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. 2023 Jan 23;13(2):323.
doi: 10.3390/life13020323.

Ephedra alata Subsp. Alenda as a Novel Source of Bioactive Phytochemicals: Characterization Based on the Mass Spectrometry and Profiling of Antioxidant and Anti-Inflammatory Properties

Affiliations

Ephedra alata Subsp. Alenda as a Novel Source of Bioactive Phytochemicals: Characterization Based on the Mass Spectrometry and Profiling of Antioxidant and Anti-Inflammatory Properties

Afoua Mufti et al. Life (Basel). .

Abstract

The aim of the present study was to examine, for the first time, the phytochemical content of Ephedra alata pulp extract (EAP) and explore its antioxidant and anti-inflammatory capacities. High-performance liquid chromatography-electrospray ionization-quadrupole-time-of-flight mass spectrometry (HPLC-ESI-QTOF/MS) was used for phytochemical analysis and three in vitro antioxidant assays together with three in vitro anti-inflammatory tests were used for the assessment of biological activity. The HPLC-ESI-QTOF/MS analysis revealed the presence of 42 metabolites, including flavonoids, sphingolipides, fatty acids, ephedrine derivatives, and amino acid derivatives. In vitro findings revealed that EAP has interesting 2,2-diphenyl-1-picrylhydrazyl (DPPH), superoxide, and ferrous ion chelating capacities (IC50 values were 0.57 mg/mL, 0.55 mg/mL, and 0.51 mg/mL for DPPH, superoxide radical, and ferrous ion, respectively). Furthermore, EAP showed a noticeable anti-inflammatory ability by inhibiting the two cyclooxygenase isoforms, COX-1 and COX-2 (IC50 of 59.1 and 58.8 µg/mL for COX-1 and COX-2, respectively), preventing protein denaturation (IC50 = 0.51 mg/mL), and protecting membrane stabilization (IC50 = 0.53 mg/mL). The results highlighted the use of Ephedra alata pulp as a potential source of natural compounds with therapeutic effects for the management of inflammatory disorders.

Keywords: COX1 and COX2; Ephedra alata; anti-inflammatory; antioxidants; high-performance liquid chromatography-electrospray ionization-quadrupole-time-of-flight mass spectrometry (HPLC–ESI–QTOF/MS).

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Base peak chromatogram of the Ephedra alata pulp (EAP) extract obtained by HPLC-DAD-QTOF-MS analysis.
Figure 2
Figure 2
Percentage enzyme inhibition and IC50 values of EAP and indomethacin against COX-1 and COX-2 enzymes. n = 3, mean ± SD values. IC50 (50% concentration of inhibitory activity).
Figure 3
Figure 3
Effect of EAP extracts on heat-induced albumin denaturation (A) and hemolysis of erythrocyte membrane (B). The data are presented as mean values (n = 3). EAP: Ephedra alata pulp extract. Ind: indomethacin. IC50 (50% concentration of inhibitory activity) values express the concentration for each sample in mg/mL. * p < 0.05 significant differences compared to indomethacin. ns: not significant.

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References

    1. Mahnashi M.H., Alyami B.A., Alqahtani Y.S., Jan M.S., Rashid U., Sadiq A., Alqarni A.O. Phytochemical Profiling of Bioactive Compounds, Anti-Inflammatory and Analgesic Potentials of Habenaria digitata Lindl.: Molecular Docking Based Synergistic Effect of the Identified Compounds. J. Ethnopharmacol. 2021;273:113976. doi: 10.1016/j.jep.2021.113976. - DOI - PubMed
    1. Tir M., Feriani A., Labidi A., Mufti A., Saadaoui E., Nasri N., Khaldi A., El Cafsi M., Tlili N. Protective effects of phytochemicals of Capparis spinosa seeds with cisplatin and CCl4 toxicity in mice. Food Biosci. 2019;28:42–48. doi: 10.1016/j.fbio.2019.01.002. - DOI
    1. Hajhashemi V., Ghanadian M., Palizaban A., Mahnam K., Eshaghi H., Gheisari B., Sadeghi-Aliabadi H. Cycloarta-23-Ene-3beta,25-Diol a Pentacyclic Steroid from Euphorbia Spinidens, as COX Inhibitor with Molecular Docking, and In Vivo Study of Its Analgesic and Anti-Inflammatory Activities in Male Swiss Mice and Wistar Rats. Prostaglandins Other Lipid Mediat. 2020;150:106473. doi: 10.1016/j.prostaglandins.2020.106473. - DOI - PubMed
    1. Tasneem S., Liu B., Li B., Choudhary M.I., Wang W. Molecular Pharmacology of Inflammation: Medicinal Plants as Anti-Inflammatory Agents. Pharmacol. Res. 2019;139:126–140. doi: 10.1016/j.phrs.2018.11.001. - DOI - PubMed
    1. Abd El-Karim S.S., Mohamed H.S., Abdelhameed M.F., Amr AE G.E., Almehizia A.A., Nossier E.S. Design, Synthesis and Molecular Docking of New Pyrazole-Thiazolidinones as Potent Anti-Inflammatory and Analgesic Agents with TNF-α Inhibitory Activity. Bioorganic Chem. 2021;111:104827. doi: 10.1016/j.bioorg.2021.104827. - DOI - PubMed