Department of Structural and Functional Biology and Neuroscience Center, University of Insubria, via A. da Giussano 10, 21052 Busto Arsizio, Varese, Italy.
Neuroscience. 2012 Mar 1;204:245-57. doi: 10.1016/j.neuroscience.2011.11.038. Epub 2011 Nov 29.
Preclinical data support the long-term adverse effects on cognition, emotionality, and psychotic-like behaviors of adolescent exposure to natural and synthetic cannabinoids. To investigate whether the long-lasting adverse effects induced by cannabinoids in adolescence are influenced by early-life stress, female and male rats were subjected to 24-h maternal deprivation at postnatal day (PND) 9 and treated with tetrahydrocannabinol (THC) during adolescence (PND 35-45) according to our previously reported protocol. At adulthood, rats were tested in the novel object recognition, social interaction, and forced swim tests, to evaluate possible alterations in recognition memory, social behavior, and coping strategy. Moreover, cannabinoid CB1 receptor density and functionality, as well as NMDA and dopamine D1 and D2 receptor densities were measured through autoradiographic binding studies. In female maternally deprived rats, THC failed to impair recognition memory, counteracted aggressiveness induced by maternal deprivation, whereas no interaction was observed in the passive coping behavior. In males, the association of the two events increased passive coping response without affecting other behaviors. This behavioral picture was accompanied by gender-dependent and region-specific alterations in NMDA, D1 and D2 receptors. In conclusion, this study demonstrates that adolescent THC exposure might have different behavioral outcomes in animals previously exposed to early-life stress compared with non-stressed controls. The interaction between the two events is not univocal, and different combinations may arise depending on the sex of the animals and the behavior considered. Alterations in NMDA, D1 and D2 receptors might be involved in the behavioral responses induced by maternal deprivation and in their modulation by THC.
动物在青春期接触天然和合成大麻素会对认知、情绪和类精神病行为产生长期的不良影响。为了研究青春期大麻素引起的长期不良影响是否受到早期生活应激的影响,雌性和雄性大鼠在出生后第 9 天(PND9)接受 24 小时的母体剥夺,并按照我们之前报道的方案在青春期(PND35-45)接受四氢大麻酚(THC)治疗。在成年期,通过新物体识别、社交互动和强迫游泳测试评估大鼠的识别记忆、社交行为和应对策略的可能变化。此外,通过放射配体结合研究测量大麻素 CB1 受体密度和功能以及 NMDA 和多巴胺 D1 和 D2 受体密度。在雌性母体剥夺大鼠中,THC 未能损害识别记忆,抵消母体剥夺引起的攻击性,而在被动应对行为中没有观察到相互作用。在雄性中,这两个事件的结合增加了被动应对反应,而不影响其他行为。这种行为模式伴随着 NMDA、D1 和 D2 受体的性别依赖性和区域特异性改变。总之,这项研究表明,与未受应激的对照组相比,青春期 THC 暴露可能在先前暴露于早期生活应激的动物中产生不同的行为结果。这两个事件的相互作用并非单一的,并且可能会根据动物的性别和所考虑的行为而产生不同的组合。NMDA、D1 和 D2 受体的改变可能参与了母体剥夺引起的行为反应及其对 THC 的调节。