dc.contributor.authors |
Sekeroglu, MR; Huyut, Z; Cokluk, E; Ozbek, H; Alp, HH; |
|
dc.date.accessioned |
2020-02-27T07:20:26Z |
|
dc.date.available |
2020-02-27T07:20:26Z |
|
dc.date.issued |
2017 |
|
dc.identifier.citation |
Sekeroglu, MR; Huyut, Z; Cokluk, E; Ozbek, H; Alp, HH; (2017). The susceptibility to autoxidation of erythrocytes in diabetic mice: Effects of melatonin and pentoxifylline. JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 31, - |
|
dc.identifier.issn |
1095-6670 |
|
dc.identifier.uri |
https://doi.org/10.1002/jbt.21976 |
|
dc.identifier.uri |
https://hdl.handle.net/20.500.12619/65500 |
|
dc.description.abstract |
Oxidative stress had a great importance in development of complications in diabetes. We investigated effects of melatonin and pentoxifylline in diabetic mice. Swiss albino mice (n=40) were divided into four groups: alloxan-induced diabetes mellitus (DM), alloxan-induced diabetes with melatonin supplementation (DM+MLT), alloxan-induced diabetes with pentoxifylline supplementation (DM+PTX), and control. Glutathione-peroxidase (GSH-Px) activity, malondialdehyde (MDA) and reduced glutathione (GSH) levels, and susceptibility to oxidation of erythrocytes were measured. MDA levels were higher than control in the DM and DM+MLT. The DM had more MDA level than the DM+MLT and DM+PTX (P<0.001). After in vitro oxidation, MDA levels of all groups were found higher than the control. However, they were significantly lower than the DM in DM+PTX and DM+MLT (P<0.001). Although GSH levels of the DM and DM+PTX were less than the control, GSH-Px activity of the DM was lower than the control and DM+PTX (P<0.05). We suggest that there is increased oxidative stress and compromised antioxidant status of erythrocytes in diabetes; however, it can be effectively prevented by melatonin or pentoxifylline supplementation. |
|
dc.language |
English |
|
dc.publisher |
WILEY |
|
dc.subject |
Toxicology |
|
dc.title |
The susceptibility to autoxidation of erythrocytes in diabetic mice: Effects of melatonin and pentoxifylline |
|
dc.type |
Article |
|
dc.identifier.volume |
31 |
|
dc.contributor.department |
Sakarya Üniversitesi/Tıp Fakültesi/Temel Tıp Bilimleri Bölümü |
|
dc.contributor.saüauthor |
Şekeroğlu, Mehmet Ramazan |
|
dc.contributor.saüauthor |
Çokluk, Erdem |
|
dc.relation.journal |
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY |
|
dc.identifier.wos |
WOS:000417915400004 |
|
dc.identifier.doi |
10.1002/jbt.21976 |
|
dc.identifier.eissn |
1099-0461 |
|
dc.contributor.author |
Şekeroğlu, Mehmet Ramazan |
|
dc.contributor.author |
Zubeyir Huyut |
|
dc.contributor.author |
Çokluk, Erdem |
|
dc.contributor.author |
Hanefi Ozbek |
|
dc.contributor.author |
Hamit Hakan Alp |
|