Chemical Characterization of Different Extracts from Artemisia annua and Their Antioxidant, Enzyme Inhibitory and Anti‐Inflammatory Properties

Author:

Acquaviva Alessandra1,Nilofar 1,Bouyahya Abdelhakim2,Zengin Gokhan3ORCID,Di Simone Simonetta Cristina1,Recinella Lucia1,Leone Sheila1,Brunetti Luigi1,Uba Abdullahi Ibrahim4,Cakilcioğlu Ugur5,Polat Rıdvan6,Darendelioglu Ekrem7,Menghini Luigi1,Ferrante Claudio1,Libero Maria Loreta1,Orlando Giustino1,Chiavaroli Annalisa1

Affiliation:

1. Department of Pharmacy G. d'Annunzio University of Chieti-Pescara 66100 Chieti Italy

2. Laboratory of Human Pathologies Biology Faculty of Sciences Department of Biology Mohammed V University in Rabat 1014 Rabat Morocco

3. Physiology and Biochemistry Laboratory Department of Biology Science Faculty Selcuk University 42130 Konya Turkey

4. Department of Molecular Biology and Genetics Istanbul AREL University 34537 Istanbul Türkiye

5. Munzur University Pertek Sakine Genç Vocational School, Tunceli Pertek 62500 Turkey

6. Department of Landscape Architecture Faculty of Agriculture Bingol University Bingöl 12000 Turkey

7. Department of Molecular Biology and Genetic Science and Art Faculty Bingol University Bingöl 12000, Turkey

Abstract

AbstractArtemisia 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.

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

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