Zavala A R, Nazarian A, Crawford C A, McDougall S A
Department of Psychology, California State University, San Bernardino 92407, USA.
Psychopharmacology (Berl). 2000 Aug;151(2-3):291-8. doi: 10.1007/s002130000377.
Repeated psychostimulant treatment has been shown to sensitize the locomotor activity of young rats, but there is conflicting evidence suggesting that this sensitized response will persist across only a few drug abstinence days.
The purpose of the present study was to determine whether: (a) young rats are capable of expressing a sensitized locomotor response after an extended drug abstinence period, and (b) the longevity of the sensitized response is critically affected by either the number of drug pretreatment days or environmental conditioning factors.
Young rats were pretreated with saline or cocaine (15 mg/kg or 30 mg/kg, i.p.) for either five or ten consecutive days [i.e., on postnatal days (PD) 16-20 or PD 11-20]. After each daily injection, rats were placed in activity chambers, and locomotion was measured for 30 min. To assess environmental conditioning factors, some rats were injected with saline prior to being placed in the activity chambers and then injected with cocaine prior to being returned to the home cage. After one or seven abstinence days (i.e., on PD 22 or PD 28), rats received a challenge injection of saline or cocaine (15 mg/kg) in the activity chamber and locomotion was assessed.
Young rats exhibit cocaine-induced locomotor sensitization after either a short (1-day) or long (7-day) drug abstinence period. When a long abstinence period was used, locomotor sensitization was only apparent when cocaine pretreatment lasted for 10 days. Conditioning factors were also important for determining whether locomotor sensitization was expressed, because young rats pretreated with cocaine in the home cage did not show a sensitized locomotor response after seven abstinence days.
Young rats are capable of showing cocaine-induced locomotor sensitization after an extended abstinence period. Both the number of drug pretreatment days and the environmental context in which cocaine was given (i.e., the activity chamber or home cage) influenced the longevity of cocaine-induced locomotor sensitization.
反复给予精神兴奋剂已被证明会使幼鼠的运动活动产生敏感化,但有相互矛盾的证据表明,这种敏感化反应仅在停药几天后就会持续存在。
本研究的目的是确定:(a)幼鼠在延长的停药期后是否能够表现出敏感化的运动反应,以及(b)敏感化反应的持续时间是否受到药物预处理天数或环境条件因素的严重影响。
幼鼠连续五天或十天用生理盐水或可卡因(15毫克/千克或30毫克/千克,腹腔注射)进行预处理[即出生后第(PD)16 - 20天或PD 11 - 20天]。每天注射后,将大鼠放入活动箱中,测量30分钟内的运动情况。为了评估环境条件因素,一些大鼠在放入活动箱前注射生理盐水,然后在返回笼舍前注射可卡因。在停药一天或七天后(即PD 22或PD 28),大鼠在活动箱中接受生理盐水或可卡因(15毫克/千克)的激发注射,并评估运动情况。
幼鼠在短期(1天)或长期(7天)停药期后均表现出可卡因诱导的运动敏感化。当采用长停药期时,运动敏感化仅在可卡因预处理持续10天时才明显。条件因素对于确定是否表现出运动敏感化也很重要,因为在笼舍中用可卡因预处理的幼鼠在停药七天后未表现出敏感化的运动反应。
幼鼠在延长的停药期后能够表现出可卡因诱导的运动敏感化。药物预处理天数和给予可卡因的环境背景(即活动箱或笼舍)均影响可卡因诱导的运动敏感化的持续时间。