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大麻二酚单独或联合利培酮在自闭症动物模型中的作用。

Effects of Cannabidiol Isolated or in Association With Risperidone in an Animal Model of Autism.

机构信息

Laboratory of Autism and Neurodevelopmental Research, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, Santa Catarina, Brazil.

Laboratory of Behavioral Neuroscience, Graduate Program in Health Sciences, University of South Santa Catarina (UNISUL), Tubarão, Santa Catarina, Brazil.

出版信息

Dev Neurobiol. 2025 Jan;85(1):e22955. doi: 10.1002/dneu.22955.

Abstract

Autism spectrum disorder (ASD) is characterized by deficits in communication, social interaction, and repetitive and stereotyped behaviors, with no specific drug therapy available. Studies have found that cannabidiol (CBD) can improve hyperactive and cognitive symptoms in children with ASD. However, little is known about the effect of CBD in combination with other medications, such as risperidone (RISP). This study aimed to evaluate the behavioral and biochemical effects of CBD in animals using a valproic acid (VPA)-induced ASD animal model. VPA was administered in pregnant Wistar rats on Day 12.5 of gestation to induce the ASD model. From the 10th to the 16th postnatal day (PND), the neurodevelopment of the animals was assessed through eye-opening, olfactory discrimination, and negative geotaxis behavioral tests. From PNDs 9 to 54, the animals were weighed. They were treated for 21 days with CBD alone (100 mg/kg, by gavage, twice a day) or in combination with RISP (0.1 mg/kg, by gavage, once a day). At PND 55, the animals were evaluated in social interaction and locomotor activity experiments. Finally, after behavioral assessment, the animals were euthanized, the brain was isolated, and oxidative stress parameters were evaluated in the hippocampus and cortex posterior. Animals exposed to VPA showed neurodevelopmental delays in opening their eyes, difficulties in turning around their axis, and took longer time to find the original nest when compared to control animals. They also exhibited impaired sociability and reduced exploratory activity, which indicates model impairments. Interestingly, animals exposed to VPA treated with CBD + RISP significantly improved sociability parameters, whereas isolated CBD did not affect this parameter. In the biochemical analysis, a significant decrease in the hippocampal sulfhydryl content was noted in the CT + CBD group and an increase in the VPA + CBD group. In conclusion, these results suggest that CBD, in combination with RISP, may be an interesting pharmacological approach to reducing ASD-related symptoms. Summary: Besides the increased prevalence of ASD cases in recent years, there are no medications to improve the central symptoms of autism. Numerous studies discuss CBD as an important medication for improving ASD symptoms; however, it is not known how CBD interacts with commonly used drugs in ASD individuals, such as RISP. This study demonstrated that CBD therapy, only when combined with RISP, improved sociability in a VPA-induced ASD animal model.

摘要

自闭症谱系障碍(ASD)的特征是沟通、社交互动以及重复和刻板行为方面的缺陷,目前尚无特定的药物治疗方法。研究发现,大麻二酚(CBD)可改善 ASD 儿童的多动和认知症状。然而,对于 CBD 与利培酮(RISP)等其他药物联合使用的效果知之甚少。本研究旨在通过丙戊酸(VPA)诱导的 ASD 动物模型评估 CBD 对动物的行为和生化影响。在妊娠第 12.5 天,向 Wistar 大鼠腹腔内注射 VPA 以诱导 ASD 模型。从出生后第 10 天到第 16 天(PND),通过睁眼、嗅觉辨别和负趋地性行为测试评估动物的神经发育情况。从 PND 9 天到 54 天,对动物进行称重。在 21 天内,它们单独接受 CBD(100mg/kg,灌胃,每天两次)或与 RISP(0.1mg/kg,灌胃,每天一次)联合治疗。在 PND 55 天,对动物进行社会互动和运动活动实验评估。最后,在行为评估后,处死动物,分离大脑,并在后脑海马体和皮质中评估氧化应激参数。与对照组相比,接触 VPA 的动物在睁眼、转身以及寻找原来的巢方面存在神经发育延迟。它们还表现出社交能力受损和探索性活动减少,这表明模型受损。有趣的是,接受 CBD+RISP 治疗的 VPA 暴露动物的社交能力参数显著改善,而单独的 CBD 则没有影响这一参数。在生化分析中,CT+CBD 组的海马硫醇含量显著降低,而 VPA+CBD 组的含量增加。综上所述,这些结果表明,CBD 联合 RISP 可能是一种减少 ASD 相关症状的有趣的药理学方法。总结:除了近年来 ASD 病例的发病率增加之外,没有药物可以改善自闭症的核心症状。许多研究都讨论了 CBD 作为改善 ASD 症状的重要药物;然而,CBD 如何与 ASD 患者常用的药物(如 RISP)相互作用尚不清楚。本研究表明,在 VPA 诱导的 ASD 动物模型中,只有当 CBD 与 RISP 联合使用时,才会改善社交能力。

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