Stojakovic Andrea, Ahmad Syed Muzzammil, Lutfy Kabirullah
Department of Pharmaceutical Sciences, College of Pharmacy, Western University of Health Sciences, 309 East 2nd Street, Pomona, CA 91766, USA.
Department of Neurology, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA.
Brain Sci. 2021 Mar 26;11(4):420. doi: 10.3390/brainsci11040420.
Evidence suggests that nicotine and alcohol can each serve as a gateway drug. We determined whether prior nicotine and alcohol treatment would alter amphetamine reward. Also, we examined whether age and dopaminergic neurotransmission are important in this regard. Male and female adolescent and adult C57BL/6J mice were tested for baseline place preference. Mice then received six conditioning with saline/nicotine (0.25 mg/kg) twice daily, followed by six conditioning with saline/ethanol (2 g/kg). Control mice were conditioned with saline/saline throughout. Finally, mice were conditioned with amphetamine (3 mg/kg), once in the nicotine-alcohol-paired chamber, and tested for place preference 24 h later. The following day, mice were challenged with amphetamine (1 mg/kg) and tested for place preference under a drugged state. Mice were then immediately euthanized, their brain removed, and nucleus accumbens isolated and processed for the level of dopamine receptors and transporter and glutamate receptors. We observed a greater amphetamine-induced place preference in naïve adolescents than adult mice with no change in state-dependent place preference between the two age groups. In contrast, amphetamine induced a significant place preference in adult but not adolescent mice with prior nicotine-alcohol exposure under the drug-free state. The preference was significantly greater in adults than adolescents under the drugged state. The enhanced response was associated with higher dopamine-transporter and D but reduced D receptors' expression in adult rather than adolescent mice, with no changes in glutamate receptors levels. These results suggest that prior nicotine and alcohol treatment differentially alters amphetamine reward in adult and adolescent mice. Alterations in dopaminergic neurotransmission may be involved in this phenotype.
有证据表明,尼古丁和酒精都可充当入门毒品。我们确定了先前的尼古丁和酒精处理是否会改变苯丙胺奖赏效应。此外,我们研究了年龄和多巴胺能神经传递在这方面是否重要。对雄性和雌性青春期及成年C57BL/6J小鼠进行基线位置偏爱测试。然后,小鼠每天接受两次生理盐水/尼古丁(0.25毫克/千克)的六次条件训练,随后接受生理盐水/乙醇(2克/千克)的六次条件训练。对照小鼠全程接受生理盐水/生理盐水的条件训练。最后,小鼠在尼古丁-酒精配对的实验箱中接受一次苯丙胺(3毫克/千克)的条件训练,并在24小时后测试位置偏爱。第二天,小鼠接受苯丙胺(1毫克/千克)激发,并在药物作用状态下测试位置偏爱。然后立即对小鼠实施安乐死,取出其大脑,分离伏隔核并进行处理,以检测多巴胺受体、转运体和谷氨酸受体的水平。我们观察到,与成年小鼠相比,未接触过药物的青春期小鼠对苯丙胺诱导的位置偏爱更强烈,且两个年龄组之间状态依赖性位置偏爱没有变化。相比之下,在无药物状态下,先前接触过尼古丁-酒精的成年小鼠对苯丙胺产生了显著的位置偏爱,而青春期小鼠则没有。在药物作用状态下,成年小鼠的偏爱明显高于青春期小鼠。这种增强的反应与成年而非青春期小鼠中较高的多巴胺转运体和D(受体)表达相关,但D(受体)表达降低,谷氨酸受体水平没有变化。这些结果表明,先前的尼古丁和酒精处理会不同程度地改变成年和青春期小鼠的苯丙胺奖赏效应。多巴胺能神经传递的改变可能与这种表型有关。