Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06510, USA.
Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06510, USA.
Neuropharmacology. 2018 Jun;135:412-423. doi: 10.1016/j.neuropharm.2018.03.036. Epub 2018 Mar 28.
Cannabis use has been associated with altered sensory gating and neural oscillations. However, it is unclear which constituent in cannabis is responsible for these effects, or whether these are cannabinoid receptor 1 (CB1R) mediated. Therefore, the present study in humans and rats examined whether cannabinoid administration would disrupt sensory gating and evoked oscillations utilizing electroencephalography (EEG) and local field potentials (LFPs), respectively. Human subjects (n = 15) completed four test days during which they received intravenous delta-9-tetrahydrocannabinol (Δ-THC), cannabidiol (CBD), Δ-THC + CBD, or placebo. Subjects engaged in a dual-click paradigm, and outcome measures included P50 gating ratio (S2/S1) and evoked power to S1 and S2. In order to examine CB1R specificity, rats (n = 6) were administered the CB1R agonist CP-55940, CP-55940+AM-251 (a CB1R antagonist), or vehicle using the same paradigm. LFPs were recorded from CA3 and entorhinal cortex. Both Δ-THC (p < 0.007) and Δ-THC + CBD (p < 0.004) disrupted P50 gating ratio compared to placebo, while CBD alone had no effect. Δ-THC (p < 0.048) and Δ-THC + CBD (p < 0.035) decreased S1 evoked theta power, and in the Δ-THC condition, S1 theta negatively correlated with gating ratios (r = -0.629, p < 0.012 (p < 0.048 adjusted)). In rats, CP-55940 disrupted gating in both brain regions (p < 0.0001), and this was reversed by AM-251. Further, CP-55940 decreased evoked theta (p < 0.0077) and gamma (p < 0.011) power to S1, which was partially blocked by AM-251. These convergent human/animal data suggest that CB1R agonists disrupt sensory gating by altering neural oscillations in the theta-band. Moreover, this suggests that the endocannabinoid system mediates theta oscillations relevant to perception and cognition.
大麻的使用与感觉门控和神经振荡的改变有关。然而,目前尚不清楚大麻中的哪种成分是导致这些影响的原因,或者这些影响是否是由大麻素受体 1(CB1R)介导的。因此,本研究在人类和大鼠中分别利用脑电图(EEG)和局部场电位(LFP)检查了大麻素给药是否会破坏感觉门控和诱发的振荡。人类受试者(n=15)在四天的测试期间完成了四项测试,在此期间他们接受了静脉内的 Delta-9-四氢大麻酚(Δ-THC)、大麻二酚(CBD)、Δ-THC+CBD 或安慰剂。受试者进行双点击范式,测量结果包括 S2/S1 的 P50 门控比和 S1 和 S2 的诱发功率。为了研究 CB1R 的特异性,使用相同的范式,用 CB1R 激动剂 CP-55940、CP-55940+AM-251(一种 CB1R 拮抗剂)或载体处理大鼠(n=6)。从 CA3 和内嗅皮层记录 LFP。与安慰剂相比,Δ-THC(p<0.007)和 Δ-THC+CBD(p<0.004)均破坏了 P50 门控比,而单独的 CBD 则没有影响。Δ-THC(p<0.048)和 Δ-THC+CBD(p<0.035)降低了 S1 诱发的θ功率,并且在 Δ-THC 条件下,S1θ与门控比呈负相关(r=-0.629,p<0.012(调整后 p<0.048))。在大鼠中,CP-55940 破坏了两个脑区的门控(p<0.0001),并且 AM-251 逆转了这一作用。此外,CP-55940 降低了 S1 的诱发θ(p<0.0077)和γ(p<0.011)功率,AM-251 部分阻断了这一作用。这些在人类和动物中得到的一致数据表明,CB1R 激动剂通过改变θ波段的神经振荡来破坏感觉门控。此外,这表明内源性大麻素系统介导了与感知和认知相关的θ振荡。