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1.
Clin Exp Obstet Gynecol ; 44(3): 398-402, 2017.
Article in English | MEDLINE | ID: mdl-29949281

ABSTRACT

OBJECTIVE: The pathological mechanisms of gestational trophoblastic disease have not yet been clearly determined. It is thought that oxidative damage contributes to the process. The aim of this study was to determine the levels of coenzyme Q10 (CoQ 10), DNA damage, and lipid peroxidation in patients with hydatidiform mole. MATERIALS AND METHODS: The authors studied the levels of CoQ10, 8-hydroxydeoxyguanosine (8-OHdG), malondialdehyde (MDA) by high-performance liquid chromatography (HPLC), and the activity of glutathione peroxidase (GPX) by spectrophotometric method in blood obtained from patients with a complete hydatidiform mole (n=29), healthy pregnant women (n=29), and healthy non-pregnant women (n=29). RESULTS: The 8-OHdG/dG ratio (2.8148 ± 0.81592) and MDA (10.8341 ± 4.64875 µmol) were significantly higher in patients with complete hydatidiform mole, while the ubiquinol-10/ubiquinone-10 ratio (0.2107 ± 0.15675) and GPX activity (43.4606 ± 18.31694 mU/mI) were lower (p < 0.001). CONCLUSION: The authors suggest that both mitochondrial oxidative and oxidative DNA damage play important roles in the pathogenesis of complete hydatidiform mole. Therefore supplementation of CoQ10 prevents recurrent gestational trophoblastic disease.


Subject(s)
Hydatidiform Mole/metabolism , Ubiquinone/analogs & derivatives , Uterine Neoplasms/metabolism , Vitamins/metabolism , 8-Hydroxy-2'-Deoxyguanosine , Adult , Case-Control Studies , Chromatography, High Pressure Liquid , DNA Damage , Deoxyguanosine/analogs & derivatives , Female , Glutathione Peroxidase/metabolism , Humans , Hydatidiform Mole/pathology , Lipid Peroxidation , Malondialdehyde/metabolism , Mitochondria/pathology , Oxidation-Reduction , Pregnancy , Ubiquinone/metabolism , Uterine Neoplasms/pathology , Young Adult
2.
Niger J Clin Pract ; 20(11): 1489-1496, 2017 Nov.
Article in English | MEDLINE | ID: mdl-29303137

ABSTRACT

OBJECTIVE: The purpose of this study was to compare the effects of thymoquinone and icodextrin in rats within the framework of an experimental adhesion model. MATERIALS AND METHODS: Rats were separated into three groups: (1) a control group consisting of rats that had 2 ml of isotonic solution administered intraperitoneally, (2) an ICO group administered with 2 ml of 4% icodextrin, and (3) a TQ group administered thymoquinone (10 mg/kg), all following cecal abrasion. The three groups underwent a reoperation on the 7th postoperative day. Hydroxyproline levels were analyzed in the resected adhesive tissues, and histopathological investigations were conducted. Blood samples were collected for biochemical analyses. RESULTS: Fewer postoperative adhesions were observed in the ICO and TQ groups compared with the control group. A comparison of the TQ and ICO groups revealed lowers levels of postoperative adhesions in the TQ group. Compared with the control group, malondialdehyde, 8-OH-deoxyguanosine/deoxyguanosine (8-OHdG/10dG), Coenzyme Q10 (CoQ10), and CoenzymeQ10/reduced CoenzymeQ10 (CoQ10/CoQ10H) values were found to be lower in the TQ and ICO groups. When the TQ and ICO groups were compared with respect to their biochemical parameters, the results for all of the four parameters were found to be statistically significantly lower in the TQ group (P < 0.000). The levels of hydroxyproline in the control, ICO, and TQ groups were found to be (mean ± standard deviation) 502.25 ± 90.39 µg/g, 342.13 ± 66.61 µg/g, and 287.88 ± 49.59 µg/g, respectively. CONCLUSIONS: A comparison of the antiadhesive effects of thymoquinone and icodextrin revealed thymoquinone to be more effective. These results indicate that thymoquinone is an efficient and strong antiadhesive molecule.


Subject(s)
Benzoquinones/pharmacology , Glucans/pharmacology , Glucose/pharmacology , Postoperative Complications , Tissue Adhesions/prevention & control , Animals , Benzoquinones/administration & dosage , Disease Models, Animal , Glucans/administration & dosage , Glucose/administration & dosage , Humans , Icodextrin , Injections, Intraperitoneal , Male , Rats , Rats, Wistar , Tissue Adhesions/etiology , Tissue Adhesions/pathology , Ubiquinone/analogs & derivatives
3.
Hum Exp Toxicol ; 35(2): 194-204, 2016 Feb.
Article in English | MEDLINE | ID: mdl-25825413

ABSTRACT

The aim of this study was to evaluate the role of α-lipoic acid (α-LA) on oxidative damage and inflammation that occur in endothelium of aorta and heart while constant consumption of high-fructose corn syrup (HFCS). The rats were randomly divided into three groups with each group containing eight rats. The groups include HFCS, HFCS + α-LA treatment, and control. HFCS was given to the rats at a ratio of 30% of F30 corn syrup in drinking water for 10 weeks. α-LA treatment was given to the rats at a dose of 100 mg/kg/day orally for the last 6 weeks. At the end of the experiment, the rats were killed by cervical dislocation. The blood samples were collected for biochemical studies, and the aortic and cardiac tissues were collected for evaluation of oxidant-antioxidant system, tissue bath, and pathological examination. HFCS had increased the levels of malondialdehyde, creatine kinase MB, lactate dehydrogenase, and uric acid and showed significant structural changes in the heart of the rats by histopathology. Those changes were improved by α-LA treatment as it was found in this treatment group. Immunohistochemical expressions of tumor necrosis factor α and inducible nitric oxide synthase were increased in HFCS group, and these receptor levels were decreased by α-LA treatment. All the tissue bath studies supported these findings. Chronic consumption of HFCS caused several problems like cardiac and endothelial injury of aorta by hyperuricemia and induced oxidative stress and inflammation. α-LA treatment reduced uric acid levels, oxidative stress, and corrected vascular responses. α-LA can be added to cardiac drugs due to its cardiovascular protective effects against the cardiovascular diseases.


Subject(s)
Antioxidants/therapeutic use , Cardiovascular System/drug effects , High Fructose Corn Syrup/toxicity , Thioctic Acid/therapeutic use , Animals , Antioxidants/metabolism , Aorta, Thoracic/pathology , Endothelium, Vascular/pathology , Female , Hyperuricemia/chemically induced , Inflammation/chemically induced , Inflammation/drug therapy , Inflammation/pathology , Myocardium/pathology , Oxidative Stress/drug effects , Rats , Rats, Wistar
4.
J Physiol Pharmacol ; 62(5): 575-82, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22204806

ABSTRACT

Ischemia is defined as cell death caused by insufficient perfusion of the tissue due to reduction in arterial or venous blood flow, depletion of cellular energy storages, and accumulation of toxic metabolites. The positive effects of controlled reperfusion are known and are used clinically. But the positive effects of controlled reperfusion on ovarian tissue have not been seen in the literature yet. The biochemical and histopathological comparative investigation of rat ovaries that were experimentally exposed to ischemia (IG), ischemia-reperfusion (I/R), and ischemia-controlled reperfusion (ICR) was aimed. Forty rats were divided into four groups (10 rats per group). First group: 3 h ischemia by vascular clips on ovarian tissue. Second group: 3 h ischemia + 1 h reperfusion. Third group: 3 h ischemia + 1 h controlled reperfusion (on-off method: controlled reperfusion by opening and closing the clips (on/off) in 10-second intervals, for 5 times for a total of 100 seconds). Fourth group: healthy rats. Biochemical (tGSH, MDA, and DNA damage level and SOD activity) and histopathological analysis were performed. The highest glutathione and superoxide dismutase measurements were found in ischemia/controlled reperfusion group among the ischemia or ischemia/reperfusion groups. Similarly the damage indicators (malondialdehyde, DNA damage level and histopathological damage grade) were the lowest in ischemia/controlled reperfusion group. These results indicate that controlled reperfusion can be helpful in minimizing ischemia-reperfusion injury in ovarian tissue exposed to ischemia for various reasons (ovarian torsion, tumor, etc.).


Subject(s)
Ischemia/complications , Ischemic Preconditioning/methods , Ovary/blood supply , Reperfusion Injury/prevention & control , Animals , Antioxidants/metabolism , DNA Damage , Female , Glutathione/metabolism , Ischemia/metabolism , Ischemia/pathology , Malondialdehyde/metabolism , Ovary/metabolism , Ovary/pathology , Rats , Rats, Wistar , Reperfusion/methods , Reperfusion Injury/etiology , Reperfusion Injury/metabolism , Reperfusion Injury/pathology , Superoxide Dismutase/metabolism
5.
Eur J Ophthalmol ; 19(1): 80-5, 2009.
Article in English | MEDLINE | ID: mdl-19123153

ABSTRACT

PURPOSE: This study examines the levels of oxidative damage in patients with retinopathy of prematurity (ROP). METHODS: Fifty patients were recruited with a birthweight below 1500 g or gestational age below 32 weeks. The cases were classified into those who developed ROP (n=25) and those without ROP (n=25). The authors obtained blood and urine samples from each infant, for measuring 8-hydroxy 2-deoxyguanosine (8-OHdG) and malondialdehyde (MDA) levels, at the time of the first examination at 4-6 postnatal weeks. RESULTS: A significant difference was observed in leukocyte and urine 8-OHdG levels in patients with ROP compared to those without ROP (p<0.001 for both). Similarly, a significant difference was observed in plasma and urine MDA levels in patients with ROP compared to those without ROP (p<0.001 for both). In addition, significant correlations were found between levels of 8-OHdG in leukocyte DNA and plasma MDA (r=0.859, p<0.001), and between levels of urine 8-OHdG excretion and urine MDA (r=0.563, p<0.001). CONCLUSIONS: 8-OHdG in leukocyte DNA and urine levels in premature infants can be useful as an indicator for ROP screening.


Subject(s)
DNA Damage , Oxidative Stress , Retinopathy of Prematurity/diagnosis , 8-Hydroxy-2'-Deoxyguanosine , Biomarkers/blood , Biomarkers/urine , Birth Weight , Chromatography, High Pressure Liquid , Deoxyguanosine/analogs & derivatives , Deoxyguanosine/blood , Gestational Age , Humans , Infant , Infant, Newborn , Infant, Very Low Birth Weight , Leukocytes/metabolism , Lipid Peroxidation , Malondialdehyde/blood , Malondialdehyde/urine , Neonatal Screening/methods
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