The effect of melatonin on oxidative stress and apoptosis in experimental diabetes mellitus-related ovarian injury

被引:10
作者
Nayki, Umit [1 ]
Onk, Didem [2 ]
Balci, Gurhan [3 ]
Nayki, Cenk [1 ]
Onk, Alper [4 ]
Cankaya, Murat [5 ]
Kafa, Ayse Humeyra Taskin [5 ]
Kuzucu, Mehmet [5 ]
机构
[1] Erzincan Univ, Sch Med, Dept Obstet & Gynecol, Erzincan, Turkey
[2] Erzincan Univ, Sch Med, Dept Anesthesiol & Reanimat, Erzincan, Turkey
[3] Erzincan Univ, Sch Med, Dept Pathol, Erzincan, Turkey
[4] Erzincan Univ, Sch Med, Dept Cardiovasc Surg, Erzincan, Turkey
[5] Erzincan Univ, Sch Med, Dept Biochem, Erzincan, Turkey
关键词
NF-kB pathway; Apoptosis; rat; ovary; oxidative stress; diabetes; ANTIOXIDANT STATUS; CASPASE-3; ACTIVATION; LIPID-PEROXIDATION; EXPRESSION; ALPHA; MECHANISMS; FAILURE; MODEL;
D O I
10.3109/09513590.2015.1126819
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We aimed to evaluate the effect of melatonin on oxidative stress and ovarian injury in rats. Twenty-four Sprague-Dawley albino rats were divided into three groups: Group 1 as nondiabetic healthy controls (n = 8), group 2 as nontreated diabetic rats (n = 8) and group 3 as melatonin-treated diabetic rats (n = 8). After overt diabetes was produced by intraperitoneal injection of streptozosin, 20 mg/kg/day of melatonin was given intraperitoneally to group 3 for a week. NF-kB and caspase-3 immunoexpressions, lipid peroxidation, the activities of antioxidative enzymes, total oxidant capacity and total antioxidant capacity were assessed. Immunoexpressions of NF-kB and caspase-3 were significantly lower in group 3 than group 2. There was a significant decrease in superoxide dismutase activity in group 2 than group 1 and a significant increase in group 3 compared with group 2. We observed a nonsignificant decrease in catalase activity between group 1 and group 2 and a nonsignificant increase between group 2 and group 3. There was a nonsignificant increase in the plasma level of total oxidant status in group 2 than group 1, but a significant decrease was observed in group 3 compared to group 2. Total antioxidant status was significantly lower in group 2 compared with group 1 and group 3. In conclusion, melatonin ameliorates the negative effects of oxidative stress on DM-related ovarian injury.
引用
收藏
页码:421 / 426
页数:6
相关论文
共 43 条
[1]  
Aebi H, 1984, Methods Enzymol, V105, P121
[2]   Effects of melatonin on oxidative-antioxidative status of tissues in streptozotocin-induced diabetic rats [J].
Aksoy, N ;
Vural, H ;
Sabuncu, T ;
Aksoy, S .
CELL BIOCHEMISTRY AND FUNCTION, 2003, 21 (02) :121-125
[3]   Mechanisms of high glucose-induced apoptosis and its relationship to diabetic complications [J].
Allen, DA ;
Yaqoob, MM ;
Harwood, SM .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2005, 16 (12) :705-713
[4]   Neurohormone melatonin prevents cell damage: Effect on gene expression for antioxidant enzymes [J].
Antolin, I ;
Rodriguez, C ;
Sainz, RM ;
Mayo, JC ;
Uria, H ;
Kotler, MI ;
RodriguezColunga, MJ ;
Tolivia, D ;
MenendezPelaez, A .
FASEB JOURNAL, 1996, 10 (08) :882-890
[5]   Comparative analysis of the protective effects of melatonin and vitamin E on streptozocin-induced diabetes mellitus [J].
Baydas, G ;
Canatan, H ;
Turkoglu, A .
JOURNAL OF PINEAL RESEARCH, 2002, 32 (04) :225-230
[6]   Role of oxidative stress in diabetic complications - A new perspective on an old paradigm [J].
Baynes, JW ;
Thorpe, SR .
DIABETES, 1999, 48 (01) :1-9
[7]   The pathobiology of diabetic complications - A unifying mechanism [J].
Brownlee, M .
DIABETES, 2005, 54 (06) :1615-1625
[8]   Efficacy and safety of exogenous melatonin for secondary sleep disorders and sleep disorders accompanying sleep restriction: meta-analysis [J].
Buscemi, N ;
Vandermeer, B ;
Hooton, N ;
Pandya, R ;
Tjosvold, L ;
Hartling, L ;
Vohra, S ;
Klassen, TP ;
Baker, G .
BMJ-BRITISH MEDICAL JOURNAL, 2006, 332 (7538) :385-388C
[9]   OXIDATIVE STRESS AS A MEDIATOR OF APOPTOSIS [J].
BUTTKE, TM ;
SANDSTROM, PA .
IMMUNOLOGY TODAY, 1994, 15 (01) :7-10
[10]   Hyperglycemia-induced apoptosis in mouse myocardium -: Mitochondrial cytochrome c-mediated caspase-3 activation pathway [J].
Cai, L ;
Li, W ;
Wang, GW ;
Guo, LP ;
Jiang, YC ;
Kang, YJ .
DIABETES, 2002, 51 (06) :1938-1948