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大麻二酚,一种治疗重度抑郁症的关键非精神活性植物大麻素:计算机模拟和体内实验探索

Cannabichromene, a key non-psychotropic phytocannabinoid in treatment of major depressive disorder: in silico and in vivo explorations.

作者信息

Sharma Abhishek, Singh Rahul, Virmani Tarun, Chouhan Neeraj Kumar, Kapoor Garima, Kumar Girish, Bhutani Rubina, Rana Neha, Sharma Shivkant

机构信息

Department of Pharmacy, School of Healthcare and Allied Sciences, G D Goenka University, Gurugram, 122103, Haryana, India.

Amity Institute of Pharmacy, Amity University, Greater Noida Campus, Knowledge Park III, Greater Noida, Uttar Pradesh, 201308, India.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 May 13. doi: 10.1007/s00210-025-04236-2.

Abstract

Cannabichromene, a non-psychotropic cannabinoid with antioxidant and neuroprotective properties, is hypothesized to possess antidepressant potential. This study aimed to evaluate cannabichromene's depression-alleviating effects in mice exposed to chronic unpredictable mild stress and unstressed mice using a combination of in silico and in vivo approaches. Initially, gene targets associated with major depressive disorder were identified through GeneCards, while cannabichromene's target genes were predicted using SwissTargetPrediction. Overlapping targets were visualized using Venny software, and protein-protein interaction networks were constructed with the STRING database. The cannabinoid receptor two genes, encoding the cannabinoid 2 receptor, emerged as a key shared target. Molecular docking studies revealed that cannabichromene exhibited a strong binding affinity to cannabinoid 2 receptors (docking score: - 9.4) compared to cannabidiol (CBD) (- 8.8) and Δ9-tetrahydrocannabinol (- 9.1). For in vivo analysis, male Swiss albino mice were subjected to chronic unpredictable mild stress for 3 weeks to induce depression-like behavior. Cannabichromene (10 and 20 mg/kg) and imipramine (15 mg/kg) were administered for 21 days. Cannabichromene at 20 mg/kg significantly reduced immobility in stressed mice, like imipramine, without affecting locomotor activity. Additionally, both cannabichromene and imipramine reduced elevated plasma nitrite and corticosterone levels and inhibited monoamine oxidase-A activity in the brain. Cannabichromene also reversed stress-induced catalase suppression. In conclusion, cannabichromene revealed a relatively substantial antidepressant character with chronic unpredictable mild stress model of depression in Swiss albino male mice, likely through interaction with cannabinoid 2 receptors encoded by the cannabinoid 2 gene, as ratified via in silico modeling and in vivo findings. This highlights cannabichromene's potential as a novel therapeutic agent for depression after further in vitro and clinical assessments in other models.

摘要

大麻二酚,一种具有抗氧化和神经保护特性的非精神活性大麻素,据推测具有抗抑郁潜力。本研究旨在通过计算机模拟和体内实验相结合的方法,评估大麻二酚对暴露于慢性不可预测轻度应激的小鼠和未应激小鼠的抗抑郁作用。最初,通过GeneCards确定与重度抑郁症相关的基因靶点,同时使用SwissTargetPrediction预测大麻二酚的靶点基因。使用Venny软件可视化重叠靶点,并使用STRING数据库构建蛋白质-蛋白质相互作用网络。编码大麻素2受体的大麻素受体2基因成为关键的共同靶点。分子对接研究表明,与大麻二酚(对接分数:-8.8)和Δ9-四氢大麻酚(-9.1)相比,大麻二酚对大麻素2受体表现出更强的结合亲和力(对接分数:-9.4)。对于体内分析,雄性瑞士白化小鼠接受3周的慢性不可预测轻度应激以诱导抑郁样行为。给予大麻二酚(10和20mg/kg)和丙咪嗪(15mg/kg)21天。20mg/kg的大麻二酚显著降低了应激小鼠的不动时间,与丙咪嗪类似,且不影响运动活性。此外,大麻二酚和丙咪嗪均降低了血浆亚硝酸盐和皮质酮水平的升高,并抑制了脑中单胺氧化酶-A的活性。大麻二酚还逆转了应激诱导的过氧化氢酶抑制作用。总之,通过计算机模拟建模和体内实验结果证实,在瑞士白化雄性小鼠的慢性不可预测轻度应激抑郁模型中,大麻二酚显示出相对显著的抗抑郁特性,可能是通过与大麻素2基因编码的大麻素2受体相互作用实现的。这突出了大麻二酚在其他模型中进一步进行体外和临床评估后作为新型抗抑郁治疗药物的潜力。

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