Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9308293 | Kidney International | 2005 | 16 Pages |
Abstract
The present data demonstrate clearly that CH3Hg-Cys is indeed a transportable substrate of OAT1. Moreover, the collective findings from the MDCK cells and NRK-52E cells infer that CH3Hg-Cys is a likely transportable mercuric species in proximal tubular epithelial cells that is taken up in vivo by both OAT1 and amino acid transporters.
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Authors
Rudolfs K. Zalups, Sarfaraz Ahmad,