2011
DOI: 10.1016/j.niox.2011.06.001
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Nitric oxide activates Nrf2 through S-nitrosylation of Keap1 in PC12 cells

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Cited by 133 publications
(92 citation statements)
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“…Wu et al [24] found that dietary protein supplementation could increase nitric oxide synthesis in the placenta of pigs. Nitric oxide could activate Nrf2 in rat pheochromocytoma cells [25]. These data indicate that there may be a correlation between dietary proteins and the function of the fish intestinal physical barriers associated with TJs, apoptosis and antioxidants as well as their related signalling pathways, which require further investigation.…”
Section: Introductionmentioning
confidence: 76%
“…Wu et al [24] found that dietary protein supplementation could increase nitric oxide synthesis in the placenta of pigs. Nitric oxide could activate Nrf2 in rat pheochromocytoma cells [25]. These data indicate that there may be a correlation between dietary proteins and the function of the fish intestinal physical barriers associated with TJs, apoptosis and antioxidants as well as their related signalling pathways, which require further investigation.…”
Section: Introductionmentioning
confidence: 76%
“…114 Several mechanisms have been described for the antiapoptotic actions of NO, such as protein activation by modification of prosthetic groups 102,115 and cysteine modification by S-nitrosylation. 29,111,112,[116][117][118] Both mechanisms can regulate signaling pathways 17,101,102,104 and gene expression. 29,118 Prosthetic group modification is related to the high NO reactivity with metal ions.…”
Section: Nitric Oxide As a Survival Molecule In Pancreatic β-Cellsmentioning
confidence: 99%
“…29,111,112,[116][117][118] Both mechanisms can regulate signaling pathways 17,101,102,104 and gene expression. 29,118 Prosthetic group modification is related to the high NO reactivity with metal ions. The activation of guanylate cyclase (GC) is a well-studied example.…”
Section: Nitric Oxide As a Survival Molecule In Pancreatic β-Cellsmentioning
confidence: 99%
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“…Nrf2 regulates the gene expression of a number of enzymes that serve to detoxify pro‐oxidative stressors,40 such as glutathione peroxidase (GPX) and HO‐1 by binding to the antioxidant response element found in the gene promoter region 34. In the same regard, there is also evidence that NO possesses antioxidant effects and can activate Nrf2 and HO‐1 41, 42. However, the mechanism by which NO reduces oxidative stress following MI/R remains unknown.…”
Section: Introductionmentioning
confidence: 99%