Title : Irisin rescues diabetic cardiac microvascular injury via ERK1/2/Nrf2/HO-1 mediated inhibition of oxidative stress.

Pub. Date : 2022 Jan

PMID : 34863716






6 Functional Relationships(s)
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1 Irisin rescues diabetic cardiac microvascular injury via ERK1/2/Nrf2/HO-1 mediated inhibition of oxidative stress. irisin nuclear factor, erythroid derived 2, like 2 Mus musculus
2 Irisin stimulated the phosphorylation of extracellular regulated protein kinases (ERK) 1/2 and nuclear factor erythroid-derived 2-like 2 (Nrf2) nuclear translocation, while U0126 (the inhibitor of ERK1/2) inhibited irisin-induced Nrf2 nuclear translocation and HO-1 expression. irisin nuclear factor, erythroid derived 2, like 2 Mus musculus
3 Irisin stimulated the phosphorylation of extracellular regulated protein kinases (ERK) 1/2 and nuclear factor erythroid-derived 2-like 2 (Nrf2) nuclear translocation, while U0126 (the inhibitor of ERK1/2) inhibited irisin-induced Nrf2 nuclear translocation and HO-1 expression. irisin nuclear factor, erythroid derived 2, like 2 Mus musculus
4 Irisin stimulated the phosphorylation of extracellular regulated protein kinases (ERK) 1/2 and nuclear factor erythroid-derived 2-like 2 (Nrf2) nuclear translocation, while U0126 (the inhibitor of ERK1/2) inhibited irisin-induced Nrf2 nuclear translocation and HO-1 expression. irisin nuclear factor, erythroid derived 2, like 2 Mus musculus
5 Nrf2 siRNA inhibited irisin"s antioxidative effects. irisin nuclear factor, erythroid derived 2, like 2 Mus musculus
6 CONCLUSION: Irisin could rescue cardiac microvessels against oxidative stress and apoptosis in diabetes via ERK1/2/Nrf2/HO-1 pathway. irisin nuclear factor, erythroid derived 2, like 2 Mus musculus