Ferioli M E, Sessa A, Rabellotti E, Tunici P, Pinotti O, Perin A
Centro di Studio sulla Patologia Cellulare, C.N.R., Milan, Italy.
Liver. 1998 Oct;18(5):326-30. doi: 10.1111/j.1600-0676.1998.tb00813.x.
AIMS/BACKGROUND: Given the important role of polyamines (putrescine, spermidine, spermine) in the modulation of macromolecular syntheses, gene expression and proteolysis, alterations in their metabolic pathways could be relevant during senescence. Since the few existing data address mainly polyamine biosynthesis, we studied the oxidative catabolism of polyamines in the liver of rats 3-36 months of age.
Polyamine oxidase activity was fluorimetrically measured using N1-acetylspermine as substrate. Spermidine/spermine N1-acetyltransferase and diamine oxidase were measured by radiochemical methods using labeled acetyl-coenzyme A and putrescine, respectively, as substrate. Polyamines were separated by HPLC and fluorimetrically quantified after post-column derivatization with o-phthaldialdehyde.
Spermidine/spermine N1-acetyltransferase activity increased in 36-month-old rats and polyamine oxidase activity in 24- and 36-month-old rats. A decline in spermine and increases in spermidine and putrescine in elderly rats suggested an activation of the interconversion pathway of higher into lower polyamines. The activity of diamine oxidase, which degrades putrescine, was enhanced starting from 12 months of age.
In the liver of aged rats, an increase in the catabolic enzymes leads to a reconversion of the higher polyamines to putrescine. This increased catabolism may represent an important age-related change and may contribute to impairment of the expression of growth-related genes in senescence.
目的/背景:鉴于多胺(腐胺、亚精胺、精胺)在调节大分子合成、基因表达和蛋白水解中发挥的重要作用,其代谢途径的改变在衰老过程中可能具有相关性。由于现有的少量数据主要涉及多胺生物合成,我们研究了3至36月龄大鼠肝脏中多胺的氧化分解代谢。
以N1-乙酰精胺为底物,采用荧光法测定多胺氧化酶活性。分别以标记的乙酰辅酶A和腐胺为底物,通过放射化学方法测定亚精胺/精胺N1-乙酰转移酶和二胺氧化酶。多胺经高效液相色谱分离,用邻苯二甲醛柱后衍生化后进行荧光定量。
36月龄大鼠的亚精胺/精胺N1-乙酰转移酶活性增加,24月龄和36月龄大鼠的多胺氧化酶活性增加。老年大鼠精胺含量下降,亚精胺和腐胺含量增加,提示高等多胺向低等多胺的相互转化途径被激活。从12月龄开始,降解腐胺的二胺氧化酶活性增强。
在老年大鼠肝脏中,分解代谢酶的增加导致高等多胺向腐胺的再转化。这种增加的分解代谢可能是与年龄相关的重要变化,可能导致衰老过程中生长相关基因表达受损。