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Age dependent changes in androgen metabolism in the rat prostate
Journal of Steroid Biochemistry
|April 1, 1985
Summary
Aging significantly alters androgen metabolism enzymes in rat prostate and seminal vesicles, with most activities decreasing. Testosterone treatment in old rats partially restored enzyme function, highlighting age-related changes in androgen processing.
Area of Science:
- Andrology
- Biochemistry
- Gerontology
Background:
- Androgen metabolism is crucial for prostate and seminal vesicle function.
- Age-related changes in androgen metabolism can impact reproductive health and disease.
- Understanding these changes is vital for addressing age-associated conditions.
Purpose of the Study:
- To investigate the age-dependent changes in androgen oxidation and reduction activities.
- To compare enzymatic activity across different male reproductive tissues in rats of varying ages.
- To assess the effect of testosterone supplementation on these age-related metabolic alterations.
Main Methods:
- Measurement of steroid oxidation/reduction in homogenates of ventral prostate (VP), dorsal prostate (DP), lateral prostate (LP), coagulating gland (CG), and seminal vesicles (SV).
- Analysis of enzyme activities in intact rats across different age groups (young mature to senescent).
- Administration of testosterone to very old rats to evaluate its impact on androgen metabolism.
Main Results:
- Enzymatic activities significantly differed between tissues and with age, with most showing decreased specific activity in older rats.
- 5 alpha-reductase activity was notably reduced in old rats, becoming undetectable in some tissues.
- 3 alpha-Hydroxysteroid oxidoreductase (3 alpha-HSOR) in the VP was the sole enzyme maintaining activity with age; testosterone administration increased most enzyme activities in old rats.
Conclusions:
- Aging profoundly impacts androgen metabolism enzymes in male reproductive organs, leading to reduced activity.
- Testosterone plays a role in modulating these age-related enzymatic changes.
- These findings provide insights into the biochemical basis of age-related alterations in the male reproductive system.