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Aging and polyamine acetylation in rat kidney
M E Ferioli1, A Sessa, P Tunici
1Centro di Studio sulla Patologia Cellulare, C.N.R., Università di Milano, Milan, Italy.
Biochimica Et Biophysica Acta
|October 7, 1996
Summary
Aging in rat kidneys activates polyamine acetylation and interconversion. This process shifts polyamine metabolism towards putrescine formation, influencing kidney function over time.
Area of Science:
- Biochemistry
- Gerontology
- Nephrology
Background:
- Polyamines are essential for cell growth and function.
- Age-related changes in polyamine metabolism can impact kidney health.
- Understanding these changes is crucial for addressing age-associated kidney dysfunction.
Purpose of the Study:
- To investigate the age-dependent changes in polyamine acetylation and interconversion in rat kidneys.
- To elucidate the role of specific enzymes in these metabolic pathways during aging.
- To determine the implications of these alterations for polyamine levels and kidney function.
Main Methods:
- Assessed the activity of key enzymes: spermidine/spermine N1-acetyltransferase, spermidine N8-acetyltransferase, and polyamine oxidase.
- Measured enzyme activities in rat kidney cytosol across different age groups (3, 24, and 36 months).
- Monitored polyamine and acetylated polyamine levels in relation to enzyme activity changes.
Main Results:
- Cytosolic spermidine/spermine N1-acetyltransferase activity increased with age, indicating enhanced acetylation.
- Spermidine N8-acetyltransferase activity also rose, suggesting increased polyamine excretion.
- Polyamine oxidase activity initially decreased, leading to N1-acetylspermidine accumulation, then increased, correlating with spermidine and putrescine increases and spermine decline.
Conclusions:
- Aging activates polyamine acetylation and interconversion pathways in the rat kidney.
- These changes favor the formation of putrescine, an alternative pathway for spermidine and putrescine.
- Age-related shifts in polyamine metabolism may contribute to functional changes in the aging kidney.