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重复戒断发作对乙醇处理大鼠乙醇耐受性获得和丧失的影响。

The effect of repeated withdrawal episodes on acquisition and loss of tolerance to ethanol in ethanol-treated rats.

作者信息

Maier D M, Pohorecky L A

出版信息

Physiol Behav. 1987;40(4):411-24. doi: 10.1016/0031-9384(87)90025-4.

Abstract

Male rats were administered ethanol via an intragastric catheter (8.0-12.0 g/kg/day) either continuously for 8 weeks or on a binge schedule with four 2 week cycles of drug administration separated from each successive cycle by a 2 week period of no drug treatment. Older rats were administered ethanol for 2 weeks, to provide an age control for the binge-treated animals as age can alter an animal's sensitivity to ethanol. Acquisition and loss of tolerance to ethanol-induced motor impairment were measured on a dowel task while acquisition and loss of tolerance to ethanol-induced hypothermia were assessed by measuring rectal temperature. Acceleration of tolerance development to both ethanol-induced motor impairment and hypothermia was observed in animals subjected to repeated withdrawal episodes (binge-Study 1) but not in the controls for total dose and duration of drug treatment who experienced withdrawal only once (continuous-Study 2). Persistence of tolerance to ethanol-induced motor impairment occurred in both binge and continuously treated animals while persistence of tolerance to ethanol-induced hypothermia was seen only in the binge treated animals. Age (3 to 7 months) did not affect tolerance development or decay. After three cycles of drug treatment (three withdrawal episodes), binge treated animals showed an impairment in motor ability when blood ethanol levels were near zero. This impairment disappeared when the animals were administered ethanol, indicating a normalizing effect of ethanol on motor behavior in animals subjected to repeated episodes of withdrawal. A similar, but not significant, effect was seen in continuously treated animals. Thus, in an animal exposed to prolonged ethanol treatment, persistent changes in responding to the drug were found. The persistence of these changes was enhanced by the experience of withdrawal from ethanol.

摘要

雄性大鼠通过胃内导管给予乙醇(8.0 - 12.0 g/kg/天),连续给药8周,或采用暴饮模式,进行四个2周的给药周期,每个连续周期之间有2周的无药物治疗期。对老年大鼠给予乙醇2周,以作为暴饮处理动物的年龄对照,因为年龄会改变动物对乙醇的敏感性。在木钉任务中测量对乙醇诱导的运动障碍的耐受性的获得和丧失,同时通过测量直肠温度评估对乙醇诱导的体温过低的耐受性的获得和丧失。在经历反复戒断发作的动物(暴饮研究1)中观察到对乙醇诱导的运动障碍和体温过低的耐受性发展加速,但在仅经历一次戒断的药物治疗总剂量和持续时间的对照组中(连续研究2)未观察到。对乙醇诱导的运动障碍的耐受性在暴饮和连续处理的动物中均持续存在,而对乙醇诱导的体温过低的耐受性仅在暴饮处理的动物中可见。年龄(3至7个月)不影响耐受性的发展或消退。在三个给药周期(三次戒断发作)后,暴饮处理的动物在血液乙醇水平接近零时表现出运动能力受损。当给动物给予乙醇时,这种损伤消失,表明乙醇对经历反复戒断发作的动物的运动行为具有正常化作用。在连续处理的动物中也观察到类似但不显著的效果。因此,在暴露于长期乙醇治疗的动物中,发现了对药物反应的持续变化。乙醇戒断的经历增强了这些变化的持续性。

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