Pittenger Steven T, Zeplin Lindsey C, Dwoskin Linda P, Bevins Rick A
Department of Psychology, University of Nebraska-Lincoln, 238 Burnett Hall, Lincoln, NE, 68588-0308, USA.
College of Pharmacy, University of Kentucky, 789 S. Limestone Street, Lexington, KY, 40536-0596, USA.
Psychopharmacology (Berl). 2015 Dec;232(23):4347-58. doi: 10.1007/s00213-015-4067-y. Epub 2015 Sep 14.
Pharmacotherapies are often utilized to aid in smoking cessation, and switching medication when treating nicotine dependence has become more commonplace. Although common, little is known about the impact of the initial therapy on the effects of the subsequent therapy.
To begin to fill this gap in our understanding, this project determined how switching compounds that share stimulus elements with nicotine during extinction altered extinction responding and generalization of this extinction back to nicotine.
Rats were trained in a discriminated goal-tracking task where nicotine administration was followed by intermittent sucrose access; sucrose was withheld following saline administration. In experiment 1, nornicotine supplanted nicotine in extinction sessions 1-3 and then a switch to varenicline on extinction sessions 4-6 was examined. In experiment 2, the reverse was investigated; varenicline to start extinction and then a switch to nornicotine. Generalization of extinction back to the nicotine stimulus was then assessed by generating a cumulative dose-effect curve.
Generalization of extinction back to the training nicotine stimulus was greater if nornicotine had been received at any point in extinction compared to only receiving varenicline. Whereas, extinction with varenicline alone showed more generalization to lower doses of nicotine.
A switch in cessation pharmacotherapy during extinction did not impede or enhance generalization back to the nicotine-training stimulus. The nornicotine stimulus appears to share more stimulus overlap with the 0.4 mg/kg nicotine stimulus and varenicline may share more overlap with lower nicotine doses.
药物疗法常用于辅助戒烟,在治疗尼古丁依赖时更换药物已变得更为常见。尽管很常见,但对于初始疗法对后续疗法效果的影响却知之甚少。
为了填补我们理解上的这一空白,本项目确定了在消退过程中更换与尼古丁具有共同刺激元素的化合物如何改变消退反应以及这种消退向尼古丁的泛化情况。
对大鼠进行辨别性目标追踪任务训练,在给予尼古丁后间歇性给予蔗糖;给予生理盐水后不给予蔗糖。在实验1中,去甲烟碱在消退阶段1 - 3取代尼古丁,然后研究在消退阶段4 - 6更换为伐尼克兰的情况。在实验2中,进行相反的研究;从伐尼克兰开始消退,然后更换为去甲烟碱。然后通过生成累积剂量 - 效应曲线来评估消退向尼古丁刺激的泛化情况。
与仅接受伐尼克兰相比,如果在消退的任何阶段接受过去甲烟碱,消退向训练用尼古丁刺激的泛化程度更高。而单独使用伐尼克兰进行消退时,对较低剂量尼古丁的泛化程度更高。
在消退过程中更换戒烟药物疗法不会阻碍或增强向尼古丁训练刺激的泛化。去甲烟碱刺激似乎与0.4mg/kg尼古丁刺激有更多的刺激重叠,而伐尼克兰可能与较低尼古丁剂量有更多的重叠。