The 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).
Influence of extraction solvents on the chemical constituents and biological activities of Astragalus aduncus from Turkey flora: In vitro and in silico insights
Giovanni Caprioli;Diletta Piatti;Massimo Ricciutelli;
2024-01-01
Abstract
The 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).I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
