Reactions steps with less specificity for bilirubin, but nevertheless involved in functions supplying UDP-glucuronate are UDP-glucose dehydrogenase (Ugdh), Phosphoglucomutase (Pgm2), and UDP-glucose pyrophosphorylase (Ugp2), all of which show

a stronger down-regulation, especially in TGFβ treated hepatocytes. It can be summarized that there is a loss of glucuronization capacity, which is enhanced by TGFβ treatment. The loss affects bilirubin conjugation but is not particularly specific to bilirubin. In pig liver, inhibition of TGFβ did not display a strong impact on bilirubin levels as compared with other liver GDC-0199 ic50 function markers (Figure 2 in [1]). This finding is in concordance Inhibitors,research,lifescience,medical with the lack

of a short term response in the bilirubin conjugation here. 2.7. Urea Synthesis Inhibitors,research,lifescience,medical Urea can be synthesized from a range of nitrogen-containing metabolites, however, the final reaction steps are common—urea cycle and carbamoyl synthase—Cps1, Otc, Ass1, Asl, Arg1 (see Figure 4A). A set of facultative reactions are often used to supply the necessary precursors (aspartate, ammonium, and carbon dioxide) from typical substrates as alanine, glutamine, glutamate, and pyruvate: Inhibitors,research,lifescience,medical Got1, Gpt/Gpt2, Glud1, and Gls2, see Figure 4B. Figure 4 Regulation of genes involved in urea synthesis. Panel (A) shows genes essential for urea synthesis, whereas panel (B) shows genes used for the supply of precursors. Arginase is one of the most down-regulated genes in the dataset. Apparently, it is switched off from a highly abundant state and TGFβ treatment makes no difference. Ornithine transcarbamylase (Otc) is down-regulated Inhibitors,research,lifescience,medical at a moderate quantity, and a further down-regulation is achieved upon TGFβ treatment. Argininosuccinate synthase (Ass1) is moderately down-regulated

but constant in TGFβ treated hepatocytes. Argininosuccinate lyase (Asl) is down-regulated by a considerable amount only in TGFβ treated hepatocytes. Carbamoyl synthetase (Cps1) is sharply down-regulated, even more so in the TGFβ treated group. Inhibitors,research,lifescience,medical Apparently, the urea cycle is not regulated in a synchronized manner. It can be predicted that hepatocytes in culture lose most of their capacity to synthesize WZ4003 molecular weight urea, and TGFβ leads to an additional down-regulation. The amount of this effect is less clear, and an estimation would depend on the information which enzymes are rate-limiting in the pathway. Among the facultative reactions, both forms of alanine aminotransferase (Gpt and Gpt2) are possibly commonly regulated. A strong decline can be found only in TGFβ treated hepatocytes. Glutamate oxaloacetate transaminase (Got) has only a slight down-regulation with time. Since these genes are also involved in many other functions, it is apparent that their regulation is very likely decoupled from the function of urea synthesis.