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This alteration is linked to a low protein expression of the canalicular bile salt transporter, Bsep.185 A posttranscriptional mechanism seems to be involved, since no changes in the levels of Bsep mRNA has been observed.186 On the other hand, mRNA levels of the bile saltuptake systems, Ntcp and Oatps (Oatp1a1 and Oatp1a4 isoforms), are decreased, although this has not been confirmed at the protein level.186 Apart from alterations in bile salt hepatic handling, Long-Evans Cinnamon rats have hyperbilirubinaemia,184,187 and impairment of the excretion of the Mrp2 substrate, BSP.188 If these alterations involve changes in the expression of Mrp2, the rate-limiting step of both bilirubin and BSP hepatic handling, this would be nontranscriptional, since Mrp2 mRNA levels are normal in these rats.186 Alternatively, the above-mentioned transcriptional downregulation of Oatps, which also transport nonbile salt organic anions such as BSP and bilirubin, may be a contributing factor

This property along with tissue/tumor expression of GT was used to develop -glutamyl prodrugs

Gene-level TPM and expected counts were quantified using RSEM v.1.3.1

Nutrients for the aging eye

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