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急性输注毒蕈碱胆碱能激动剂槟榔碱对阿尔茨海默型痴呆患者言语记忆和视觉空间功能的影响。

Effects of acute infusion of the muscarinic cholinergic agonist arecoline on verbal memory and visuo-spatial function in dementia of the Alzheimer type.

作者信息

Raffaele K C, Berardi A, Morris P P, Asthana S, Haxby J V, Schapiro M B, Rapoport S I, Soncrant T T

机构信息

Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health, Bethesda, Maryland.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 1991;15(5):643-8. doi: 10.1016/0278-5846(91)90054-5.

Abstract
  1. Treatment of patients with dementia of the Alzheimer type (DAT) with arecoline, a muscarinic cholinergic receptor agonist, reportedly improves performance on a picture recognition memory task, but not on other memory measures. To examine further possible performance improvements following arecoline treatment, patients with DAT were treated with a 30 min intravenous infusion of arecoline (5 mg). 2. Psychometric testing was done at five time points (two before and three following the infusion). Patients were tested on a memory task (Buschke selective reminding) and a test of visuo-spatial performance (figure copying). 3. No net change from baseline was seen in mean scores following arecoline infusion. However, the changes in performance on the two tasks were correlated (p less than 0.02) over subjects at 10 min but not at 1.5 or 5.5 hr following the infusion. 4. This result suggests that although individual patients vary in their response to a given dose of arecoline, their responses are consistent across types of tasks. Thus the lack of a mean drug effect may be due to individual differences in response rather than to a lack of response.
摘要
  1. 据报道,用毒蕈碱胆碱能受体激动剂槟榔碱治疗阿尔茨海默型痴呆(DAT)患者,可改善其在图片识别记忆任务中的表现,但对其他记忆指标无改善作用。为进一步研究槟榔碱治疗后可能出现的表现改善情况,对DAT患者进行了30分钟的槟榔碱(5毫克)静脉输注治疗。2. 在五个时间点进行了心理测量测试(输注前两个时间点,输注后三个时间点)。对患者进行了一项记忆任务测试(布施克选择性回忆测试)和一项视觉空间表现测试(图形临摹)。3. 槟榔碱输注后,平均得分与基线相比未见净变化。然而,在输注后10分钟时,两项任务表现的变化在受试者中具有相关性(p小于0.02),但在输注后1.5小时或5.5小时时无相关性。4. 这一结果表明,尽管个体患者对给定剂量槟榔碱的反应存在差异,但其反应在不同类型的任务中是一致的。因此,缺乏平均药物效应可能是由于个体反应差异,而非无反应。

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