RESUMO
When respiring rat liver mitochondria are incubated in the presence of Fe(III) gluconate, their DNA (mtDNA) relaxes from the supercoiled to the open circular form dependent on the iron dose. Anaerobiosis or antioxidants fail to completely inhibit the unwinding. High-resolution field-emission in-lens scanning electron microscopy imaging, in concert with backscattered electron detection, pinpoints nanometer-range iron colloids bound to mtDNA isolated from iron-exposed mitochondria. High-resolution field-emission in-lens scanning electron microscopy with backscattered electron detection imaging permits simultaneous detailed visual analysis of DNA topology, iron dose-dependent mtDNA unwinding, and assessment of iron colloid formation on mtDNA strands.
Assuntos
DNA Mitocondrial/ultraestrutura , Ferro/farmacologia , Conformação de Ácido Nucleico/efeitos dos fármacos , Animais , DNA Circular/ultraestrutura , DNA Mitocondrial/efeitos dos fármacos , DNA Mitocondrial/isolamento & purificação , Feminino , Microscopia Eletrônica de Varredura/métodos , Mitocôndrias Hepáticas/metabolismo , Plasmídeos/efeitos dos fármacos , Plasmídeos/ultraestrutura , Ratos , Ratos WistarRESUMO
Reactive oxygen species (ROS: superoxide radical, O2.-; hydrogen peroxide, H2O2; hydroxyl radical, OH.), which arise from the univalent reduction of dioxygen are formed in mitochondria. We summarize here results which indicate that ROS, and also the radical nitrogen monoxide ('nitric oxide', NO), act as physiological modulators of some mitochondrial functions, but may also damage mitochondria. Hydrogen peroxide, which originates in mitochondria predominantly from the dismutation of superoxide, causes oxidation of mitochondrial pyridine nucleotides and thereby stimulates a specific Ca2+ release from intact mitochondria. This release is prevented by cyclosporin A (CSA). Hydrogen peroxide thus contributes to the maintenance of cellular Ca2+ homeostasis. A stimulation of mitochondrial ROS production followed by an enhanced Ca2+ release and re uptake (Ca2+ 'cycling') by mitochondria causes apoptosis and necrosis, and contributes to hypoxia/reperfusion injury. These kinds of cell injury can be attenuated at the mitochondrial level by CSA. When ROS are produced in excessive amounts in mitochondria nucleic acids, proteins, and lipids are extensively modified by oxidation. Physiological (sub-micromolar) concentrations of NO potently and reversibly deenergize mitochondria at oxygen tensions that prevail in cells by transiently binding to cytochrome oxidase. This is paralleled by mitochondrial Ca2+ release and uptake. Higher NO concentrations or prolonged exposure of cells to NO causes their death. It is concluded that ROS and NO are important physiological reactants in mitochondria and become toxic only when present in excessive amounts.
Assuntos
Doença , Mitocôndrias/metabolismo , Óxido Nítrico/fisiologia , Oxidantes/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Animais , Apoptose , Cálcio/metabolismo , Sobrevivência Celular/efeitos dos fármacos , Glutationa/análogos & derivados , Glutationa/farmacologia , Humanos , Fígado/citologia , Fígado/efeitos dos fármacos , Compostos Nitrosos/farmacologia , Estresse Oxidativo , Valores de Referência , S-NitrosoglutationaRESUMO
A new laser configuration has been devised utilizing a mercury mirror as one reflector. When the laser is oriented vertically, lasing occurs. This beam can thus be used for the precision alignment of vertical structures.