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Reactive oxygen species peroxidation

One of the important consequences of neuronal stimulation is increased neuronal aerobic metabolism which produces reactive oxygen species (ROS). ROS can oxidize several biomoiecules (carbohydrates, DNA, lipids, and proteins). Thus, even oxygen, which is essential for aerobic life, may be potentially toxic to cells. Addition of one electron to molecular oxygen (O,) generates a free radical [O2)) the superoxide anion. This is converted through activation of an enzyme, superoxide dismurase, to hydrogen peroxide (H-iO,), which is, in turn, the source of the hydroxyl radical (OH). Usually catalase... [Pg.280]

Azelaic acid is effective on P. acnes suppression, even if less than benzoyl peroxide. The anti-inflammatory effect of azelaic acid seems to be related to a decreased production of reactive oxygen species by neutrophils. Azelaic acid may also regulate the ductal cell keratinization, reducing the number of comedones, ft is not sebosuppressive. [Pg.124]

In the last few decades, several epidemiological studies have shown that a dietary intake of foods rich in natural antioxidants correlates with reduced risk of coronary heart disease particularly, a negative association between consumption of polyphenol-rich foods and cardiovascular diseases has been demonstrated. This association has been partially explained on the basis of the fact that polyphenols interrupt lipid peroxidation induced by reactive oxygen species (ROS). A large body of studies has shown that oxidative modification of the low-density fraction of lipoprotein (LDL) is implicated... [Pg.5]

Glutathione-peroxidase (GSH-Pxase) is an enzyme found in erythroqrtes and other tissues that has an essential selenocysteine residue involved in the catalytic decomposition of reactive oxygen species. In the erythrocyte, hydrogen peroxide is the principle reactive oxygen species available. [Pg.300]

At the present time it is difficult to single out any one factor that could be held ultimately responsible for cell death after cerebral ischaemia. Recent studies, however, have provided us with sufficient evidence to conclude that free radical damage is at least one component in a chain of events that leads to cell death in ischaemia/reperfiision injury. As noted earlier in this review, much of the evidence for free radicals in the brain and the sources of free radicals come from studies in animals subjected to cerebral ischaemia. Perhaps the best evidence for a role for free radicals or reactive oxygen species in cerebral ischaemia is derived from studies that demonstrate protective effects of antioxidants. Antioxidants and inhibitors of lipid peroxidation have been shown to have profound protective effects in models of cerebral ischaemia. Details of some of these studies will be mentioned later. Several reviews have been written on the role of oxygen radicals in cerebral ischaemia (Braughler and HaU, 1989 Hall and Btaughler, 1989 Kontos, 1989 Floyd, 1990 Nelson ef /., 1992 Panetta and Clemens, 1993). [Pg.77]

Lipid peroxidation (see Fig. 17.2) is a chain reaction that can be attacked in many ways. The chain reaction can be inhibited by use of radical scavengers (chain termination). Initiation of the chain reaction can be blocked by either inhibiting synthesis. of reactive oxygen species (ROS) or by use of antioxidant enzymes like superoxide dismutase (SOD), complexes of SOD and catalase. Finally, agents that chelate iron can remove free iron and thus reduce Flaber-Weiss-mediated iron/oxygen injury. [Pg.263]

Different mechanisms to explain the disinfection ability of photocatalysts have been proposed [136]. One of the first studies of Escherichia coli inactivation by photocatalytic Ti02 action suggested the lipid peroxidation reaction as the mechanism of bacterial death [137]. A recent study indicated that both degradation of formaldehyde and inactivation of E. coli depended on the amount of reactive oxygen species formed under irradiation [138]. The action with which viruses and bacteria are inactivated by Ti02 photocatalysts seems to involve various species, namely free hydroxyl radicals in the bulk solution for the former and free and surface-bound hydroxyl radicals and other oxygen reactive species for the latter [139]. Different factors were taken into account in a study of E. coli inactivation in addition to the presence of the photocatalyst treatment with H202, which enhanced the inactivation... [Pg.106]

The cholinesterase activity is determined in the presence of alllelochemicals-alkaloids (Fig. 4) and reactive oxygen species ozone and peroxides (Table 1). [Pg.158]

Figure 28.19 The cleavage reaction of FeBABE involves a catalytic process using peroxide and ascorbate to form reactive oxygen species. Any protein structure in the immediate vicinity of the FeBABE label on the bait protein will undergo peptide bond cleavage. Figure 28.19 The cleavage reaction of FeBABE involves a catalytic process using peroxide and ascorbate to form reactive oxygen species. Any protein structure in the immediate vicinity of the FeBABE label on the bait protein will undergo peptide bond cleavage.
The use of hydrogen peroxide as an oxidant is not compatible with the operation of a biocatalytic fuel cell in vivo, because of low levels of peroxide available, and the toxicity associated with this reactive oxygen species. In addition peroxide reduction cannot be used in a membraneless system as it could well be oxidized at the anode. Nevertheless, some elegant approaches to biocatalytic fuel cell electrode configuration have been demonstrated using peroxidases as the biocatalyst and will be briefly reviewed here. [Pg.413]

As the superoxide radical is a precursor of the other reactive oxygen species and interacts with blood plasma components under physiological and pathological conditions as well, systems related to its generation are biologically relevant. It should be noted, however, that with respect to the initiation of lipid peroxidation as one of the main causes of oxidative cell damage, its own reactivity is very weak and that only in protonized form is its toxicity comparable to that of lipid peroxyl radicals [18]. [Pg.501]

The formation of hydroxyl or hydroxyl-like radicals in the reaction of ferrous ions with hydrogen peroxide (the Fenton reaction) is usually considered as a main mechanism of free radical damage. However, Qian and Buettner [172] have recently proposed that at high [02]/ [H202] ratios the formation of reactive oxygen species such as perferryl ion at the oxidation of ferrous ions by dioxygen (Reaction 46) may compete with the Fenton reaction (2) ... [Pg.708]


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See also in sourсe #XX -- [ Pg.26 , Pg.28 ]




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Oxygen peroxide species

Oxygen peroxides

Oxygen species

Oxygenated species

Peroxide species

Reactive oxygen

Reactive oxygen reactivity

Reactive oxygen species

Reactive species

Reactive species reactivity

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