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Raloxifene and Tamoxifen Reduce PARP Activity, Cytokine and Oxidative Stress Levels in the Brain and Blood of Ovariectomized Rats

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dc.creator Ovey, Ishak Suat
dc.creator Yazgan, Yener
dc.creator Yazgan, Betul
dc.creator NAZIROĞLU, Mustafa
dc.date 2016-09-30T21:00:00Z
dc.date.accessioned 2020-10-06T10:31:49Z
dc.date.available 2020-10-06T10:31:49Z
dc.identifier 6facfe32-037d-443d-a292-e26c3533273c
dc.identifier 10.1007/s12031-016-0785-9
dc.identifier https://avesis.sdu.edu.tr/publication/details/6facfe32-037d-443d-a292-e26c3533273c/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/63069
dc.description It is well known that 17 beta-estradiol (E2) has an antioxidant role on neurological systems in the brain. Raloxifene (RLX) and tamoxifen (TMX) are selective estrogen receptor modulators. An E2 deficiency stimulates mitochondrial functions for promoting apoptosis and increasing reactive oxygen species (ROS) production. However, RLX and TMX may reduce the mitochondrial ROS production via their antioxidant properties in the brain and erythrocytes of ovariectomized (OVX) rats. We aimed to investigate the effects of E2, RLX, and TMX on oxidative stress, apoptosis, and cytokine production in the brain and erythrocytes of OVX rats.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Raloxifene and Tamoxifen Reduce PARP Activity, Cytokine and Oxidative Stress Levels in the Brain and Blood of Ovariectomized Rats
dc.type info:eu-repo/semantics/article


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