Le Merrer Julie, Stephens David N
Department of Psychology, University of Sussex, Falmer, Brighton BN1 9QG, United Kingdom.
J Neurosci. 2006 Jul 5;26(27):7163-71. doi: 10.1523/JNEUROSCI.5345-05.2006.
Repeated administration of abused drugs sensitizes their stimulant effects and results in a drug-paired environment eliciting conditioned activity. We tested whether food induces similar effects. Food-deprived male mice were given novel food during 30 min tests in a runway (FR group) that measured locomotor activity. Whereas the activity of this group increased with repeated testing, that of a group exposed to the runways but that received the food in the home cage (FH group), or of a group satiated by prefeeding before testing (SAT group), decreased. When exposed to the runways in the absence of food, the paired group was more active than the other groups (conditioned activity); no activity differences were seen in an alternative, non-food-paired, apparatus. Conditioned activity survived a 3-week period without runway exposure. Conditioned activity was selectively reduced by the opiate antagonist naltrexone (10-20 mg/kg) and by the noncompetitive AMPA receptor antagonist GYKI 52466 [1-(4-aminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine hydrochloride] (5-10 mg/kg). The D1 antagonist SCH23390 [R(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride] (15-30 microg/kg) and D2 antagonist sulpiride (25-125 mg/kg) reduced activity nonspecifically. A single intraperitoneal dose of cocaine (10 mg/kg) or morphine (20 mg/kg) increased activity compared with saline, the stimulant effect being larger in the FR group, suggesting "cross-sensitization" to these drugs. However, pretreatment with GYKI 52466 or naltrexone at doses that suppressed conditioned activity in FR animals suppressed cross-sensitization to cocaine. When allowed ad libitum access to food in the runway, FR mice consumed more pellets in a time-limited test. Thus, many of the features of behavioral sensitization to drugs can be demonstrated using food reward and may contribute to excessive eating.
反复使用滥用药物会使其刺激作用敏感化,并导致药物配对环境引发条件性活动。我们测试了食物是否会引发类似的效果。在一个测量运动活动的跑道上,对禁食的雄性小鼠进行30分钟的测试,期间给予它们新的食物(FR组)。该组的活动随着反复测试而增加,而另一组小鼠虽暴露于跑道,但在其笼舍中进食(FH组),或者一组在测试前通过预喂达到饱腹状态(SAT组),其活动则减少。当在没有食物的情况下暴露于跑道时,配对组比其他组更活跃(条件性活动);在另一个非食物配对的装置中未观察到活动差异。在没有跑道暴露的情况下,条件性活动持续了3周。阿片类拮抗剂纳曲酮(10 - 20毫克/千克)和非竞争性AMPA受体拮抗剂GYKI 52466 [1 - (4 - 氨基苯基)-4 - 甲基 - 7,8 - 亚甲基二氧基 - 5H - 2,3 - 苯并二氮杂卓盐酸盐](5 - 10毫克/千克)可选择性地降低条件性活动。D1拮抗剂SCH23390 [R(+)-7 - 氯 - 8 - 羟基 - 3 - 甲基 - 1 - 苯基 - 2,3,4,5 - 四氢 - 1H - 3 - 苯并氮杂卓盐酸盐](15 - 30微克/千克)和D2拮抗剂舒必利(25 - 125毫克/千克)非特异性地降低活动。与生理盐水相比,单次腹腔注射可卡因(10毫克/千克)或吗啡(20毫克/千克)会增加活动,FR组的刺激作用更大,这表明对这些药物存在“交叉敏感化”。然而,以抑制FR动物条件性活动的剂量用GYKI 52466或纳曲酮预处理可抑制对可卡因的交叉敏感化。当在跑道上允许FR小鼠自由进食时,在限时测试中它们消耗的颗粒更多。因此,使用食物奖励可以证明行为对药物敏感化的许多特征,并且可能导致过度进食。