Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Bahar, Tunctan"'
Autor:
Beyza Ozgen, Sefika Pinar Senol, Dilsah Ezgi Yilmaz, Meryem Temiz-Resitoglu, Omer Bahceli, Bahar Tunctan
Publikováno v:
Pharmacia, Vol 70, Iss 4, Pp 1345-1354 (2023)
Objectives: This study aimed to investigate the effect of the gasdermin D (GSDMD) and mixed lineage kinase domain-like pseudokinase (MLKL) inhibitor, necrosulfonamide (NSA), on lipopolysaccharide (LPS)-induced hyperalgesia in mice. Methods: Reaction
Externí odkaz:
https://doaj.org/article/d3682546f2bc4a95a1924a6cfab0b36d
Autor:
Omer Bahceli, Sefika Pinar Seno, Meryem Temiz-Resi, Mehmet Furkan Hor, Seyhan Sahan-Fira, Bahar Tunctan
Publikováno v:
International Journal of Pharmacology. 18:1171-1188
Autor:
Deniz Kibar, Meryem Temiz-Resitoglu, Demet Sinem Guden, Şakir Necat Yılmaz, Kafait U. Malik, Sefika Pinar Senol, Seyhan Sahan-Firat, Bahar Tunctan
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 99:921-934
Neuroinflammation plays a critical role during sepsis triggered by microglial activation. Mammalian target of rapamycin (mTOR) has gained attraction in neuroinflammation, however, the mechanism remains unclear. Our goal was to assess the effects of m
Autor:
Beyza Ozgen, Sefika Pinar Senol, Dilsah Ezgi Yilmaz, Meryem Temiz-Resitoglu, Omer Bahceli, Bahar Tunctan
Recent studies have demonstrated that two distinct forms of necrotic cell death, pyroptosis, and necroptosis, triggered by the lipid A part of lipopolysaccharide (LPS) are involved in the pathogenesis of several neurodegenerative diseases associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a288769e52451f4c3e0ee29b3200f12
https://doi.org/10.21203/rs.3.rs-1727695/v1
https://doi.org/10.21203/rs.3.rs-1727695/v1
Autor:
Seyhan Sahan-Firat, Ali Cagli, Sefika Pinar Senol, Meryem Temiz-Resitoglu, Bahar Tunctan, Ayse Nihal Sari, Demet Sinem Guden
Publikováno v:
Drug Development Research. 82:815-825
Epoxyeicosatrienoic acids (EETs) have anti-inflammatory effects and soluble epoxide hydrolase (sEH) inhibition might be a useful therapeutic approach to manage inflammatory disorders. The purpose of the study was to investigate whether nucleotide-bin
Autor:
Meryem Temiz-Resitoglu, Seyhan Sahan-Firat, Sefika Pinar Senol, Demet Sinem Guden, Ayse Nihal Sari, Bahar Tunctan
Publikováno v:
Neurochemical Research. 46:624-637
A selective RXR agonist, bexarotene, has been shown to have anti-inflammatory, anti-nociceptive, and neuroprotective effects in several models of numerous neurological diseases characterized by systemic inflammation. The mechanisms underlying these e
Publikováno v:
Journal of Literature Pharmacy Sciences. 10:153-165
Autor:
Dilsah Ezgi Yilmaz, Sefika Pinar Senol, Meryem Temiz-Resitoglu, Seyhan Sahan-Firat, Bahar Tunctan
Objective The nucleotide-binding oligomerization domain-like receptor X1 (NLRX1) has been associated with various anti-inflammatory mechanisms. We investigated whether the NLRX1 ligand docosahexaenoic acid (DHA) ameliorates lipopolysaccharide (LPS)-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b603a9ed81187d766293db6fa66ad27d
https://doi.org/10.21203/rs.3.rs-1403191/v1
https://doi.org/10.21203/rs.3.rs-1403191/v1
Autor:
Seyhan Sahan-Firat, Senay Balci, Özden Vezir, Lulufer Tamer-Gumus, Bahar Tunctan, Meryem Temiz-Resitoglu, Kafait U. Malik, Zumrut Kocak, Demet Sinem Guden, Nehir Sucu
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 97:1193-1203
Mammalian target of rapamycin (mTOR) has been recognized with potential immunomodulatory properties playing an important role in various physiopathological processes including ischemia–reperfusion (I/R) injury. I/R injury stimulate reactive oxygen
Autor:
Bahar Tunctan, Sefika Pinar Senol, Meryem Temiz-Resitoglu, Dilsah Ezgi Yilmaz, Demet Sinem Guden, Omer Bahceli, Mehmet Furkan Horat, Seyhan Sahan-Firat, Ayse Nihal Sari, John R. Falck, Raghunath Reddy Anugu, Kafait U. Malik
Publikováno v:
Journal of cardiovascular pharmacology. 80(2)
The orphan receptor, G protein-coupled receptor (GPR) 75, which has been shown to mediate various effects of 20-hydroxyeicosatetraenoic acid (20-HETE), is considered as a therapeutic target in the treatment of cardiovascular diseases in which changes