Department of Theoretical and Applied Sciences, Biomedical Research Division, University of Insubria, via Manara 7, 21052 Busto Arsizio VA, Italy.
Department of Theoretical and Applied Sciences, Biomedical Research Division, University of Insubria, via Manara 7, 21052 Busto Arsizio VA, Italy.
Prog Neuropsychopharmacol Biol Psychiatry. 2014 Jul 3;52:41-4. doi: 10.1016/j.pnpbp.2013.07.020. Epub 2013 Aug 1.
Epidemiological studies suggest that Cannabis use during adolescence confers an increased risk for developing psychotic symptoms later in life. However, despite their interest, the epidemiological data are not conclusive, due to their heterogeneity; thus modeling the adolescent phase in animals is useful for investigating the impact of Cannabis use on deviations of adolescent brain development that might confer a vulnerability to later psychotic disorders. Although scant, preclinical data seem to support the presence of impaired social behaviors, cognitive and sensorimotor gating deficits as well as psychotic-like signs in adult rodents after adolescent cannabinoid exposure, clearly suggesting that this exposure may trigger a complex behavioral phenotype closely resembling a schizophrenia-like disorder. Similar treatments performed at adulthood were not able to produce such phenotype, thus pointing to a vulnerability of the adolescent brain towards cannabinoid exposure. The neurobiological substrate of the adolescent vulnerability is still largely unknown and experimental studies need to elucidate the cellular and molecular mechanism underlying these effects. However, the few data available seem to suggest that heavy adolescent exposure to cannabinoids is able to modify neuronal connectivity in specific brain areas long after the end of the treatment. This is likely due to disruption of maturational events within the endocannabinoid system during adolescence that in turn impact on the correct neuronal refinement peculiar of the adolescent brain, thus leading to altered adult brain functionality and behavior.
流行病学研究表明,青少年时期使用大麻会增加日后出现精神病症状的风险。然而,尽管人们对此很感兴趣,但由于其异质性,流行病学数据并不具有结论性;因此,在动物中模拟青少年阶段对于研究大麻使用对青少年大脑发育偏差的影响是有用的,这些偏差可能会导致日后出现精神病障碍的易感性。尽管数量有限,但临床前数据似乎支持在青少年期大麻素暴露后成年啮齿动物中存在受损的社交行为、认知和感觉运动门控缺陷以及类精神病迹象,这清楚地表明这种暴露可能引发一种复杂的行为表型,类似于精神分裂症样障碍。在成年期进行类似的治疗并不能产生这种表型,这表明青少年期的大脑对大麻素暴露很敏感。青少年易感性的神经生物学基础在很大程度上仍然未知,需要进行实验研究来阐明这些影响的细胞和分子机制。然而,现有的少量数据似乎表明,青少年期大量接触大麻素能够在治疗结束后很长时间改变特定大脑区域的神经元连接。这可能是由于青少年时期内内源性大麻素系统的成熟事件中断,进而影响青少年大脑特有的正确神经元细化,从而导致成年期大脑功能和行为的改变。