Sala M, Braida D, Calcaterra P, Leone M P, Comotti F A, Gianola S, Gori E
Institute of Pharmacology, Faculty of Mathematical, Physical and Natural Sciences, University of Milan, Italy.
Eur J Pharmacol. 1991 Feb 26;194(1):45-9. doi: 10.1016/0014-2999(91)90122-7.
The effect of two anticholinergic drugs administered intracerebroventricularly on acquisition of an 8-arm radial maze task was examined in the rat. Increasing doses of atropine (1, 4.5, 22.5, 45 micrograms/rat) and pirenzepine (4.5, 15, 60, 90 micrograms/rat) significantly impaired performance in the working-memory components of the task. For both drugs this impairment was linearly related to the log of the administered doses and log-dose-response relationship were parallel. The regression lines calculated for each parameter for both drugs were parallel to each other, thus allowing us to calculate the potency of atropine versus pirenzepine: atropine was 5.4 times more potent than pirenzepine for correct arm entries, 10 times more potent for the number of errors and 4 times more potent for the total time taken to complete the task. The relevance of M1 and M2 subtype central acetylcholine receptors in cognitive processes is discussed.
研究了向大鼠脑室内注射两种抗胆碱能药物对其在八臂放射状迷宫任务学习中的影响。递增剂量的阿托品(1、4.5、22.5、45微克/只大鼠)和哌仑西平(4.5、15、60、90微克/只大鼠)显著损害了该任务工作记忆部分的表现。对于这两种药物,这种损害与给药剂量的对数呈线性相关,且对数剂量反应关系平行。为两种药物的每个参数计算的回归线相互平行,因此我们能够计算出阿托品相对于哌仑西平的效价:在正确进入臂数方面,阿托品的效价比哌仑西平高5.4倍;在错误数量方面,高10倍;在完成任务所需的总时间方面,高4倍。文中讨论了M1和M2亚型中枢乙酰胆碱受体在认知过程中的相关性。