Bruno G, Mohr E, Gillespie M, Fedio P, Chase T N
Arch Neurol. 1986 Jul;43(7):659-61. doi: 10.1001/archneur.1986.00520070017009.
Cholinergic projections to the cerebral cortex from certain basal forebrain nuclei degenerate in Alzheimer's disease. Nevertheless, attempts to alleviate this disorder through the administration of drugs that increase the availability of acetylcholine to postsynaptic receptor sites have generally yielded disappointing results. In an attempt to evaluate the therapeutic efficacy of cholinomimetics that act independently of the presynaptic cholinergic terminals, a double-blind, placebo-controlled trial of the muscarinic agonist RS-86 (2-ethyl-8 methyl-2,8 diazospiro [4.5]-decane-1,3-dione hydrobromide) was undertaken. Eight patients with Alzheimer's disease with mild to moderately advanced dementia received RS-86 orally at maximum individually tolerated dose levels for eight days. Although some verbal and visuospatial tests showed slight alterations, no consistent overall change in cognitive performance could be discerned. These results lend further support to the view that short-term administration of cholinomimetic monotherapies may fail in the symptomatic treatment of Alzheimer's dementia.
在阿尔茨海默病中,来自某些基底前脑核团的胆碱能投射会退化至大脑皮层。然而,试图通过给予能增加乙酰胆碱对突触后受体位点可用性的药物来缓解这种疾病,总体上却产生了令人失望的结果。为了评估独立于突触前胆碱能终末起作用的拟胆碱药的治疗效果,进行了一项关于毒蕈碱激动剂RS - 86(2 - 乙基 - 8 - 甲基 - 2,8 - 二氮杂螺[4.5]癸烷 - 1,3 - 二酮氢溴酸盐)的双盲、安慰剂对照试验。8名患有轻度至中度晚期痴呆的阿尔茨海默病患者以个体最大耐受剂量口服RS - 86,持续8天。尽管一些语言和视觉空间测试显示有轻微变化,但在认知表现上未发现一致的总体变化。这些结果进一步支持了这样一种观点,即短期给予拟胆碱单药治疗可能无法有效治疗阿尔茨海默病性痴呆的症状。