Reactive oxygen species inhibitors

Reactive oxygen species inhibitors consisting of curcumin derivatives, (IV), were prepared by Pandol (4) and are used in treating inflammation disorders associated with pancreatitis. 

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). 

That the oxidative burst is directly involved in the chemical defense of these algae is clear. This reaction can be inhibited by diphenyleneiodonium, a suicide inhibitor of NADPH-oxidase which suppresses both the production of reactive oxygen species and the natural resistance to epiphytic bacteria. In addition a role in the defense against endophytes was indicated, since pre-treatment with oligomeric guluronates resulted in decreased infection of L. digitata with the pathogen Laminariocolax tomentosoides [141]. 

Ganguly A, Das B, Roy A, Sen N, Dasgupta SB, Mukhopadhayay S, Majumder HK. (2007) Betulinic acid, a catalytic inhibitor of topoisomerase I, inhibits reactive oxygen species-mediated apoptotic topoisomerase I-DNA cleavable complex formation in prostate cancer cells but does not affect the process of cell death. Cancer Res 67 11848-11858. 

Already in 1982, it was suggested that the intermediate chromium(V) state is involved in the carcinogenic process.9 Reactive Cr(V) and Cr(IV) intermediates may be harmful in many ways acting as tyrosine phosphatase inhibitors, or by forming organic radicals upon reaction with cellular reductants, which in turn can react with O2 and lead to reactive oxygen species.10 Reaction of chromium(VI) with... 

There are specific fiuorescent dyes for specific pathologies created by specific drug classes, such as phospholipidosis from cationic amphiphilic drugs [18, 19], mitochondrial DNA depletion by nucleoside reverse transcriptase inhibitors that also inhibit mitochondrial DNA polymerase gamma and redox cyclers that produce reactive oxygen species. The complex mechanism of statin-induced toxicity is demonstrated vith early sublethal effects on apoptosis, mitochondrial function and calcium homeostasis [20]. 

Several pathophysiological mechanisms have been proposed, including adverse effects of protease inhibitors on hepatocyte and fat cell function (143), mitochondrial toxicity from nucleoside analogues (144), excess of reactive oxygen species (145), and cytokine-mediated events... 

Reactive oxygen species such as the hydroxyl radical, superoxide anion, and peroxynitrite are involved in many cellular processes including the inflammatory response. The best known antiinflammatory compound is ebselen (59, R = Ph). It is shown to be a neuroprotective agent and an inhibitor of free radical-induced apoptosis [20, 248, 249], It has undergone phase III clinical trials and is soon to become the first synthetic organoselenium therapeutic released on the market. 

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