Ellgren M, Artmann A, Tkalych O, Gupta A, Hansen H S, Hansen S H, Devi L A, Hurd Y L
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Eur Neuropsychopharmacol. 2008 Nov;18(11):826-34. doi: 10.1016/j.euroneuro.2008.06.009.
Adolescence is a critical phase of active brain development often characterized by the initiation of marijuana (Cannabis sativa) use. Limited information is known regarding the endogenous cannabinoid system of the adolescent brain as well as related neurotransmitters that appear sensitive to cannabis exposure. We recently observed that adult rats pre-exposed to Delta-9-tetrahydrocannabinol (THC) during adolescence self-administered higher amounts of heroin and had selective impairments of the enkephalin opioid system within the nucleus accumbens (NAc) implicated in reward-related behavior. To explore the ontogeny of the cannabinoid and opioid neuronal systems in association with adolescence THC exposure, rats were examined at different adolescent stages during an intermittent THC paradigm (1.5 mg/kg i.p. every third day) from postnatal days (PNDs) 28-49. Rat brains were examined 24 h after injection at PND 29 (early adolescence), PND 38 (mid adolescence) and PND 50 (late adolescence) and analyzed for endocannabinoids (anandamide and 2-arachidonoylglycerol), Met-enkephalin, cannabinoid CB(1) receptors and micro opioid receptors (microOR) in the NAc, caudate-putamen and prefrontal cortex (PFC). Of the markers studied, the endocannabinoid levels had the most robust alterations throughout adolescence and were specific to the PFC and NAc. Normal correlations between anandamide and 2-arachidonoylglycerol concentrations in the NAc (positive) and PFC (negative) were reversed by THC. Other significant THC-induced effects were confined to the NAc - increased anandamide, decreased Met-enkephalin and decreased microORs. These findings emphasize the dynamic nature of the mesocorticolimbic endocannabinoid system during adolescence and the selective mesocorticolimbic disturbance as a consequence of adolescent cannabis exposure.
青春期是大脑积极发育的关键阶段,其特点通常是开始使用大麻( Cannabis sativa)。关于青少年大脑的内源性大麻素系统以及对大麻暴露敏感的相关神经递质,已知信息有限。我们最近观察到,青春期期间预先接触Δ-9-四氢大麻酚(THC)的成年大鼠会自我注射更多量的海洛因,并且伏隔核(NAc)内的脑啡肽阿片系统存在选择性损伤,这与奖励相关行为有关。为了探讨与青春期THC暴露相关的大麻素和阿片样物质神经元系统的个体发生,在出生后第28至49天的间歇性THC范式(每三天腹腔注射1.5mg/kg)期间,对处于不同青春期阶段的大鼠进行了检查。在出生后第29天(青春期早期)、第38天(青春期中期)和第50天(青春期晚期)注射后24小时检查大鼠大脑,并分析伏隔核、尾状核-壳核和前额叶皮质(PFC)中的内源性大麻素(花生四烯乙醇胺和2-花生四烯酸甘油酯)、甲硫氨酸脑啡肽、大麻素CB(1)受体和微小阿片受体(microOR)。在所研究的标志物中,内源性大麻素水平在整个青春期变化最为显著,并且在PFC和NAc中具有特异性。THC使NAc(正相关)和PFC(负相关)中花生四烯乙醇胺和2-花生四烯酸甘油酯浓度之间的正常相关性发生了逆转。THC诱导的其他显著影响仅限于NAc——花生四烯乙醇胺增加、甲硫氨酸脑啡肽减少和微小阿片受体减少。这些发现强调了青春期期间中脑边缘内源性大麻素系统的动态性质以及青春期大麻暴露导致的选择性中脑边缘系统紊乱。