Okinawa propolis components might be beneficial in the treatment of inflammation, type 2 diabetes mellitus, and Alzheimer's disease. - GreenMedInfo Summary

Okinawa propolis (OP) and its major ingredients were reported to have anti-cancer effects and lifespan-extending effects onthrough inactivation of the oncogenic kinase, p21-activated kinase 1 (PAK1). Herein, five prenylated flavonoids from OP, nymphaeol-A (NA), nymphaeol-B (NB), nymphaeol-C (NC), isonymphaeol-B (INB), and 3'-geranyl-naringenin (GN), were evaluated for their anti-inflammatory, anti-diabetic, and anti-Alzheimer's effects using in vitro techniques. They showed significant anti-inflammatory effects through inhibition of albumin denaturation (half maximal inhibitory concentration (IC) values of 0.26⁻1.02 µM), nitrite accumulation (ICvalues of 2.4⁻7.0 µM), and cyclooxygenase-2 (COX-2) activity (ICvalues of 11.74⁻24.03 µM). They also strongly suppressed in vitro α-glucosidase enzyme activity with ICvalues of 3.77⁻5.66 µM. However, only INB and NA inhibited acetylcholinesterase significantly compared to the standard drug donepezil, with ICvalues of 7.23 and 7.77µM, respectively. Molecular docking results indicated that OP compounds have good binding affinity to the α-glucosidase and acetylcholinesterase proteins, making non-bonded interactions with their active residues and surrounding allosteric residues. In addition, none of the compounds violated Lipinski's rule of five and showed notable toxicity parameters. Density functional theory (DFT)-based global reactivity descriptors demonstrated their high reactive nature along with the kinetic stability. In conclusion, this combined study suggests that OP components might be beneficial in the treatment of inflammation, type 2 diabetes mellitus, and Alzheimer's disease.