Keehn J D, Coulson G E, Klieb J
J Exp Anal Behav. 1976 Jan;25(1):105-12. doi: 10.1901/jeab.1976.25-105.
In dose-related amounts, the drug haloperidol attenuated schedule-induced drinking by rats prefed with 0.01-mg drug added to 0, 25, 50, 75 or all of 100 Noyes 45-mg pellets. Drug pellets also induced less drinking than did regular Noyes pellets by rats that obtained these pellets at 1-min intervals by bar pressing. Haloperidol also reduced bar pressing and, temporarily, rate of reinforcement. The results appeared not to be due to a general sedative effect of haloperidol but to its selective power to reduce angiotensin-induced drinking. Thus, schedule-induced drinking, which is abnormal in not causing satiation, is controllable by a drug that interferes with the renin-angiotensin hormone system thought to regulate normal drinking.
以与剂量相关的量,药物氟哌啶醇减轻了预先喂食添加了0.01毫克药物的大鼠的定时诱导饮水,这些药物分别添加到0、25、50、75或全部100颗45毫克的诺伊斯丸剂中。通过按压杠杆以1分钟的间隔获取这些丸剂的大鼠,药物丸剂诱导的饮水也比普通诺伊斯丸剂少。氟哌啶醇还减少了按压杠杆的行为,并暂时降低了强化率。结果似乎不是由于氟哌啶醇的一般镇静作用,而是由于其降低血管紧张素诱导饮水的选择性能力。因此,定时诱导饮水这种不会引起饱腹感的异常饮水行为,可被一种干扰被认为调节正常饮水的肾素-血管紧张素激素系统的药物所控制。