RTI International, 3040 Cornwallis Road, Research Triangle Park, NC 27709, USA.
RTI International, 3040 Cornwallis Road, Research Triangle Park, NC 27709, USA.
Neuropharmacology. 2018 Jul 15;137:133-140. doi: 10.1016/j.neuropharm.2018.04.018. Epub 2018 May 3.
Edible cannabis-infused products are an increasingly popular method of using cannabis in the United States. Yet, preclinical research to determine mechanisms underlying abuse of Δ-tetrahydrocannabinol (THC), the primary psychoactive constituent of cannabis, has focused primarily on the effects of parenteral administration. The purpose of this study was to examine the rewarding and aversive effects of oral THC in a novel rodent voluntary ingestion model. Adult male and female Sprague Dawley rats were given access to sucrose-sweetened solutions during daily sessions. A range of THC concentrations, each paired with a unique flavor previously tested alone, was introduced into these solutions for four-session exposure periods and drinking volumes were measured. Injected (i.p.) THC doses were also paired with unique flavors to compare the effects of route of THC administration on drinking. Introduction of THC into sucrose solutions dose-dependently decreased drinking upon initial exposure, though drinking generally increased in subsequent sessions. By contrast, i.p. THC produced sustained dose-dependent decreases in drinking in rats of both sexes. Subsequent exposure to paired flavors in the absence of THC resulted in further decreases in drinking, suggesting route-specific aversion. Additional testing using saccharin-sweetened solutions in a two-bottle choice paradigm was also conducted, with THC producing sustained dose-dependent decreases in drinking after initial exposure in rats of both sexes. Though self-administration of ingested THC was not demonstrated, evidence of route-specific THC aversion was observed, which suggests that certain routes and/or rates of THC administration may mitigate some of its aversive effects.
食用含大麻素的产品是美国越来越流行的一种使用大麻的方法。然而,用于确定 Δ-四氢大麻酚(THC)滥用机制的临床前研究主要集中在该药物的注射给药效应上。该研究的目的是在新型啮齿动物自愿摄入模型中检查口服 THC 的奖赏和厌恶效应。成年雄性和雌性 Sprague Dawley 大鼠在每日的实验中可接触到含糖的蔗糖溶液。将一系列 THC 浓度与之前单独测试过的独特味道配对引入这些溶液中,进行了为期四个实验期的暴露,并测量了摄水量。同时也将注射(i.p.)THC 剂量与独特的味道配对,以比较 THC 给药途径对摄水的影响。最初暴露于 THC 会使蔗糖溶液的摄水量呈剂量依赖性地减少,但随后的实验中摄水量通常会增加。相比之下,i.p. THC 会使雌雄大鼠的摄水量持续产生剂量依赖性的减少。随后在没有 THC 的情况下接触配对的味道会导致摄水量进一步减少,表明存在特定途径的厌恶。使用蔗糖溶液在双瓶选择范式中进行了额外的测试,结果显示雌雄大鼠在初次暴露后,THC 会持续产生剂量依赖性的摄水量减少。尽管未证明摄入 THC 的自我给药,但观察到了特定途径的 THC 厌恶的证据,这表明某些途径和/或 THC 给药速率可能会减轻其一些厌恶效应。