EFFECT OF BRANCHED-CHAIN AMINO-ACIDS ON ALBUMIN GENE-EXPRESSION IN THE LIVER OF GALACTOSAMINE-TREATED RATS

Citation
M. Kuwahata et al., EFFECT OF BRANCHED-CHAIN AMINO-ACIDS ON ALBUMIN GENE-EXPRESSION IN THE LIVER OF GALACTOSAMINE-TREATED RATS, Journal of nutritional biochemistry, 9(4), 1998, pp. 209-214
Citations number
21
Categorie Soggetti
Nutrition & Dietetics",Biology
ISSN journal
09552863
Volume
9
Issue
4
Year of publication
1998
Pages
209 - 214
Database
ISI
SICI code
0955-2863(1998)9:4<209:EOBAOA>2.0.ZU;2-4
Abstract
Acute liver injury was induced in mts by the administration of galacto samine, which brought about inhibition of RNA synthesis and protein sy nthesis in the liver The galactosamine-treated rats were infused with total parenteral nutrition solutions containing various proportions of branched-chain amino acids and the recovery from the galactosamine in toxication was followed by measuring albumin mRNA levels and polysome profiles. The levels of total cytoplasmic albumin mRNA were markedly d ecreased on day 2 after the galactosamine treatment, but the levels we re restored to almost the control value by day 4 in all the groups irr espective of the content of branched-chain amino acids in the infusion solutions. On the contrary, the levels of beta-actin mRNA changed in the opposite direction to those of albumin mRNA. It was also found tha t polysomes ill the liver were extensively disaggregated on day 2 afte r the galactosamine treatment, but the polysome profiles returned to n ormal on day 4 in all the groups. However, when the levels of polysome -associated albumin mRNA were quantitated, we found that the extent of the recovery was dependent on the content of branched-chain amino aci ds in the infusion solutions; as the content of branched-chain amino a cids increased the level of polysome-associated albumin mRNA increased . These results suggest that the integration of albumin mRNA into func tional polysomes in the liver is regulated by the supply of branched-c hain amino acids. (C) Elsevier Science Inc. 1998.