Abstract
We have examined the endogenous nuclease activity of the liver of intact, castrated and testosterone-treated mice of different ages. Both Mg2+- and Ca2+-dependent endogenous nuclease activities decline in old age. Withdrawal of the hormone increases nuclease activity in the immature and young. However, testosterone administration prevents the digestion of nuclei to different extents in all ages. These findings suggest a possible protective role of testosterone in the cleavage of liver chromatin by endogenous nucleases during the aging of mice.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 59-61 |
| Number of pages | 3 |
| Journal | Molecular Biology Reports |
| Volume | 22 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 1995 |
| Externally published | Yes |
Keywords
- aging
- androgen
- endogenous nuclease
- mice liver
ASJC Scopus subject areas
- Molecular Biology
- Genetics
Fingerprint
Dive into the research topics of 'Androgen treatment protects mouse liver chromatin from cleavage by endogenous nucleases during aging: Androgen and nuclease activity'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS