Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Peroxide various, toxicity

Studies carried out with complete cells in vivo, cell membranes and other cell fractions point to the selective oxidation of phosphatidylserine (26) to a hydroperoxide (PS-OOH) on oxidative stress caused by toxic agents such as H2O2, t-BuOOH and cumyl hydroperoxide (27). Formation of PS-OOH is observed during apoptosis. These phenomena are important because of the cytotoxic effects of various peroxides used in commercial products coming into direct contact with the human body, as is the case of epidermal keratinocytes in contact with cosmetic formulations" ". The toxic effects of f-BuOOH are associated with vasoconstriction and damage to the vascular smooth muscles ". Global determination methods for primary lipid oxidation products are discussed in Section IV.B. [Pg.613]

Increase of free cytosolic calcium is toxic for various reasons. Among them are the diminution of ATP levels (Tsuji et al. 1994), the protease and lipase activation, and the FR production that causes a peroxidation of lipids. The inflow of calcium in the terminals could also increase the release of endogenous excitatory amino acids and propagate neuronal damage through positive feedback (Choi and Hartley 1993). Glutamic neurotoxicity mediated by calcium follows three stages ... [Pg.510]

Figure 6.10 Production of various reactive oxygen species, the role in tissue damage, and their detoxication and toxication. Reactive species shown are hydrogen peroxide, superoxide, and hydroxyl radical. Figure 6.10 Production of various reactive oxygen species, the role in tissue damage, and their detoxication and toxication. Reactive species shown are hydrogen peroxide, superoxide, and hydroxyl radical.
The cellular injury, which underlies target organ toxicity, may result from various underlying events primary, secondary, and tertiary events. Primary events result from initial damage, for example, lipid peroxidation, enzyme inhibition, covalent binding to crucial macromolecules, ischemia, and changes in thiol status. [Pg.283]

Carbon tetrachloride causes centrilobular liver necrosis and steatosis after acute exposure, and liver cirrhosis, liver tumors, and kidney damage after chronic administration. The mechanism underlying the acute toxicity to the liver involves metabolic activation by cytochrome P-450 to yield a free radical (trichloromethyl free radical). This reacts with unsaturated fatty acids in the membranes of organelles and leads to toxic products of lipid peroxidation including malondialdehyde and hydroxynonenal. This results in hepatocyte necrosis and inhibition of various metabolic processes including protein synthesis. The latter leads to steatosis as a result of inhibition of the synthesis of lipoproteins required for triglyceride export. [Pg.432]

Top) Toxicity of various resveratrol concentrations against Salmonella typhimurium tester strain TA-102 in a histidine-containing medium. (Bottom) Antimutagenic effect of resveratrol concentrations in a modified Ames test employing strain TA-102 and hydrogen peroxide. [Pg.151]


See other pages where Peroxide various, toxicity is mentioned: [Pg.244]    [Pg.363]    [Pg.244]    [Pg.130]    [Pg.504]    [Pg.731]    [Pg.271]    [Pg.1061]    [Pg.416]    [Pg.80]    [Pg.237]    [Pg.249]    [Pg.54]    [Pg.417]    [Pg.1161]    [Pg.1163]    [Pg.1164]    [Pg.75]    [Pg.445]    [Pg.346]    [Pg.58]    [Pg.160]    [Pg.485]    [Pg.613]    [Pg.746]    [Pg.747]    [Pg.508]    [Pg.1161]    [Pg.1164]    [Pg.485]    [Pg.613]    [Pg.613]    [Pg.614]    [Pg.746]    [Pg.747]    [Pg.272]    [Pg.310]    [Pg.22]    [Pg.148]    [Pg.1193]    [Pg.58]    [Pg.246]    [Pg.14]    [Pg.488]   
See also in sourсe #XX -- [ Pg.83 ]




SEARCH



Peroxides toxicity

© 2024 chempedia.info