» Articles » PMID: 32991579

Alkaloids of Abuta Panurensis Eichler: In Silico and in Vitro Study of Acetylcholinesterase Inhibition, Cytotoxic and Immunomodulatory Activities

Abstract

Natural products obtained from species of the genus Abuta (Menispermaceae) are known as ethnobotanicals that are attracting increasing attention due to a wide range of their pharmacological properties. In this study, the alkaloids stepharine and 5-N-methylmaytenine were first isolated from branches of Abuta panurensis Eichler, an endemic species from the Amazonian rainforest. Structure of the compounds was elucidated by a combination of 1D and 2D NMR spectroscopic and MS and HRMS spectrometric techniques. Interaction of the above-mentioned alkaloids with acetylcholinesterase enzyme and interleukins IL-6 and IL-8 was investigated in silico by molecular docking. The molecules under investigation were able to bind effectively with the active sites of the AChE enzyme, IL-6, and IL-8 showing affinity towards the proteins. Along with the theoretical study, acetylcholinesterase enzyme inhibition, cytotoxic, and immunomodulatory activity of the compounds were assessed by in vitro assays. The data obtained in silico corroborate the results of AChE enzyme inhibition, the IC50 values of 61.24μM for stepharine and 19.55μM for 5-N-methylmaytenine were found. The compounds showed cytotoxic activity against two tumor cell lines (K562 and U937) with IC50 values ranging from 11.77 μM to 28.48 μM. The in vitro assays revealed that both alkaloids were non-toxic to Vero and human PBMC cells. As for the immunomodulatory activity, both compounds inhibited the production of IL-6 at similar levels. Stepharine inhibited considerably the production of IL-8 in comparison to 5-N-methylmaytenine, which showed a dose dependent action (inhibitory at the IC50 dose, and stimulatory at the twofold IC50 one). Such a behavior may possibly be explained by different binding modes of the alkaloids to the interleukin structural fragments. Occurrence of the polyamine alkaloid 5-N-methylmaytenine was reported for the first time for the Menispermaceae family, as well as the presence of stepharine in A. panurensis.

Citing Articles

Optimization of Fermentation Conditions of for Enhanced Acetylcholinesterase and Butyrylcholinesterase.

Choi J, Yoon J, Kim M Foods. 2022; 11(15).

PMID: 35954035 PMC: 9368701. DOI: 10.3390/foods11152268.


In Vitro and In Silico Evaluation of Cholinesterase Inhibition by Alkaloids Obtained from Branches of Eichler.

da Silva Mesquita R, Kyrylchuk A, Cherednichenko A, Costa Sa I, Macedo Bastos L, da Silva F Molecules. 2022; 27(10).

PMID: 35630611 PMC: 9144276. DOI: 10.3390/molecules27103138.


Extending the lore of curcumin as dipteran Butyrylcholine esterase (BChE) inhibitor: A holistic molecular interplay assessment.

Rao P, Goswami D, Rawal R PLoS One. 2022; 17(5):e0269036.

PMID: 35617284 PMC: 9135230. DOI: 10.1371/journal.pone.0269036.


Recent Developments in New Therapeutic Agents against Alzheimer and Parkinson Diseases: In-Silico Approaches.

Cruz-Vicente P, Passarinha L, Silvestre S, Gallardo E Molecules. 2021; 26(8).

PMID: 33920326 PMC: 8069930. DOI: 10.3390/molecules26082193.

References
1.
Melchiorre C, Andrisano V, Bolognesi M, Budriesi R, Cavalli A, Cavrini V . Acetylcholinesterase noncovalent inhibitors based on a polyamine backbone for potential use against Alzheimer's disease. J Med Chem. 1998; 41(22):4186-9. DOI: 10.1021/jm9810452. View

2.
Gorbalenya A, Svitkin Y, Kazachkov Y, Agol V . Encephalomyocarditis virus-specific polypeptide p22 is involved in the processing of the viral precursor polypeptides. FEBS Lett. 1979; 108(1):1-5. DOI: 10.1016/0014-5793(79)81164-3. View

3.
Soares E, Silva F, de Almeida R, de Lima B, da Silva Filho F, Barison A . Direct infusion ESI-IT-MSn alkaloid profile and isolation of tetrahydroharman and other alkaloids from Bocageopsis pleiosperma maas (Annonaceae). Phytochem Anal. 2015; 26(5):339-45. DOI: 10.1002/pca.2568. View

4.
Houghton P, Ren Y, Howes M . Acetylcholinesterase inhibitors from plants and fungi. Nat Prod Rep. 2006; 23(2):181-99. DOI: 10.1039/b508966m. View

5.
Steele J, Simmonds M, Veitch N, Warhurst D . Evaluation of the anti-plasmodial activity of bisbenzylisoquinoline alkaloids from Abuta grandifolia. Planta Med. 1999; 65(5):413-6. DOI: 10.1055/s-1999-14017. View