2011
DOI: 10.1134/s0006350911030171
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Redox regulation of cellular processes: A biophysical model and experiment

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Cited by 9 publications
(4 citation statements)
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“…On the one hand, this adaptogen can reduce the expression level of inflammatory cytokines (TNF-α, IL-6, and COX-2) and fibrotic markers (PC1 and TGF-β) by inhibiting the NF-κB enzyme. On the other hand, it can initiate antioxidant protection in mononuclear cells (14) by increasing the expression of CAT and MnSOD, NADPH oxidase (p22 and NOX2)/and other antioxidant enzymes (15). MT activates mitochondrial oxidative phosphorylation (13), preventing the formation of free radicals and depletion of cellular energy reserves (14), thereby exhibiting powerful cardio-, vaso-and neuroprotective properties.…”
Section: Introductionmentioning
confidence: 99%
“…On the one hand, this adaptogen can reduce the expression level of inflammatory cytokines (TNF-α, IL-6, and COX-2) and fibrotic markers (PC1 and TGF-β) by inhibiting the NF-κB enzyme. On the other hand, it can initiate antioxidant protection in mononuclear cells (14) by increasing the expression of CAT and MnSOD, NADPH oxidase (p22 and NOX2)/and other antioxidant enzymes (15). MT activates mitochondrial oxidative phosphorylation (13), preventing the formation of free radicals and depletion of cellular energy reserves (14), thereby exhibiting powerful cardio-, vaso-and neuroprotective properties.…”
Section: Introductionmentioning
confidence: 99%
“…All biological systems contain redox elements that play an important role in transcriptional regulation, cell proliferation, apoptosis, hormonal signaling, and other fundamental cell functions [3]. Organization and coordination of the redox activity of these elements occur through redox circuits and depend on the intracellular concentration of redox-active molecules [4, 5]. Redox active molecules may cause both regulatory and toxic effects depending on the value of cellular redox state parameters [5, 6].…”
Section: Introductionmentioning
confidence: 99%
“…Organization and coordination of the redox activity of these elements occur through redox circuits and depend on the intracellular concentration of redox-active molecules [4, 5]. Redox active molecules may cause both regulatory and toxic effects depending on the value of cellular redox state parameters [5, 6]. However, little is known about mechanisms of regulation, structural organization, and interaction between electron-transport participants inside the cell and other signal and regulatory systems.…”
Section: Introductionmentioning
confidence: 99%
“…Согласно предложенному механизму, кроме редокс-активных соединений и их мишеней в редокс-регуляторных процессах участвуют также белки-ферменты -оксидоредуктазы, локализация которых вблизи белков-мишеней определяет специфический отклик клеток. При этом регуляторный эффект действия редокс-активных соединений определяется не конкретной молекулой, а группой взаимодействующих участников, образующих электрон-транспортные цепи (редокс-цепи), и зависит от величин параметров редокс-гомеостаза [11]. Компонентами биологических электрон-транспортных цепей являются оксидоредуктазы и эндогенные редокс-активные соединения, включая АФК и антиоксиданты.…”
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