Phytochemical analysis and anticholinesterase activity of aril of Myristica fragrans Houtt

In this study, the ethyl acetate fraction of Myristica fragrans Houtt. was investigated for its in vitro anticholinesterase activity as well as neuroprotectivity against H2O2-induced cell death in PC12 neuronal cells and the ability to chelate bio-metals (Zn2+, Fe2+, and Cu2+). The fraction was inactive toward acetylcholinesterase (AChE); however, it inhibited the butyrylcholinesterase (BChE) with IC50 value of 68.16 mu g/mL, compared with donepezil as the reference drug (IC50 = 1.97 mu g/mL) via Ellman's method. It also showed good percentage of neuroprotection (86.28% at 100 mu g/mL) against H2O2-induced neurotoxicity and moderate metal chelating ability toward Zn2+, Fe2+, and Cu2+. The phytochemical study led to isolation and identification of malabaricone A (1), malabaricone C (2), 4-(4-(3,4-dimethoxyphenyl)-2,3-dimethylbutyl)benzene-1,2-diol (3), nectandrin B (4), macelignan (5), and 4-(4-(benzo[d][1,3]dioxol-5-yl)-1-methoxy-2,3-dimethylbutyl)-2-methoxyphenol (6) which were assayed for their cholinesterase (ChE) inhibitory activity. Compounds 1 and 3 were not previously reported for M. fragrans. Among isolated compounds, compound 2 showed the best activity toward both AChE and BChE with IC50 values of 25.02 and 22.36 mu M, respectively, compared with donepezil (0.07 and 4.73 mu M, respectively).

Automated summary

This study found that the ethyl acetate fraction of Myristica fragrans has inhibitory activity against BChE and neuroprotective effects against H2O2-induced cell death. Compound 2 from Myristica fragrans showed the best inhibitory activity against both AChE and BChE.