CNRS, EPHE, INCIA, UMR 5287, Univ. Bordeaux, 33000 Bordeaux, France.
Department of Molecular and Translational Medicine, University of Brescia, 25123 Brescia, Italy.
Cells. 2023 Jul 25;12(15):1927. doi: 10.3390/cells12151927.
Phytocannabinoids, including the non-addictive cannabis component cannabidivarin (CBDV), have been reported to hold therapeutic potential in several neurodevelopmental disorders (NDDs). Nonetheless, the therapeutic value of phytocannabinoids for treating Fragile X syndrome (FXS), a major NDD, remains unexplored. Here, we characterized the neurobehavioral effects of CBDV at doses of 20 or 100 mg/kg in the -knockout (-KO) mouse model of FXS using two temporally different intraperitoneal regimens: subchronic 10-day delivery during adulthood (Study 1: rescue treatment) or chronic 5-week delivery at adolescence (Study 2: preventive treatment). Behavioral tests assessing FXS-like abnormalities included anxiety, locomotor, cognitive, social and sensory alterations. Expression of inflammatory and plasticity markers was investigated in the hippocampus and prefrontal cortex. When administered during adulthood (Study 1), the effects of CBDV were marginal, rescuing at the lower dose only the acoustic hyper-responsiveness of -KO mice and at both doses their altered hippocampal expression of neurotrophins. When administered during adolescence (Study 2), CBDV at both doses prevented the cognitive, social and acoustic alterations of adult -KO mice and modified the expression of several inflammatory brain markers in both wild-type littermates and mutants. These findings warrant the therapeutic potential of CBDV for preventing neurobehavioral alterations associated with FXS, highlighting the relevance of its early administration.
植物大麻素,包括非成瘾性大麻成分大麻二酚(CBDV),已被报道在几种神经发育障碍(NDD)中具有治疗潜力。然而,植物大麻素治疗脆性 X 综合征(FXS)的治疗价值,作为一种主要的 NDD,仍未得到探索。在这里,我们使用两种不同时间的腹腔内方案,在 FXS 的 - 敲除(-KO)小鼠模型中表征了 CBDV 在 20 或 100mg/kg 剂量下的神经行为效应:成年期的亚慢性 10 天给药(研究 1:挽救治疗)或青春期的慢性 5 周给药(研究 2:预防治疗)。评估 FXS 样异常的行为测试包括焦虑、运动、认知、社交和感觉改变。在海马体和前额叶皮层中研究了炎症和可塑性标志物的表达。当在成年期(研究 1)给予时,CBDV 的作用是微不足道的,仅在较低剂量下挽救了 -KO 小鼠的听觉超敏反应,在两种剂量下均挽救了其海马体神经生长因子表达的改变。当在青春期(研究 2)给予时,两种剂量的 CBDV 均可预防成年 -KO 小鼠的认知、社交和听觉改变,并改变了野生型同窝仔和突变体的几种炎症性脑标志物的表达。这些发现证明了 CBDV 预防与 FXS 相关的神经行为改变的治疗潜力,强调了其早期给药的相关性。