Basit öğe kaydını göster

dc.contributor.authorAltinoz, Meric A.
dc.contributor.authorElmaci, Ilhan
dc.date.accessioned2021-03-06T09:44:37Z
dc.date.available2021-03-06T09:44:37Z
dc.identifier.citationElmaci I., Altinoz M. A. , "Thymoquinone: An edible redox-active quinone for the pharmacotherapy of neurodegenerative conditions and glial brain tumors. A short review", BIOMEDICINE & PHARMACOTHERAPY, cilt.83, ss.635-640, 2016
dc.identifier.issn0753-3322
dc.identifier.otherav_e6f3baf6-f347-49a8-998a-44a25ca21286
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/151910
dc.identifier.urihttps://doi.org/10.1016/j.biopha.2016.07.018
dc.description.abstractThere exist few efficient agents in the neurological and neurosurgical armamentarium for treatment of neurotrauma, refractory seizures and high grade glial tumors. Pathophysiological conditions of diverse neural injuries have converging common pathways including oxidative stress and apoptosis. Targeted therapies have been throughly investigated, but limited success has been achieved until now. Phytochemical drugs may provide easily achievable and cheap adjunctive sources. Thymoquinone is an edible quinone obtained from Nigella sativa seed oil and exerts powerful antiinflammatory, antioxidant and antitumor activities in experimental models. Recently emerging studies conducted with animal models suggest that thymoquinone - bearing a very simple molecular structure - significantly crosses the blood brain barrier and exerts neuromodulatory activities. Indeed, in animal studies, the following actions of thymoquinone were demonstrated: 1-Protection against ischemic brain damage. 2-Reduction of epileptic seizures and associated cerebral oxidative injury. 3-Reduction of morphine tolerance and associated oxidative brain damage. 4-Anxiolytic effects and reduction of immobility stress-associated cerebral oxidative injury. 5-Reduction of diabetes-induced cerebral oxidative stress, 6-Reduction of cerebral oxidative injuries induced by noxious exposures including toluene, lead and ionizing radiation. Substantial in vitro data suggest that thymoquinone may be beneficial in treatment of glial tumors. However, there is no clinical study investigating its antitumor effects. In fact, thymoquinone suppresses growth and invasion, and induces apoptosis of glial tumor cells via degrading tubulins and inhibiting 20S proteasome, telomerase, autophagy, FAK and metalloproteinases. A simple and easily available agent may be a promising adjunctive treatment option in neurological and neurosurgical practice. (C) 2016 Elsevier Masson SAS. All rights reserved.
dc.language.isoeng
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.subjectYaşam Bilimleri
dc.titleThymoquinone: An edible redox-active quinone for the pharmacotherapy of neurodegenerative conditions and glial brain tumors. A short review
dc.typeMakale
dc.relation.journalBIOMEDICINE & PHARMACOTHERAPY
dc.contributor.departmentMemorial Healthcare Group , ,
dc.identifier.volume83
dc.identifier.startpage635
dc.identifier.endpage640
dc.contributor.firstauthorID235342


Bu öğenin dosyaları:

DosyalarBoyutBiçimGöster

Bu öğe ile ilişkili dosya yok.

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster