Abstract
Mouse renal cortical tubule cells in primary culture exposed to cadmium (Cd2+) develop decreased Na+-glucose cotransport activity as measured by uptake of the glucose analogue α-methylglucoside. RNA was isolated from kidney cell cultures, and after reversed transcription, the DNA was amplified with primers to rat SGLT1 (the high affinity isoform of the sodium glucose cotransporter) and mouse β-actin. Only one product was identified after amplification with the rat SGLT1 primers, which on sequencing was 96% identical to rat SGLT1. Compared to β-actin, the intensity of the SGLT1 message declined progressively as CdCl2concentration in the medium increased from 0 to 10 μM. Similar decreases in SGLT1 mRNA were also observed as media zinc (Zn2+) concentrations rose from 0 to 75 μM or as copper (Cu) concentrations increased from 0 to 150 μM. Exposure to 8 μM Cd as Cd-metallothionein (Cd7-MT) also caused a fall in relative SGLT1 mRNA abundance, and at nearly identical internal Cd concentrations of 40-43 pmol/μg DNA, both Cd7-MT and CdCl2reduced SGLT1 mRNA to 33% of control. In general, the fall in SGLT1 mRNA was more rapid than the decline in Na+-dependent glucose uptake after cells were exposed to Cd2+. These findings suggest that the effects of Cd2+and other metals on renal glucose transport are related to decreased expression of SGLT1 message.
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