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急性和重复给药后大麻二酚与 Δ-9-四氢大麻酚的相互作用:反弹过度活跃、感觉运动门控以及中脑边缘通路中的表观遗传和神经适应性变化。

Interactions between cannabidiol and Δ-THC following acute and repeated dosing: Rebound hyperactivity, sensorimotor gating and epigenetic and neuroadaptive changes in the mesolimbic pathway.

机构信息

Brain and Mind Centre, University of Sydney, Sydney, Australia; Discipline of Pharmacology, School of Medical Science, University of Sydney, Sydney, Australia.

Brain and Mind Centre, University of Sydney, Sydney, Australia; Discipline of Pharmacology, School of Medical Science, University of Sydney, Sydney, Australia; The Lambert Initiative of Cannabinoid Therapeutics, University of Sydney, Sydney, Australia.

出版信息

Eur Neuropsychopharmacol. 2017 Feb;27(2):132-145. doi: 10.1016/j.euroneuro.2016.12.004. Epub 2016 Dec 31.

Abstract

The evidence base for the use of medical cannabis preparations containing specific ratios of cannabidiol (CBD) and Δ-tetrahydrocannabinol (THC) is limited. While there is abundant data on acute interactions between CBD and THC, few studies have assessed the impact of their repeated co-administration. We previously reported that CBD inhibited or potentiated the acute effects of THC dependent on the measure being examined at a 1:1 CBD:THC dose ratio. Further, CBD decreased THC effects on brain regions involved in memory, anxiety and body temperature regulation. Here we extend on these finding by examining over 15 days of treatment whether CBD modulated the repeated effects of THC on behaviour and neuroadaption markers in the mesolimbic dopamine pathway. After acute locomotor suppression, repeated THC caused rebound locomotor hyperactivity that was modestly inhibited by CBD. CBD also slightly reduced the acute effects of THC on sensorimotor gating. These subtle effects were found at a 1:1 CBD:THC dose ratio but were not accentuated by a 5:1 dose ratio. CBD did not alter the trajectory of enduring THC-induced anxiety nor tolerance to the pharmacological effects of THC. There was no evidence of CBD potentiating the behavioural effects of THC. However we demonstrated for the first time that repeated co-administration of CBD and THC increased histone 3 acetylation (H3K9/14ac) in the VTA and ΔFosB expression in the nucleus accumbens. These changes suggest that while CBD may have protective effects acutely, its long-term molecular actions on the brain are more complex and may be supradditive.

摘要

使用含有特定比例大麻二酚 (CBD) 和 Δ-四氢大麻酚 (THC) 的医用大麻制剂的证据基础有限。虽然有大量关于 CBD 和 THC 急性相互作用的数据,但很少有研究评估它们重复共同给药的影响。我们之前的研究报告称,CBD 以剂量比为 1:1 的 CBD:THC 抑制或增强 THC 的急性作用,此外,CBD 降低了 THC 对参与记忆、焦虑和体温调节的大脑区域的影响。在这里,我们通过检查超过 15 天的治疗,扩展了这些发现,以研究 CBD 是否调节了 THC 在中脑边缘多巴胺通路中的重复作用和神经适应标志物。在急性运动抑制后,重复给予 THC 引起运动过度活跃,而 CBD 适度抑制了这种反应。CBD 还略微降低了 THC 对感觉运动门控的急性影响。这些细微的影响在 CBD:THC 剂量比为 1:1 时发现,但在 5:1 剂量比时并未加剧。CBD 没有改变 THC 引起的焦虑的持续轨迹,也没有改变对 THC 药理作用的耐受性。没有证据表明 CBD 增强了 THC 的行为影响。然而,我们首次证明,重复共同给予 CBD 和 THC 增加了 VTA 中的组蛋白 3 乙酰化 (H3K9/14ac) 和核伏隔核中的 ΔFosB 表达。这些变化表明,虽然 CBD 可能具有急性保护作用,但它对大脑的长期分子作用更为复杂,可能是超相加的。

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