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. 2024 Jun 14;24(1):232.
doi: 10.1186/s12906-024-04520-3.

Metabolic profiling of Vitex Pubescens Vahl bark via UPLC-ESI-QTOF/MS/MS analysis and evaluation of its antioxidant and acetylcholinesterase inhibitory activities

Affiliations

Metabolic profiling of Vitex Pubescens Vahl bark via UPLC-ESI-QTOF/MS/MS analysis and evaluation of its antioxidant and acetylcholinesterase inhibitory activities

Safa Abdelbaset et al. BMC Complement Med Ther. .

Abstract

Background: Alzheimer's disease is a neurodegenerative age-related disease that primarily affects the elderly population leading to progressive memory impairments and neural deficits. It is counted as a major cause of geriatric dependency and disability. The pathogenesis of Alzheimer's disease incidence is complex and involves various hypotheses, including the cholinergic hypothesis, deposition of β-amyloid plaques, neuroinflammation, oxidative stress, and apoptosis. Conventional treatments such as donepezil aim to delay the symptoms but do not affect the progression of the disease and may cause serious side effects like hepatoxicity. The use of natural candidates for Alzheimer's disease treatment has drawn the attention of many researchers as it offers a multitargeted approach.

Methods: This current study investigates the metabolic profiles of total defatted methanolic extract of Vitex pubescens bark and its polar fractions, viz. ethyl acetate and n-butanol, using ultra-performance liquid chromatography-electrospray ionization-quadrupole time-of-flight tandem mass spectrometry(UPLC-ESI-QTOF/MS/MS) technique as well as evaluate the antioxidant using free radical scavenging assays, viz. DPPH and ABTS assays and in-vitro acetylcholinesterase inhibitory activities using Ellman's microplate assay.

Results: Metabolic profiling revealed a total of 71, 43, and 55 metabolites tentatively identified in the defatted methanolic extract, ethyl acetate, and n-butanol fractions, respectively. Phenolic acids were the most abundant class, viz. benzoic acids, and acyl quinic acid derivatives followed by flavonoids exemplified mainly by luteolin-C-glycosides and apigenin-C-glycosides. Quantification of the total phenolic and flavonoid contents in the total defatted methanolic extract confirmed its enrichment with phenolics and flavonoids equivalent to 138.61 ± 9.39 µg gallic acid/mg extract and 119.63 ± 4.62 µg rutin/mg extract, respectively. Moreover, the total defatted methanolic extract exhibited promising antioxidant activity confirmed through DPPH and ABTS assays with a 50% inhibitory concentration (IC50) value equivalent to 52.79 ± 2.16 µg/mL and 10.02 ± µg/mL, respectively. The inhibitory activity of acetylcholine esterase (AchE) was assessed using in-vitro Ellman's colorimetric assay, the total defatted methanolic extract, ethyl acetate, and n-butanol fractions exhibited IC50 values of 52.9, 15.1 and 108.8 µg/mL that they proved the significant inhibition of AchE activity.

Conclusion: The results obtained herein unraveled the potential use of the total methanolic extract of Vitex pubescens bark and its polar fractions as natural candidates for controlling Alzheimer's disease progression.

Keywords: Vitex pubescens bark; Acetylcholinesterase; AchE inhibitory activity; Alzheimer’s; Antioxidant; Ellman’s assay; Polar fractions; UPLC-ESI-QTOF/MS/MS.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
UPLC-ESI-QTOF/MS/MS chromatograms of V. pubescens methanol extract (A) total defatted methanol extract in the negative ion mode, B defatted methanol extract in the positive ion mode, C ethyl acetate fraction in the negative ion mode and D n-butanol fraction. The peaks are annotated as listed in Table 1
Fig. 2
Fig. 2
The structures of major identified peaks using UPLC-ESI-QTOF/MS/MS from the defatted methanol extract, ethyl acetate and n-butanol fractions of V. pubescens bark
Fig. 3
Fig. 3
DPPH percent inhibition of V. pubescens extract versus Trolox standard
Fig. 4
Fig. 4
Acetylcholinesterase inhibitory activity of V. pubescens total defatted methanol extract and its polar fractions at different concentrations using dose response nonlinear regression test. VT: total defatted methanol extract, VE: polar ethyl acetate fraction and VB: polar n-butanol fraction of V. pubescens barksversus donepezil control
Fig. 5
Fig. 5
Acetylcholinesterase inhibitory calculated IC50 ofV. pubescens total defatted methanol extract and its polar fractions at different concentrations versus donepezil control using one way ANOVA followed by Tukey’s post hoc test. VT: total defatted methanol extract, VE: polar ethyl acetate fraction and VB: polar n-butanol fraction of V. pubescens bark.*,$: significant different with P<0.05

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