4.6 Article

LC-MS/MS Phytochemical Profiling, Antioxidant Activity, and Cytotoxicity of the Ethanolic Extract of Atriplex halimus L. against Breast Cancer Cell Lines: Computational Studies and Experimental Validation

Journal

PHARMACEUTICALS
Volume 15, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/ph15091156

Keywords

Atriplex halimus L.; antioxidant activity; cytotoxicity; breast cancer; computational study; ADMET analysis; toxicity prediction

Funding

  1. Moroccan Ministry of Higher Education, Scientific Research and Innovation (Mohamed Premier University, Faculty of Science, Oujda) - Conseil Departemental d'Eure et Loir
  2. Conseil Regional Centre-Val de Loire (program Biomedicaments, EtopoCentre)

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Atriplex halimus L., commonly known as Mediterranean saltbush, is a plant used for treating various ailments in Morocco. This study investigated the antioxidant activity and cytotoxicity of the ethanolic extract of A. halimus leaves. The extract was found to contain phenolic acids and flavonoids, and exhibited strong antioxidant properties. It also showed significant inhibitory activity against cancer cells in vitro.
Atriplex halimus L., also known as Mediterranean saltbush, and locally as Lgtef, an halophytic shrub, is used extensively to treat a wide variety of ailments in Morocco. The present study was undertaken to determine the antioxidant activity and cytotoxicity of the ethanolic extract of A. halimus leaves (AHEE). We first determined the phytochemical composition of AHEE using a liquid chromatography (LC)-tandem mass spectrometry (MS/MS) technique. The antioxidant activity was evaluated using different methods including DPPH scavenging capacity, beta-carotene bleaching assay, ABTS scavenging, iron chelation, and the total antioxidant capacity assays. Cytotoxicity was investigated against human cancer breast cells lines MCF-7 and MDA-MB-231. The results showed that the components of the extract are composed of phenolic acids and flavonoids. The DPPH test showed strong scavenging capacity for the leaf extract (IC50 of 0.36 +/- 0.05 mg/mL) in comparison to ascorbic acid (IC50 of 0.19 +/- 0.02 mg/mL). The beta-carotene test determined an IC50 of 2.91 +/- 0.14 mg/mL. The IC50 values of ABTS, iron chelation, and TAC tests were 44.10 +/- 2.92 TE mu mol/mL, 27.40 +/- 1.46 mg/mL, and 124 +/- 1.27 mu g AAE/mg, respectively. In vitro, the AHE extract showed significant inhibitory activity in all tested tumor cell lines, and the inhibition activity was found in a dose-dependent manner. Furthermore, computational techniques such as molecular docking and ADMET analysis were used in this work. Moreover, the physicochemical parameters related to the compounds' pharmacokinetic indicators were evaluated, including absorption, distribution, metabolism, excretion, and toxicity prediction (Pro-Tox II).

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