Riley A L, Wetherington C L
Pharmacol Biochem Behav. 1987 Apr;26(4):677-81. doi: 10.1016/0091-3057(87)90595-8.
Rats injected with the opiate antagonist, naloxone hydrochloride (10 mg/kg), 15 min prior to sessions in which they were given free food on a fixed time 75-sec schedule, displayed retarded acquisition of schedule-induced polydipsia relative to vehicle-injected subjects. Rats injected with naloxone after schedule-induced polydipsia had been acquired were unaffected, i.e., they continued to drink at control levels. Given that schedule-induced polydipsia has been considered non-opioid in nature, because of previous reports of its insensitivity to naloxone, the present report of differential effects of naloxone on the acquisition and maintenance of schedule-induced polydipsia suggests that some modification of this conclusion is necessary. Possible alternative mechanisms for these differential effects are discussed.
在按固定时间75秒的时间表给予大鼠自由食物的实验环节前15分钟,注射阿片类拮抗剂盐酸纳洛酮(10毫克/千克)的大鼠,相对于注射赋形剂的大鼠,在条件诱导性多饮的习得方面表现出延迟。在习得条件诱导性多饮后注射纳洛酮的大鼠未受影响,即它们继续以对照水平饮水。鉴于由于先前有报道称条件诱导性多饮对纳洛酮不敏感,其本质一直被认为是非阿片类的,本报告中纳洛酮对条件诱导性多饮的习得和维持产生不同影响,表明有必要对这一结论进行一些修正。文中讨论了这些不同影响可能的替代机制。