Title : Farrerol Ameliorated Cisplatin-Induced Chronic Kidney Disease Through Mitophagy Induction via Nrf2/PINK1 Pathway.

Pub. Date : 2021

PMID : 34858188






6 Functional Relationships(s)
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1 Farrerol Ameliorated Cisplatin-Induced Chronic Kidney Disease Through Mitophagy Induction via Nrf2/PINK1 Pathway. farrerol nuclear factor, erythroid derived 2, like 2 Mus musculus
2 Previously, Our study has showed that farrerol can activate Nrf2 and ameliorate cisplatin-induced acute kidney injury (AKI). farrerol nuclear factor, erythroid derived 2, like 2 Mus musculus
3 In this study, we evaluated the correlation between mitophagy and the protective effect of the Nrf2 activator farrerol on cisplatin-induced CKD by using C57BL/6 wild-type and Nrf2 knockout mice. farrerol nuclear factor, erythroid derived 2, like 2 Mus musculus
4 Similar to previous results, farrerol activated Nrf2 on the 38th day of cisplatin administration, subsequently stimulating the Nrf2-targeted antioxidant enzymes HO-1 and NQO1. farrerol nuclear factor, erythroid derived 2, like 2 Mus musculus
5 Similar to previous results, farrerol activated Nrf2 on the 38th day of cisplatin administration, subsequently stimulating the Nrf2-targeted antioxidant enzymes HO-1 and NQO1. farrerol nuclear factor, erythroid derived 2, like 2 Mus musculus
6 These data indicated that farrerol effectively inhibited cisplatin-induced inflammation and renal fibrosis by activating Nrf2 and PINK1/Parkin-mediated mitophagy, which provides a potential novel therapeutic target for CKD. farrerol nuclear factor, erythroid derived 2, like 2 Mus musculus