GC-MS ANALYSIS, CHOLINESTERASE INHIBITORY AND ANTIOXIDANT POTENTIALS OF ZAPOTECA PORTORICENSIS (JACQ.) H.M. HERN (FABACEAE) ROOT EXTRACTS

GC-MS ANALYSIS, CHOLINESTERASE INHIBITORY AND ANTIOXIDANT POTENTIALS OF ZAPOTECA PORTORICENSIS (JACQ.) H.M. HERN (FABACEAE) ROOT EXTRACTS


JOEL OJOGBANE ONOJA1,2,3,*, JULIUS IDOWU OLAWUNI4, MALACHUKWU CHIBUNDU UMEOKOLI1

1. Department of Pharmacognosy and Environmental Medicine, Faculty of Pharmaceutical Sciences, University of Nigeria Nsukka, Nigeria.
2. Institute of Drug-Herbal Medicine-Excipient Research and Development, University of Nigeria, Nsukka, Nigeria.
3. Center for Drug Discovery, University of Buea, Buea, Cameroon
4. Department of Biochemistry and Molecular Biology, Faculty of Sciences, Obafemi Awolowo University Ile-Ife, Nigeria.

Afr. J Pharm Res Dev; Volume 16(4): 69-80   ; 2024

ABSTRACT

The age-related neurodegenerative illness known as Alzheimer’s disease (AD) is typified by the unavoidable decline in cognitive function. Existing drugs has limitations, therefore there is an urgent need for new neurotherapeutic agents. There has been a lot of excitement in recent years about finding therapeutic herbs that can restore cognitive impairment due to their lower side effects. The aim of the study is to evaluate the cholinesterase inhibitory and antioxidant potentials of Zapoteca portoricensis (Jacq.) H.M. Hern root extracts and also identify the bioactive molecules present. Ellman colorimetric assay was used to evaluate the cholinesterase inhibitory potentials of various extracts at 1 mg/mL. The antioxidant potentials of extracts were evaluated using in-vitro chemical analysis. GC-MS was used to identify bioactive molecules from  most active extract. One-way ANOVA at α0.05 was adopted. Ethyl acetate extract showed the highest acetylcholinesterase (IC50 = 0.149±0.00 mg/mL) and butyrylcholinesterase (IC50 = 0.393±0.02 mg/mL) inhibitory potential as compared to eserine for AChE (IC50 = 0.051±0.01 mg/mL) and for BuChE (IC50 = 0.049±0.00 mg/mL). Ethyl acetate extract also demonstrated its potential to chelate metals (IC50 = 0.106±0.02 mg/mL) as compared to EDTA (IC50 = 0.086±0.00 mg/mL). The DPPH radical scavenging potential was higher in ethyl acetate extract (IC50 = 0.082±0.05 mg/mL) when compared to vitamin C (IC50 = 0.008±0.00 mg/mL). The total antioxidant capacity of extracts revealed that ethyl acetate extract also has the highest concentration (125.5±14.3 mg/g AAE/g of extract (R2=0.9276)). The GC-MS analysis of ethyl acetate extract revealed the presence of 62 compounds which includes n-Hexadecanoic acid (RT 14.81, Area % 10.03), 9,12-Octadecadienoic acid (Z,Z)- (RT 15.97, Area % 10.03), cis-9-Hexadecenal (RT 16.01, Area % 8.36). The ethyl acetate extract from the root of Zapoteca portoricensis has the aptitude to prolong the half-life of acetylcholine by its ability to inhibit cholinesterase enzyme.

 

Keywords: Fabaceae, Zapoteca portoricensis, Cholinesterase inhibition, Antioxidant, GC-MS

Email of correspondence: joel.onoja@unn.edu.ng;

https://doi.org/10.59493/ajopred/2024.1.8                                     ISSN: 0794-800X (print); 1596-2431 (online)

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