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Effect of phenylalanine derivatives on the main regulatory enzymes of hepatic cholesterogenesis

✍ Scribed by M. Castillo; M. Martinez-Cayuela; M. F. Zafra; E. Garcia-Peregrin


Book ID
104674123
Publisher
Springer
Year
1991
Tongue
English
Weight
333 KB
Volume
105
Category
Article
ISSN
0300-8177

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✦ Synopsis


Phenylalanine, phenylpyruvate and phenylacetate produced a considerable inhibition of chick liver mevalonate 5-pyrophosphate decarboxylase while mevalonate kinase and mevalonate 5-phosphate kinase were not significantly affected. Phenolic derivatives of phenylalanine produced a similar inhibition of decarboxylase activity than that found in the presence of phenyl metabolites. The degree of inhibition was progressive with increasing concentrations of inhibitors (1.25-5.00 mM). Simultaneous supplementation of different metabolites in conditions similar to those in experimental phenylketonuria (0.25 mM each) produced a clear inhibition of liver decarboxylase and 3-hydroxy-3-methylglutaryl-CoA reductase. To our knowledge, this is the first report on the in vitro inhibition of both liver regulatory enzymes of cholesterogenesis in phenylketonuria-like conditions. Our results show a lower inhibition of decarboxylase than that of reductase but suggest an important regulatory role of decarboxylase in cholesterol synthesis.


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## Abstract Three phenylalanine derivatives, Ac‐Phe‐NHMe, H‐Phe‐NHMe, and Ac‐Phe‐OH, were selected as models of Phe residues situated at the internal, the N‐terminal, and the C‐terminal positions of peptide chains, respctively. The side‐chain conformations of the three compounds were analyzed from