Kurumun Atıf Alan Makalesi
Atıf Alan Yayın
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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Atıf Yapan Yayın
Decoding chemical profiles and biological activities of aerial parts and roots of Eryngium thorifolium Boiss by HPLC-MS/MS, GC-MS and in vitro chemical assays
Scopus
Havuzumuzda 34 atıf almış
Eryngium species are widely distributed and primarily utilised for medicinal and culinary purposes. This study aimed to evaluate the chemical composition, antioxidant, enzyme inhibition, and cytotoxic properties of various extracts from the aerial parts and roots of E. thorifolium Boiss. The chemical composition of ethyl acetate, methanol, and water extracts was analysed using High-Performance Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (HPLC-ESI-MS/MS), while the hexane ones were examined using Gas Chromatography-Mass Spectrometry (GC-MS) analysis. The most predominant class of secondary metabolites identified were fatty acid amides and flavonoids as hexose conjugates. Extracts from the aerial parts exhibited the highest antioxidant activity, with the methanol and water extracts showing the best anti- 2,2-diphenyl-1-picrylhydrazyl (DPPH) (21.9 mg trolox equivalent (TE)/g) and anti- 2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) (89.26 mg TE/g) activities. Enzyme inhibition tests revealed that the hexane extract from the roots had the highest anti-acetylcholinesterase activity (2.49 mg galantamine equivalent (GALAE)/g). Additionally, both the hexane and ethyl acetate extracts from the aerial parts demonstrated the highest anti-butyrylcholinesterase activity (3.13 and 3.71 mg GALAE/g, p ≥ 0.05). At a concentration of 100 μg/mL, all extracts from the roots and aerial parts, except the water one, displayed potent cytotoxicity against the human embryonic (HEK 293) and murine macrophages (RAW 264.7) cell lines, with cellular viability ranging from 1.66 to 2.62% compared to the control (0.5% DMSO) (89.2 and 95.1%, respectively). Through network pharmacology and molecular docking, the phytochemicals of E. thorifolium show significant potential as natural compounds targeting key proteins involved in cancer progression, including Bcl-2, c-KIT, PI3K, and AKT. Their binding affinities and predicted interactions highlight their possible therapeutic applications in managing various cancers. These findings suggested E. thorifolium is a promising source of phytochemicals targeting specific oxidative stress-linked diseases, including cancer, diabetes and neurodegenerative disorders.
Atıf Yapan Makale Bilgileri
Kurumlar (10)
Ain Shams University
Cairo, Egypt
Balikesir Üniversitesi
Balikesir, Turkey
Faculty of Pharmacy, Ain Shams University
Cairo, Egypt
Khartoum University
Khartoum, Sudan
Ponnaiya's Code and Genome Pvt Ltd
Madurai, India
School of Pharmacy
Badr, Egypt
Selçuk Üniversitesi
Selçuklu, Turkey
Universidade do Algarve
Faro, Portugal
Università degli Studi di Padova
Padua, Italy
Université de Lorraine
Nancy, France