Zernig Gerald, Harbig Philipp, Weiskirchner Ilka, Auffinger Margit, Wakonigg Gudrun, Saria Alois
Division of Neurochemistry, Department of Psychiatry, University of Innsbruck, Austria.
J Mol Neurosci. 2002 Feb-Apr;18(1-2):135-42. doi: 10.1385/JMN:18:1-2:135.
Alley running has been successfully used as an operant to demonstrate both the positive and negative reinforcing effect of intravenously administered drugs of abuse in a bona fide operant conditioning paradigm, the Ettenberg runway, in which confounding drug effects on motor performance and drug accumulation are avoided. While Ettenberg and colleagues focus on the intravenous route of drug administration, we tested the practicability of the subcutaneous route of administration in this runway paradigm in Sprague Dawley rats, using morphine as the investigated drug of abuse. We also modified the Ettenberg runway, most notably in that either food (sweetened condensed milk), no food, morphine, or saline was presented outside the runway in a separate cage. This made shaping, i.e., the initial presentation of a food reinforcer within the runway, necessary to establish responding. The manipulations necessary to administer subcutaneous (sc) injections were well tolerated by over 90% of the tested rats (n = 93). However, sc injections increased runtimes to the experimenter cutoff of 60 s within 20 once-daily sessions. Because of strong experimenter effects, all morphine doses or saline had to be adminstered blind. Under these experimenter-blind conditions, 0.1 and 1 mg/kg subcutaneous morphine proved to be reinforcing in that these doses significantly slowed down the gradual increase in runtimes imposed upon by the sc injection procedure. Thus, morphine can be demonstrated to be a positive reinforcer in a modified Ettenberg runway even when given subcutaneously. This effect, however, is eventually overcome by the negative reinforcing effect of subjecting the animals to sc injection procedure.
在一种真正的操作性条件反射范式——埃滕伯格跑道实验中,巷跑已成功用作一种操作性行为,以证明静脉注射滥用药物的正性和负性强化作用,该实验避免了药物对运动表现的混杂影响和药物蓄积。虽然埃滕伯格及其同事专注于药物的静脉注射途径,但我们在斯普拉格-道利大鼠的这种跑道范式中测试了皮下注射途径的可行性,使用吗啡作为被研究的滥用药物。我们还对埃滕伯格跑道进行了改进,最显著的是在跑道外的一个单独笼子里呈现食物(甜炼乳)、无食物、吗啡或生理盐水。这使得塑造行为成为必要,即在跑道内最初呈现食物强化物以建立反应。超过90%的受试大鼠(n = 93)对皮下注射所需的操作耐受性良好。然而,在每天一次的20次实验中,皮下注射会增加跑到实验者设定的60秒截止时间的时长。由于存在强烈的实验者效应,所有吗啡剂量或生理盐水都必须在盲态下给药。在这些实验者盲态的条件下,0.1和1毫克/千克皮下注射吗啡被证明具有强化作用,因为这些剂量显著减缓了皮下注射程序导致的时长逐渐增加。因此,即使皮下给药,吗啡在改良的埃滕伯格跑道实验中也可被证明是一种正性强化物。然而,这种效应最终会被让动物接受皮下注射程序的负性强化作用所克服。