Person: ŞENKARDEŞ, İSMAİL
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ŞENKARDEŞ
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İSMAİL
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Publication Metadata only Chemical characterization and pharmacological profile of tribulus terrestris extracts: A novel source of cosmeceuticals and pharmaceuticals(2023-04-01) ŞENKARDEŞ, İSMAİL; UYSAL Ş., ŞENKARDEŞ İ., Jekő J., Cziáky Z., Zengin G.© 2023 Elsevier LtdTribulus terrestris is widely used in traditional medicine and in dietary supplements. Therefore, this research aims to obtain comprehensive information on antioxidant properties, enzyme inhibitory activity and chemical composition of T. terrestris leaves. HPLC-MS/MS was used to further extensively characterize the chemical composition of T. terrestris extracts. 27, 75, and 51 chemical components were identifed in ethyl acetate, methanol and water extract, respectively. The radical scavenging activity results showed that water extract had the strongest acvitiy (DPPH: 30.50 mgTE/g, ABTS: 44.49 mgTE/g). The reducing power activity was assessed by FRAP and CUPRAC assays. The highest CUPRAC activity is shown by the ethyl acetate extract (79.01 mgTE/g). Water extract showed the highest metal chelating activity compared with other extract. In general, the highest antioxidant capacity were obtained in the water extract. Ethyl acetate extract exhibited the highest enzyme inhibition activity (AChE: 1.56 mgGAE/g; BChE: 2.14 mgGALAE/g; α-amylase: 0.73 mmolACE/g; Tyrosinase: 30.14 mgKAE/g) compared with other extracts. This research provides a scientific basis for the development of natural antioxidant and enzyme inhibiton sources from T. terrestris.Publication Metadata only Chemical composition and bio-functional perspectives of Erica arborea L. extracts obtained by different extraction techniques: Innovative insights(ELSEVIER, 2019) DOĞAN, AHMET; Zengin, Gokhan; Cvetanovic, Aleksandra; Gasic, Uros; Stupar, Alena; Bulut, Gizem; Senkardes, Ismail; Dogan, Ahmet; Seebaluck-Sandoram, Roumita; Rengasamy, Kannan R. R.; Sinan, Kouadio Ibrahime; Mahomoodally, Mohamad FawziErica arborea L., also known as Estrella Gold, is traditionally used for several purposes. In this research, five different extraction techniques: accelerated solvent extraction (ASE), microwave-assisted extraction (MAE), maceration (MAC), soxhlet (SOE) and ultrasound-assisted extraction (UAE) were used to compare the total phenolic, flavonoids, total antioxidant activity and enzymatic activities of E. arborea extracts obtained different extraction techniques. The total phenolic and flavonoid contents were in the order of ASE > MAE > SOE > MAC > UAE. All extracts showed antioxidant, anticholinesterase, anti-tyrosinase and anti-diabetic activities. A highly sensitive method using ultra-high-pressure liquid chromatography coupled with linear ion trap-Orbitrap tandem mass spectrometry (UHPLC-LTQ-Orbitrap-MS) has been used for the qualitative analysis of obtained extracts. Seventy-two polyphenolic compounds were identified in all extracts. However, 20 components were quantified among the extracts. ASE was found to be a better extraction technique as compared to the other extraction techniques. E. arborea can be exploited in the discovery of bioactive natural products for the treatment of Alzheimer's disease, diabetes and pigmentation problems.Publication Metadata only Utilisation of Rhododendron luteum Sweet bioactive compounds as valuable source of enzymes inhibitors, antioxidant, and anticancer agents(PERGAMON-ELSEVIER SCIENCE LTD, 2020) ŞENKARDEŞ, İSMAİL; Mahomoodally, Mohamad Fawzi; Sieniawska, Elwira; Sinan, Kouadio Ibrahime; Picot-Allain, Marie Carene Nancy; Yerlikaya, Serife; Baloglu, Mehmet Cengiz; Altunoglu, Yasemin Celik; Senkardes, Ismail; Rengasamy, Kannan R. R.; Zengin, GokhanEthnobotanical evidences report the use of Rhododendron luteum Sweet (Ericaceae) in traditional medicinal systems. However, R. luteum has been associated to the occurrence of 'mad honey' poisoning. In the present study, the ethyl acetate, methanol, and water extracts of R. luteum were investigated for their in vitro antioxidant, enzyme inhibition, and cytotoxic properties. The cytotoxicity of R. luteum extracts on A549 lung cancer cell line was evaluated using MTT cell viability assay. Besides, HPLC-ESI-MSn approach was employed to elucidate the secondary metabolite profiles of R. luteum in order to establish any structure-activity relationship. Methanol and water extracts of R. luteum possessed highest radical scavenging and reducing properties while the ethyl acetate extract showed highest metal chelating properties. In terms of enzyme inhibition, the methanol and ethyl acetate extracts of R. luteum, possessing epigallocatechin, were active inhibitors of cholinesterase enzymes, a-glucosidase, and tyrosinase. Water extract caused growth inhibition of A549 cells with 207.2 mu g/ml IC50 value. Though R. luteum has received little scientific attention due to the occurrence of grayanotoxins in the plant, however, data presented in this work shows promising biological activity of R. luteum and highlighted its role as a potential source of antioxidant and key enzyme inhibitors.Publication Metadata only Multidirectional biological investigation and phytochemical profile of Rubus sanctus and Rubus ibericus(PERGAMON-ELSEVIER SCIENCE LTD, 2019) ŞENKARDEŞ, İSMAİL; Zengin, Gokhan; Ferrante, Claudio; Senkardes, Ismail; Gevrenova, Reneta; Zheleva-Dimitrova, Dimitrina; Menghini, Luigi; Orlando, Giustino; Recinella, Lucia; Chiavaroli, Annalisa; Leone, Sheila; Brunetti, Luigi; Picot-Allain, Carene Marie Nancy; Rengasamy, Kannan R. R.; Mahomoodally, Mohamad FawziIn the present study, the biological properties, including, the enzyme inhibitory and antioxidant activities, as well as, the phytochemical profile of the ethyl acetate, methanol, and water extracts of Rubus sanctus Schreb. and Rubus ibericus Juz. leaves were determined using in vitro bioassays. Wide range of phytochemicals, including, hydroxybenzoic acids, hydroxycinnamic acids, acylquinic acids, ellagitannins, flavonoids, and triterpenoid saponins were determined using UHPLC-ESI/HRMS technique. The ethyl acetate and methanol extracts of the studied Rubus species effectively inhibited acetyl and butyryl cholinesterase. On the other hand, R. sanctus water extract showed low inhibition against alpha-amylase and prominent inhibitory action against alpha-glucosidase. Data collected from this study reported the radical scavenging and reducing potential of the studied Rubus species. Investigation of the protective effects of the different extracts of R. sanctus and R. ibericus in experimental model of ulcerative colitis was performed. The extracts were also tested on spontaneous migration of human colon cancer cells (HCT116) in wound healing experimental paradigm. Only R. sanctus methanol extract inhibited spontaneous HCT116 migration in the wound healing test. Our results suggested that R. sanctus and R. ibericus may be potential candidates as sources of biologically-active compounds for the development of nutraceuticals, pharmaceuticals, and/or cosmetics.Publication Metadata only Metabolomics-based profiling with chemometric approach to delineate the bio-pharmaceutical properties of fruit extracts from Ligustrum vulgare L(ELSEVIER, 2019) ŞENKARDEŞ, İSMAİL; Rocchetti, Gabriele; Senizza, Biancamaria; Zengin, Gokhan; Senkardes, Ismail; Sadeer, Nabeelah Bibi; Mahomoodally, Mohamad Fawzi; Lucini, LuigiLigustrum vulgare L. (Family: Oleaceae) is an evergreen shrub native to North-west Africa, Europe and Western Asia. In the present work, infusion (water), ethyl acetate, methanol and n-hexane extracts of the fruits of L. vulgare L. were studied for their in vitro antioxidant and enzyme inhibitory properties along with their untargeted polyphenolic profile (using an ultra-high-performance liquid chromatography-quadrupole time-of-flight (UHPLC-QTOF) mass spectrometry approach). Untargeted metabolomics coupled to multivariate statistics showed that Ligustrum fruit extracts were very abundant in polyphenols, such as flavonoids, tyrosols and lignans, with ethyl acetate allowing the highest recovery among the extraction solvents tested. The methanolic extract inhibited the highest acetylcholinesterase (AChE), tyrosinase and glucosidase activity (4.23 mg galatamine equivalent (GALAE)/g, 132.85 mg kojic acid equivalent (KAE)/g and 1.94 mmol acarbose equivalent (ACAE)/g respectively) while the ethyl acetate extract inhibited the highest butyrylcholinesterase (BChE) and amylase activity (4.92 mg GALAE/g and 0.73 mmol ACAE/g, respectively). However, the infusion showed the weakest activity against all the enzymes studied. However, the extract showed highest antioxidant property in'the antioxidant assays (except for phosphomolybdenum). The present paper is the first comprehensive report on L. vulgare fruits and thus our findings are of considerable interest to design new bioproducts for the pharmaceutical and cosmeceutical industry in the future.Publication Metadata only Investigation on biological activities of Melissa officinalis subsp. altissima(2022-05-25) RAYAMAN, ERKAN; YILMAZ, BEYZA NUR; ŞENKARDEŞ, İSMAİL; TAŞKIN, TURGUT; Koç G., RAYAMAN E., ÖZDATLI KURTULUŞ Ş., Ermanoğlu M., YILMAZ B. N., ŞENKARDEŞ İ., TAŞKIN T.Publication Metadata only Untargeted metabolomic profiling of three Crataegus species (hawthorn) and their in vitro biological activities(WILEY, 2020) ŞENKARDEŞ, İSMAİL; Rocchetti, Gabriele; Senizza, Biancamaria; Zengin, Gokhan; Mahomodally, Mohamad Fawzi; Senkardes, Ismail; Lobine, Devina; Lucini, LuigiBACKGROUND In this investigation, the chemical and biological profiles of three Turkish Crataegus species (Crataegus orientalis, Crataegus szovitsii and Crataegus tanacetifolia) were studied in order to provide the first comprehensive characterization and their health-promoting potential. In this respect, polyphenolic profiles were evaluated using ultrahigh-performance liquid chromatography-quadrupole time-of-flight mass spectrometry. The in vitro antioxidant activities of the Crataegus samples were evaluated by using free-radical scavenging, phosphomolybdenum, ferrous-ion chelating, and reducing power assays. The inhibitory activities against alpha-glucosidase, amylase, cholinesterases (acetylcholinesterase (AChE) and butyrylcholinesterase (BChE)), and tyrosinase were also established. RESULTS The untargeted metabolomic approach highlighted the effect of both extraction types and species on the phenolic profiles of different Crateagus tissues (i.e. leaves and twigs). The methanolic extracts showed the maximum radical scavenging and reducing activity in all test systems, whereas for ferrous-ion chelating assays the decocted and infused extracts showed the highest activity. Only the methanolic extracts were effective against AChE and BChE. The extract tested showed remarkable inhibitory effects against tyrosinase and alpha-glucosidase, whereas all the extracts exhibited modest inhibition against alpha-amylase. Overall, the twig extracts of the three species studied showed superior antioxidant and enzyme inhibitory activities. CONCLUSION On the basis of these results, the three Crataegus species can be classified as potent bioresources for high-value phytochemicals, which warrant further investigations for developing novel nutraceuticals. (c) 2019 Society of Chemical IndustryPublication Metadata only Chemical profiles and biological potential of tuber extracts from Cyclamen coum Mill(ELSEVIER, 2021) ŞENKARDEŞ, İSMAİL; Mahomoodally, Mohamad Fawzi; Picot-Allain, Marie Carene Nancy; Zengin, Gokhan; Llorent-Martinez, Eulogio J.; Stefanucci, Azzurra; Gunes, Ak; Senkardes, Ismail; Tomczyk, Michal; Mollica, AdrianoCyclamen coum Mill. used in traditional medicine has been reported to exhibit interesting biological activities. In this study, the ability of the C. coum tuber extracts to inhibit clinical enzymes, namely, cholinesterases, ty-rosinase, alpha-amylase, and alpha-glucosidase, as well as the antioxidant properties were assessed. High -performance liquid chromatography/electrospray ionization quadrupole-time -of-flight mass spectrometer (HPLC- ESI-Q -TOF-MS) was employed to obtain detailed phytochemical proiles and in silico studies were performed against the key clinical enzymes. HPLC- ESI-Q -TOF -MS results conirmed the presence of saponins cyclacoumin and cy-claminorin, which were previously identiied from C. coum tuber extracts. In addition, other phenolic com-pounds, namely, phloretin C -dihexoside, quercetin 3 -galactoside, and catechin, were also identiied from C. coum tuber extracts. The methanol extract showed interesting inhibition against tyrosinase (6 5. 87 mg kojic acid equivalent/g extract) and alpha-glucosidase (3 4. 41 mg acarbose equivalent / g extract). Low inhibition was observed against cholinesterases and alpha-amylase. The methanol also showed active antioxidant properties (expressed as Trolox equivalent [TE]), namely, radical scavenging and reducing potential (1 5. 17 and 21 .8 6 mg TE / g extract, for 2, 2 '- azino- bis(3-ethylbenzthiazoline -6 -sulfonic acid) and cupric reducing antioxidant capacity assays, re-spectively). In order to highlight the possible bioactive compounds responsible of the biological effect, phloretin C -diglucoside, catechin and quercetin 3 -galactoside were docked via in silico molecular modelling ap-proaches. For tyrosinase, quercetin 3 -galactoside showed better docking and free binding energy which was found to bind very strongly to the enzymatic cavity of tyrosinase (via hydrogen bonds to Glu322, His85, His263, Gly281 and pi-pi stacks to His263 and His259). Findings from this study tend to advocate for further in-vestigations focusing on the isolation of bioactive compounds from the methanol extract of C. coum tuber ex-tracts and assessment of their cytotoxicity and their bioactivity.Publication Metadata only Antioxidant abilities, key enzyme inhibitory potential and phytochemical profile of Tanacetum poteriifolium Grierson(ELSEVIER, 2019) ŞENKARDEŞ, İSMAİL; Zengin, Gokhan; Sieniawska, Elwira; Senkardes, Ismail; Picot-Allain, Marie Carene Nancy; Sinan, Kouadio Ibrahime; Mahomoodally, Mohamad FawziThe members of the genus Tanacetum have a long history in traditional medicine to manage several diseases. Thus, the present study attempts to determine the chemical composition and to probe into the biological activities of Tanacetum poteriifolium Grierson, a poorly studied medicinal plant. The enzyme inhibitory and antioxidant properties of the ethyl acetate, methanol, and water extracts were assessed using standard in vitro assays. Biological data were further investigated by multivariate analysis tools. The water extract showed the highest concentration of phenolics (83.38 mg gallic acid equivalent (GAE)/g extract), and was a potent radical scavenger (238.12 and 282.54 mg Trolox equivalent (TE)/g extract, towards 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid (ABTS), respectively) and had potent reducing power (555.03 and 285.79 mg TE/g extract, towards cupric reducing antioxidant capacity (CUPRAC) and ferric reducing antioxidant power (FRAP), respectively). The ethyl acetate extract (41.07 mg ethylenediaminetetraacetic acid equivalent (EDTAE)/g extract), rich in flavonoids (43.55 mg rutin equivalent (RE)/g extract), was a potent metal chelator. Besides, the ethyl acetate extract exhibited strong inhibitory action on cholinesterases (3.47 and 3.46 mg galantamine equivalent (GALAE)/g extract) and alpha-glucosidase (23.67 mmol acarbose equivalent (ACAE)/g extract). Tyrosinase was actively inhibited in the presence of the methanol extract of T. poteriifolium (128.54 mg kojic acid equivalent (KAE)/g extract). Liquid chromatography-electrospray ionisation quadrupole time-of-flight mass spectrometry analysis revealed the presence of quinic acid and methylquercetin derivatives in T. poteriifolium ethyl acetate extract. Two unknown compounds having m/z values 289.17, 267.23, 235.13, 211.14, 185.12, 121.06 and 275.21, 211.15, 171.11, 121.11 were identified from the T. poteriifolium methanol extract. Principal component analysis was performed to obtain an overview of the influence of solvents on T. poteriifolium biological activities which were satisfactorily discriminated. This study provides valuable baseline data on the biological activity of T. poteriifolium towards important enzymes targeted in the management of global health problems, such as Alzheimer's disease, diabetes, and epidermal hyperpigmentation problems.Publication Metadata only Anti-quorum sensing and anti-biofilm activities of Hypericum perforatum extracts against Pseudomonas aeruginosa(ELSEVIER IRELAND LTD, 2019) DOĞAN, AHMET; Dogan, Sule; Gokalsin, Baris; Senkardes, Ismail; Dogan, Ahmet; Sesal, N. CenkEthnopharmacological relevance: Hypericum perforatum L. (Hypericaceae) has been used as a traditional therapeutic for skin wounds, burns, cuts and stomach ailments including stomach ache, ulcers for a long time in many societies. Although many studies about its antibacterial properties can be found, there is a lack of studies about its quorum sensing inhibition properties, which effects bacterial vulnerability directly, on Pseudomonas aeruginosa. Aim of the study: Evaluation of anti-quorum sensing (anti-QS) and anti-biofilm activity of ethanol, methanol, acetone and ultra-sonicated extracts of Hypericum perforatum L. (HP) which is a well-known wound healer, against P. aeruginosa. Materials and methods: Aerial parts of HP were extracted with ethanol, methanol and acetone. In addition, separate extractions with ultrasonication were carried out with same solvents. Anti-QS activity tests with different doses of HP extracts were performed by employing biomonitor strains, of which the promoter of QS regulating and green fluorescent protein (GFP) genes were fusioned. For anti-biofilm activity, HP extracts were applied to wild type PAO1 strains and biofilm inhibition was quantified via crystal violet staining method. Results: HP's ethanol, methanol and acetone extracts (250 mu g/ml doses) inhibited LasIR signalling pathway up to 65.43%, 59.60%, 55.95% and same solvent extracts obtained with ultrasonication inhibited 71.33%, 64.47%, 57.35% respectively. Moreover, inhibition rates of Rh1IR pathway were 28.80%, 50.83%, 45.84% for ethanol, methanol, acetone extracts (250 mu g/ml doses) and 51.43%, 57.41%, 50.02% for ultrasonication extracts (250 mu g/ml doses), compared to untreated controls. In the experiments, ethanol, methanol, acetone and ultra-sonicated extracts of HP did not inhibit biofilm formation. Conclusions: This study shows that HP plant is capable for blocking of las and rhl QS systems of P. aeruginosa. However, it was observed that ethanol, methanol and acetone extract of the plant samples did not show anti-biofilm activity against P. aeruginosa. This led us to thinking that biofilm formation was caused via another pathway such as IQS or PQS. Further studies with isolated active compounds of HP might give a better understanding of the effects on biofilm formation of P. aeruginosa.
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