Pregled bibliografske jedinice broj: 555
Nephrotoxic heavy metals increase expression of mdr1 in rat kidney cortex brush-border membrane
Nephrotoxic heavy metals increase expression of mdr1 in rat kidney cortex brush-border membrane // Journal of the American Society of Nephrology / American Society of Nephrology (ur.).
Kansas City (MI): Williams and Wilkins, 1997. (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Nephrotoxic heavy metals increase expression of mdr1 in rat kidney cortex brush-border membrane
(Nephrotoxic heavy metals increase expression of mdr1 in rat kideny cortex brush-border membrane)
Autori
Herak-Kramberger, Carol Mirna ; Blanuša, Maja ; Milković-Kraus, Sanja ; Thevenod, Frank ; Sabolić, Ivan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Journal of the American Society of Nephrology
/ American Society of Nephrology - Kansas City (MI) : Williams and Wilkins, 1997
Skup
30th Annual Meeting of the American Society of Nephrology
Mjesto i datum
San Antonio (TX), Sjedinjene Američke Države, 02.11.1997. - 05.11.1997
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
multidrug resistance; mdr1; heavy metals; kidney; rat
Sažetak
NEPHROTOXIC HEAVY METALS INCREASE EXPRESSION OF MDR1 IN RAT KIDNEY CORTEX BRUSH-BORDER MEMBRANE
Herak-Kramberger CM*, Blanusa M*, Milkovic-Kraus S*, Thevenod F*, and Sabolic I* (introduced by D. Brown), IMI, Zagreb, Croatia & II. Physiology, University of Saarland, Homburg/Saar, Germany
The multidrug resistance P-glycoprotein (mdr1), an efflux pump for various xenobiotics, is expressed on the apical membrane of excretory epitelial cells, including the kidney proximal tubule (PT). The physiological role of mdr1 in PT is not known. Mdr1 expression in cells may be affected by environmental stress and cytotoxic heavy metals (Chin et al., J. Biol. Chem, 265:221-226, 1990). Using an anti-mdr1 antibody (C219), we studied mdr1 expression in PT by immunohistochemistry and in isolated renal cortical brush-border membranes (BBM) by western blotting in control rats and in rats treated in vivo with various metals for 5 (cis-Pt) or 14 days (Pb, Hg, Cd, Cu, Zn, Mn, Ca, Mg, Al, La). The amount of mdr1 in BBM was correlated to the metal concentration in the renal cortical tissue measured by atomic absorption spectrometry. In control rats, a very low tissue concentration of the metals and a heterogeneous expression of mdr1 in BBM along the PT (S1<S2<S3) was detected. In experimental rats, concentration of all metals in the tissue increased between 7- (Mn) and 3000-fold (Cd). Only cis-Pt, Pb, Cd and Hg increased mdr1 expression in BBM by 3-, 6-, 15-, and 18-fold, respectively. Conclusion: a) nephrotoxic heavy metals increase mdr1 expression in the rat kidney BBM in vivo, b) this increase may be part of a specific cytoprotective response of PT cells to oxidative stress induced by nephrotoxic heavy metals.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Javno zdravstvo i zdravstvena zaštita
POVEZANOST RADA
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb
Profili:
Ivan Sabolić
(autor)
Carol Mirna Herak-Kramberger
(autor)
Sanja Milković-Kraus
(autor)
Maja Blanuša
(autor)