In Vitro Evaluation, Chemical Profiling, and In Silico ADMET Prediction of the Pharmacological Activities of Artemisia absinthium Root Extract

<i>Artemisia absinthium</i> L., is a plant with established pharmacological properties, but the <i>A. absinthium</i> root extract (AARE) remains unexplored. The aim of this study was to examine the chemical composition of AARE and assess its biological activity, which included antidiabetic, antibacterial, anticancer, and antioxidant properties. GC-MS was used to analyze the chemical components. The antioxidant activity of the total phenolic and flavonoid content was evaluated. Antibacterial activity and cytotoxic effects were identified. Enzyme inhibition experiments were performed to determine its antidiabetic potential. Molecular docking was utilized to evaluate the potential antioxidant, antibacterial, and anticancer activities of the compounds from AARE using Maestro 11.5 from the Schrödinger suite. AARE exhibited moderate antioxidant activity in DPPH (IC<sub>50</sub>: 172.41 ± 3.15 μg/mL) and ABTS (IC<sub>50</sub>: 378.94 ± 2.18 μg/mL) assays. Cytotoxicity tests on MCF-7 and HepG2 cancer cells demonstrated significant anticancer effects, with IC<sub>50</sub> values of 150.12 ± 0.74 μg/mL and 137.11 ± 1.33 μg/mL, respectively. Apoptotic studies indicated an upregulation of pro-apoptotic genes (<i>caspase</i>-<i>3</i>, <i>8</i>, <i>9</i>, <i>Bax</i>) and a downregulation of anti-apoptotic markers (<i>Bcl-2</i> and <i>Bcl-Xl</i>). AARE also inhibited α-amylase and α-glucosidase, suggesting potential antidiabetic effects, with IC<sub>50</sub> values of 224.12 ± 1.17 μg/mL and 243.35 ± 1.51 μg/mL. Antibacterial assays revealed strong activity against Gram-positive bacteria. Molecular docking and pharmacokinetic analysis identified promising inhibitory effects of key AARE compounds on NADPH oxidase, <i>E. coli</i> Gyrase B, and Topoisomerase IIα, with favorable drug-like properties. These findings suggest AARE's potential in treating cancer, diabetes, and bacterial infections, warranting further in vivo and clinical studies.

Authors

Institutions

Publication Details

Journal
Pharmaceuticals
Published
2024-12-07
DOI
https://doi.org/10.3390/ph17121646
Citations
4
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
1.87
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

In Vitro Evaluation, Chemical Profiling, and In Silico ADMET Prediction of the Pharmacological Activities of Artemisia absinthium Root Extract

Noorah Abdulaziz Othman Alkubaisi, Reem M. Aljowaie, Asma N. Alsaleh, Mourad A. M. Aboul‐Soud et al.
4 citations
Pharmaceuticals
Drug-Induced Hepatotoxicity and Protection
1.87
article

In Vitro Evaluation, Chemical Profiling, and In Silico ADMET Prediction of the Pharmacological Activities of Artemisia absinthium Root Extract

Noorah Abdulaziz Othman Alkubaisi, Reem M. Aljowaie, Asma N. Alsaleh, Mourad A. M. Aboul‐Soud, Ibrahim M. Aziz, Rawan M. Alshalan
article en
4 citations

Abstract

<i>Artemisia absinthium</i> L., is a plant with established pharmacological properties, but the <i>A. absinthium</i> root extract (AARE) remains unexplored. The aim of this study was to examine the chemical composition of AARE and assess its biological activity, which included antidiabetic, antibacterial, anticancer, and antioxidant properties. GC-MS was used to analyze the chemical components. The antioxidant activity of the total phenolic and flavonoid content was evaluated. Antibacterial activity and cytotoxic effects were identified. Enzyme inhibition experiments were performed to determine its antidiabetic potential. Molecular docking was utilized to evaluate the potential antioxidant, antibacterial, and anticancer activities of the compounds from AARE using Maestro 11.5 from the Schrödinger suite. AARE exhibited moderate antioxidant activity in DPPH (IC<sub>50</sub>: 172.41 ± 3.15 μg/mL) and ABTS (IC<sub>50</sub>: 378.94 ± 2.18 μg/mL) assays. Cytotoxicity tests on MCF-7 and HepG2 cancer cells demonstrated significant anticancer effects, with IC<sub>50</sub> values of 150.12 ± 0.74 μg/mL and 137.11 ± 1.33 μg/mL, respectively. Apoptotic studies indicated an upregulation of pro-apoptotic genes (<i>caspase</i>-<i>3</i>, <i>8</i>, <i>9</i>, <i>Bax</i>) and a downregulation of anti-apoptotic markers (<i>Bcl-2</i> and <i>Bcl-Xl</i>). AARE also inhibited α-amylase and α-glucosidase, suggesting potential antidiabetic effects, with IC<sub>50</sub> values of 224.12 ± 1.17 μg/mL and 243.35 ± 1.51 μg/mL. Antibacterial assays revealed strong activity against Gram-positive bacteria. Molecular docking and pharmacokinetic analysis identified promising inhibitory effects of key AARE compounds on NADPH oxidase, <i>E. coli</i> Gyrase B, and Topoisomerase IIα, with favorable drug-like properties. These findings suggest AARE's potential in treating cancer, diabetes, and bacterial infections, warranting further in vivo and clinical studies.

PharmaceuticalsVol. 17(12)
King Saud University (SA)
Openalex Percentile: Top 15%
Drug-Induced Hepatotoxicity and Protection
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.