Establishing a link between the chemical composition and biological activities of Gladiolus italicus Mill. from the Turkish flora utilizing in vitro, in silico and network pharmacological methodologies

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Özet

Objectives: Five solvent extracts (n-hexane, ethyl acetate, ethanol, ethanol/water (70%), and water) of Gladiolus italicus Mill. from Turkey were evaluated for chemical and biological properties. Methods: Antioxidant activities, inhibitory properties against key enzymes involved in the etiology of chronic diseases were tested, as well as cytotoxic effects on different cell lines. Chemical characterization was also carried out to determine the most abundant compounds of each extract. Results: The highest total phenolic content (TPC) was observed in the water extract while highest TFC in ethanol/water extract. The most abundant compounds in the extracts were hyperoside (69041.06 mg kg−1), isoquercitrin (46239.49 mg kg−1), delphindin-3,5-diglucoside (42043.81 mg kg−1), myricetin (21486.61 mg kg−1), and kaempferol-3-glucoside (21199.76 mg kg−1). Molecular dynamic (MD) simulations confirmed the structural stability and dynamic conformational integrity of these complexes over a period of 100 ns. In network pharmacology, A total of 657 unique target genes were screened: 52 associated with programmed cell death-1 (PD-1), 85 with vascular endothelial growth factor receptor-2 (VEGFR2), and 130 with fibroblast growth factor receptor-2 (FGFR2), identifying crucial gene interactions for these proteins. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted, revealing significant interactions and pathways such as the advanced glycation end products (AGE) and their receptors (RAGE) signaling pathway in diabetic complications and T- helper 17 (Th17) cell differentiation, among others. This elucidation of complex networks involving key genes like AKT Serine/Threonine Kinase 1 (AKT1), MYC proto-oncogene (MYC), tumor protein 53 (TP53), Interleukin 6 (IL6), and tumor necrosis factor (TNF) provides a promising foundation for the development of targeted therapies in the treatment of non-communicable diseases. Conclusion: These results show that G. italicus could be a natural source of potent antioxidants and enzyme inhibitors which need to be further explored for the development of biopharmaceuticals.

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dc.contributor.authorZengin, Gokhan
dc.contributor.authorCetiz, Mehmet Veysi
dc.contributor.authorAbul, Nurgul
dc.contributor.authorGulcin, Ilhami
dc.contributor.authorCaprioli, Giovanni
dc.contributor.authorPiatti, Diletta
dc.contributor.authorRicciutelli, Massimo
dc.contributor.authorKoyuncu, Ismail
dc.contributor.authorYuksekdag, Ozgur
dc.contributor.authorBahşi, Muammer
dc.contributor.authorGüler, Osman
dc.contributor.authorAumeeruddy, Muhammad Zakariyyah
dc.contributor.authorMahomoodally, Mohamad Fawzi
dc.date.accessioned2026-10-28T14:55:02.803136003Z
dc.date.available2026-10-28T14:55:02.803136003Z
dc.date.issued2025
dc.description.abstractObjectives: Five solvent extracts (n-hexane, ethyl acetate, ethanol, ethanol/water (70%), and water) of Gladiolus italicus Mill. from Turkey were evaluated for chemical and biological properties. Methods: Antioxidant activities, inhibitory properties against key enzymes involved in the etiology of chronic diseases were tested, as well as cytotoxic effects on different cell lines. Chemical characterization was also carried out to determine the most abundant compounds of each extract. Results: The highest total phenolic content (TPC) was observed in the water extract while highest TFC in ethanol/water extract. The most abundant compounds in the extracts were hyperoside (69041.06 mg kg−1), isoquercitrin (46239.49 mg kg−1), delphindin-3,5-diglucoside (42043.81 mg kg−1), myricetin (21486.61 mg kg−1), and kaempferol-3-glucoside (21199.76 mg kg−1). Molecular dynamic (MD) simulations confirmed the structural stability and dynamic conformational integrity of these complexes over a period of 100 ns. In network pharmacology, A total of 657 unique target genes were screened: 52 associated with programmed cell death-1 (PD-1), 85 with vascular endothelial growth factor receptor-2 (VEGFR2), and 130 with fibroblast growth factor receptor-2 (FGFR2), identifying crucial gene interactions for these proteins. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted, revealing significant interactions and pathways such as the advanced glycation end products (AGE) and their receptors (RAGE) signaling pathway in diabetic complications and T- helper 17 (Th17) cell differentiation, among others. This elucidation of complex networks involving key genes like AKT Serine/Threonine Kinase 1 (AKT1), MYC proto-oncogene (MYC), tumor protein 53 (TP53), Interleukin 6 (IL6), and tumor necrosis factor (TNF) provides a promising foundation for the development of targeted therapies in the treatment of non-communicable diseases. Conclusion: These results show that G. italicus could be a natural source of potent antioxidants and enzyme inhibitors which need to be further explored for the development of biopharmaceuticals.
dc.identifier.doi10.1080/15376516.2024.2397387
dc.identifier.eissn1537-6524
dc.identifier.endpage166
dc.identifier.issn1537-6516
dc.identifier.issue2
dc.identifier.pmid39246014
dc.identifier.scopus2-s2.0-85203374150
dc.identifier.startpage146
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2181
dc.identifier.volume35
dc.identifier.wosWOS:001309214900001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofToxicology Mechanisms and Methods
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantioxidant
dc.subjectenzyme inhibitors
dc.subjectGladiolus italicus
dc.subjecthyperoside
dc.subjectmolecular dynamics
dc.subjectnetwork pharmacology
dc.subject.otherAnimals
dc.subject.otherAntioxidants
dc.subject.otherCell Survival
dc.subject.otherComputer Simulation
dc.subject.otherHumans
dc.subject.otherMolecular Docking Simulation
dc.subject.otherNetwork Pharmacology
dc.subject.otherPlant Extracts
dc.subject.otherTurkey
dc.subject.other1,1 diphenyl 2 picrylhydrazyl
dc.subject.other2,2' azinobis(3 ethylbenzothiazoline 6 sulfonic acid)
dc.subject.other3 hydroxybenzoic acid
dc.subject.other3,5 dicaffeoylquinic acid
dc.subject.other4 hydroxybenzoic acid
dc.subject.otheracetic acid ethyl ester
dc.subject.otheradvanced glycation end product
dc.subject.otherastragalin
dc.subject.otheraurantiin
dc.subject.otherchlorogenic acid
dc.subject.othercinnamic acid
dc.subject.othercoumaric acid
dc.subject.otherdelphinidin
dc.subject.otherellagic acid
dc.subject.otherferulic acid
dc.subject.otherfibroblast growth factor receptor 2
dc.subject.otherGladiolus italicus extract
dc.subject.otherhyperin
dc.subject.otherinterleukin 6
dc.subject.otherisoquercetin
dc.subject.otherisorhamnetin
dc.subject.otherkaempferol
dc.subject.otherligand
dc.subject.othermyricetin
dc.subject.otherphloretin
dc.subject.otherphytochemical
dc.subject.otherplant extract
dc.subject.otherprogrammed death 1 receptor
dc.subject.otherprotein serine threonine kinase
dc.subject.otherprotein tyrosine kinase inhibitor
dc.subject.otherquercetin
dc.subject.otherrutoside
dc.subject.othertumor necrosis factor
dc.subject.otherunclassified drug
dc.subject.othervasculotropin receptor 2
dc.subject.otherantioxidant
dc.subject.otherantioxidant activity
dc.subject.otherantioxidant assay
dc.subject.otherapoptosis
dc.subject.otherArticle
dc.subject.otherbiological activity
dc.subject.otherblood brain barrier
dc.subject.othercancer cell line
dc.subject.othercell differentiation
dc.subject.othercell viability assay
dc.subject.otherchemical composition
dc.subject.othercolorectal cancer
dc.subject.othercomputer model
dc.subject.otherconformational transition
dc.subject.othercontrolled study
dc.subject.othercytotoxicity
dc.subject.otherdrug absorption
dc.subject.otherdrug distribution
dc.subject.otherdrug excretion
dc.subject.otherdrug metabolism
dc.subject.otherdrug targeting
dc.subject.otherenergy
dc.subject.otherenzyme activity
dc.subject.otherenzyme inhibition
dc.subject.otherextraction
dc.subject.otherflora
dc.subject.othergene interaction
dc.subject.othergene ontology
dc.subject.otherGladiolus
dc.subject.otherhigh performance liquid chromatography
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherin vitro study
dc.subject.otherintestine absorption
dc.subject.otherKEGG
dc.subject.otherKG-1 cell line
dc.subject.otherliver toxicity
dc.subject.othermass spectrometry
dc.subject.othermelanoma
dc.subject.othermethodology
dc.subject.othermolecular docking
dc.subject.othermolecular dynamics
dc.subject.otherMTT assay
dc.subject.othernonhuman
dc.subject.otherpathway enrichment analysis
dc.subject.otherpharmacokinetic parameters
dc.subject.otherPi3K/Akt signaling
dc.subject.otherprediction
dc.subject.otherprostate cancer
dc.subject.otherproto oncogene
dc.subject.otherrisk
dc.subject.othersignal transduction
dc.subject.othersystems pharmacology
dc.subject.othertemperature
dc.subject.otherTh17 cell
dc.subject.otherTurkey (republic)
dc.titleEstablishing a link between the chemical composition and biological activities of Gladiolus italicus Mill. from the Turkish flora utilizing in vitro, in silico and network pharmacological methodologies
dc.typeArticle
rdl.citation.openalex13
rdl.citation.scopus15
rdl.departmentDepartment of Biology, Faculty of Science, Selcuk University, Konya, Turkey
rdl.departmentDepartment of Bioinformatics, Biozentrum der Universität Würzburg, Würzburg, Germany
rdl.departmentDepartment of Chemistry, Faculty of Sciences, Ataturk University, Erzurum
rdl.departmentCHemistry Interdisciplinary Project (CHip), School of Pharmacy, University of Camerino, Camerino, Italy
rdl.departmentDepartment of Medical Biochemistry, Faculty of Medicine, Harran University, Sanliurfa, Turkey
rdl.departmentFaculty of Education, Department of Primary Education, Firat University, Elazig, Turkey
rdl.departmentPertek Sakine Genç Vocational School, Munzur University, Pertek, Tunceli, Turkey
rdl.departmentDepartment of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit, Mauritius
rdl.departmentInstitute of Research and Development, Duy Tan University, Da Nang, Vietnam
rdl.departmentSchool of Engineering & Technology, Duy Tan University, Da Nang, Vietnam
rdl.oa.statusgreen
rdl.oa.statusclosed
rdl.oa.urlhttps://figshare.com/articles/journal_contribution/Establishing_a_link_between_the_chemical_composition_and_biological_activities_of_i_Gladiolus_italicus_i_Mill_from_the_Turkish_flora_utilizing_i_in_vitro_i_i_in_silico_i_and_network_pharmacological_methodologies/26968286
rdl.scopus.quartileQ3
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED