Leander J D
Psychopharmacology (Berl). 1981;75(1):5-8. doi: 10.1007/BF00433492.
The effects of benztropine, scopolamine, atropine, methylatropine, amitriptyline, phencyclidine, and meperidine were determined alone and in conjunction with a behaviorally suppressing dose (0.05 mg/kg IM) of oxotremorine in pigeons responding under a multiple fixed-ratio 30 fixed-interval 5-min schedule of grain presentation. Benztropine, scopolamine, atropine, and amitriptyline antagonized the behavioral suppressing effects of oxotremorine at doses that alone decreased responding. In contrast, methylatropine, phencyclidine, and meperidine did not antagonize the effects of oxotremorine. These results suggest that benztropine, scopolamine, atropine, and amitripytline decrease responding due to an action at central muscarinic receptors, whereas the behavioral effects of methylatropine, phencyclidine, and meperidine are due to actions other than at central muscarinic receptors.
在鸽子按照多重固定比率30固定间隔5分钟谷物呈现时间表做出反应的情况下,分别测定了苯海索、东莨菪碱、阿托品、甲阿托品、阿米替林、苯环利定和哌替啶的作用,以及它们与行为抑制剂量(0.05毫克/千克,肌肉注射)的氧化震颤素联合使用时的作用。苯海索、东莨菪碱、阿托品和阿米替林在单独使用时能降低反应的剂量下,拮抗了氧化震颤素的行为抑制作用。相比之下,甲阿托品、苯环利定和哌替啶并未拮抗氧化震颤素的作用。这些结果表明,苯海索、东莨菪碱、阿托品和阿米替林由于作用于中枢毒蕈碱受体而降低反应,而甲阿托品、苯环利定和哌替啶的行为效应则归因于中枢毒蕈碱受体以外的作用。