Dept. of Theoretical and Applied Sciences, Biomedical Division and Center of Neuroscience, Univ. of Insubria, Busto Arsizio (VA), Italy.
Dept. of Medical Sciences, Section of Pharmacology, University of Ferrara, Ferrara, Italy.
Neurobiol Dis. 2014 Mar;63:35-47. doi: 10.1016/j.nbd.2013.10.028. Epub 2013 Nov 4.
Although several findings indicate an association between adolescent cannabis abuse and the risk to develop schizophrenia later in life, the evidence for a causal relationship is still inconclusive. In the present study, we investigated the emergence of psychotic-like behavior in adult female rats chronically exposed to delta-9-tetrahydrocannabinol (THC) during adolescence. To this aim, female Sprague-Dawley rats were treated with THC during adolescence (PND 35-45) and, in adulthood (PND 75), a series of behavioral tests and biochemical assays were performed in order to investigate the long-term effects of adolescent THC exposure. Adolescent THC pretreatment leads to long-term behavioral alterations, characterized by recognition memory deficits, social withdrawal, altered emotional reactivity and sensitization to the locomotor activating effects of acute PCP. Moreover, since cortical disinhibition seems to be a key feature of many different animal models of schizophrenia and GABAergic hypofunction in the prefrontal cortex (PFC) has been observed in postmortem brains from schizophrenic patients, we then investigated the long-lasting consequences of adolescent THC exposure on GABAergic transmission in the adult rat PFC. Biochemical analyses revealed that adolescent THC exposure results in reduced GAD67 and basal GABA levels within the adult PFC. GAD67 expression is reduced both in parvalbumin (PV)- and cholecystokinin (CCK)-containing interneurons; this alteration may be related to the altered emotional reactivity triggered by adolescent THC, as silencing PFC GAD67 expression through a siRNA-mediated approach is sufficient to impact rats' behavior in the forced swim test. Finally, the cellular underpinnings of the observed sensitized response to acute PCP in adult THC-treated rats could be ascribed to the increased cFos immunoreactivity and glutamate levels in the PFC and dorsal striatum. The present findings support the hypothesis that adolescent THC exposure may represent a risk factor for the development of a complex psychotic-like behavior in adulthood.
尽管有几项研究结果表明青少年滥用大麻与成年后患精神分裂症的风险之间存在关联,但因果关系的证据仍不确定。在本研究中,我们研究了在青春期长期暴露于大麻素 delta-9-四氢大麻酚(THC)的成年雌性大鼠中出现类精神病行为的情况。为此,雌性 Sprague-Dawley 大鼠在青春期(PND 35-45)期间接受 THC 治疗,然后在成年期(PND 75)进行一系列行为测试和生化分析,以研究青春期 THC 暴露的长期影响。青春期 THC 预处理会导致长期的行为改变,表现为识别记忆缺陷、社会回避、情绪反应改变以及对急性 PCP 致运动激活作用的敏感性增加。此外,由于皮质抑制解除似乎是许多不同精神分裂症动物模型的一个关键特征,并且在精神分裂症患者的死后大脑中观察到前额叶皮层(PFC)中的 GABA 能功能低下,因此我们随后研究了青春期 THC 暴露对成年大鼠 PFC 中 GABA 能传递的长期影响。生化分析显示,青春期 THC 暴露导致成年 PFC 中 GAD67 和基础 GABA 水平降低。GAD67 表达减少发生在包含 GABA 能神经元的 PV-和 CCK-中;这种改变可能与青春期 THC 引发的情绪反应改变有关,因为通过 siRNA 介导的方法沉默 PFC GAD67 表达足以影响大鼠在强迫游泳测试中的行为。最后,成年 THC 处理大鼠对急性 PCP 表现出的敏化反应的细胞基础可以归因于 PFC 和背侧纹状体中 cFos 免疫反应性和谷氨酸水平的增加。这些发现支持了以下假设:青春期 THC 暴露可能是成年后患复杂类精神病行为的一个风险因素。