Chemical Characterization of Different Extracts from Artemisia annua and Their Antioxidant, Enzyme Inhibitory and Anti-Inflammatory Properties
Özet
Artemisia annua L. (Asteraceae Family) is an important plant in Asia that has been used for treating different diseases, including fever due to malaria, wounds, tubercolisis, scabues, pain, convulsions, diabetes, and inflammation. In this study we aimed to evaluate the effects of different polarity extracts (hexane, dichloromethane, ethyl acetate, ethanol, ethanol/water (70 %) and water) from A. annua against the burden of inflammation and oxidative stress occurring in colon tissue exposed to LPS. In parallel, chemical composition, antiradical, and enzyme inhibition effects against α-amylase, α-glucosidase, tyrosinase, and cholinesterases were evaluated. The water extract contained the highest content of the total phenolic with 34.59 mg gallic acid equivalent (GAE)/g extract, while the hexane had the highest content of the total flavonoid (20.06 mg rutin equivalent (RE)/g extract). In antioxidant assays, the polar extracts (ethanol, ethanol/water and water) exhibited stronger radical scavenging and reducing power abilities when compared to non-polar extracts. The hexane extract showed the best AChE, tyrosinase and glucosidase inhibitory effects. All extracts revealed effective anti-inflammatory agents, as demonstrated by the blunting effects on COX-2 and TNFα gene expression. These effects seemed to be not related to the only phenolic content. However, it is worthy of interest to highlight how the higher potency against LPS-induced gene expression was shown by the water extract; thus suggesting a potential phytotherapy application in the management of clinical symptoms related to inflammatory colon diseases, although future in vivo studies are needed to confirm such in vitro and ex vivo observations.
Anahtar Kelimeler
- Scopus
- 45
- OpenAlex
- 43
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Acquaviva, Alessandra | |
| dc.contributor.author | Nilofar | |
| dc.contributor.author | Bouyahya, Abdelhakim | |
| dc.contributor.author | Zengin, Gokhan | |
| dc.contributor.author | Di Simone, Simonetta Cristina | |
| dc.contributor.author | Recinella, Lucia | |
| dc.contributor.author | Leone, Sheila | |
| dc.contributor.author | Brunetti, Luigi | |
| dc.contributor.author | Uba, Abdullahi Ibrahim | |
| dc.contributor.author | Cakilcioğlu, Ugur | |
| dc.contributor.author | Polat, Rıdvan | |
| dc.contributor.author | Darendelioglu, Ekrem | |
| dc.contributor.author | Menghini, Luigi | |
| dc.contributor.author | Ferrante, Claudio | |
| dc.contributor.author | Libero, Maria Loreta | |
| dc.contributor.author | Orlando, Giustino | |
| dc.contributor.author | Chiavaroli, Annalisa | |
| dc.date.accessioned | 2026-10-28T14:55:07.424663743Z | |
| dc.date.available | 2026-10-28T14:55:07.424663743Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Artemisia annua L. (Asteraceae Family) is an important plant in Asia that has been used for treating different diseases, including fever due to malaria, wounds, tubercolisis, scabues, pain, convulsions, diabetes, and inflammation. In this study we aimed to evaluate the effects of different polarity extracts (hexane, dichloromethane, ethyl acetate, ethanol, ethanol/water (70 %) and water) from A. annua against the burden of inflammation and oxidative stress occurring in colon tissue exposed to LPS. In parallel, chemical composition, antiradical, and enzyme inhibition effects against α-amylase, α-glucosidase, tyrosinase, and cholinesterases were evaluated. The water extract contained the highest content of the total phenolic with 34.59 mg gallic acid equivalent (GAE)/g extract, while the hexane had the highest content of the total flavonoid (20.06 mg rutin equivalent (RE)/g extract). In antioxidant assays, the polar extracts (ethanol, ethanol/water and water) exhibited stronger radical scavenging and reducing power abilities when compared to non-polar extracts. The hexane extract showed the best AChE, tyrosinase and glucosidase inhibitory effects. All extracts revealed effective anti-inflammatory agents, as demonstrated by the blunting effects on COX-2 and TNFα gene expression. These effects seemed to be not related to the only phenolic content. However, it is worthy of interest to highlight how the higher potency against LPS-induced gene expression was shown by the water extract; thus suggesting a potential phytotherapy application in the management of clinical symptoms related to inflammatory colon diseases, although future in vivo studies are needed to confirm such in vitro and ex vivo observations. | |
| dc.identifier.articlenumber | e202300547 | |
| dc.identifier.doi | 10.1002/cbdv.202300547 | |
| dc.identifier.eissn | 1612-1880 | |
| dc.identifier.issn | 1612-1872 | |
| dc.identifier.issue | 8 | |
| dc.identifier.pmid | 37306942 | |
| dc.identifier.scopus | 2-s2.0-85165011265 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/munzur/2233 | |
| dc.identifier.volume | 20 | |
| dc.identifier.wos | WOS:001031770700001 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | Chemistry and Biodiversity | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | anti-inflammatory effects | |
| dc.subject | antioxidant effects | |
| dc.subject | Artemisia annua | |
| dc.subject | enzyme inhibition | |
| dc.subject | specialized metabolites | |
| dc.subject.other | Anti-Inflammatory Agents | |
| dc.subject.other | Antioxidants | |
| dc.subject.other | Artemisia annua | |
| dc.subject.other | Ethanol | |
| dc.subject.other | Hexanes | |
| dc.subject.other | Inflammation | |
| dc.subject.other | Lipopolysaccharides | |
| dc.subject.other | Monophenol Monooxygenase | |
| dc.subject.other | Phenols | |
| dc.subject.other | Plant Extracts | |
| dc.subject.other | Water | |
| dc.subject.other | alpha glucosidase | |
| dc.subject.other | amylase | |
| dc.subject.other | Artemisia annua extract | |
| dc.subject.other | artemisin | |
| dc.subject.other | cholinesterase | |
| dc.subject.other | cyclooxygenase 2 | |
| dc.subject.other | epicatechin | |
| dc.subject.other | flavone | |
| dc.subject.other | flavonoid | |
| dc.subject.other | hesperetin | |
| dc.subject.other | interleukin 6 | |
| dc.subject.other | interleukin 8 | |
| dc.subject.other | naringenin | |
| dc.subject.other | quercetin | |
| dc.subject.other | thymol | |
| dc.subject.other | tumor necrosis factor | |
| dc.subject.other | alcohol | |
| dc.subject.other | antiinflammatory agent | |
| dc.subject.other | antioxidant | |
| dc.subject.other | hexane | |
| dc.subject.other | lipopolysaccharide | |
| dc.subject.other | n-hexane | |
| dc.subject.other | phenol derivative | |
| dc.subject.other | plant extract | |
| dc.subject.other | animal experiment | |
| dc.subject.other | animal model | |
| dc.subject.other | animal tissue | |
| dc.subject.other | antidiabetic activity | |
| dc.subject.other | antiinflammatory activity | |
| dc.subject.other | antioxidant activity | |
| dc.subject.other | antioxidant assay | |
| dc.subject.other | Article | |
| dc.subject.other | chemical composition | |
| dc.subject.other | colitis | |
| dc.subject.other | colon tissue | |
| dc.subject.other | colorimetry | |
| dc.subject.other | controlled study | |
| dc.subject.other | crystal structure | |
| dc.subject.other | disease burden | |
| dc.subject.other | enzyme inhibition | |
| dc.subject.other | gene expression | |
| dc.subject.other | human | |
| dc.subject.other | in vitro study | |
| dc.subject.other | in vivo study | |
| dc.subject.other | molecular docking | |
| dc.subject.other | mouse | |
| dc.subject.other | nonhuman | |
| dc.subject.other | oxidative stress | |
| dc.subject.other | phytotherapy | |
| dc.subject.other | chemistry | |
| dc.title | Chemical Characterization of Different Extracts from Artemisia annua and Their Antioxidant, Enzyme Inhibitory and Anti-Inflammatory Properties | |
| dc.type | Article | |
| rdl.citation.openalex | 43 | |
| rdl.citation.scopus | 45 | |
| rdl.department | Department of Pharmacy, G. d'Annunzio University of Chieti-Pescara, 66100, Chieti, Italy | |
| rdl.department | Laboratory of Human Pathologies Biology, Faculty of Sciences, Department of Biology, Mohammed V University in Rabat, 1014, Rabat, Morocco | |
| rdl.department | Physiology and Biochemistry Laboratory, Department of Biology, Science Faculty, Selcuk University, 42130, Konya, Turkey | |
| rdl.department | Department of Molecular Biology and Genetics, Istanbul AREL University, 34537, Istanbul, Türkiye | |
| rdl.department | Munzur University, Pertek Sakine Genç Vocational School, Tunceli, Pertek, 62500, Turkey | |
| rdl.department | Department of Landscape Architecture, Faculty of Agriculture, Bingol University, Bingöl, 12000, Turkey | |
| rdl.department | Department of Molecular Biology and Genetic, Science and Art Faculty, Bingol University, Bingöl, 12000, Turkey | |
| rdl.oa.status | closed | |
| rdl.scopus.quartile | Q2 | |
| rdl.sdg | SDG03 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED |

