Title : Hydrogen Sulfide Induces Keap1 S-sulfhydration and Suppresses Diabetes-Accelerated Atherosclerosis via Nrf2 Activation.

Pub. Date : 2016 Oct

PMID : 27335232






5 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Hydrogen Sulfide Induces Keap1 S-sulfhydration and Suppresses Diabetes-Accelerated Atherosclerosis via Nrf2 Activation. Hydrogen Sulfide kelch-like ECH-associated protein 1 Mus musculus
2 H2S increased S-sulfhydration of Keap1, induced Nrf2 dissociation from Keap1, enhanced Nrf2 nuclear translocation, and inhibited O2 (-) generation, which were abrogated after Keap1 mutated at Cys151, but not Cys273, in endothelial cells. Hydrogen Sulfide kelch-like ECH-associated protein 1 Mus musculus
3 H2S increased S-sulfhydration of Keap1, induced Nrf2 dissociation from Keap1, enhanced Nrf2 nuclear translocation, and inhibited O2 (-) generation, which were abrogated after Keap1 mutated at Cys151, but not Cys273, in endothelial cells. Hydrogen Sulfide kelch-like ECH-associated protein 1 Mus musculus
4 H2S increased S-sulfhydration of Keap1, induced Nrf2 dissociation from Keap1, enhanced Nrf2 nuclear translocation, and inhibited O2 (-) generation, which were abrogated after Keap1 mutated at Cys151, but not Cys273, in endothelial cells. Hydrogen Sulfide kelch-like ECH-associated protein 1 Mus musculus
5 Collectively, H2S attenuates diabetes-accelerated atherosclerosis, which may be related to inhibition of oxidative stress via Keap1 sulfhydrylation at Cys151 to activate Nrf2 signaling. Hydrogen Sulfide kelch-like ECH-associated protein 1 Mus musculus