Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Apr;36(4):653-667.
doi: 10.1007/s11011-021-00674-y. Epub 2021 Jan 26.

Computational exploration of vicine - an alkaloid glycoside mediated pathological hallmark of adenosine kinase to promote neurological disorder

Affiliations

Computational exploration of vicine - an alkaloid glycoside mediated pathological hallmark of adenosine kinase to promote neurological disorder

SathishKumar Paramashivam et al. Metab Brain Dis. 2021 Apr.

Abstract

Epilepsy disease is characterized by the neuronal dysfunction or abnormal neuronal activity of the brain which is regulated by astrocytes. These are glial cells and found to be the major regulators of the brain which are guided by the occurrence of adenosine kinase (ADK) enzyme in the central nervous system (CNS). During the normal physiological environment, ADK maintains the level of adenosine in the CNS. Dysfunction of ADK levels results in accumulation of adenosine levels in the CNS that leads to the pathophysiology of the brain such as astrogliosis which is a pathological hallmark of epileptic seizures. Vicine, an alkaloid glycoside in bitter gourd juice (Momordica charantia) is found to be toxic to the human system if the bitter gourd juice is consumed more. This compound inhibits ADK enzyme activity to lead epilepsy and seizure. Here, the toxic effect of vicine targeting ADK using computational predictions was investigated. The 3-dimensional structure of ADK has been constructed using I-Tasser, which has been refined by ModRefiner, GalaxyRefine, and 3D refine and it was endorsed using PROCHECK, ERRAT, and VADAR. 3D structure of the ligand molecule has been obtained from PubChem. Molecular docking has been achieved using AutoDock 4.2 software, from which the outcome showed the effective interaction between vicine and ADK, which attains binding free energy (∆G) of - 4.13 kcal/mol. Vicine molecule interacts with the active region ARG 149 of ADK and inhibits the functions of ADK that may cause imbalance in energy homeostasis. Also, pre-ADMET results robustly propose in which vicine possesses toxicity, and meanwhile, from the Ames test, it was shown as mutagenic. Hence, the results from our study suggest that vicine was shown to be toxic that suppresses the ADK activity to undergo pathological conditions in the neuronal junctions to lead epilepsy.

Keywords: ADK; AutoDock; Bitter gourd; Epilepsy; Stroke; Vicine.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Aamir M, Singh VK, Dubey MK, Meena M, Kashyap SP, Katari SK, Upadhyay RK, Umamaheswari A, Singh S (2018) In silico prediction, characterization, molecular docking, and dynamic studies on fungal SDRs as novel targets for searching potential fungicides against Fusarium wilt in tomato. Front Pharmacol 9:1038. https://doi.org/10.3389/fphar.2018.01038 - DOI - PubMed - PMC
    1. Afifi TH, Riyadh SM, Deawaly AA, Naqvi A (2019) Novel chromenes and benzochromenes bearing arylazo moiety: molecular docking, in silico admet, in vitro antimicrobial and anticancer screening. Med Chem Res 28:1471–1487. https://doi.org/10.1007/s00044-019-02387-5 - DOI
    1. Bhattacharya D, NowotnyJ CR, Cheng J (2016) 3Drefine: an interactive web server for efficient protein structure refinement. Nucleic Acids Res 44:W406–W409. https://doi.org/10.1093/nar/gkw336 - DOI - PubMed - PMC
    1. Boison D (2010a) Adenosine dysfunction and adenosine kinase in epileptogenesis. Open Neurosci J 4:93–101. https://doi.org/10.2174/1874082001004020093 - DOI - PubMed - PMC
    1. Boison D (2010b) The adenosine kinase hypothesis of epileptogenesis. Prog Neurobiol 84:249–262. https://doi.org/10.1016/j.pneurobio.2007.12.002 - DOI

Publication types

MeSH terms

LinkOut - more resources