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In vitro enzyme inhibitory properties, antioxidant activities, and phytochemical profile of Potentilla thuringiaca
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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From Metabolites to Mechanisms: Scorzonera parviflora Aerial Parts and Roots Extracts Profiled by UPLC-ESI-MS/MS, In Vitro/In Silico Tests, and Network Analysis
Scopus
Havuzumuzda Open Access
In the present study, the extraction of Scorzonera parviflora aerial parts and roots was performed using four solvents, namely ethyl acetate (EA), ethanol, ethanol/water, and water. The total phenolic and flavonoid contents were evaluated by Folin–Ciocalteu and AlCl₃ assays, while the chemical profile of extracts was determined by ultra performance liquid chromatography tandem mass spectrometry (UPLC–MS/MS). Antioxidant activities were assessed by radical scavenging, reducing power and metal chelating assays, whereas enzyme inhibition activity was tested against cholinesterases (acetylcholinesterase (AChE), butyrylcholinesterase (BChE)), tyrosinase, and carbohydrate-digesting enzymes (α-amylase and α-glucosidase). Additionally, molecular docking and network pharmacology analyses were conducted to elucidate the potential targets and mechanisms underlying the observed bioactivities. The enzyme inhibition, cytotoxicity and network pharmacology components were combined within a single study to link the chemical profile of the extracts to their multi-target biological effects and to identify the molecular targets underlying the observed activities. The results showed that the highest total phenolic content was found in the aerial part water extract (33.28 mg gallic acid equivalent (GAE)/g), followed by the ethanol/water extract (29.63 mg GAE/g), while the EA extract contained the highest amount of flavonoids (22.88 mg rutin equivalent (RE)/g). The phytochemical profile consisted of several classes, with flavonoids being the most abundant, followed by phenolic acids, glycosides and fatty acids. Aerial part extracts exhibited higher antioxidant activity than root extracts in most assays. Among all extracts, the aerial part water extract had the highest 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) (89.44 mg trolox equivalent (TE)/g) and metal chelating activity (MCA) (19.31 mg ethylenediaminetetraacetate equivalent (EDTAE)/g), while the ethanol/water extract demonstrated the strongest overall antioxidant capacity. The highest inhibition of AChE and BChE was observed for the roots ethanol extracts, measuring 3.04 mg and 3.66 mg galantamine equivalent (GALAE)/g, respectively. The ethanol/water extracts displayed the strongest tyrosinase inhibition, recorded with 59.57 mg kojic acid equivalent (KAE)/g. In conclusion, S. parviflora extracts exhibit notable antioxidant and enzyme inhibitory activities, highlighting their remarkable therapeutic potential, making them promising candidates for applications in the pharmaceutical, nutraceutical and natural product industries.
Atıf Yapan Makale Bilgileri
Kurumlar (9)
Ain Shams University
Cairo, Egypt
Central Hospital of Shanghai Jiading District
Shanghai, China
Faculty of Pharmacy, Ain Shams University
Cairo, Egypt
Renji Hospital
Shanghai, China
School of Pharmacy
Badr, Egypt
Selçuk Üniversitesi
Selçuklu, Turkey
Universidade do Algarve
Faro, Portugal
University of G. d'Annunzio Chieti and Pescara
Chieti, Italy
University of Novi Sad
Novi Sad, Serbia