Beggiato Sarah, Borelli Andrea Celeste, Tomasini Maria Cristina, Morgano Lucia, Antonelli Tiziana, Tanganelli Sergio, Cuomo Vincenzo, Ferraro Luca
Department of Life Sciences and Biotechnology, University of Ferrara, Italy.
Department of Medical Sciences, University of Ferrara, Italy.
Neurobiol Learn Mem. 2017 Mar;139:135-143. doi: 10.1016/j.nlm.2016.12.023. Epub 2017 Jan 16.
The long-lasting effects of gestational cannabinoids exposure on the adult brain of the offspring are still controversial. It has already been shown that pre- or perinatal cannabinoids exposure induces learning and memory disruption in rat adult offspring, associated with permanent alterations of cortical glutamatergic neurotransmission and cognitive deficits. In the present study, the risk of long-term consequences induced by perinatal exposure to cannabinoids on rat hippocampal GABAergic system of the offspring, has been explored. To this purpose, pregnant rats were treated daily with Delta-tetrahydrocannabinol (Δ-THC; 5mg/kg) or its vehicle. Perinatal exposure to Δ-THC induced a significant reduction (p<0.05) in basal and K-evoked [H]-GABA outflow of 90-day-old rat hippocampal slices. These effects were associated with a reduction of hippocampal [H]-GABA uptake compared to vehicle exposed group. Perinatal exposure to Δ-THC induced a significant reduction of CB1 receptor binding (B) in the hippocampus of 90-day-old rats. However, a pharmacological challenge with either Δ-THC (0.1μM) or WIN55,212-2 (2μM), similarly reduced K-evoked [H]-GABA outflow in both experimental groups. These reductions were significantly blocked by adding the selective CB1 receptor antagonist SR141716A. These findings suggest that maternal exposure to cannabinoids induces long-term alterations of hippocampal GABAergic system. Interestingly, previous behavioral studies demonstrated that, under the same experimental conditions as in the present study, perinatal cannabinoids exposure induced cognitive impairments in adult rats, thus resembling some effects observed in humans. Although it is difficult and sometimes misleading to extrapolate findings obtained from animal models to humans, the possibility that an alteration of hippocampus aminoacidergic transmission might underlie, at least in part, some of the cognitive deficits affecting the offspring of marijuana users, is supported.
孕期接触大麻素对后代成年大脑的长期影响仍存在争议。已有研究表明,产前或围产期接触大麻素会导致大鼠成年后代的学习和记忆障碍,这与皮质谷氨酸能神经传递的永久性改变和认知缺陷有关。在本研究中,探讨了围产期接触大麻素对后代大鼠海马体GABA能系统产生长期影响的风险。为此,对怀孕大鼠每日给予Δ-四氢大麻酚(Δ-THC;5mg/kg)或其溶剂。围产期接触Δ-THC导致90日龄大鼠海马切片基础和钾诱发的[H]-GABA外流显著减少(p<0.05)。与溶剂暴露组相比,这些效应与海马体[H]-GABA摄取减少有关。围产期接触Δ-THC导致90日龄大鼠海马体中CB1受体结合(B)显著减少。然而,用Δ-THC(0.1μM)或WIN55,212-2(2μM)进行药理学刺激,在两个实验组中同样降低了钾诱发的[H]-GABA外流。添加选择性CB1受体拮抗剂SR141716A可显著阻断这些减少。这些发现表明,母体接触大麻素会导致海马体GABA能系统的长期改变。有趣的是,先前的行为学研究表明,在与本研究相同的实验条件下,围产期接触大麻素会导致成年大鼠出现认知障碍,因此类似于在人类中观察到的一些效应。尽管将从动物模型中获得的结果外推至人类既困难又有时会产生误导,但海马体氨基酸能传递改变可能至少部分地是影响大麻使用者后代的一些认知缺陷的基础这一可能性得到了支持。