Riley A L, Pournaghash S
Department of Psychology, American University, Washington, DC 20016, USA.
Pharmacol Biochem Behav. 1995 Dec;52(4):779-87. doi: 10.1016/0091-3057(95)00180-5.
Rats trained to discriminate the mixed mu agonist/kappa antagonist buprenorphine from its vehicle generalize buprenorphine control to morphine. Buprenorphine, however, does not generalize to MR2266. The generalization to morphine suggests that buprenorphine's mu agonist properties mediated in part its discriminative control. The failure to generalize to MR2266, a compound reported to block kappa-mediated effects, however, suggests that its kappa antagonist activity was not involved in its discriminative effects. The ability of buprenorphine's mu (but not kappa) activity to establish stimulus control may be a function of the overshadowing of the kappa properties of buprenorphine by its concurrent mu activity. To test this possibility, in the present experiment rats were chronically exposed to morphine prior to buprenorphine discrimination training. This procedure has been reported to result in tolerance to buprenorphine's mu agonist effects and a more pronounced display of its kappa antagonist properties. The rats were then tested for the generalization of buprenorphine control to morphine, MR2266, and pentobarbital. As expected, buprenorphine failed to generalize to the nonopioid pentobarbital. Although subjects were tolerant to morphine (as evidenced by reductions in morphine-induced behavioral effects and a rightward shift in the doses of morphine substituting for buprenorphine), buprenorphine still failed to generalize to MR2266. The failure of buprenorphine to generalize to MR2266 under conditions that should have allowed for the development of stimulus control by buprenorphine's kappa antagonist activity was discussed in terms of the general inability of kappa antagonist activity to support discrimination learning.
经过训练能区分混合μ激动剂/κ拮抗剂丁丙诺啡与其溶媒的大鼠,会将丁丙诺啡的效应泛化至吗啡。然而,丁丙诺啡不会泛化至MR2266。向吗啡的泛化表明,丁丙诺啡的μ激动剂特性部分介导了其辨别性效应。然而,未能向MR2266泛化,MR2266是一种据报道可阻断κ介导效应的化合物,这表明其κ拮抗剂活性未参与其辨别性效应。丁丙诺啡的μ(而非κ)活性建立刺激控制的能力,可能是其同时存在的μ活性掩盖了丁丙诺啡κ特性的结果。为了验证这种可能性,在本实验中,大鼠在丁丙诺啡辨别训练前长期接触吗啡。据报道,该程序会导致对丁丙诺啡的μ激动剂效应产生耐受性,并更明显地表现出其κ拮抗剂特性。然后测试大鼠对丁丙诺啡效应向吗啡、MR2266和戊巴比妥的泛化情况。正如预期的那样,丁丙诺啡未能泛化至非阿片类药物戊巴比妥。尽管实验对象对吗啡产生了耐受性(表现为吗啡诱导的行为效应降低以及替代丁丙诺啡的吗啡剂量向右移动),但丁丙诺啡仍未能泛化至MR2266。在本应允许丁丙诺啡的κ拮抗剂活性发展出刺激控制的条件下,丁丙诺啡未能泛化至MR2266,这一点根据κ拮抗剂活性普遍无法支持辨别学习进行了讨论。