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记忆损害与血浆氟硝西泮水平

Impairment of memory and plasma flunitrazepam levels.

作者信息

Bareggi S R, Ferini-Strambi L, Pirola R, Smirne S

机构信息

Department of Pharmacology, State University, School of Medicine, Milano, Italy.

出版信息

Psychopharmacology (Berl). 1998 Nov;140(2):157-63. doi: 10.1007/s002130050753.

Abstract

Flunitrazepam was administered to volunteers in three different oral doses. The effects on psychomotor sedation, attention, working memory and explicit memory were then assessed at various intervals after dosing and compared with levels of the drug in the plasma. Three groups of 12 healthy males with similar levels of education were given placebo or flunitrazepam (1, 2 or 4 mg) in a double-blind, random-sequence study. Volunteers completed a battery of tests at night, 3.5 h after taking the drug and in the morning, 10 h afterward. Blood samples were collected for drug analysis before and after the nocturnal tests and before morning tests. At night, only the highest dose of flunitrazepam (4 mg) induced significant changes in psychomotor sedation, attention, working memory, and prose immediate recall. Doses of 2 and 4 mg flunitrazepam significantly reduced the mean scores of explicit memory (morning tests). Z-scores, calculated from differences between flunitrazepam and placebo, revealed that 2 mg flunitrazepam impaired memory but not alertness or attention. Linear regression analysis of the relationship between plasma levels of flunitrazepam and its effects (Z-scores) indicated that there was a significant positive correlation between peak levels of flunitrazepam at night and impairment of night attention and explicit memory, i.e. delayed recall of prose (r = 0.59, P < 0.01) and trigrams (r = 0.55, P < 0.01). However, memory and attention Z-scores as a function of plasma levels fitted with nonlinear regression analysis to the Emax model had higher correlation coefficients. To produce an effect equal to 50% of the maximum effect for memory impairment, concentrations (EC50) were 6.1 and 6.4 ng/ml for prose and trigrams delayed recall; but for attention they were much higher, at 13.2 ng/ml. The overall results indicate that higher concentrations were needed to impair attention than were required to impair memory.

摘要

向志愿者服用三种不同口服剂量的氟硝西泮。给药后在不同时间间隔评估其对精神运动性镇静、注意力、工作记忆和外显记忆的影响,并与血浆中的药物水平进行比较。在一项双盲、随机序列研究中,三组各12名受教育程度相似的健康男性被给予安慰剂或氟硝西泮(1、2或4毫克)。志愿者在夜间、服药后3.5小时以及10小时后的早晨完成一系列测试。在夜间测试前后和早晨测试前采集血样进行药物分析。夜间,只有最高剂量的氟硝西泮(4毫克)会引起精神运动性镇静、注意力、工作记忆和散文即时回忆的显著变化。2毫克和4毫克剂量的氟硝西泮显著降低了外显记忆的平均得分(早晨测试)。根据氟硝西泮与安慰剂之间的差异计算出的Z分数显示,2毫克氟硝西泮损害记忆,但不损害警觉性或注意力。氟硝西泮血浆水平与其效应(Z分数)之间关系的线性回归分析表明,夜间氟硝西泮峰值水平与夜间注意力损害和外显记忆之间存在显著正相关,即散文延迟回忆(r = 0.59,P < 0.01)和三字母组延迟回忆(r = 0.55,P < 0.01)。然而,作为血浆水平函数的记忆和注意力Z分数与Emax模型的非线性回归分析拟合具有更高的相关系数。为了产生相当于记忆损害最大效应50%的效果,散文和三字母组延迟回忆的浓度(EC50)分别为6.1和6.4纳克/毫升;但对于注意力,浓度要高得多,为13.2纳克/毫升。总体结果表明,损害注意力所需的浓度高于损害记忆所需的浓度。

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