Bevins R A, Besheer J, Pickett K S
Department of Psychology, University of Nebraska-Lincoln, Lincoln, NE 68588-0308, USA.
Pharmacol Biochem Behav. 2001 Jan;68(1):135-45. doi: 10.1016/s0091-3057(00)00451-2.
Little is known about the processes that mediate acquisition and expression of conditioned associations between contextual cues and psychomotor effects of nicotine. In four separate experiments using rats, an environment repeatedly paired with nicotine acquired the ability to elicit increases in activity even in the absence of drug. This conditioned effect was sensitive to nicotine dose. Rats that had 0.6 or 1.2 mg/kg nicotine, but not 0.3 mg/kg, paired with the environment were more active than an unpaired control group (Experiment 1). In Experiment 2, control groups eliminated accounts based on nonspecific effects of nicotine and inhibitory conditioning decreasing activity in the unpaired controls of Experiment 1. Pretreatment on the test day with 100 mg/kg of gamma vinyl-GABA (GVG), a compound that inhibits the enzyme required to breakdown GABA, partially blocked the expression of locomotor conditioning without impairing activity in controls (Experiment 3). In Experiment 4, pretreatment on the test day with the dopamine D(1) receptor antagonist SCH-23390 (0.03 mg/kg) blocked expression of nicotine-conditioned locomotor activity; the D(2)/D(3) receptor antagonist eticlopride did not. Thus, the dopamine D(1) receptor subtype appears to play a role in context-elicited increases in activity conditioned by nicotine; GABA may also modulate the expression of this conditioned effect.
关于介导情境线索与尼古丁精神运动效应之间条件性关联的习得和表达的过程,人们所知甚少。在四项以大鼠为对象的独立实验中,一个与尼古丁反复配对的环境获得了即使在无药物情况下也能引发活动增加的能力。这种条件性效应对尼古丁剂量敏感。与环境配对给予0.6或1.2mg/kg尼古丁(而非0.3mg/kg)的大鼠比未配对的对照组更活跃(实验1)。在实验2中,对照组排除了基于尼古丁非特异性效应和抑制性条件作用降低实验1中未配对对照组活动的解释。在测试当天用100mg/kg的γ-乙烯基-GABA(GVG)进行预处理,GVG是一种抑制分解GABA所需酶的化合物,它部分阻断了运动条件反射的表达,而不影响对照组的活动(实验3)。在实验4中,在测试当天用多巴胺D(1)受体拮抗剂SCH-23390(0.03mg/kg)进行预处理可阻断尼古丁条件性运动活动的表达;D(2)/D(3)受体拮抗剂依托必利则无此作用。因此,多巴胺D(1)受体亚型似乎在尼古丁条件性引发的情境诱发活动增加中起作用;GABA也可能调节这种条件性效应的表达。