Format

Send to

Choose Destination
Biochem Pharmacol. 1997 Jun 15;53(12):1889-900.

Binding of mercury in renal brush-border and basolateral membrane-vesicles.

Author information

1
Division of Basic Medical Sciences, Mercer University School of Medicine, Macon, GA 31207, USA.

Abstract

The influence of the thiols L-cysteine (CYS), glutathione (GSH), and 2,3-dimercapto-1-propanesulfonate (DMPS) on the binding and transport of inorganic mercury (Hg2+) in luminal (brush-border) and basolateral membrane-vesicles isolated from the kidneys of rats was studied using radiolabeled mercury (203HgCl2). Membrane-vesicles were exposed to 1, 10, or 100 microM Hg2+ in the presence or absence of a 3:1 or 10:1 mole-ratio of CYS, GSH, or DMPS relative to Hg2+. Equilibration of mercury with the membrane-vesicles occurred very rapidly, essentially being complete within 5 sec. By 60 sec, binding accounted for 87-97% of intravesicular Hg2+ in the absence of exogenous thiols. All three thiols significantly reduced the fraction of binding, with DMPS being the most effective agent. CYS enhanced the association of Hg2+ with luminal membrane-vesicles relative to that when Hg2+ was added alone, suggesting that conjugation of Hg2+ with CYS promotes the transport of low concentrations of Hg2+. In contrast, an excess of either GSH or DMPS relative to Hg2+ interfered significantly with both the binding and transport of Hg2+ into either luminal or basolateral membrane-vesicles. In summary, the present study is the first to describe the association of Hg2+ with renal luminal and basolateral membrane-vesicles. Evidence was obtained for the involvement of a Hg2+-CYS conjugate as a mechanism by which Hg2+ uptake and binding to luminal membranes occur and for an inhibitory effect of GSH and the chelator DMPS with regard to Hg2+ uptake and binding, demonstrating that extracellular thiols can modulate significantly the renal accumulation of Hg2+.

PMID:
9256164
DOI:
10.1016/s0006-2952(97)00138-x
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center