Staben Jenika, Koch Megan, Reid Keelee, Muckerheide Jessica, Gilman Lauren, McGuinness Finn, Kiesser Sarina, Oswald Iain W H, Koby Kevin A, Martin Thomas J, Kaplan Joshua S
Department of Psychology, Behavioral Neuroscience Program, Western Washington University, Bellingham, WA, United States.
Scientific Technical Services, Western Washington University, Bellingham, WA, United States.
Front Neurosci. 2023 Jun 16;17:1185737. doi: 10.3389/fnins.2023.1185737. eCollection 2023.
Cannabidiol (CBD) is a non-intoxicating phytocannabinoid with increasing popularity due to its purported therapeutic efficacy for numerous off-label conditions including anxiety and autism spectrum disorder (ASD). Those with ASD are commonly deficient in endogenous cannabinoid signaling and GABAergic tone. CBD has a complex pharmacodynamic profile that includes enhancing GABA and endocannabinoid signaling. Thus, there is mechanistic justification for investigating CBD's potential to improve social interaction and related symptoms in ASD. Recent clinical trials in children with ASD support CBD's beneficial effects in numerous comorbid symptoms, but its impact on social behavior is understudied.
Here, we tested the prosocial and general anxiolytic efficacy of a commercially available CBD-rich broad spectrum hemp oil delivered by repeated puff vaporization and consumed via passive inhalation in the female cohort of the BTBR strain, a common inbred mouse line for preclinical assessment of ASD-like behaviors.
We observed that CBD enhanced prosocial behaviors using the 3-Chamber Test with a different vapor dose-response relationship between prosocial behavior and anxiety-related behavior on the elevated plus maze. We also identified that inhalation of a vaporized terpene blend from the popular OG Kush cannabis strain increased prosocial behavior independently of CBD and acted together with CBD to promote a robust prosocial effect. We observed similar prosocial effects with two additional cannabis terpene blends from the Do-Si-Dos and Blue Dream strains, and further reveal that these prosocial benefits rely on the combination of multiple terpenes that comprise the blends.
Our results illustrate the added benefit of cannabis terpene blends for CBD-based treatment of ASD.
大麻二酚(CBD)是一种无致幻作用的植物大麻素,因其对包括焦虑症和自闭症谱系障碍(ASD)在内的多种未标明用途的疾病具有治疗功效而越来越受欢迎。患有ASD的人通常内源性大麻素信号传导和γ-氨基丁酸能张力不足。CBD具有复杂的药效学特征,包括增强γ-氨基丁酸和内源性大麻素信号传导。因此,有机制依据来研究CBD改善ASD社交互动及相关症状的潜力。最近针对ASD儿童的临床试验支持了CBD对多种共病症状的有益作用,但其对社交行为的影响研究不足。
在此,我们测试了一种市售的富含CBD的广谱大麻油的亲社会和一般抗焦虑功效,该大麻油通过重复 puff 汽化给药,并通过被动吸入在BTBR品系的雌性小鼠群体中使用,BTBR品系是一种常用于临床前评估ASD样行为的近交小鼠品系。
我们观察到,使用三室试验,CBD增强了亲社会行为,在高架十字迷宫上亲社会行为与焦虑相关行为之间存在不同的汽化剂量反应关系。我们还发现,吸入来自流行的OG Kush大麻品种的汽化萜烯混合物可独立于CBD增加亲社会行为,并与CBD共同作用以促进强大的亲社会效应。我们用来自Do-Si-Dos和Blue Dream品种的另外两种大麻萜烯混合物观察到了类似的亲社会效应,并进一步揭示这些亲社会益处依赖于构成混合物的多种萜烯的组合。
我们的结果说明了大麻萜烯混合物对基于CBD治疗ASD的附加益处。