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In vitro enzyme inhibitory properties, antioxidant activities, and phytochemical profile of Potentilla thuringiaca
Phytochemistry Letters Cilt 20 ss. 365-372
Scopus Toplam 432 atıf DOI
The genus Potentilla is interesting for the pharmaceutical field due to its valuable medicinal properties, which have been observed in complementary and alternative medicine. In recent years, studies conducted to estimate the biological activity of several of the Potentilla species have shown a wide spectrum of therapeutic properties. In particular, in the present paper, different extracts obtained from the herb P. thuringiaca were analysed for antioxidant and enzyme inhibitory activities. The UHPLC-DAD-MS3 hyphenated techniques reported herein allow for the identification of phytoconstituents. The analyses showed the presence of flavonoids and ellagitannins as major components. Furthermore, the data demonstrated that the analysed extracts revealed a high total antioxidant capacity in the phosphomolybdenum assay. The free radical scavenging activity of the extracts was evaluated using DPPH and ABTS assays. The reducing power activity of P. thuringiaca was also determined by FRAP and CUPRAC assays, as well as metal chelating activity. In addition, the total extracts and the different fractions of P. thuringiaca revealed potent inhibitory activities against α-amylase and α-glucosidase, AChE, tyrosinase and lipase. Surprisingly, no activity against BChE was shown. P. thuringiaca could be a valuable natural source of antioxidants with interesting inhibitory actions against the key enzymes involved in several human diseases, and could represent a valid starting point for the development of new treatment and management strategies, including its use as a food supplement.
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Bioactive agents from Parkia biglobosa (Jacq.) R.Br. ex G. Don bark extracts for health promotion and nutraceutical uses
Journal of the Science of Food and Agriculture Cilt 104 ss. 2820-2831
Scopus Havuzumuzda Open Access 8 atıf almış
BACKGROUND: Parkia biglobosa stem bark extracts were prepared using methanol, methanol 80%, water and ethyl acetate to investigate their phytochemical contents, as well as antioxidant and enzyme inhibitory properties. RESULTS: Liquid chromatography (LC) quadrupole time-of-flight mass spectrometry (MS) and LC-MSn revealed the presence of flavonoids, hydroxycinnamic acid derivatives and gallotannins. Particularly, the water extract contained rutin (480 μg per 100 mg) and 3-caffeoylquinic acid (1109 μg per 100 mg) in higher amounts, whereas the 80% methanol extract contains methoxyluteolin-7-O-rutinoside and catechin derivatives as major compounds. Total phenolic and flavonoid contents of the extracts were yielded in the range of 32.26–119.88 mg gallic acid equivalents g−1 and 0.60–2.39 mg rutin equivalents g−1, respectively. Total antioxidant capacity was also displayed in the range of 0.53–6.34 mmol Trolox equivalents (TE) g−1. Both the methanolic extracts showed higher total antioxidant capacity that could be related to the total phenolic contents. Radical scavenging capacity in DPPH (2,2-diphenyl-2-picryl-hydrazyl) (37.21–508.30 mg TE g−1) and ABTS [2,2-azinobis(3-ethylbenzothiazoline- 6-sulfonic acid)] (60.95–1068.06 mg TE g−1) assays, reducing power in cupric ion reducing antioxidant capacity (54.23–1002.78 mg TE g−1) and ferric ion reducing antioxidant power (33.18–558.68 mg TE g−1) assays, as well as metal chelating activity (2.45–11.28 mg EDTA equivalents g−1), were exhibited by all extracts. All extracts were found to inhibit acetylcholinesterase [0.23–2.47 mg galanthamine equivalents (GALAE) g−1], tyrosinase [27.20–83.33 mg kojic acid equivalents g−1], amylase [mmol acarbose equivalents (ACAE) g−1]. On the other hand, all extracts, except the water extract, inhibited butyrylcholinesterase (5.38–6.56 mg GALAE g−1), whereas only the water and ethyl acetate extract showed glucosidase inhibitory potential (1.96 and 1.82 mmol ACAE g−1). In general, the water extract was found to be a weaker enzyme inhibitor suggesting that water is not the preferrable extraction solvent to obtain active products. CONCLUSION: The present study demonstrated that the stem bark extracts of P. biglobosa contains good amount of phytochemical and extracts present significant antioxidant, as well as reasonable enzyme inhibitory effects. Hence, these findings suggest that further studies can be performed on more specific biological targets and models of bioactivity to determine their safe usage as a nutraceutical or for the preparation functional foods. © 2023 The Authors. Journal of The Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.
Atıf Yapan Makale Bilgileri
Kurumlar (6)
Duy Tan University Da Nang, Viet Nam
İstanbul Arel Üniversitesi Istanbul, Turkey
Selçuk Üniversitesi Selçuklu, Turkey
Università degli Studi di Padova Padua, Italy
Université Félix Houphouët-Boigny Abidjan, Cote d'Ivoire
University of Mauritius Reduit, Mauritius