Justinova Zuzana, Ferré Sergi, Barnes Chanel, Wertheim Carrie E, Pappas Lara A, Goldberg Steven R, Le Foll Bernard
Preclinical Pharmacology Section, Behavioral Neuroscience Research Branch, Intramural Research Program, National Institute on Drug Abuse, NIH, DHHS, Biomedical Research Center, 251 Bayview Blvd., Baltimore, MD 21224, USA.
Psychopharmacology (Berl). 2009 Apr;203(2):355-67. doi: 10.1007/s00213-008-1270-0. Epub 2008 Aug 8.
Adenosine receptors are involved in cocaine and methamphetamine discrimination and exposure to caffeine can affect behavioral effects of nicotine in rats.
Here we investigated the relative involvement of adenosine A(1) and A(2A) receptors in nicotine, cocaine, and methamphetamine discrimination, before and/or during chronic caffeine exposure.
The nonselective adenosine receptor antagonist caffeine, the A(1)-receptor antagonist cyclopentyltheophylline (CPT), and the A(2A)-receptor antagonist MSX-3 were evaluated in rats trained to discriminate 0.4 mg/kg nicotine from saline under a fixed-ratio schedule of food delivery. Effects of adenosine receptor antagonists were then compared in rats discriminating nicotine, methamphetamine, or cocaine from saline during chronic caffeine exposure in their drinking water.
Caffeine, CPT, and MSX-3 partially generalized to nicotine and shifted nicotine dose-response curves leftwards. During chronic caffeine exposure, however, all three ligands failed to generalize to nicotine and failed to shift nicotine dose-response curves. In previous experiments, CPT and MSX-3 partially generalized to methamphetamine and cocaine and shifted dose-response curves leftwards. In the present experiments, CPT neither generalized nor shifted dose-response curves for methamphetamine or cocaine during chronic caffeine exposure. However, MSX-3 partially generalized to both psychostimulants and shifted their dose-response curves leftwards. Caffeine partially generalized to cocaine, but not methamphetamine, and shifted both dose-response curves leftwards.
Both adenosine A(1) and A(2A) receptors are capable of modulating the discriminative-stimulus effects of nicotine. Chronic caffeine exposure produces complete tolerance to both A(1)- and A(2A)-mediated effects in nicotine-trained rats. In contrast, chronic caffeine exposure produces tolerance to adenosine A(1)-mediated, but not A(2A)-mediated, effects in methamphetamine- and cocaine-trained rats.
腺苷受体参与可卡因和甲基苯丙胺辨别,且接触咖啡因会影响大鼠体内尼古丁的行为效应。
在此,我们研究了慢性咖啡因暴露之前和/或期间,腺苷A(1)和A(2A)受体在尼古丁、可卡因和甲基苯丙胺辨别中的相对参与情况。
在按固定比率食物投递方案训练以区分0.4毫克/千克尼古丁和生理盐水的大鼠中,评估了非选择性腺苷受体拮抗剂咖啡因、A(1)受体拮抗剂环戊基茶碱(CPT)和A(2A)受体拮抗剂MSX-3。然后比较了在饮用水中进行慢性咖啡因暴露期间,腺苷受体拮抗剂对区分尼古丁、甲基苯丙胺或可卡因与生理盐水的大鼠的影响。
咖啡因、CPT和MSX-3部分泛化至尼古丁,并使尼古丁剂量反应曲线左移。然而,在慢性咖啡因暴露期间,所有三种配体均未泛化至尼古丁,也未使尼古丁剂量反应曲线移动。在先前的实验中,CPT和MSX-3部分泛化至甲基苯丙胺和可卡因,并使剂量反应曲线左移。在本实验中,在慢性咖啡因暴露期间,CPT既未泛化至甲基苯丙胺或可卡因,也未使其剂量反应曲线移动。然而,MSX-3部分泛化至两种精神兴奋剂,并使它们的剂量反应曲线左移。咖啡因部分泛化至可卡因,但未泛化至甲基苯丙胺,并使两种剂量反应曲线左移。
腺苷A(1)和A(2A)受体均能够调节尼古丁的辨别刺激效应。慢性咖啡因暴露使尼古丁训练大鼠对A(1)和A(2A)介导的效应产生完全耐受性。相比之下,慢性咖啡因暴露使甲基苯丙胺和可卡因训练大鼠对腺苷A(1)介导的效应产生耐受性,但对A(2A)介导的效应未产生耐受性。