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dc.contributor.authorDolanbey, Serap Niğdelioğlu
dc.contributor.authorKoçancı, Fatma Gonca
dc.contributor.authorAslım, Belma
dc.date.accessioned2022-09-22T06:18:52Z
dc.date.available2022-09-22T06:18:52Z
dc.date.issued2021en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12868/1648
dc.description.abstractBackground: Oxidative stress is a significant feature in the pathomechanism of neurodegenerative diseases. Thus, the search for an effective and safe novel antioxidant agent with neuroprotective properties has increased the interest in medicinal plant products as a bioactive phytochemical source. However, little is known about the potential effects of the medically important Glaucium corniculatum as a natural antioxidant. Objective: In the present study, it was aimed to investigate the anti-oxidative, anti-apoptotic, and cell cycle regulatory mechanisms underlying the neuroprotective effects of alkaloid extracts (chloroform, methanol, and water) from G. corniculatum, which was profiled for major alkaloid/alkaloids, against H2O2-induced neuronal damage in differentiated PC12 cells. Materials and methods: The profiles of the alkaloid extracts were analyzed by GC-MS. The effects of the alkaloid extracts on intracellular ROS production, level of apoptotic cells, and cell cycle dysregulation were analyzed by flow cytometry; the effects on mRNA expression of apoptosis-related genes were also analyzed by qRT-PCR. Results: The same alkaloid components, allocryptopine, tetrahydropalmatine, and tetrahydroberberine N-oxide were obtained in all three solvents, but the ratios of the components differed according to the solvents. Allocryptopine was determined to be the major alkaloid ingredient in the alkaloid extracts, with the highest amount of allocryptopine (497 mu g/mg) being found in the chloroform alkaloid extract (CAE) (*p < 0.05). The best results were obtained from CAE, which has the highest amount of allocryptopine among alkaloid extracts in all studies. CAE suppressed intracellular ROS production (5.7-fold), percentage of apoptotic cells (3.0-fold), and cells in the sub G1 phase (6.8-fold); additionally, it increased cells in the G1 phase (1.5-fold) (**p < 0.01). CAE remarkably reduced the expressions of Bax, Caspase-9/-3 mRNA (2.4-3.5-fold) while increasing the expression of Bcl-2 mRNA (3.0-fold) (*p < 0.05). Conclusions: Our results demonstrated that alkaloid extracts from G. corniculatum, which contain allocryptopine, tetrahydropalmatine, and tetrahydroberberine N-oxide suppressed oxidative stress-induced neuronal apoptosis, possibly by suppressing the mitochondrial apoptotic pathway and regulating the cell cycle. These results are the first report that related alkaloids have played a neuroprotective role by regulating multiple mechanisms. Thus, our study indicated that these alkaloids especially allocryptopine could offer an efficient and novel strategy to explore novel drugs for neuroprotection and cognitive improvement.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1016/j.biopha.2021.111690en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAlkaloiden_US
dc.subjectAllocryptopineen_US
dc.subjectCell cycleen_US
dc.subjectNeuronal apoptosisen_US
dc.subjectNeuroprotective effecten_US
dc.subjectOxidative stressen_US
dc.titleNeuroprotective effects of allocryptopine-rich alkaloid extracts against oxidative stress-induced neuronal damageen_US
dc.typearticleen_US
dc.contributor.departmentALKÜ, Meslek Yüksekokulları, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Hizmetler ve Teknikler Bölümüen_US
dc.identifier.volume140en_US
dc.relation.journalBiomedicine & Pharmacotheraphyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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