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dc.contributor.authorAgoren, Busra Karpuz
dc.contributor.authorErez, Mahmut Sinan
dc.contributor.authorKozan, Esma
dc.contributor.authorDagyaran, Aydin
dc.contributor.authorAkdag, Mevlut
dc.contributor.authorSobarzo-Sanchez, Eduardo
dc.contributor.authorAkkol, Esra Kupeli
dc.date.accessioned2025-12-28T16:40:50Z
dc.date.available2025-12-28T16:40:50Z
dc.date.issued2025
dc.identifier.issn2076-0817
dc.identifier.urihttps://doi.org/10.3390/pathogens14010077
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2732
dc.description.abstractGastrointestinal nematodes (GINs) inflict significant economic losses on sheep and goat farming globally due to reduced productivity and the development of anthelmintic resistance. Sustainable control strategies are urgently needed including the exploration of medicinal plants as safer alternatives to chemical anthelmintics. This genus of plants is used for anti-inflammatory, antioxidant, and antimicrobial activities. In this study, we aimed to evaluate the anthelmintic activities of Nepeta racemosa Lam. MeOH extract, n-hexane, dichloromethane (DCM), ethyl acetate (EtOAc), n-buthanol (n-BuOH) and aqueous (H2O) subextracts, and quantify rosmarinic acid in the active extract by the HPLC method, and perform in silico molecular docking studies of rosmarinic acid to examine its binding interactions with tubulin. The anthelmintic activity of the plant extracts on gastrointestinal nematode eggs and larvae (L3) of the sheep was assessed using in vitro test methods such as the egg hatch assay and larval motility assay, conducted over a 24 h period (1, 2, 3, 4, 6, 8, 24). All extracts exhibited 100% effectiveness in the egg hatch inhibition assay, regardless of concentration (50-1.5625 mg/mL). The EtOAc subextract shows the highest effectiveness at 79.66%, followed by the MeOH extract at 74.00%, water at 64.00%, n-hexane at 67.00%, and DCM at 61.00%, and the lowest effectiveness is observed with n-BuOH at 51.66% in the larval motility assay. The major compound of EtOAc extract, the most active extract of N. racemosa, was determined as rosmarinic acid and its amount in the extract was determined as 14.50 mg/100 mg dry extract. The amount of rosmarinic acid in the MeOH extract was found to be 0.21 mg/100 mg dry extract. n-Hexane, DCM, n-BuOH, and H2O extracts' rosmarinic acid content was lower than the LOQ value. As tubulin plays an important role in the mechanism of anthelmintics, the major compound of the most active extract (NR-EtOAc) rosmarinic acid was docked onto the colchicine-binding site of the tubulin (5OV7) protein. Rosmarinic acid showed a similar activity spectrum to the anthelmintic drug albendazole. The discovery of low-cost and low-toxicity anthelmintic compounds is very important.
dc.language.isoen
dc.publisherMdpi
dc.relation.ispartofPathogens
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectNepeta racemosa
dc.subjectLamiaceae
dc.subjectanthelmintic
dc.subjectrosmarinic acid
dc.subjectin silico
dc.subjecttubulin
dc.subjectHPLC
dc.titleThe Anthelmintic Activity of Nepeta racemosa Lam. Against Gastrointestinal Nematodes of Sheep: Rosmarinic Acid Quantification and In Silico Tubulin-Binding Studies
dc.typeArticle
dc.identifier.orcid0000-0002-5829-7869
dc.identifier.orcid0000-0002-2790-2544
dc.identifier.orcid0009-0001-7872-3482
dc.identifier.orcid0000-0002-8783-6139
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.3390/pathogens14010077
dc.identifier.volume14
dc.identifier.issue1
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Agoren, Busra Karpuz] Baskent Univ, Fac Pharm, Dept Pharmacognosy, TR-06810 Ankara, Turkiye; [Erez, Mahmut Sinan; Kozan, Esma] Afyon Kocatepe Univ, Fac Vet Med, Dept Parasitol, TR-03200 Afyonkarahisar, Turkiye; [Dagyaran, Aydin] Cay Directorate Agr & Forestry, TR-03706 Afyonkarahisar, Turkiye; [Akdag, Mevlut] Afyonkarahisar Hlth Sci Univ, Fac Pharm, Dept Pharmaceut Chem, TR-03030 Afyonkarahisar, Turkiye; [Sobarzo-Sanchez, Eduardo] Univ Cent Chile, Fac Ciencias Salud, Ctr Invest Ingn Mat, Santiago 8370292, Chile; [Sobarzo-Sanchez, Eduardo] Univ Santiago De Compostela, Fac Pharm, Dept Organ Chem, Santiago De Compostela 15782, Spain; [Akkol, Esra Kupeli] Gazi Univ, Fac Pharm, Dept Pharmacognosy, TR-06330 Ankara, Turkiye
dc.identifier.pmid39861038
dc.identifier.scopus2-s2.0-85215823745
dc.identifier.scopusqualityQ1
dc.identifier.wosWOS:001403837400001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.snmzKA_WoS_20251227


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