Uncovering chemical profiles, biological potentials, and protection effect against ECM destruction in H2O2-treated HDF cells of the extracts of Stachys tundjeliensis

MakaleYalnız künyeScopus SJRQ2
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

The genus Stachys L., one of the largest genera of the Lamiaceae family, is highly represented in Turkey. This study was conducted to determine the bio-pharmaceutical potential and phenolic contents of six different extracts from aerial parts of Stachys tundjeliensis. The obtained results showed that the ethanol extract exhibited the highest antioxidant activity in the antioxidant assays. Meanwhile, the ethanol extract displayed strong inhibitory activity against α-tyrosinase, the dichloromethane extract exhibited potent inhibition against butyrylcholinesterase, and the n-hexane extract against α-amylase. Based on ultra-high performance liquid chromatography coupled to high-resolution mass spectrometry analysis, more than 90 secondary metabolites, including hydroxybenzoic acid, hydroxycinnamic acid, and their glycosides, acylquinic acids, phenylethanoid glycosides, and various flavonoids were identified or tentatively annotated in the studied S. tundjeliensis extracts. It was observed that the application of S. tundjeliensis eliminated H2O2-induced oxidative stress. It was determined that protein levels of phospho-nuclear factor kappa B (NF-κB), receptor for advanced glycation endproducts, and activator protein-1, which are activated in the nucleus, decreased, and the synthesis of matrix metalloproteinase (MMP)-2 and MMP-9 also decreased to basal levels. Overall, these findings suggest that S. tundjeliensis contains diverse bioactive compounds for the development of nutraceuticals or functional foods with potent biological properties.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/munzur/2101Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/ardp.202300528Yayıncı resmi DOI adresi
İndeks kayıtları
Kaydın indeks veri tabanlarındaki sayfası (aktarımda alınan kayıt numarasıyla). Erişim, indeksin kendi koşullarına bağlıdır.
Atıflar
Scopus
12
OpenAlex
12
Her kaynağın kendi saydığı toplam atıf; aktarım ve zenginleştirme sırasında alındı.
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKurt-Celep, Inci
dc.contributor.authorZheleva-Dimitrova, Dimitrina
dc.contributor.authorSinan, Kouadio Ibrahime
dc.contributor.authorUba, Abdullahi Ibrahim
dc.contributor.authorNilofar
dc.contributor.authorMahomoodally, Mohamad Fawzi
dc.contributor.authorAumeeruddy, Muhammad Zakariyyah
dc.contributor.authorCakilcioglu, Ugur
dc.contributor.authorDall'Acqua, Stefano
dc.contributor.authorZengin, Gokhan
dc.date.accessioned2026-10-28T14:54:56.226734966Z
dc.date.available2026-10-28T14:54:56.226734966Z
dc.date.issued2024
dc.description.abstractThe genus Stachys L., one of the largest genera of the Lamiaceae family, is highly represented in Turkey. This study was conducted to determine the bio-pharmaceutical potential and phenolic contents of six different extracts from aerial parts of Stachys tundjeliensis. The obtained results showed that the ethanol extract exhibited the highest antioxidant activity in the antioxidant assays. Meanwhile, the ethanol extract displayed strong inhibitory activity against α-tyrosinase, the dichloromethane extract exhibited potent inhibition against butyrylcholinesterase, and the n-hexane extract against α-amylase. Based on ultra-high performance liquid chromatography coupled to high-resolution mass spectrometry analysis, more than 90 secondary metabolites, including hydroxybenzoic acid, hydroxycinnamic acid, and their glycosides, acylquinic acids, phenylethanoid glycosides, and various flavonoids were identified or tentatively annotated in the studied S. tundjeliensis extracts. It was observed that the application of S. tundjeliensis eliminated H2O2-induced oxidative stress. It was determined that protein levels of phospho-nuclear factor kappa B (NF-κB), receptor for advanced glycation endproducts, and activator protein-1, which are activated in the nucleus, decreased, and the synthesis of matrix metalloproteinase (MMP)-2 and MMP-9 also decreased to basal levels. Overall, these findings suggest that S. tundjeliensis contains diverse bioactive compounds for the development of nutraceuticals or functional foods with potent biological properties.
dc.description.sponsorshipEuropean Union-NextGenerationEU
dc.description.sponsorshipEuropean Union‐NextGenerationEU
dc.description.sponsorshipNational Recovery and Resilience Plan of the Republic of Bulgaria, (BG‐RRP‐2.004‐0004‐C01)
dc.identifier.articlenumber2300528
dc.identifier.doi10.1002/ardp.202300528
dc.identifier.eissn1521-4184
dc.identifier.issn0365-6233
dc.identifier.issue2
dc.identifier.pmid37974540
dc.identifier.scopus2-s2.0-85176951451
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2101
dc.identifier.volume357
dc.identifier.wosWOS:001107056100001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofArchiv der Pharmazie
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectantioxidant
dc.subjectenzyme inhibition
dc.subjectphenolics
dc.subjectphospho-NF-κB
dc.subjectStachys
dc.subject.otherAntioxidants
dc.subject.otherButyrylcholinesterase
dc.subject.otherEthanol
dc.subject.otherGlycosides
dc.subject.otherPlant Extracts
dc.subject.otherReceptor for Advanced Glycation End Products
dc.subject.otherStachys
dc.subject.otherStructure-Activity Relationship
dc.subject.other3 feruloylquinic acid
dc.subject.other4',7 dihydroxy 5,6 dimethoxyflavone
dc.subject.other5,6,7 trimethoxy 3,3',4' trihydroxyflavone
dc.subject.otheracetylnaringenin
dc.subject.otheracteoside
dc.subject.otheradvanced glycation end product receptor
dc.subject.otheramylase
dc.subject.otherantioxidant
dc.subject.otherapigenin
dc.subject.otherapigenin derivative
dc.subject.otherbetonyoside d
dc.subject.othercaffeic acid
dc.subject.otherchlorogenic acid
dc.subject.othercholinesterase
dc.subject.otherchrysin
dc.subject.othercirsiliol
dc.subject.othercirsimaritin
dc.subject.othercoumaric acid
dc.subject.otherdarendoside B
dc.subject.otherdichloromethane
dc.subject.otheresculetin
dc.subject.othereupatilin
dc.subject.otherflavonoid
dc.subject.othergelatinase A
dc.subject.othergelatinase B
dc.subject.othergentisic acid
dc.subject.otherglycoside
dc.subject.otherhydrogen peroxide
dc.subject.otherhydroxybenzoic acid
dc.subject.otherhypolaetin
dc.subject.otherimmunoglobulin enhancer binding protein
dc.subject.otherisoquercetin
dc.subject.otherisoscutellarein
dc.subject.otherisoverbascoside
dc.subject.otherkaempferol
dc.subject.otherleucosceptoside A
dc.subject.otherluteolin
dc.subject.otherluteolin 7 glucoside
dc.subject.othermartynoside
dc.subject.othermatrix metalloproteinase
dc.subject.othermethylisoscutellarein 7 o hexoside
dc.subject.othermonophenol monooxygenase
dc.subject.othernaringenin
dc.subject.othernutraceutical
dc.subject.otherpara coumaric acid
dc.subject.otherphytochemical
dc.subject.otherplant extract
dc.subject.otherprotocatechuic acid
dc.subject.otherquinic acid
dc.subject.otherrhamnazin
dc.subject.otherrosmarinic acid
dc.subject.othershikimic acid
dc.subject.othersitogluside
dc.subject.otherStachys tundjeliensis extract
dc.subject.othersyringic acid
dc.subject.othertranscription factor AP 1
dc.subject.otherunclassified drug
dc.subject.othervitexin
dc.subject.otheralcohol
dc.subject.otheraerial plant part
dc.subject.otherantioxidant activity
dc.subject.otherArticle
dc.subject.otherbiological activity
dc.subject.othercell proliferation
dc.subject.otherchemical fingerprinting
dc.subject.othercontrolled study
dc.subject.othercytotoxicity
dc.subject.otherdrug isolation
dc.subject.otherenzyme inhibition
dc.subject.otherextracellular matrix
dc.subject.otherfunctional food
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.othermass spectrometry
dc.subject.othermolecular docking
dc.subject.othernonhuman
dc.subject.otheroxidative stress
dc.subject.otherplant cell
dc.subject.otherprotein expression
dc.subject.otherprotein synthesis
dc.subject.otherskin fibroblast
dc.subject.otherStachys tundjeliensis
dc.subject.otherultra performance liquid chromatography
dc.subject.otherchemistry
dc.subject.otherstructure activity relation
dc.titleUncovering chemical profiles, biological potentials, and protection effect against ECM destruction in H2O2-treated HDF cells of the extracts of Stachys tundjeliensis
dc.typeArticle
rdl.citation.openalex12
rdl.citation.scopus12
rdl.departmentDepartment of Pharmacognosy, Faculty of Pharmacy, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey
rdl.departmentDepartment of Pharmacognosy, Faculty of Pharmacy, Medical University of Sofia, Sofia, Bulgaria
rdl.departmentDepartment of Biology, Science Faculty, Selcuk University, Konya, Turkey
rdl.departmentDepartment of Molecular Biology and Genetics, Istanbul AREL University, Istanbul, Turkey
rdl.departmentDepartment of Pharmacy, Botanic Garden "Giardino dei Semplici", Università degli Studi "Gabriele d'Annunzio", Chieti, Italy
rdl.departmentInstitute of Research and Development, Duy Tan University, Da Nang, Vietnam
rdl.departmentSchool of Engineering & Technology, Duy Tan University, Da Nang, Vietnam
rdl.departmentDepartment of Health Sciences, Faculty of Medicine and Health Sciences, University of Mauritius, Réduit, Mauritius
rdl.departmentPertek Sakine Genç Vocational School, Munzur University, Pertek, Tunceli, Turkey
rdl.departmentDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy
rdl.oa.statusclosed
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED