2011
DOI: 10.1016/j.ejphar.2011.07.043
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Eicosapentaenoic acid regulates IκBα and prevents tubulointerstitial injury in kidney

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Cited by 10 publications
(8 citation statements)
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“…In the current study, we showed that linseed-enriched diet up-regulated the expression of genes ( SLC20A1 , TRAF3IP2 , TP53INP1 , TNFRSF12A , TLR9 and BIRC2 ) which involved in IκB inhibition in porcine skeletal muscle, and might lead to decrease NF-κB activation (Table 5 ). Recent studies indicated that activation of NF-κB is inhibited by n-3 PUFAs in lymphomonocyte [ 45 ], and the decreased IKK activation is likely to contribute to the suppressed NF-κB activation [ 46 ]. Our results provided an alternative explanation why n-3 PUFAs could suppress NF-κB activation.…”
Section: Discussionmentioning
confidence: 99%
“…In the current study, we showed that linseed-enriched diet up-regulated the expression of genes ( SLC20A1 , TRAF3IP2 , TP53INP1 , TNFRSF12A , TLR9 and BIRC2 ) which involved in IκB inhibition in porcine skeletal muscle, and might lead to decrease NF-κB activation (Table 5 ). Recent studies indicated that activation of NF-κB is inhibited by n-3 PUFAs in lymphomonocyte [ 45 ], and the decreased IKK activation is likely to contribute to the suppressed NF-κB activation [ 46 ]. Our results provided an alternative explanation why n-3 PUFAs could suppress NF-κB activation.…”
Section: Discussionmentioning
confidence: 99%
“…Based on this, we believe that the absent reduction in proteinuria was not due to insufficient DPP4 inhibition and GLP-1R stimulation but rather because of the robust degree of renal injury in which a reduction in macrophage infiltration alone was not sufficient to influence the disease course. Takase et al (35) used eicosapentaenoic acid (EPA) in the same model. Treatment with EPA significantly reduced CD68positive macrophage infiltration into the tubulointerstitial area, which was associated with the prevention of tubulointerstitial injury.…”
Section: Discussionmentioning
confidence: 99%
“…5 An et al in 2009 showed that omega-3 supplement could reduce the upregulation of profibrotic, proinflammatory and prooxidant routes and modified tubulointersititial fibrosis [23]. In the study done by Takase et al in 2011 it was indicated that EPA blocked the development of tubulointersititial damage in models with Thy-1 nephritis and had inhibitory effects on inflammatory molecules by regulating IKBa in cultured renal cells [24]. The study that Abdou et al conductd in 2014 declared that omega-3 fatty acids prevented renal toxicity induced by lead in rats [25].…”
Section: Discussionmentioning
confidence: 99%