Selenomethionine induces polyamine biosynthesis in regenerating rat liver tissue

被引:3
作者
Bjelakovic, G. [1 ]
Beninati, S.
Pavlovic, D.
Sokolovic, D.
Stojanovic, I.
Jevtovic, T.
Bjelakovic, G. B.
Nikolic, J.
Basic, J.
机构
[1] Univ Nis, Fac Med, Inst Biochem, Nish, Serbia
[2] Univ Roma Tor Vergata, Dept Biol, Rome, Italy
[3] Univ Nis, Fac Med, Dept Gastroenterol Hepatol, Nish, Serbia
关键词
Se-methionine; polyamines; polyamine oxidase; diamine oxidase; liver regeneration; rats; CANCER CHEMOPREVENTION; CELL-GROWTH; METABOLISM; SPERMIDINE; SELENIUM; APOPTOSIS; OXIDASE; PUTRESCINE; MECHANISMS;
D O I
10.1007/s00726-006-0392-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mu g/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.
引用
收藏
页码:525 / 529
页数:5
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