Slow-down of age-dependent telomere shortening is executed in human skin keratinocytes by hormesis-like-effects of trace hydrogen peroxide or by anti-oxidative effects of pro-vitamin C in common concurrently with reduction of intracellular oxidative stress

2004 ◽  
Vol 93 (3) ◽  
pp. 588-597 ◽  
Author(s):  
Seiichi Yokoo ◽  
Kayo Furumoto ◽  
Eiso Hiyama ◽  
Nobuhiko Miwa
Life Sciences ◽  
1998 ◽  
Vol 63 (11) ◽  
pp. 935-948 ◽  
Author(s):  
Kayo Furumoto ◽  
Eiji Inoue ◽  
Norio Nagao ◽  
Eiso Hiyama ◽  
Nobuhiko Miwa

2016 ◽  
Vol 91 (7) ◽  
pp. 480-491 ◽  
Author(s):  
S Ben Khedir ◽  
D Moalla ◽  
N Jardak ◽  
M Mzid ◽  
Z Sahnoun ◽  
...  

Author(s):  
Gang Wang ◽  
Shurui Chen ◽  
Zhenya Shao ◽  
Yankun Li ◽  
Wei Wang ◽  
...  

Metformin, the first medication that is often prescribed for the treatment of Type-2 Diabetes Mellitus (T2DM), was recently found to be neuroprotective. To study the mechanism underlying the neuroprotective effect of metformin, we pre-treated primary spinal cord neurons with 50 µM or 100 µM µM metformin for 2 hours prior to treatment with hydrogen peroxide (H2O2) for up to 48 hours. Our results showed that H2O2 increased the expression of purinergic receptor P2X7 (P2X7R) in spinal cord neurons, which promoted the downstream pro-inflammatory cytokines release and oxidative stress. We found that metformin could reverse these pro-inflammatory and pro-oxidative effects of H2O2. Besides, P2X7R knockdown by siRNA suppressed H2O2-induced proinflammatory cytokine release and oxidative stress response. In conclusion, our results show that metformin can alleviate H2O2-induced inflammation and oxidative stress via modulating the P2X7R signaling pathway.


2012 ◽  
Vol 36 (0A) ◽  
pp. 32-42
Author(s):  
محمودسالم محمدشيت المعاضيدي

The present study was designed to investigate the effect of Vitamin C (450 mg/kg diet) and sodium selenite (0.5 mg/kg diet) in adult white Leghorn male chickens (30 weeks of age), whose concomitantly exposed to oxidative stress induced by hydrogen peroxide (0.5%) supplemented with drinking water for 6 weeks on reproductive performance. Semen were collected at 0, 2, 4 and 6weeks, The study results showed that hydrogen peroxide treatment caused a significant decrease in the body weight, sperm concentration, mass motility and individual motility during experimental period. Also a decrease in testosterone and testis glutathione concentration at the 6th week of the treatment, accompanied with a significant increase in dead and abnormal sperm percentage, testis malondialdehyde level compared with the control group. Histopathological changes revealed presence of necrosis and sloughing in the epithelial lining of the semineferous tubules and vacuolar degeneration of the supporting cells that fall in the lumen of the semineferous tubules and necrosis of interstitial cells. Vitamin C and sodium selenite with hydrogen peroxide caused a significant increase in body weight, sperm concentration, mass motility and individual motility during the experimental period, testosterone and glutathione level, accompanied with a significant decrease in dead and abnormal sperm percentages and Malondialdehyde level compared with hydrogen peroxide. In addition to the improvement in the histological picture of the semineferous tubules, mitosis germ cells were observed through their arrangement in circular tubules. It was concluded from this study that Vitamin C and Sodium selenite reverse the adverse effects produced by hydrogen peroxide on certain physiological and reproductive aspects in adult male chickens.


Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 4228-4228
Author(s):  
Phillip D Knouse ◽  
Mayurika Pise ◽  
Jalissa N Furr ◽  
Rhea Li ◽  
Donna A Bell ◽  
...  

Abstract Abstract 4228 Pediatric leukemia patients undergoing treatment are often malnourished due to nausea, food aversions, and mucositis. Clinical observations suggest that poor nutrition worsens outcomes for this patient population. Oxidative stress may be a key intermediary linking nutrition and clinical outcomes. Previous reports suggest that diet may modulate the balance of cellular pro- and antioxidants and that oxidative stress may influence the efficacy of cancer treatment. Taken together, these data suggest that dietary changes might modulate oxidative stress and consequently impact the efficacy of therapies used to treat children with cancer. We hypothesize that age-appropriate nutrition may augment oxidative stress induced by chemotherapy and improve patient response to therapy. To address this hypothesis, we commenced a pilot study evaluating the interrelationship between nutrition and oxidative stress in children who are receiving therapy for leukemia. Twenty-four hour dietary recalls were completed and analyzed using the Minnesota Nutrition Data System for Research (NDSR) dietary analysis program to ascertain nutritional information, including caloric intake and dietary antioxidant consumption. Accordingly, the levels of pro- and anti-oxidants in mononuclear cells isolated from peripheral blood were quantified to measure oxidative stress. Levels of the reactive oxygen species (ROS) superoxide and hydrogen peroxide were measured with dihydroethidium (HE) and 2′,7′-dichlorofluorescin diacetate (DCF-DA) staining, respectively. As oxidative stress results from an imbalance of pro- and anti-oxidants, the quantity of the most common cellular antioxidant glutathione (GSH) was also measured by monochlorobimane staining. Assessments of nutrition and oxidative stress were completed for each patient at regularly scheduled intervals over a six month period. The first assessment occurred either before the patient received chemotherapy or during a prolonged break from chemotherapy whereas later assessments were conducted one month, two months, and six months after the patient began or resumed chemotherapy. Consequently, changes in nutrition and oxidative stress were monitored in response to treatment. To date, analyses have been completed for 12 patients. The median age of our patient population at the time of enrollment is 28.5 months. The oldest patient was 53 months at the time of enrollment and the youngest patient was 22 months. Seven patients are male and 6 are female. All subjects are receiving therapy for acute lymphoblastic leukemia (ALL); 7 have been diagnosed with standard risk ALL and 6 have been diagnosed with high risk ALL. Preliminary results show that ROS were increased in mononuclear cells isolated from the majority of subjects during the course of their treatment. An increase was defined as a two-fold or greater elevation in ROS at any subsequent visit compared to the baseline visit. An increase in superoxides was detected in 72.7% of patients (8 of 11). Also, an increase in hydrogen peroxide was detected in 50% of patients (6 of 12). Interestingly, the antioxidant GSH was decreased in mononuclear cells isolated from many of our patients during the course of their treatment. A decrease was defined as a drop in the quantity of GSH at all subsequent visits compared to the baseline visit. A decrease in GSH was seen in 50% of patients (6 of 12) and 33% (4 of 12) demonstrated a decrease in GSH coincident with an increase in both superoxides and hydrogen peroxide. This increase in ROS and decrease in GSH suggests that the majority of our patients experience oxidative stress during therapy. To investigate the impact of diet on oxidant status, NDSR software was used to compare the consumption of dietary antioxidants, such as vitamins A, B3, C, and E, selenium, and glutamic acid, to the corresponding amounts of ROS from the same visit. The strongest correlation was between vitamin C consumption and hydrogen peroxide levels. An inverse relationship between vitamin C consumption and hydrogen peroxide levels was apparent in 58.3% of patients (7 of 12). Though this data is preliminary, our hope is that the findings from this pilot study will begin to illuminate the relationship between diet and oxidative stress in pediatric leukemia patients and justify future work which will aid in devising dietary interventions that will modulate oxidant status to favor improved survival of children with leukemia. Disclosures: No relevant conflicts of interest to declare.


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