Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/1735
Title: NF-kappa B activation mediates crystal translocation and interstitial inflammation in adenine overload nephropathy
Authors: OKABE, CristieneBORGES, Raquel LernerALMEIDA, Danilo Candido deFANELLI, CamillaBARLETTE, Grasiela PedreiraMACHADO, Flavia GomesARIAS, Simone Costa AlarconMALHEIROS, Denise Maria Avancini CostaCAMARA, Niels Olsen SaraivaZATZ, RobertoFUJIHARA, Clarice Kazue
Citation: AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, v.305, n.2, p.F155-F163, 2013
Abstract: Adenine overload promotes intratubular crystal precipitation and interstitial nephritis. We showed recently that these abnormalities are strongly attenuated in mice knockout for Toll-like receptors-2, -4, MyD88, ASC, or caspase-1. We now investigated whether NF-kappa B activation also plays a pathogenic role in this model. Adult male Munich-Wistar rats were distributed among three groups: C (n = 17), receiving standard chow; ADE (n = 17), given adenine in the chow at 0.7% for 1 wk and 0.5% for 2 wk; and ADE + pyrrolidine dithiocarbamate (PDTC; n = 14), receiving adenine as above and the NF-kappa B inhibitor PDTC (120 mg.kg(-1).day(-1) in the drinking water). After 3 wk, widespread crystal deposition was seen in tubular lumina and in the renal interstitium, along with granuloma formation, collagen accumulation, intense tubulointerstitial proliferation, and increased interstitial expression of inflammatory mediators. Part of the crystals were segregated from tubular lumina by a newly formed cell layer and, at more advanced stages, appeared to be extruded to the interstitium. p65 nuclear translocation and IKK-alpha increased abundance indicated activation of the NF-kappa B system. PDTC treatment prevented p65 migration and normalized IKK-alpha, limited crystal shift to the interstitium, and strongly attenuated interstitial fibrosis/inflammation. These findings indicate that the complex inflammatory phenomena associated with this model depend, at least in part, on NF-kappa B activation, and suggest that the NF-kappa B system may become a therapeutic target in the treatment of chronic kidney disease.
Appears in Collections:Artigos e Materiais de Revistas Científicas - FM/MCM
Artigos e Materiais de Revistas Científicas - HC/ICHC
Artigos e Materiais de Revistas Científicas - LIM/16

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