Ahsan Hafiz Muhammad, de la Peña June Bryan I, Botanas Chrislean Jun, Kim Hee Jin, Yu Gu Yong, Cheong Jae Hoon
Uimyung Research Institute for Neuroscience, Department of Pharmacy, Sahmyook University, Seoul 139-742.
Department of Chemistry, Sahmyook University, Seoul 139-742, Republic of Korea.
Biomol Ther (Seoul). 2014 Sep;22(5):460-6. doi: 10.4062/biomolther.2014.056. Epub 2014 Sep 30.
Nicotine addiction is a worldwide problem. However, previous studies characterizing the rewarding and reinforcing effects of nicotine in animal models have reported inconsistent findings. It was observed that the addictive effects are variable on different factors (e.g. route, dose, and age). Here, we evaluated the rewarding and reinforcing effects of nicotine in different routes of administration, across a wide dose range, and in different age groups. Two of the most widely used animal models of drug addiction were employed: the conditioned place preference (CPP) and self-administration (SA) tests. Nicotine CPP was evaluated in different routes [intraperitoneal (i.p.) and subcutaneous (s.c.)], doses (0.05 to 1.0 mg/kg) and age [adolescent and adult rats]. Similarly, intravenous nicotine SA was assessed in different doses (0.01 to 0.06 mg/kg/infusion) and age (adolescent and adult rats). In the CPP test, s.c. nicotine produced greater response than i.p. The 0.2 mg/kg dose produced highest CPP response in adolescent, while 0.6 mg/kg in adult rats; which were also confirmed in 7 days pretreated rats. In the SA test, adolescent rats readily self-administer 0.03 mg/kg/infusion of nicotine. Doses that produced nicotine CPP and SA induced blood nicotine levels that corresponded well with human smokers. In conclusion, we have demonstrated that nicotine produces reliable CPP [0.2 mg/kg dose (s.c.)] in adolescents and [0.6 mg/kg dose (s.c.)] in adults, and SA [0.03 mg/kg/infusion] in adolescent rats. Both tests indicate that adolescent rats are more sensitive to the rewarding and reinforcing effects of nicotine.
尼古丁成瘾是一个全球性问题。然而,以往在动物模型中表征尼古丁奖赏和强化作用的研究报告结果并不一致。据观察,成瘾效应在不同因素(如给药途径、剂量和年龄)上存在差异。在此,我们评估了尼古丁在不同给药途径、广泛剂量范围以及不同年龄组中的奖赏和强化作用。采用了两种最常用的药物成瘾动物模型:条件性位置偏爱(CPP)和自身给药(SA)试验。在不同给药途径[腹腔注射(i.p.)和皮下注射(s.c.)]、剂量(0.05至1.0毫克/千克)和年龄[青春期和成年大鼠]条件下评估尼古丁CPP。同样,在不同剂量(0.01至0.06毫克/千克/输注)和年龄(青春期和成年大鼠)条件下评估静脉注射尼古丁SA。在CPP试验中,皮下注射尼古丁比腹腔注射产生的反应更大。0.2毫克/千克剂量在青春期大鼠中产生最高的CPP反应,而在成年大鼠中为0.6毫克/千克;这在预处理7天的大鼠中也得到了证实。在SA试验中,青春期大鼠容易自身给药0.03毫克/千克/输注的尼古丁。产生尼古丁CPP和SA的剂量所诱导的血液尼古丁水平与人类吸烟者相当。总之,我们已经证明,尼古丁在青春期大鼠中产生可靠的CPP[0.2毫克/千克剂量(皮下注射)],在成年大鼠中产生[