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A double‐blind, placebo‐controlled single dose trial of intravenous flumazenil in Alzheimer's disease
Author(s) -
Templeton Lisa,
Barker Andrew,
Wesnes Keith,
Wilkinson David
Publication year - 1999
Publication title -
human psychopharmacology: clinical and experimental
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.461
H-Index - 78
eISSN - 1099-1077
pISSN - 0885-6222
DOI - 10.1002/(sici)1099-1077(199906)14:4<239::aid-hup94>3.0.co;2-r
Subject(s) - flumazenil , benzodiazepine , placebo , antagonist , anesthesia , alzheimer's disease , cognition , medicine , crossover study , cholinergic , psychology , pharmacology , neuroscience , disease , receptor , pathology , alternative medicine
Benzodiazepine agonists have been shown to reduce cognitive functioning by producing attentional deficits similar to those produced by muscarinic antagonists. It has therefore been postulated that benzodiazepine antagonists may improve cognitive function in patients with Alzheimer's disease by indirectly increasing cholinergic function. Eleven patients with mild to moderate Alzheimer's disease took part in a double‐blind placebo‐controlled crossover study of the effects of a single 1 mg injection of the benzodiazepine antagonist flumazenil on cognitive function. Validated computer tests were used to assess change in cognitive function over time after each injection. No adverse effects of the drug were experienced. Speed on both a simple reaction time task and a picture recognition task was significantly slowed by flumazenil compared to placebo at 15 min ( p =0.027 and p =0.01). Accuracy of recalling pictures was significantly reduced compared to baseline ( p =0.0002), but this was not statistically significant when compared to placebo. Possible reasons for these findings are discussed and it is concluded that a single injection of 1 mg flumazenil produces cognitive slowing in patients with Alzheimer's disease. It is suggested that further research is needed into central benzodiazepine receptor density and function, as well as dose–response studies using flumazenil. Copyright © 1999 John Wiley & Sons, Ltd.