Selenomethionine induces polyamine biosynthesis in regenerating rat liver tissue

Amino Acids. 2007 Sep;33(3):525-9. doi: 10.1007/s00726-006-0392-0. Epub 2006 Oct 10.

Abstract

Our study was undertaken to elucidate the effects of selenomethionine (SeMet) on polyamine metabolism in regenerating rat liver tissue, as useful model of rapidly growing normal tissue. We have examined the levels of spermine, spermidine and putrescine in liver tissue. At the same time we have evaluated the activities of polyamine oxidase (PAO) and diamine oxidase (DAO), the catabolic enzymes of polyamine metabolism. The obtained results suggest that polyamine levels in regenerating liver tissue, at 7(th) day after two-thirds partial hepatectomy, were higher in comparison with control group. The administration of selenomethionine to hepatectomized animals during seven days, in a single daily dose of 2.5 microg/100 g body weight, increases the amount of spermine and spermidine; the level of putrescine does not change under the influence of SeMet in regenerating rat liver tissue.PAO activity is lower in regenerating hepatic tissue than in control group. Supplementation of hepatectomized animals with SeMet significantly decreases the activity of this enzyme. DAO activity was significantly higher in hepatectomized and in operated animals treated with SeMet compared to the sham-operated and control ones. The differential sensitivity observed in our model of highly proliferating normal tissue to SeMet, compared with the reported anticancer activity of this molecule is discussed.

MeSH terms

  • Amine Oxidase (Copper-Containing) / metabolism
  • Animals
  • Hepatectomy
  • Humans
  • Liver* / enzymology
  • Liver* / pathology
  • Liver* / physiology
  • Male
  • Oxidoreductases Acting on CH-NH Group Donors / metabolism
  • Polyamine Oxidase
  • Polyamines / metabolism*
  • Rats
  • Rats, Wistar
  • Regeneration*
  • Selenomethionine / metabolism*

Substances

  • Polyamines
  • Selenomethionine
  • Amine Oxidase (Copper-Containing)
  • Oxidoreductases Acting on CH-NH Group Donors