sleep seems to be essential for a sleep-related facilitation of declarative memory.
为研究糖皮质激素在夜间早期和晚期睡眠对陈述性记忆和程序性记忆影响中的作用,在健康男性保留睡眠前7小时给予2毫克地塞米松(对比安慰剂)。保留睡眠时段覆盖夜间睡眠的早期或晚期。服用安慰剂后,配对联想列表的回忆(陈述性记忆)从早期睡眠中获益更多,而镜像追踪技能的回忆(程序性记忆)从晚期睡眠中获益更多。地塞米松不影响早期睡眠中占主导的慢波睡眠,但阻断了早期睡眠对配对联想回忆的有益作用。相反,地塞米松减少了晚期睡眠中占主导的快速眼动睡眠,但不影响晚期睡眠对镜像追踪技能的有益作用。早期睡眠期间内源性糖皮质激素分泌的自然抑制似乎对睡眠相关的陈述性记忆促进至关重要。