4.7 Article

Reversal of radiocontrast medium toxicity in human renal proximal tubular cells by white grape juice extract

Journal

CHEMICO-BIOLOGICAL INTERACTIONS
Volume 229, Issue -, Pages 17-25

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.cbi.2014.12.035

Keywords

Signaling; Renal cell; Vitis spp.; Kinase; Cell injury

Funding

  1. Italian Ministry of University and Scientific Research [2008B99E7M]
  2. Italian Society of Nephrology
  3. Sicily Region (PO FESR Sicilia) [CUP G73F11000050004]
  4. Sicily Region (project MEPRA of Linea d'Intervento 4.1.1.1) [133]
  5. Italian Medicines Agency (Agenzia Italiana del Farmaco, AIFA)
  6. Regione Calabria Project Rete Regionale di informazione sul farmaco: informazione, formazione, e farmacovigilanza

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Radiocontrast media (RCM)-induced nephrotoxicity (CIN) is a major clinical problem accounting for 12% of all hospital-acquired cases of acute kidney injury. The pathophysiology of CIN is not well understood, but direct toxic effects on renal cells have been postulated as contributing to CIN. We have investigated the effect of a white grape (Vitis vinifera) juice extract (WGJe) on human renal proximal tubular (HK-2) cells treated with the radiocontrast medium (RCM) sodium diatrizoate. WGJe caused an increase in phosphorylation of the prosurvival kinases Akt and ERK1/2 in HK-2 cells. Treatment of HK-2 cells with 75 mg I/ml sodium diatrizoate for 2.5 h and then further incubation (for 27.5 h) after removal of the RCM caused a drastic decrease in cell viability. However, pre-treatment with WGJe, prior to incubation with diatrizoate, dramatically improved cell viability. Analysis of key signaling molecules by Western blotting showed that diatrizoate caused a drastic decrease in phosphorylation of Akt (Ser473), FOXO1 (Thr24) and FOXO3a (Thr32) during the initial 2.5 h incubation period, and WGJe pre-treatment caused a reversal of these effects. Further analysis by Western blotting of samples from HK-2 cells cultured for longer periods of time (for up to 27.5 h after an initial 2.5 h exposure to diatrizoate with or without WGJe pre-treatment) showed that WGJe pre-treatment caused a negative effect on phosphorylation of p38, NF-kappa B (Ser276) and pERK1/2 whilst having a positive effect on the phosphorylation of Akt, FOXO1/FOXO3a and maintained levels of Pim-1 kinase. WGJe may alleviate RCM toxicity through modulation of signaling molecules that are known to be involved in cell death and cell survival and its possible beneficial effects should be further investigated. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

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