Co-administration of Vitamins E and C protects against stress-induced hepatorenal oxidative damage and effectively improves lipid profile at both low and high altitude

The aim of this study was to evaluate the effect of co- administration of vitamins E and C on exhaustive exercise induced-stress in regards to hepatorenal function in rats native to low altitude (LA) and high altitude (HA). In both LA and HA areas, native wistar rats of each area were divided into three groups of 6 rats each, which include stress-free control, forced swimming-induced experimental stress and experimental stress plus vitamins E and C treatment. Lipid profile and Liver and kidney functions were assessed in both groups. HA and LA rats exhibit similar baseline levels of liver and kidney function as well as lipid metabolism profiles. However, HA rats showed decreased levels of antioxidant markers with an increased level of lipid peroxidation. Exhaustive swimming exercise induced a significant increase in the liver and kidney function of rats at both altitudes accompanied with a decrease in antioxidants levels. However, the magnitude of change observed in HA rats was more profound. Also at LA, forced swimming exercise resulted in a significant increase in serum total cholesterol (TChol), triacylglycerides (TAG) and high-density lipoprotein cholesterol (HDL). However, in HA rats, forced swimming exercise caused a significant decrease in serum TChol and low-density lipoprotein (LDL), except for HDL levels which were significantly elevated. Pre- and co-administration of vitamins E and C counteracted the induction of liver and/or kidney function by exhaustive exercise, and lowered TChol and LDL levels in rats at either altitude. In conclusion, at native high altitude: kidney and liver function essentially remained stable; response to stress included more profound oxidative damage to liver and kidney tissues as well as augmented deterioration in lipid metabolism compared to low altitude; and combined administration of vitamins E and C protected against observed oxidative stress damage to liver and kidney tissues and preserved lipid metabolism. At low altitude, combined administration of vitamin E and C protected against stress-induced oxidative damage to the liver and kidney and did preserve normal lipid metabolism, except for HDL. These novel findings reveal the pathophysiological changes in the liver function, kidney function and lipid metabolism occurring at high altitude specifically under stress, and demonstrate the efficacy of combined supplementation of vitamins E and C to normalize these changes.Key words: Exercise, oxidative stress, vitamin E, vitamin C, altitude, rats

Complications of diabetes: an unsolicited epigenetic memory

Diabetes is a multifactorial disease, characterized by hyperglycemia and insulin resistance. Diabetic microvascular end points such as retinopathy, cardiomyopathy and nephropathy; and macrovascular complications such as myocardial infarction and strokes, causing premature death in diabetic populations. Despite strong familial clustering is associated with diabetes, the essential role of epigenetic component in the development of diabetes and its complications is inevitable. Several clinical trials and experimental animal studies show the persistence of diabetic vascular complications even after the normalization of glucose in diabetic patients, indicating the role of epigenetic or metabolic memory. Although previous researches on diabetes implicated the role of reactive oxygen species in the pathogenesis and development of diabetic complications, lifestyle factors including diet and exercise and environmental factors are strongly associated in inducing epigenetic changes related to diabetic risk

Crataegus Aronia protects and reverses vascular inflammation in a high fat diet rat model by an antioxidant mechanism and modulating serum levels of oxidized low-density lipoprotein

Context: Crataegus aronia (Willd.) Bosc (Rosaceae) (syn. Azarolus L) is traditionally used to treat cardiovascular disorders. Objectives: To investigate C. aronia protection against a high-fat diet (HFD)-induced vascular inflammation in rats. Materials and methods: Wistar Male rats (180–220 g) were divided (n = 10/group) as control fed a standard diet (STD), STD + C. aronia (200 mg/kg, orally), HFD, HFD + C. aronia and HFD post-treated with C. aronia. Simvastatin (20 mg/kg) was co- or post-administered as a positive control drug. HFD was given for 8 weeks, and all other treatments were administered for 4 weeks. Results: Most significantly, co-administration of C. aronia to HFD-fed rats reduced the thickness of aorta tunica media (90 ± 5 vs. 160 ± 11.3 µm) and adventitia (54.3 ± 3.8 vs. 93.6 ± 9.4 µm). It also lowered protein levels of TNF-α (0.51 ± 0.15 and 0.15 ± 0.16 vs. 0.1 ± 0.09%) and IL-6 (0.52 ± 0.19 vs. 1.0 ± 0.2%) in their aorta or serum (5.9 ± 0.91 vs. 12.98 ± 1.3 ng/mL and 78.1 ± 6.7 vs. 439 ± 78 pg/mL, respectively). It also lowered all serum lipids and increased aorta levels of GSH levels (70.4 ± 4.0 vs. 40.7 µM) and activity of SOD (5.7 ± 0.7 vs. 2.9 ± 0.6 U/mg) and decreased serum levels of ox-LDL-c (566.7 ± 46 vs. 1817 ± 147 ng/mL). Such effects were more profound than all other treatments. Conclusions: C. aronia inhibits the HFD-induced vascular inflammation and its use in clinical trials is recommended

Nutrition, Physical Activity, and Gender Risks for Adolescent Obesity in Southwestern Saudi Arabia

Background/Aim: The aim of the study was to investigate gender differences in obesity and related behavior among adolescent school boys and girls in southwestern Saudi Arabia. Patients and Methods: A cross-sectional study on a stratified sample of 1,249 adolescent boys and 620 adolescent girls, was conducted in southwestern Saudi Arabia. They were interviewed and examined for weight and height using standardized techniques. Results: The prevalence of obesity and overweight in the present study amounted to 23.2% among boys and 29.4% among girls. The following significant risk factors were identified; being a female [adjusted odds ratio (aOR) =1.372, 95% confidence interval (CI) =1.099-1.753] and lack of class physical exercise (aOR =1.452, 95% CI =1.149-2.117). Conclusion: Obesity among adolescents is a public health problem in Southwestern Saudi Arabia. The problem is more prevalent among girls. Thus, there is a need for a national programme in the country to prevent and control obesity among adolescents

Curcumin attenuates doxorubicin-induced cardiotoxicity via suppressing oxidative Stress, preventing inflammation and apoptosis: Ultrastructural and computational approaches

Currently, doxorubicin (DOX) is one of the medications commonly used in chemotherapy to treat different types of tumors.Nonetheless, despite being effective in multiple tumors, yet its use is limited owing to its cytotoxic effects, the therapeutic use of DOX has been limited. This work aimed to explore whether curcumin (CMN) can prevents DOX-induced cardiotoxicity in rats. Four groups of rats were created, with the first functioning as a control, while the second group received CMN. DOX alone was administered to the third group, whereas CMN and DOX were administered to the fourth group. Lipid peroxidation assessed as Malondialdehyde (MDA), aspartate aminotransferase (AST), alanine aminotransferase (ALT), oxidative stress markers as catalase (CAT), superoxide dismutase (SOD), and inflammatory markers as tumor necrosis factor-alpha (TNF-α) in heart homogenates, each one was assessed. Heart specimens was investigated histologically and ultrastructurally. Increased, AST, and ALT serum levels, increased MDA levels, decreased SOD and CAT levels, and increased TNF-α concentrations in heart homogenates were all signs of DOX-induced myocardial injury. Histological and ultrastructural examinations revealed vacuoles and larger, swollen mitochondria in the cytoplasm. Furthermore, DOX caused significant changes in the myocardium, most notably nuclei disintegration, myofibrillar loss, and myocyte vacuolization. Using CMN with DOX reduced the harmful consequences of DOX on the myocardium by returning the increased AST and ALT levels to their original levels as compared to the control and reducing them. In cardiac tissue, CMN significantly increased the concentrations of SOD and CAT and significantly decreased the concentrations of MDA and TNF-α. Biochemical and histological studies have demonstrated that CMN has a heart-protective effect that might be related to its antioxidant and anti-inflammatory capabilities

Metformin ameliorates ROS-p53-collagen axis of fibrosis and dyslipidemia in type 2 diabetes mellitus-induced left ventricular injury

Background: The link between oxidative stress (ROS), apoptosis (p53) and fibrosis (collagen) in type 2 diabetes mellitus (T2DM)-induced cardiac injury in the presence and absence of the antidiabetic drug, metformin has not been investigated before. Material and methods: T2DM was induced in rats by a combination of high carbohydrate and fat diets (HCFD) and streptozotocin (50 mg/kg) injection. The protection group started metformin (200 mg/kg) treatment 14 days prior to the induction of diabetes and continued on metformin and HCFD until being sacrificed at week 12. Results: Diabetes significantly induced blood levels of ROS and left ventricular p53 and collagen expression that was inhibited by metformin. Metformin also significantly reduced glycated haemoglobin and dyslipidemia induced by diabetes. In addition, a significant correlation between ROS-p53-collagen axis and glycaemia and hyperlipidaemia was observed. Conclusions: These findings show that metformin provides substantial protection against diabetic cardiomyopathy-induced ROS-p53 mediated fibrosis and dyslipidemia.</p

Metformin ameliorates ROS-p53-collagen axis of fibrosis and dyslipidemia in type 2 diabetes mellitus-induced left ventricular injury

Background: The link between oxidative stress (ROS), apoptosis (p53) and fibrosis (collagen) in type 2 diabetes mellitus (T2DM)-induced cardiac injury in the presence and absence of the antidiabetic drug, metformin has not been investigated before. Material and methods: T2DM was induced in rats by a combination of high carbohydrate and fat diets (HCFD) and streptozotocin (50 mg/kg) injection. The protection group started metformin (200 mg/kg) treatment 14 days prior to the induction of diabetes and continued on metformin and HCFD until being sacrificed at week 12. Results: Diabetes significantly induced blood levels of ROS and left ventricular p53 and collagen expression that was inhibited by metformin. Metformin also significantly reduced glycated haemoglobin and dyslipidemia induced by diabetes. In addition, a significant correlation between ROS-p53-collagen axis and glycaemia and hyperlipidaemia was observed. Conclusions: These findings show that metformin provides substantial protection against diabetic cardiomyopathy-induced ROS-p53 mediated fibrosis and dyslipidemia.</p