Anxiolytic Activity of Morellic Acid: Modulation of Diazepam's Anxiolytic Effects, Possibly Through GABAergic Interventions

IF 5 1区 医学 Q1 NEUROSCIENCES CNS Neuroscience & Therapeutics Pub Date : 2025-02-17 DOI:10.1111/cns.70276
Md. Shimul Bhuia, Tanzila Akter Eity, Raihan Chowdhury, Siddique Akber Ansari, Mehedi Hasan Bappi, Md. Anin Nayeem, Farjana Akter, Muhammad Torequl Islam
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Abstract

Background

Numerous studies suggest that morellic acid (MOR), highly available in Garcinia plants, has different physiological activities, including anti-cancer, anti-oxidant, and anti-microbial activity.

Aim

In this investigation, we aimed to demonstrate the anxiolytic activity, along with the mechanism behind this activity of MOR, using in vivo and in silico studies.

Methods

For this, we used different doses of MOR (5 and 10 mg/kg) and administered this drug intraperitoneally to Swiss albino mice (male and female). Diazepam (DZP), a positive allosteric modulator of the GABAA receptor, was used as a positive control at a dose of 2 mg/kg (i.p), and vehicle was used as a control group. In this test, various test protocols are used to assess the behavioral patterns of mice, including swing, hole cross, light–dark testing, and open field testing.

Results

This investigation revealed that MOR remarkably reduced the locomotor activity of mice in a dose-dependent manner and produced calming behaviors like DZP. However, the findings showed that the combination of MOR and DZP synergistically reduced the locomotion of mice compared to the single therapy. On the other hand, from the computational study, the result demonstrated that MOR exhibited the highest binding scores (−9.2 kcal/mol) towards the GABAA receptor α3 subunit and −7.6 kcal/mol towards the GABAA α2 receptor. Whereas, DZP showed −6.6 and −7.3 kcal/mol docking affinity and FLU exerted −6.2 and −6.3 kcal/mol docking scores towards the GABAA receptor α2 and α3 subunits, respectively. The ligand interacted with the receptor by forming different hydrogen and hydrophobic bonds.

Conclusion

However, it is recommended that more precise and comprehensive preclinical investigations be required to demonstrate the exact mechanism behind the anxiolytic effects and conduct clinical trials to determine efficacy and safety.

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戊酸的抗焦虑活性:调节安定的抗焦虑作用,可能通过gaba能干预
背景大量研究表明,在藤黄属植物中大量存在的摩尔酸(morellic acid, MOR)具有多种生理活性,包括抗癌、抗氧化、抗微生物等。目的在本研究中,我们旨在通过体内和计算机研究来证明MOR的抗焦虑活性及其作用机制。方法采用不同剂量的MOR(5和10 mg/kg)腹腔注射瑞士白化小鼠(雄性和雌性)。以GABAA受体的正变构调节剂地西泮(DZP)为阳性对照,剂量为2mg /kg (i.p),对照组为对照。在本试验中,采用了多种试验方案来评估小鼠的行为模式,包括摇摆试验、孔交叉试验、光暗试验和开阔场地试验。结果MOR以剂量依赖的方式显著降低小鼠的运动活动,并产生镇静行为,如DZP。然而,研究结果表明,与单一治疗相比,MOR和DZP联合治疗可协同降低小鼠的运动能力。另一方面,计算研究结果表明,MOR对GABAA受体α3亚基的结合得分最高(- 9.2 kcal/mol),对GABAA α2受体的结合得分为- 7.6 kcal/mol。而DZP对GABAA受体α2和α3亚基的对接亲和力分别为−6.6和−7.3 kcal/mol, FLU对GABAA受体α2和α3亚基的对接评分分别为−6.2和−6.3 kcal/mol。配体通过形成不同的氢键和疏水键与受体相互作用。结论需要更精确、更全面的临床前研究来揭示其抗焦虑作用的确切机制,并开展临床试验来确定其有效性和安全性。
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来源期刊
CNS Neuroscience & Therapeutics
CNS Neuroscience & Therapeutics 医学-神经科学
CiteScore
7.30
自引率
12.70%
发文量
240
审稿时长
2 months
期刊介绍: CNS Neuroscience & Therapeutics provides a medium for rapid publication of original clinical, experimental, and translational research papers, timely reviews and reports of novel findings of therapeutic relevance to the central nervous system, as well as papers related to clinical pharmacology, drug development and novel methodologies for drug evaluation. The journal focuses on neurological and psychiatric diseases such as stroke, Parkinson’s disease, Alzheimer’s disease, depression, schizophrenia, epilepsy, and drug abuse.
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