Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/30085
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DC Field | Value | Language |
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dc.contributor.author | Gundogdu, G. | - |
dc.contributor.author | Dodurga, Yavuz | - |
dc.contributor.author | Küçükatay, Vural | - |
dc.date.accessioned | 2020-06-08T12:11:10Z | |
dc.date.available | 2020-06-08T12:11:10Z | |
dc.date.issued | 2019 | - |
dc.identifier.issn | 0301-4851 | - |
dc.identifier.uri | https://hdl.handle.net/11499/30085 | - |
dc.identifier.uri | https://doi.org/10.1007/s11033-019-04850-3 | - |
dc.description.abstract | Homocysteine (hcy) is an amino acid that contains sulfur species. In healthy individuals, plasma hcy levels are low. The aim of this study was to investigate the potential neurotoxic effects of hcy and sulfite (sft) molecules alone and in their combination, and also to identify the relationship of these substances on oxidative stress. SH-SY5Y cells were used as an invitro neurodegenerative disease model. The SH-SY5Y cells were treated with various concentrations of hcy alone, sft alone (final concentrations in the well were 10–250 µM and 0.1–5 mM, respectively) and a combination of both (hcy + sft). Their cytotoxicity and genotoxic effects were investigated using the XTT test and Comet assay and, their impact on oxidative stress was examined using total antioxidant–oxidant status (TAS-TOS) kits. The highest toxic doses of hcy and sft were found to be 250 µM and 5 mM, respectively, but the maximum toxic effect was observed for hcy + sft (p < 0.001). In addition, an increase in DNA damage was evident in all groups, but maximal damage was inflicted using in hcy + sft (p < 0.001). The oxidative stress index was significantly increased in hcy + sft (p < 0.05). Determining the increase in sft and hcy levels may contribute to delaying the occurrence of diseases before symptoms of neurodegenerative disease appear. © 2019, Springer Nature B.V. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springer Netherlands | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Homocysteine | en_US |
dc.subject | Neurodegenerative diseases | en_US |
dc.subject | Neurotoxicity | en_US |
dc.subject | Sulfite | en_US |
dc.subject | homocysteine | en_US |
dc.subject | sulfite | en_US |
dc.subject | antioxidant | en_US |
dc.subject | sulfite oxidase | en_US |
dc.subject | sulfur amino acid | en_US |
dc.subject | Article | en_US |
dc.subject | comet assay | en_US |
dc.subject | controlled study | en_US |
dc.subject | cytotoxicity | en_US |
dc.subject | DNA damage | en_US |
dc.subject | genotoxicity | en_US |
dc.subject | human | en_US |
dc.subject | human cell | en_US |
dc.subject | in vitro study | en_US |
dc.subject | nerve degeneration | en_US |
dc.subject | neurotoxicity | en_US |
dc.subject | oxidative stress | en_US |
dc.subject | SH-SY5Y cell line | en_US |
dc.subject | XTT assay | en_US |
dc.subject | degenerative disease | en_US |
dc.subject | drug effect | en_US |
dc.subject | lipid peroxidation | en_US |
dc.subject | metabolism | en_US |
dc.subject | tumor cell line | en_US |
dc.subject | Amino Acids, Sulfur | en_US |
dc.subject | Antioxidants | en_US |
dc.subject | Cell Line, Tumor | en_US |
dc.subject | Comet Assay | en_US |
dc.subject | DNA Damage | en_US |
dc.subject | Humans | en_US |
dc.subject | Lipid Peroxidation | en_US |
dc.subject | Neurodegenerative Diseases | en_US |
dc.subject | Oxidative Stress | en_US |
dc.subject | Sulfite Oxidase | en_US |
dc.subject | Sulfites | en_US |
dc.title | The sulfite molecule enhances homocysteine toxicity in SH-SY5Y cells | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 46 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.startpage | 4017 | |
dc.identifier.startpage | 4017 | en_US |
dc.identifier.endpage | 4025 | en_US |
dc.identifier.doi | 10.1007/s11033-019-04850-3 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 31079315 | en_US |
dc.identifier.scopus | 2-s2.0-85065701172 | en_US |
dc.identifier.wos | WOS:000478684300038 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
crisitem.author.dept | 14.03. Basic Medical Sciences | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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