Sürdürülebilir Kalkınma Amaçları

Yazarlar

  • MakaleAçık Erişim2026Scopus SJRQ1
    Biochemical effects and theoretical study of a metformin in the carp (Cyprinus carpio) fry

    İSPİR, Ünal; Tüzün, Burak; KIRICI, Muammer; Poustforoosh, Alireza; YONAR, Muhammet Enis; YONAR, Serpil MİŞE; ŞEKER, Engin

    Pharmaceutical chemicals are frequently detected in wastewater, and metformin, an oral hypoglycemic agent, is among the most common. In this study, the effects of metformin on biochemical (total protein, glycogen, lipid) and antioxidant (malondialdehyde (MDA), glutathione (GSH), glutathione S-transferase (GST), catalase (CAT)) parameters were investigated in carp ( Cyprinus carpio ) fry. Fish were exposed to 40 and 80 µg/L metformin for 96 h, 14 and 21 days. No mortalities occurred in any group. At 80 µg/L for 21 days, total protein activity and lipid levels significantly decreased. Glycogen activity showed no significant differences compared to controls. Antioxidant parameters measured spectrophotometrically revealed that MDA levels, CAT and GST activities decreased with time but increased with dose, while GSH levels rose with time yet decreased with dose. Overall, significant time- and dose-dependent effects ( p < 0.05) were observed. In silico analyses were also performed. The activity of metformin against antioxidant proteins was evaluated, and molecular dynamics simulations confirmed strong interactions with the most active protein. ADME/T analysis provided pharmacokinetic insights, and Gaussian-based quantum chemical calculations (EHOMO, ELUMO, ΔE, dipole, etc.) characterized electronic and structural properties. These combined results indicate that metformin alters key biochemical pathways in carp fry and has significant reactivity toward antioxidant proteins. Findings suggest potential ecotoxicological risks in aquatic systems and relevance to pharmacological profiling.

    • SDG 3 · Sağlık ve Kaliteli Yaşam
    AtıfScopus1OpenAlex1
    ScopusWeb of SciencePubMedİncele
  • MakaleAçık Erişim2025Scopus SJRQ3
    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

    Zengin, Gokhan; Cetiz, Mehmet Veysi; Abul, Nurgul; Gulcin, Ilhami; Caprioli, Giovanni; Piatti, Diletta; Ricciutelli, Massimo; Koyuncu, Ismail; Yuksekdag, Ozgur; Bahşi, Muammer

    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.

    • SDG 3 · Sağlık ve Kaliteli Yaşam
    AtıfScopus15OpenAlex13
    ScopusWeb of SciencePubMedİncele