Levin Edward D, Lawrence Susan Slade, Petro Ann, Horton Kofi, Rezvani Amir H, Seidler Frederic J, Slotkin Theodore A
Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, USA; Department of Pharmacology and Cancer Biology, Duke University Medical Center, USA.
Neurotoxicol Teratol. 2007 Jul-Aug;29(4):458-65. doi: 10.1016/j.ntt.2007.02.002. Epub 2007 Mar 2.
Adolescence is the life stage when tobacco addiction typically begins. Adolescent neurobehavioral development may be altered by nicotine self-administration in a way that persistently potentiates addiction. Previously, we showed that female adolescent rats self-administer more nicotine than do adults and that the increased nicotine intake then persists through the transition to adulthood [E.D. Levin, A. Rezvani, D. Montoya, J. Rose, H. Swartzwelder, Adolescent-onset nicotine self-administration modeled in female rats, Psychopharmacology 169 (2003) 141-149.]. In the current study, male Sprague-Dawley rats were given access to nicotine via the standard operant IV self-administration procedure (nicotine bitartrate dose of 0.03 mg/kg/infusion). One group of male rats started during adolescence the other group started in young adulthood. After the end of the four-week period of self-administration brain regions of the rats were assessed for alpha4beta2 nicotinic receptor binding. We found that male rats, like females, show higher nicotine self-administration when starting during adolescence as compared to starting in adulthood (p<0.001). Indeed, the effect in adolescent males was even greater than that in females, with more than triple the rate of nicotine self-administration vs. the adult-onset group during the first 2 weeks. The adolescent onset nicotine-self-administering rats also had significantly greater high affinity nicotinic receptor binding in the midbrain and the striatum, whereas hippocampal binding did not differ between the age groups. Striatal values significantly correlated with nicotine self-administration during the first 2 weeks in the adult-onset group but not the adolescent-onset rats, suggesting that the differences in self-administration may depend in part on underlying disparities in synaptic responses to nicotine. After the initial 2 weeks, nicotine self-administration in male rats declined toward adult-like levels, as the adolescent rats approached adulthood. This study showed that adolescent male rats self-administer significantly more nicotine than do male adult rats, but that adolescent-onset nicotine self-administration in male rats declines over weeks of continued use to approach adult-onset levels. In a previous study, we found that female rats also show greater nicotine self-administration with adolescent onset vs. adult onset, but that the females continued higher rates of self-administration into adulthood. Our results thus reinforce the concept that the adolescent brain is unusually receptive to the effects of nicotine in a manner that reinforces the potential for addiction.
青春期是烟草成瘾通常开始的生命阶段。尼古丁自我给药可能会改变青少年的神经行为发育,以一种持续增强成瘾性的方式。此前,我们发现雌性青少年大鼠比成年大鼠自我给药更多的尼古丁,并且增加的尼古丁摄入量会持续到成年期 [E.D. 莱文、A. 雷兹瓦尼、D. 蒙托亚、J. 罗斯、H. 斯瓦茨韦尔德,《雌性大鼠模拟青少年期开始的尼古丁自我给药》,《精神药理学》169 (2003) 141 - 149]。在当前研究中,雄性斯普拉格 - 道利大鼠通过标准操作性静脉自我给药程序获取尼古丁(酒石酸尼古丁剂量为0.03 mg/kg/输注)。一组雄性大鼠在青春期开始,另一组在成年早期开始。在四周的自我给药期结束后,评估大鼠的脑区α4β2烟碱型受体结合情况。我们发现,与成年期开始相比,雄性大鼠在青春期开始时也表现出更高的尼古丁自我给药量(p<0.001)。实际上,青春期雄性大鼠的这种效应甚至比雌性大鼠更大,在最初两周内,尼古丁自我给药率是成年期开始组的三倍多。青春期开始尼古丁自我给药的大鼠在中脑和纹状体中也具有显著更高的高亲和力烟碱型受体结合,而不同年龄组之间海马体的结合没有差异。在成年期开始组中,纹状体的值在最初两周内与尼古丁自我给药显著相关,但在青春期开始组中则不然,这表明自我给药的差异可能部分取决于对尼古丁突触反应的潜在差异。在最初的两周后,随着青春期大鼠接近成年期,雄性大鼠的尼古丁自我给药量下降至类似成年的水平。这项研究表明,青春期雄性大鼠自我给药的尼古丁量明显多于成年雄性大鼠,但青春期开始的尼古丁自我给药在持续使用数周后会下降至成年期开始的水平。在之前的一项研究中,我们发现雌性大鼠与成年期开始相比,青春期开始时也表现出更高的尼古丁自我给药量,但雌性大鼠在成年后仍保持较高的自我给药率。因此,我们的结果强化了这样一个概念,即青少年大脑对尼古丁的影响异常敏感,这种方式增强了成瘾的可能性。