4.6 Article

In Vitro and In Silico Evaluation of Anticholinesterase and Antidiabetic Effects of Furanolabdanes and Other Constituents from Graptophyllum pictum (Linn.) Griffith

Journal

MOLECULES
Volume 28, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/molecules28124802

Keywords

Graptophyllum pictum; furanolabdanes; anticholinesterase; alpha-amylase; alpha-glucosidase; molecular docking

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In this study, seven compounds were isolated from Graptophyllum pictum and evaluated for their anticholinesterase activities and antidiabetic potential. The results showed that G. pictum and its compounds could be used in the development of therapies for Alzheimer's disease and diabetes.
Graptophyllum pictum is a tropical plant noticeable for its variegated leaves and exploited for various medicinal purposes. In this study, seven compounds, including three furanolabdane diterpenoids, i.e., Hypopurin E, Hypopurin A and Hypopurin B, as well as with Lupeol, beta-sitosterol 3-O-beta-D-glucopyranoside, stigmasterol 3-O-beta-D-glucopyranoside and a mixture of beta-sitosterol and stigmasterol, were isolated from G. pictum, and their structures were deduced from ESI-TOF-MS, HR-ESI-TOF-MS, 1D and 2D NMR experiments. The compounds were evaluated for their anticholinesterase activities against acetylcholinesterase (AChE) and butyrylcholinesterase (BchE), as well as their antidiabetic potential through inhibition of alpha-glucosidase and alpha-amylase. For AChE inhibition, no sample had IC50 within tested concentrations, though the most potent was Hypopurin A, which had a percentage inhibition of 40.18 +/- 0.75%, compared to 85.91 +/- 0.58% for galantamine, at 100 mu g/mL. BChE was more susceptible to the leaves extract (IC50 = 58.21 +/- 0.65 mu g/mL), stem extract (IC50 = 67.05 +/- 0.82 mu g/mL), Hypopurin A (IC50 = 58.00 +/- 0.90 mu g/mL), Hypopurin B (IC50 = 67.05 +/- 0.92 mu g/mL) and Hypopurin E (IC50 = 86.90 +/- 0.76 mu g/mL). In the antidiabetic assay, the furanolabdane diterpenoids, lupeol and the extracts had moderate to good activities. Against alpha-glucosidase, lupeol, Hypopurin E, Hypopurin A and Hypopurin B had appreciable activities but the leaves (IC50 = 48.90 +/- 0.17 mu g/mL) and stem (IC50 = 45.61 +/- 0.56 mu g/mL) extracts were more active than the pure compounds. In the alpha-amylase assay, stem extract (IC50 = 64.47 +/- 0.78 mu g/mL), Hypopurin A (IC50 = 60.68 +/- 0.55 mu g/mL) and Hypopurin B (IC50 = 69.51 +/- 1.30 mu g/mL) had moderate activities compared to the standard acarbose (IC50 = 32.25 +/- 0.36 mu g/mL). Molecular docking was performed to determine the binding modes and free binding energies of Hypopurin E, Hypopurin A and Hypopurin B in relation to the enzymes and decipher the structure-activity relationship. The results indicated that G. pictum and its compounds could, in general, be used in the development of therapies for Alzheimer's disease and diabetes.

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