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1.
FEBS Lett ; 492(1-2): 29-32, 2001 Mar 09.
Artigo em Inglês | MEDLINE | ID: mdl-11248231

RESUMO

The free radicals generated from the iron containing system of xanthine oxidase and hypoxanthine (Fe-XO/HX) were directly detected by using spin trapping. It was found that not only superoxide anion (O(2)*-) and hydroxyl radical (OH*), but also alkyl or alkoxyl radicals (R*) were formed when saccharides such as glucose, fructose and sucrose were added into the Fe-XO/HX system. The generated amount of R* was dependent on the kind and concentration of saccharides added into the Fe-XO/HX system and no R* were detected in the absence of saccharides, indicating that there is an interaction between the saccharide molecules and the free radicals generated from the Fe-XO/HX system and saccharide molecules are essential for generating R* in the Fe-XO/HX system. It is expected that the toxicity of R* would be greater than of hydrophilic O(2)*- and OH* because they are liposoluble and their lives are longer and the active sites of biomolecules are closely related with lipophilic phase, thus they can damage cells more seriously than O(2)*- and OH*. The R* generated from the saccharide containing Fe-XO/HX can be effectively scavenged by selenium containing abzyme (Se-abzyme), indicating Se-abzyme is a promising antioxidant.


Assuntos
Radicais Livres/química , Frutose/química , Glucose/química , Hipoxantina/química , Sacarose/química , Xantina Oxidase/química , Animais , Carboidratos/química , Bovinos , Espectroscopia de Ressonância de Spin Eletrônica/métodos , Ferro/química , Mitocôndrias Cardíacas/metabolismo , Óxidos de Nitrogênio/química , Piridinas , Selênio/química
2.
Appl Biochem Biotechnol ; 82(3): 167-73, 1999 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-10813024

RESUMO

Selenium-containing abzyme (m4G3) was prepared and its protection of myocardial mitochondria against oxidative damage was studied using the swelling of mitochondria, quantity of lipid peroxidation products, and change in cytochrome-c oxidase activity as a measure of mitochondrial damage. The results showed that m4G3 could inhibit mitochondrial damage caused by the hypoxanthine-xanthine oxidase system in vitro. Electronic spin resonance (ESR) studies demonstrated that m4G3 could decrease the amount of free radicals generated in the damage system.


Assuntos
Anticorpos Catalíticos/farmacologia , Glutationa Peroxidase/farmacologia , Mitocôndrias Cardíacas/metabolismo , Selênio/farmacologia , Animais , Bovinos , Espectroscopia de Ressonância de Spin Eletrônica , Complexo IV da Cadeia de Transporte de Elétrons/metabolismo , Radicais Livres , Peroxidação de Lipídeos , Malondialdeído/metabolismo , Mitocôndrias Cardíacas/enzimologia , Estresse Oxidativo/efeitos dos fármacos , Fatores de Tempo , Xantina Oxidase/metabolismo
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