Acetylcholinesterase inhibitory activities of some flavonoids from the root bark of Pinus krempfii Lecomte: in vitro and in silico study

Abstract

From the root bark of Pinus krempfii Lecomte, four flavonoids were isolated and evaluated for their inhibitory activities against AChE and BChE enzymes in vitro and in silico. Tectochrysin (1) was found to inhibit AChE with an IC₅₀ value of 33.69 ± 2.80 μM. The docking study results also showed agreement with the in vitro test results. All four compounds also showed the best binding affinity for the AChE enzyme, characterised by binding energy (ΔG) values as low as −8.1 to −9.3 kcal/mol, in which, the compound tectochrysin had the best binding affinity for the AChE protein with a ΔG value of −9.329 kcal/mol. Tectochrysin (1) was also bound to the amino acid Phe295 of AChE with a bond length of 2.8 Å, similar to the control dihydrotanshinone-I. Galangin (2) also showed its in vitro inhibitory activity against BChE with an IC₅₀ value of 82.21 ± 2.70 μM. In silico, it also had the best binding energy value of −9.072 kcal/mol with BChE and formed hydrogen bonds with the His438 (2.85 Å) residues of BChE like the positive control (tacrine). The steered molecular dynamics (SMD) simulation results of these two complexes revealed a mechanistic insight that the protein-ligand complexes showed stable trajectories throughout the 20 and 150 ns simulations. Moreover, the drug likeliness suggested that both flavonoids (1 and 2) were expected to be drug-like and have an LD₅₀ toxicity level of 5. This study has contributed new results for drug discovery and the development of substances with neuroprotective effects, especially for the treatment of Alzheimer’s disease.

Communicated by Ramaswamy H. Sarma

Keywords:

• Acetylcholinesterase
• Alzheimer’s disease
• butyrylcholinesterase
• Pinus krempfii
• flavonoid

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This research was partly financially supported by VAST through the project No. QTSK01.01/21.22 (PI Pham Ngọc Khanh), the Institute of Chemistry (ICH/23, TT Thuy), and by a VAST grant, coded KHCBSS.01/21-23 (for PI Nguyen Manh Cuong).