Millington W R, McCall A L, Wurtman R J
Ann Neurol. 1978 Oct;4(4):302-6. doi: 10.1002/ana.410040403.
Competition by deanol (dimethylaminoethanol) with choline for uptake from the bloodstream into the brain was demonstrated by simultaneous intracarotid administration of carbon 14-labeled choline with deanol (plus tritiated water and indium 113m, to calculate a brain uptake index) and by measuring the brain uptake of 14C-labeled choline mixed with sera from rats pretreated with deanol (300 or 500 mg/kg 8 or 30 minutes earlier). The inhibition constant for inhibition of choline uptake by deanol (159 micrograms) was actually lower than the Michaelis constant for choline itself (442 micrograms); hence, the affinity of the carrier mechanism for deanol is at least as great as it is for choline. Deanol administration also elevated blood choline levels; thus, the effect of the drug on brain choline (and acetylcholine) levels is the result of the increase it produces in blood choline and the suppression it causes in choline uptake. These findings may explain discrepant results from laboratories seeking increases in brain acetylcholine or clinical improvement in patients with tardive dyskinesia after deanol treatment.
通过将碳14标记的胆碱与二甲氨基乙醇(同时给予氚化水和铟113m以计算脑摄取指数)经颈内动脉同时给药,以及通过测量与经二甲氨基乙醇(300或500mg/kg,提前8或30分钟)预处理的大鼠血清混合的14C标记胆碱的脑摄取,证明了二甲氨基乙醇与胆碱在从血流摄取进入脑方面存在竞争。二甲氨基乙醇(159微克)抑制胆碱摄取的抑制常数实际上低于胆碱自身的米氏常数(442微克);因此,载体机制对二甲氨基乙醇的亲和力至少与对胆碱的亲和力一样大。给予二甲氨基乙醇也会提高血胆碱水平;因此,该药物对脑胆碱(和乙酰胆碱)水平的影响是它所引起的血胆碱增加以及对胆碱摄取的抑制作用的结果。这些发现可能解释了在寻求通过二甲氨基乙醇治疗增加脑乙酰胆碱或改善迟发性运动障碍患者临床症状的实验室中出现的不一致结果。