Marco Eva Maria, Llorente Ricardo, Pérez-Alvarez Laura, Moreno Enrique, Guaza Carmen, Viveros Maria Paz
Departamento de Fisiología (Fisiología Animal II), Facultad de Biología, Universidad Complutense, C/Jose Antonio Novais 2, Ciudad Universitaria, Madrid, Spain.
Behav Brain Res. 2005 Sep 8;163(2):212-8. doi: 10.1016/j.bbr.2005.05.005.
The kappa (kappa) opioid system appears to interact with nicotine in the modulation of locomotion and addiction related processes. In this study we have investigated the possible implication of the kappa-opioid system in the effects of nicotine on anxiety and adrenocortical activity. In two different experiments, we analysed the possible interaction between nicotine (0.5 mg/kg i.p.) and either the kappa-opioid receptor antagonist nor-binaltorphimine (5 mg/kg i.p.) or the kappa-opioid receptor agonist U50,488H (1 mg/kg s.c.). Behavioural and endocrine experiments were performed in different groups of animals. Animals were exposed to the holeboard immediately followed by the plus-maze. Serum corticosterone levels were determined by radioimmunoassay. Nicotine induced an anxiogenic-like effect in the plus-maze and a significant decrease of holeboard activity. The anxiogenic-like effect in the plus-maze was not modified by any of the kappa-opioid receptor ligands. Nicotine also induced a significant increase in the corticosterone levels, and the kappa antagonist, which did not exert any effect per se, antagonised this effect. The kappa-agonist U50,488H induced a significant increase in corticosterone concentration when administered alone. We provide the first evidence for the involvement of the kappa-opioid receptor in the stimulatory effect of nicotine on adrenocortical activity.
κ(kappa)阿片系统似乎在运动及成瘾相关过程的调节中与尼古丁相互作用。在本研究中,我们调查了κ阿片系统在尼古丁对焦虑和肾上腺皮质活动影响中的可能作用。在两个不同实验中,我们分析了尼古丁(0.5毫克/千克腹腔注射)与κ阿片受体拮抗剂 nor - 纳洛酮啡(5毫克/千克腹腔注射)或κ阿片受体激动剂U50,488H(1毫克/千克皮下注射)之间的可能相互作用。在不同组动物中进行了行为和内分泌实验。动物先被置于洞板中,随后立即放入十字迷宫。通过放射免疫分析法测定血清皮质酮水平。尼古丁在十字迷宫中诱发了类似焦虑的效应,并使洞板活动显著减少。十字迷宫中类似焦虑的效应未被任何一种κ阿片受体配体改变。尼古丁还导致皮质酮水平显著升高,而本身无任何作用的κ拮抗剂拮抗了这一效应。单独给予κ激动剂U50,488H时,可使皮质酮浓度显著升高。我们首次提供了证据表明κ阿片受体参与了尼古丁对肾上腺皮质活动的刺激作用。