Department of Anesthesiology, Perioperative, and Pain Medicine, Children's Hospital Boston, and Department of Anaesthesia, Harvard Medical School, Boston, MA 02115, USA.
Neuroscience. 2011 Apr 14;179:1-8. doi: 10.1016/j.neuroscience.2011.01.032. Epub 2011 Jan 26.
Adolescence is a critical vulnerable period during which exposure to nicotine greatly enhances the possibility to develop drug addiction. Growing evidence suggests that serotonergic (5-HT) neurotransmission may contribute to the initiation and maintenance of addictive behavior. As the dorsal raphe (DR) and median raphe (MnR) nuclei are the primary 5-HT source to the forebrain, the current study tested the hypothesis that there are age-dependent effects of acute nicotine administration on activation of 5-HT neurons within these regions. Both adolescent (Postnatal day 30) and adult (Postnatal day 70) male Sprague-Dawley rats received subcutaneous injection of either saline or nicotine (0.2, 0.4, or 0.8 mg/kg). Subsequently, the number of 5-HT cells that were double-labeled for Fos and tryptophan hydroxylase was counted in seven subregions within the DR and the entire MnR. The results show that acute nicotine injection induces Fos expression in 5-HT neurons in a region-specific manner. In addition, adolescents show broader regional activations at either a lower (0.2 mg/kg) and a higher (0.8 mg/kg) dose of nicotine, displaying a unique U-shape response curve across doses. In contrast, 5-HT cells with activated Fos expression were restricted to fewer regions in adults, and the patterns of expression were more consistent across doses. The results reveal dose-dependent effects of nicotine during adolescence with apparent sensitization at different ends of the dosage spectrum examined compared to adults. These data indicate that initial exposure to nicotine may have unique effects in adolescence on the ascending 5-HT system, with the potential for consequences on the affective-motivational qualities of the drug and the subsequent propensity for repeated use.
青春期是一个关键的脆弱时期,在此期间接触尼古丁会大大增加产生药物成瘾的可能性。越来越多的证据表明,5-羟色胺(5-HT)能神经传递可能有助于成瘾行为的开始和维持。由于背侧中缝核(DR)和中缝核(MnR)是前脑 5-HT 的主要来源,本研究检验了这样一个假设,即急性尼古丁给药对这些区域内 5-HT 神经元的激活有年龄依赖性的影响。青春期(出生后第 30 天)和成年(出生后第 70 天)雄性 Sprague-Dawley 大鼠分别接受皮下注射生理盐水或尼古丁(0.2、0.4 或 0.8mg/kg)。随后,在 DR 的七个亚区和整个 MnR 中计数 Fos 和色氨酸羟化酶双重标记的 5-HT 细胞数。结果表明,急性尼古丁注射以区域特异性方式诱导 5-HT 神经元中的 Fos 表达。此外,青少年在较低(0.2mg/kg)和较高(0.8mg/kg)剂量的尼古丁下表现出更广泛的区域激活,表现出跨剂量的独特 U 形反应曲线。相比之下,在成年人中,具有激活的 Fos 表达的 5-HT 细胞局限于较少的区域,并且表达模式在各剂量之间更为一致。这些结果揭示了青春期尼古丁的剂量依赖性效应,与成年相比,在研究的剂量范围内,在不同的剂量端表现出明显的敏化现象。这些数据表明,与成年相比,初始接触尼古丁可能在青春期对上行 5-HT 系统产生独特的影响,从而对药物的情感动机特性产生潜在影响,并随后增加重复使用的倾向。