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香豆素的类焦虑效应,可能通过与GABAkine的相互作用途径:基于计算机模拟方法的动物研究

Anxiogenic-like effects of coumarin, possibly through the GABAkine interaction pathway: Animal studies with in silico approaches.

作者信息

Prottay Abdullah Al Shamsh, Ripu Tawfik Rakaiyat, Sarwar Md Nazim, Rahman Towfiqur, Ahmmed Md Shakil, Bappi Mehedi Hasan, Emon Md, Ansari Siddique Akber, Coutinho Henrique D M, Islam Muhammad Torequl

机构信息

Department of Pharmacy, Bangabandhu Sheikh Mujibur Rahman Science and Technology University, Gopalganj 8100, Bangladesh; Bioinformatics and Drug Innovation Laboratory, BioLuster Research Center Ltd., Gopalganj 8100, Bangladesh.

Department of Pharmacy, Bangabandhu Sheikh Mujibur Rahman Science and Technology University, Gopalganj 8100, Bangladesh.

出版信息

Behav Brain Res. 2025 Mar 5;480:115392. doi: 10.1016/j.bbr.2024.115392. Epub 2024 Dec 10.

Abstract

BACKGROUND

Anxiety disorder is the most common mental illness and a major contributor to impairment. Thus, there is an urgent need to find novel lead compounds to mitigate anxiety. It is widely recognized that the neurobiology of anxiety-related behavior involves GABAergic systems.

OBJECTIVES

This research aimed to examine the anxiogenic action of coumarin (CMN), a natural benzopyrone derived from plants, and determine its underlying mechanism through in vivo and in silico investigations.

METHODS

This was accomplished by using a variety of behavioral procedures, including open field, swing, hole cross, and light-dark tests, on male and female Swiss albino mice that had been orally administered three experimental doses of CMN (1, 2, and 4 mg/kg). The CMN group was also examined with the GABA receptor agonist diazepam (DZP, 2 mg/kg) and flumazenil antagonist (FLU, 0.1 mg/kg). Furthermore, CMN and standards were subjected to a molecular docking analysis to determine their binding affinities for the GABA receptor subunits (α1, α4, β2, γ2, and δ). Several software programs were used to visualize the ligand-receptor interaction and analyze the pharmacokinetic profile.

RESULTS

Compared to typical treatments, our results show that CMN (1 mg/kg) significantly (p < 0.05) increases the locomotor activity of animals. Furthermore, CMN exerted the highest binding affinity (-6.5 kcal/mol) with the GABA-α1 receptor compared to conventional DZP. Along with FLU, CMN displayed several hydrophobic and hydrogen bonds with GABA receptor subunits. The pharmacokinetic and drug-like properties of CMN are also remarkable. In animal studies, CMN worked synergistically with FLU to provide anxiogenic-like effects.

CONCLUSION

We conclude that, based on in vivo and in silico data, CMN, alone or in combination with FLU, may be employed in future neurological clinical studies. However, further research is needed to confirm this behavioral activity and elucidate the possible mechanism of action.

摘要

背景

焦虑症是最常见的精神疾病,也是导致功能障碍的主要因素。因此,迫切需要寻找新的先导化合物来减轻焦虑。人们普遍认识到,与焦虑相关行为的神经生物学涉及γ-氨基丁酸(GABA)能系统。

目的

本研究旨在研究香豆素(CMN)(一种从植物中提取的天然苯并吡喃酮)的致焦虑作用,并通过体内和计算机模拟研究确定其潜在机制。

方法

通过对口服三种实验剂量(1、2和4mg/kg)CMN的雄性和雌性瑞士白化小鼠进行多种行为学实验,包括旷场实验、摆动实验、洞板实验和明暗箱实验来完成。CMN组还与GABA受体激动剂地西泮(DZP,2mg/kg)和氟马西尼拮抗剂(FLU,0.1mg/kg)进行了比较。此外,对CMN和标准品进行分子对接分析,以确定它们对GABA受体亚基(α1、α4、β2、γ2和δ)的结合亲和力。使用多个软件程序来可视化配体-受体相互作用并分析药代动力学特征。

结果

与典型治疗相比,我们的结果表明,CMN(1mg/kg)显著(p<0.05)增加了动物的自发活动。此外,与传统的DZP相比,CMN与GABA-α1受体具有最高的结合亲和力(-6.5kcal/mol)。与FLU一起,CMN与GABA受体亚基显示出多个疏水键和氢键。CMN的药代动力学和类药性质也很显著。在动物研究中,CMN与FLU协同作用,产生类似致焦虑的效果。

结论

我们得出结论,基于体内和计算机模拟数据,CMN单独或与FLU联合使用,可能会用于未来的神经临床研究。然而,需要进一步的研究来证实这种行为活性并阐明可能的作用机制。

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