ABSTRACT
Although the pathogenesis of ischemia reperfusion (IR) injury is based on complex mechanisms, free radicals play a central role. We evaluated membrane fluidity and lipid peroxidation during pancreas transplantation (PT) performed in 12 pigs (six donors and six recipients). Fluidity was measured by fluorescence spectroscopy, and malondialdehyde (MDA) and 4-hydroxyalkenals (4-HDA) concentrations were used as an index of lipid oxidation. Pancreatic tissues were collected as follows: (A) donor, immediately before vascular clamping; (B) graft, following perfusion lavage with University of Wisconsin preservation fluid; (C) graft, after 16 h of cold ischemia; and (D) recipient, 30 min vascular postreperfusion. Fluidity and MDA and 4-HDA concentrations were similar in cases A, B, and C. However, there was significant membrane rigidity and increased lipid peroxidation after reperfusion (D). These findings suggest that reperfusion exaggerates oxidative damage and may account for the rigidity in the membranes of allografts during PT.
Subject(s)
Lipid Peroxidation , Membrane Fluidity , Pancreas Transplantation , Pancreas/metabolism , Reperfusion Injury/metabolism , Animals , Female , Malondialdehyde/metabolism , Microscopy, Fluorescence/methods , Pancreas/pathology , Reperfusion Injury/pathology , Swine , Transplantation, HomologousABSTRACT
Antioxidant defences are essential for cellular redox regulation. Since free-radical production may be enhanced by physical activity, herein, we evaluated the effect of acute exercise on total antioxidant status (TAS) and the plasma activities of catalase, glutathione reductase, glutathione peroxidase, and superoxide dismutase and its possible relation to oxidative stress resulting from exercise. Healthy untrained male subjects (n = 34) performed three cycloergometric tests, including maximal and submaximal episodes. Venous blood samples were collected before and immediately after each different exercise. TAS and enzyme activities were assessed by spectrophotometry. An increase of the antioxidant enzyme activities in plasma was detected after both maximal and submaximal exercise periods. Moreover, under our experimental conditions, exercise also led to an augmentation of TAS levels. These findings are consistent with the idea that acute exercise may play a beneficial role because of its ability to increase antioxidant defense mechanisms through a redox sensitive pathway.
Subject(s)
Antioxidants/metabolism , Exercise/physiology , Oxidative Stress/physiology , Oxidoreductases/blood , Adult , Analysis of Variance , Antioxidants/analysis , Exercise Test , Humans , MaleABSTRACT
The protective in vivo effects of melatonin or pinoline on carbon tetrachloride (CCl(4))-induced oxidative damage were investigated in liver of rats and compared to rats injected only with CCl(4) (5 mL/kg body weight). Hepatic cell membrane fluidity, monitored using fluorescence spectroscopy, exhibited a significant decrease in animals exposed to CCl(4) compared to control rats. Increases in lipid and protein oxidation, as assessed by concentrations of malondialdehyde (MDA) and 4-hydroxyalkenals (4-HDA), and protein carbonylation, respectively, were also seen in hepatic homogenates of animals exposed to CCl(4). The administration of melatonin (10 mg/kg body weight) or pinoline injected 30 min before and 1 hr after CCl(4), fully prevented membrane rigidity and protein oxidation. However, treatment with melatonin was more effective in terms of reducing lipid peroxidation than pinoline, as the increases in MDA+4-HDA levels because of CCl(4) were reduced by 93.4% and 34.4% for melatonin or pinoline, respectively. Livers from CCl(4)-injected rats showed several histopathological alterations; above all, there were signs of necrosis and ballooning degeneration. The concurrent administration of melatonin or pinoline reduced the severity of these morphological changes. On the basis of the biochemical and histopathological findings, we conclude that both melatonin and pinoline were highly effective in protecting the liver against oxidative damage and membrane rigidity because of CCl(4). Therefore, these indoles may be useful as cotreatments for patients with hepatic intoxication induced by CCl(4).
Subject(s)
Carbolines/pharmacology , Carbon Tetrachloride Poisoning/drug therapy , Carbon Tetrachloride/toxicity , Chemical and Drug Induced Liver Injury/drug therapy , Liver/drug effects , Melatonin/pharmacology , Oxidative Stress/drug effects , Animals , Carbon Tetrachloride Poisoning/metabolism , Carbon Tetrachloride Poisoning/pathology , Chemical and Drug Induced Liver Injury/metabolism , Chemical and Drug Induced Liver Injury/pathology , Histocytochemistry , Lipid Peroxidation/drug effects , Liver/metabolism , Male , Malondialdehyde/metabolism , Membrane Fluidity/drug effects , Photomicrography , Protein Carbonylation/drug effects , Rats , Rats, Sprague-DawleyABSTRACT
No disponible
Subject(s)
Humans , Synaptosomes , Melatonin , Pineal Gland/physiology , Oxidative Stress/physiology , Free RadicalsABSTRACT
No disponible
Subject(s)
Humans , Lipid Peroxidation/physiology , Central Nervous System Neoplasms/physiopathology , Brain Neoplasms/physiopathologyABSTRACT
No disponible
