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Sökning: L773:0031 6768 OR L773:1432 2013 > (2010-2014) > Cationic uremic tox...

Cationic uremic toxins affect human renal proximal tubule cell functioning through interaction with the organic cation transporter

Schophuizen, Carolien M. S. (författare)
Wilmer, Martijn J. (författare)
Jansen, Jitske (författare)
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Gustavsson, Lena (författare)
Lund University,Lunds universitet,Institutionen för translationell medicin,Medicinska fakulteten,Department of Translational Medicine,Faculty of Medicine
Hilgendorf, Constanze (författare)
Hoenderop, Joost G. J. (författare)
van den Heuvel, Lambert P. (författare)
Masereeuw, Rosalinde (författare)
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 (creator_code:org_t)
2013-06-29
2013
Engelska.
Ingår i: Pflügers Archiv. - : Springer Science and Business Media LLC. - 0031-6768. ; 465:12, s. 1701-1714
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Several organic cations, such as guanidino compounds and polyamines, have been found to accumulate in plasma of patients with kidney failure due to inadequate renal clearance. Here, we studied the interaction of cationic uremic toxins with renal organic cation transport in a conditionally immortalized human proximal tubule epithelial cell line (ciPTEC). Transporter activity was measured and validated in cell suspensions by studying uptake of the fluorescent substrate 4-(4-(dimethylamino)styryl)-N-methylpyridinium-iodide (ASP(+)). Subsequently, the inhibitory potencies of the cationic uremic toxins, cadaverine, putrescine, spermine and spermidine (polyamines), acrolein (polyamine breakdown product), guanidine, and methylguanidine (guanidino compounds) were determined. Concentration-dependent inhibition of ASP(+) uptake by TPA, cimetidine, quinidine, and metformin confirmed functional endogenous organic cation transporter 2 (OCT2) expression in ciPTEC. All uremic toxins tested inhibited ASP(+) uptake, of which acrolein required the lowest concentration to provoke a half-maximal inhibition (IC50 = 44 +/- 2 mu M). A Dixon plot was constructed for acrolein using three independent inhibition curves with 10, 20, or 30 mu M ASP(+), which demonstrated competitive or mixed type of interaction (K (i) = 93 +/- 16 mu M). Exposing the cells to a mixture of cationic uremic toxins resulted in a more potent and biphasic inhibitory response curve, indicating complex interactions between the toxins and ASP(+) uptake. In conclusion, ciPTEC proves a suitable model to study cationic xenobiotic interactions. Inhibition of cellular uptake transport was demonstrated for several uremic toxins, which might indicate a possible role in kidney disease progression during uremia.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Human proximal tubule cell
OCT
Uremic toxin
Polyamines
Guanidine
Acrolein

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