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Cultured mammary epithelial monolayers (BME‐UV) express functional organic anion and cation transporters
Author(s) -
ALBATAINEH M. M.,
Van Der MERWE D.,
SCHULTZ B. D.,
GEHRING R.
Publication year - 2009
Publication title -
journal of veterinary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.527
H-Index - 60
eISSN - 1365-2885
pISSN - 0140-7783
DOI - 10.1111/j.1365-2885.2009.01057.x
Subject(s) - transporter , monolayer , organic anion transporter 1 , chemistry , organic cation transport proteins , biochemistry , microbiology and biotechnology , biophysics , biology , gene
There is ongoing concern about the potential adverse effects of xenobiotic residues in cows’ milk to the human consumer. Although drugs that are intentionally administered to lactating dairy cattle are rigorously regulated to prevent harmful residues, there are numerous other potential sources of exposure that are not as easily controlled. For example, cattle may be exposed to mycotoxins, pesticides and/or persistent organic pollutants through feed, water and inhalation of polluted air. Accurate estimates of the rate and extent of excretion of these compounds into milk is important to assess the risk of exposure through cows’ milk. In the present study, the expression of carrier mediated transport processes in cultured monolayers of an immortalized bovine mammary epithelial cell line (BME‐UV) was determined using a flow‐through diffusion cell system, selective substrates and inhibitors of organic cation transporters (OCT) and organic anion transporters (OAT). The basal‐to‐apical (BL‐to‐Ap) flux of tetraethylammonium and estrone sulfate significantly exceeded their flux in the opposite direction. The addition of selective inhibitors to the donor compartment significantly decreased the BL‐to‐Ap flux of either selective substrate. These results suggest that both OCT and OAT are functionally expressed by BME‐UV cells.

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