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1.
CNS Neurosci Ther ; 18(10): 811-8, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22934841

ABSTRACT

AIMS: Manganese superoxide dismutase (MnSOD), one of the most crucial antioxidant enzymes in the central nervous system, is thought to be one of the major mechanisms by which cells counteract the injuries of reactive oxygen species after cerebral ischemia. In this study, we used a novel synthesized compound (MnTm4PyP) with highly effective superoxide dismutase activity to study the therapeutic potential of MnSOD and the possible underlying mechanisms in cerebral ischemia. METHODS: Primary cultured cortical neurons were used to examine the protective effect of the compounds. Mice with middle cerebral artery occlusion were used as ischemic stroke animal model. Animals were pretreated with MnTm4PyP intravenously 30 min before surgery. At 24 h after surgery, neurological behavior and histological function were observed. Infarcted cortex tissues and cultured neurons were collected for investigation of the oxidative stress signaling pathways. RESULTS: In vitro studies revealed that MnSOD mimic MnTm4PyP pretreatment significantly increased viability of neurons after injury by H(2) O(2) . Intracellular superoxide radical levels were eliminated. In vivo experiments demonstrated MnTm4PyP pretreatment reduced infarct volume and improved neurological function. The MnSOD mimic alleviated oxidative stress and apoptosis. CONCLUSION: MnSOD is an effective therapeutic target in ischemic stroke prevention because of its antioxidant effects and oxidative stress regulation.


Subject(s)
Chlorophyll/therapeutic use , Infarction, Middle Cerebral Artery/complications , Infarction, Middle Cerebral Artery/prevention & control , Neuroprotective Agents/therapeutic use , Oxidative Stress/physiology , Superoxide Dismutase/chemistry , Animals , Brain Infarction/etiology , Brain Infarction/prevention & control , Calcium/metabolism , Cell Survival/drug effects , Cells, Cultured , Cerebral Cortex/cytology , Chlorophyll/chemistry , Cyclic AMP Response Element-Binding Protein/metabolism , Disease Models, Animal , Embryo, Mammalian , Endoplasmic Reticulum Chaperone BiP , Gene Expression Regulation/drug effects , Heat-Shock Proteins/metabolism , Hydrogen Peroxide/metabolism , Male , Mice , Mice, Inbred C57BL , Nervous System Diseases/drug therapy , Nervous System Diseases/etiology , Neurons/drug effects , Neurons/metabolism , Neuroprotective Agents/chemistry , Oxygen Compounds/metabolism , Superoxide Dismutase/metabolism , Transcription Factor CHOP/metabolism
3.
Water Sci Technol ; 55(6): 39-46, 2007.
Article in English | MEDLINE | ID: mdl-17486833

ABSTRACT

The hot acid hydrolysis followed by chlorine dioxide (A/D*) and hot chlorine dioxide (D*) technologies have proven very useful for bleaching of eucalyptus kraft pulp. Although the characteristics and biodegradability of effluents from conventional chlorine dioxide bleaching are well known, such information is not yet available for effluents derived from hot acid hydrolysis and hot chorine dioxide bleaching. This study discusses the characteristics and biodegradability of such effluents. Combined whole effluents from the complete sequences DEpD, D*EpD, A/D*EpD and ADEpD, and from the pre-bleaching sequences DEp, D*Ep, A/D*Ep and ADEp were characterized by quantifying their colour, AOX and organic load (BOD, COD, TOC). These effluents were also evaluated for their treatability by simulation of an activated sludge system. It was concluded that treatment in the laboratory sequencing batch reactor was efficient for removal of COD, BOD and TOC of all effluents. However, colour increased after biological treatment, with the greatest increase found for the effluent produced using the AD technology. Biological treatment was less efficient at removing AOX of effluents from the sequences with D*, A/D* and AD as the first stages, when compared to the reference D stage; there was evidence of the lower treatability of these organochlorine compounds from these sequences.


Subject(s)
Acids/chemistry , Chlorine Compounds/chemistry , Hot Temperature , Industrial Waste , Oxides/chemistry , Waste Disposal, Fluid/methods , Water Pollutants, Chemical/isolation & purification , Biodegradation, Environmental , Bioreactors , Coloring Agents/isolation & purification , Eucalyptus/chemistry , Hydrocarbons, Chlorinated/chemistry , Hydrocarbons, Chlorinated/metabolism , Hydrolysis , Oxygen Compounds/chemistry , Oxygen Compounds/metabolism , Paper , Reference Standards
4.
Cell Transplant ; 14(7): 441-8, 2005.
Article in English | MEDLINE | ID: mdl-16285252

ABSTRACT

One impediment for a wider application of islet transplantation is the limited number of donor pancreata for islet isolation. A more efficient utilization of available organs could in part alleviate this problem. Perfluorocarbons (PFCs) have a high oxygen solubility coefficient and maintain high oxygen partial pressures for extended time. They serve also as oxygen "reservoirs" for harvested organs in pancreas organ transplantation. The aim of this study was to test whether the use of PFCs could also be beneficial for the secretory activity and overall viability of cultured purified islets before transplantation. Purified rat islets were cultured in static conditions with or without oxygen-saturated PFCs for 1 or 7 days. Cell death and apoptosis were assessed by trypan blue staining, DNA strand breaks, and caspase 3/7 activity. mRNA levels of insulin and ICA512/IA-2, a membrane marker of secretory granules (SGs), were quantitated by real-time PCR, whereas insulin content and secretion were measured by RIA. Polypyrimidine tract binding protein (PTB), which promotes SG biogenesis, was assessed by Western blotting. The number of SGs and the ultrastructural appearance of beta5-cells were analyzed by cryoimmunoelectronmicroscopy for insulin. Various parameters, including caspase activity, insulin and ICA512/IA-2 mRNA levels, PTB expression, number of secretory granules, and ultrastructural appearance did not significantly differ between control and PFC-cultured islets. On the other hand, PFC culture islets showed significantly increased DNA fragmentation and a reduced insulin stimulation index at both time points compared to control islets. While advantageous for the transport of human harvested organs, the use of PFH in the culture may be comparable to and/or not provide advantage over conventional protocols for culture of islets for transplantation.


Subject(s)
DNA/analysis , Fluorocarbons/pharmacology , Islets of Langerhans/drug effects , Oxygen Compounds/pharmacology , Animals , Cell Survival/drug effects , Cells, Cultured , Female , Fluorocarbons/metabolism , Gene Expression , Insulin/biosynthesis , Insulin-Secreting Cells/ultrastructure , Islets of Langerhans/chemistry , Oxygen Compounds/metabolism , Rats , Rats, Inbred BB
5.
Artif Organs ; 28(9): 795-9, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15320942

ABSTRACT

This article briefly discusses a few key issues related to transfusion, the concept of hemoglobin-based red blood cell substitutes (HBOCs), and some parameters useful in evaluating the current properties of solutions. Potential uses of HBOCs in civilian applications are identified and listed. Use of HBOCs as a hemodiluent for intraoperative autologous blood donation (IAD) is a particular application that has relevance in many surgical settings and this is discussed in some detail. Data from a Phase III clinical trial is presented to show the potential for avoiding the use of allogeneic blood and blood products in a clinical model of large volume red cell use. Extrapolation to a general use model, primarily based in the potential for surgery, will be noted. Some general parametric values of HBOCs are presented. These values are by no means considered optimal for all HBOCs and are subject to exploration, fine tuning, correction, or even rejection.


Subject(s)
Blood Substitutes/therapeutic use , Erythrocyte Transfusion , Hemoglobins/metabolism , Oxygen Compounds/administration & dosage , Clinical Trials, Phase III as Topic , Erythrocyte Transfusion/methods , Humans , Oxygen Compounds/metabolism
6.
J Nutr Sci Vitaminol (Tokyo) ; 49(4): 217-20, 2003 Aug.
Article in English | MEDLINE | ID: mdl-14598906

ABSTRACT

The antioxidant activities of natural d-alpha-tocopherol, mixed tocopherols and tocotrienols, and formulations comprising all forms of vitamin E, providing 400 IU, were determined employing an improved oxygen radical absorbance capacity (ORAC) assay using fluorescein (FL) as the fluorescent probe, randomly methylated beta-cyclodextrin (RMCD), 2,2'-azobis(2-amidino-propane)dihydrochloride (AAPH) as the peroxyl radical generator, and Trolox as the standard in 75 mM phosphate buffer. The antioxidant activities, expressed in micromol Trolox equivalent per gram, of d-alpha-tocopherol (87%), mixed tocopherols (70%), and tocotrienols (30%) were found to be 1,293, 1,948, and 1,229, respectively. Some of the vitamin E formulations showed antioxidant activities superior to d-alpha-tocopherol.


Subject(s)
Antioxidants/metabolism , Oxygen Compounds/metabolism , Vitamin E/metabolism , Amidines/metabolism , Antioxidants/analysis , Chromans/metabolism , Cyclodextrins/metabolism , Fluorescein/analysis , Free Radicals/metabolism , Humans , Indicators and Reagents , Peroxides/metabolism , Tocopherols/chemistry , Tocopherols/metabolism , Tocotrienols/chemistry , Tocotrienols/metabolism , Vitamin E/analogs & derivatives , Vitamin E/chemistry
8.
Zh Mikrobiol Epidemiol Immunobiol ; (4 Suppl): 65-71, 2000.
Article in Russian | MEDLINE | ID: mdl-12712517

ABSTRACT

The review deals with the analysis of the properties of active forms of oxygen (AFO), generated by phagocytic cells, and their role in the development of a number of human diseases. Bacterial and viral infections contribute to the activation of the oxidizing metabolism of phagocytes. In the process of this metabolism the formation of toxic oxygen and nitrogen metabolites occurs. The defect of the system of activation calls prolonged microbial persistence whose most severe manifestation is chronic granulomatosis. On the contrary, the uncontrolled production of oxidants cause tissue lesions. The role of AFO in the pathogenesis of cardiovascular diseases, peptic ulcer, the syndrome of respiratory insufficiency and bronchial asthma is discussed.


Subject(s)
Oxygen/metabolism , Phagocytes/metabolism , Reactive Oxygen Species/metabolism , Asthma/etiology , Asthma/pathology , Bacterial Infections/metabolism , Cardiovascular Diseases/etiology , Cardiovascular Diseases/pathology , Free Radicals , Granulomatous Disease, Chronic/etiology , Granulomatous Disease, Chronic/pathology , Humans , Nitro Compounds/metabolism , Nitro Compounds/toxicity , Oxidants/metabolism , Oxygen Compounds/metabolism , Oxygen Compounds/toxicity , Peptic Ulcer/etiology , Peptic Ulcer/pathology , Respiratory Insufficiency/etiology , Respiratory Insufficiency/pathology , Virus Diseases/metabolism
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