Thiébot M H, Le Bihan C, Soubrié P, Simon P
Psychopharmacology (Berl). 1985;86(1-2):147-52. doi: 10.1007/BF00431700.
This study investigated whether benzodiazepines reduce the capacity of animals to wait for food reward. Rats trained in a T-maze were allowed to choose between two magnitudes of reward: immediate, but small (two pellets) vs delayed, but large (eight pellets). The rats learned within ten sessions to select (80-100%) the arm leading to the largest reward. Separate groups of rats were then confined for 15, 30 or 60 s in the arm associated with the largest reward before gaining access to the spacially contiguous goal-box. The choice of the other arm was not followed by a period of waiting. Under these conditions, the frequency with which the small-reward arm was chosen increased linearly as a function of the duration of the waiting period. Diazepam (2-4 mg/kg IP) dose-dependently increased the number of times the small-reward arm was chosen during the sessions for which the waiting period was fixed at 15 or 30 s. Nitrazepam (2 mg/kg IP), chlordiazepoxide (16 mg/kg IP) and clobazam (16 mg/kg IP) had similar effects. The action of diazepam was counteracted by simultaneous administration of flumazepil (Ro 15-1788, 8 mg/kg PO). In the absence of confinement, these benzodiazepines, diazepam (4 mg/kg) excepted, did not modify selection of the large-reward arm. Conversely, the serotonin uptake blockers indalpine (2-4 mg/kg IP) and zimelidine (8-16 mg/kg IP) dose-dependently increased preference for the arm leading to the delayed (25 s) but large reward. These results suggest that benzodiazepines, perhaps by increasing impulsivity, render the animals less prone than controls to tolerate delayed access to reward.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究调查了苯二氮䓬类药物是否会降低动物等待食物奖励的能力。在T型迷宫中训练的大鼠可以在两种奖励幅度之间进行选择:即时但量小(两颗食丸)与延迟但量大(八颗食丸)。大鼠在十次训练内学会选择(80 - 100%)通向最大奖励的臂。然后将单独的几组大鼠在与最大奖励相关的臂中禁闭15、30或60秒,之后才能进入空间相邻的目标箱。选择另一臂则无需等待。在这些条件下,选择小奖励臂的频率随等待期持续时间呈线性增加。地西泮(2 - 4毫克/千克腹腔注射)剂量依赖性地增加了在等待期固定为15或30秒的训练过程中选择小奖励臂的次数。硝西泮(2毫克/千克腹腔注射)、氯氮䓬(16毫克/千克腹腔注射)和氯巴占(16毫克/千克腹腔注射)有类似作用。同时给予氟马西尼(Ro 15 - 1788,8毫克/千克口服)可抵消地西泮的作用。在没有禁闭的情况下,除地西泮(4毫克/千克)外,这些苯二氮䓬类药物不会改变对大奖励臂的选择。相反,5-羟色胺摄取阻滞剂吲哚哌胺(2 - 4毫克/千克腹腔注射)和齐美利定(8 - 16毫克/千克腹腔注射)剂量依赖性地增加了对通向延迟(25秒)但量大奖励的臂的偏好。这些结果表明,苯二氮䓬类药物可能通过增加冲动性,使动物比对照组更不容易耐受延迟获得奖励。(摘要截短于250字)