
Epoxyeicosatrienoic acids (EETs) are arachidonic acid metabolites with biological effects, including anti-apoptotic, anti-inflammatory, and anti-fibrotic functions. Soluble epoxide hydrolase (sEH)-mediated hydrolysis of EETs to dihydroxyeicosatrienoic acids (DHET) attenuates these effects. In addition, EETs administration and sEH inhibition significantly reduced M1 macrophage markers, while M2 macrophage markers were highly upregulated. The findings provide a mechanistic understanding of how EETs prevent kidney fibrogenesis during obstructive nephropathy and suggest EETs treatment as a potential therapeutic strategy for treating fibrotic diseases.
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