Influence of extraction solvents on the chemical constituents and biological activities of Astragalus aduncus from Turkey flora: In vitro and in silico insights

Author:

Lazarova Irina1,Nilofar 23,Caprioli Giovanni4,Piatti Diletta4,Ricciutelli Massimo4,Ulusan Musa Denizhan5,Koyuncu Ismail6,Yuksekdag Ozgur6,Mollica Adriano7,Stefanucci Azzurra7,Zengin Gokhan2ORCID

Affiliation:

1. Department of Chemistry, Faculty of Pharmacy Medical University‐Sofia Sofia Bulgaria

2. Physiology and Biochemistry Research Laboratory, Department of Biology, Science Faculty Selcuk University Konya Turkey

3. Department of Pharmacy, Botanic Garden “Giardino dei Semplici” “Gabriele d'Annunzio” University Chieti Italy

4. Department of Chemical and Pharmaceutical Sciences and Biotechnology, CHemistry Interdisciplinary Project (CHip), School of Pharmacy University of Camerino Camerino Italy

5. Department of Forest Engineering, Faculty of Forestry, Department of Forest Engineering Isparta University of Applied Sciences Isparta Turkey

6. Department of Medical Biochemistry, Faculty of Medicine Harran University Sanliurfa Turkey

7. Department of Pharmacy “G. D'Annunzio” University of Chieti‐Pescara Chieti Italy

Abstract

AbstractThe n‐hexane, ethyl acetate, ethanol, ethanol/water (70% ethanol), and water extracts of Astragalus aduncus aerial parts were investigated for their antioxidant potential, enzyme inhibition activity (anti‐acetylcholinesterase [AChE], anti‐butyrylcholinesterase [BChE], antityrosinase, antiamylase, and antiglucosidase) and antiproliferative effect (against colon adenocarcinoma cell line [HT‐29], gastric cancer cell line [HGC‐27], prostate carcinoma cell line [DU‐145], breast adenocarcinoma cell line [MDA‐MB‐231], and cervix adenocarcinoma cell line [HeLa]). In addition, the phytochemical profile of the extracts was evaluated using validated spectrophotometric and high‐pressure liquid chromatography‐electrospray ionization/tandem mass spectroscopy methods. Generally, the 70% ethanol extract demonstrated the strongest antioxidant properties, and it was the richest source of total phenolic constituents. Our findings indicated that the ethyl acetate extract was the most potent BChE inhibitor (11.44 mg galantamine equivalents [GALAE]/g) followed by the ethanol extract (8.51 mg GALAE/g), while the ethanol extract was the most promising AChE inhibitor (3.42 mg GALAE/g) followed by the ethanol/water extract (3.17 mg GALAE/g). Excellent tyrosinase inhibitory activity (66.25 mg kojic acid equivalent/g) was observed in ethanol/water extracts of the aerial part of A. aduncus. Тhese results showed that the most cytotoxic effects were exhibited by the ethyl acetate extract against HGC‐27 cells (IC50: 36.76 µg/mL), the ethanol extract against HT‐29 cells (IC50: 30.79 µg/mL), and the water extract against DU‐145 cells (IC50: 37.01 µg/mL). A strong correlation was observed between the highest total flavonoid content and the highest content of individual compounds in the ethanol extract, including rutin, hyperoside, isoquercitrin, delphinidin‐3,5‐diglucoside (delphinidin‐3,5‐O‐diglucoside), and kaempferol‐3‐glucoside (kaempferol‐3‐O‐glucoside). In the present study, the A. aduncus plant was considered a new source of antioxidants, enzyme inhibitors, and anticancer agents and could be used as a future health‐benefit natural product.

Publisher

Wiley

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