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作为大鼠乙醇耐受性发展和丧失指标的定时控制行为

Schedule-controlled behavior as an index of the development and loss of ethanol tolerance in the rat.

作者信息

Bird D C, Holloway F A, Carney J M

出版信息

Psychopharmacology (Berl). 1985;87(4):414-20. doi: 10.1007/BF00432505.

DOI:10.1007/BF00432505
PMID:3936099
Abstract

Twelve male Sprague-Dawley rats, following training on one of two food-motivated operant schedules (Fixed-Ratio 30 or Variable Interval 30 s), were exposed to an escalating regimen of daily ethanol (1.125-3.0 g/kg, IP) administration. This increasing dose regimen continued until the maximally tolerable dose for each subject was reached. Tolerance was then monitored for approximately 6 months by periodic ethanol challenge doses (1.5 g/kg). Dose-effect curves (DECs) were obtained prior to chronic ethanol (DEC1), immediately after ethanol tolerance development (DEC2), and 6 months (DEC3) following termination of ethanol exposure. At DEC1, ethanol produced dose-dependent decreases in rate on both schedules with no significant schedule differences in ED50 (the dose effective at reducing the maximal response rate by one-half) values. Maximal tolerance was achieved in means of 46 and 55 days on the VI and FR schedules, respectively. Differences in rate of tolerance acquisition on the initial dose of the chronic regimen (1.125 g/kg) account for most of the difference in the overall rate of acquisition. Comparison of the ED50 data from DECs 1 and 2 indicated that daily ethanol exposure resulted in a 2-fold decrease in ethanol sensitivity (i.e., tolerance) on both operant schedules. The ED50 data from DECs 1 and 3 demonstrated a 1.7-fold decrease in ethanol potency on DEC3. This duration of tolerance was considerably longer than that generally reported, and possibly related to the extended ethanol exposure and the sensitivity of operant schedules to drug effects.

摘要

12只雄性斯普拉格-道利大鼠,在两种以食物为动机的操作性条件反射程序(固定比率30或可变间隔30秒)之一上接受训练后,暴露于每日递增的乙醇给药方案(1.125 - 3.0克/千克,腹腔注射)中。这种递增剂量方案持续进行,直到达到每个受试者的最大耐受剂量。然后通过定期给予乙醇激发剂量(1.5克/千克)监测耐受性约6个月。在慢性乙醇给药前(DEC1)、乙醇耐受性发展后立即(DEC2)以及乙醇暴露终止后6个月(DEC3)获得剂量效应曲线(DEC)。在DEC1时,乙醇在两种程序上均产生剂量依赖性的反应率降低,ED50(使最大反应率降低一半的有效剂量)值在两种程序之间无显著差异。在可变间隔和固定比率程序上,分别在平均46天和55天达到最大耐受性。慢性给药方案初始剂量(1.125克/千克)时耐受性获得速率的差异占总体获得速率差异的大部分。DEC1和DEC2的ED50数据比较表明,每日乙醇暴露导致两种操作性条件反射程序上乙醇敏感性(即耐受性)降低2倍。DEC1和DEC3的ED50数据表明,DEC3时乙醇效力降低1.7倍。这种耐受性持续时间比一般报道的要长得多,可能与延长的乙醇暴露以及操作性条件反射程序对药物效应的敏感性有关。

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本文引用的文献

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