| Abstrakt: |
Acetyl-CoA carboxylase (ACC) catalyzes the rate-limiting step in the synthesis of long-chain fatty acids. Since aging Influences adiposity, we studied the activity of ACC and its mRNA content in livers of 4-, 12-, and 24-month-old male Fischer 344 rats. The mean (± SEM) activity of ACC (mU/mg protein) in liver homogenates from 4-month-old rats was 1.01 ± 0.14. There was an 80% Increase in activity (1.83 ± 0.27) in 12-month-old rats (P < 0.01). However, there was significantly less activity (0.46 ± 0.06) in livers of 24-month-old rats (P < 0.001). The total activity of ACC (per g liver) followed the same trend. The enzyme from all age groups was purified by avidin-affinity chromatography. The purified preparation migrated as a major protein band (Mr262,000) on sodium dodecyl sulfate (SDS)-polyacrylamide gels. The specific activity of the purified preparation was 1.5,1.8, and 1.8 U7/mg for 4-, 12-, and 24-month-old rats, respectively. The alkali-labile phosphate content was 5.66 ± 0.17,5.64 ± 0.21, and 6.21 ± 0.35 mois P1/mole subunit for 4-, 12-, and 24-month-old rats, respectively. These age-related differences were not significant. The hepatic ACC mRNA measured by ribonuclease protection assay when corrected for G3PDH mRNA was significantly reduced in 24-month-old rats (0.24 ± 0.03) compared with 12-month-old (0.58 ± 0.04) or 4-month-old rats (0.43 ± 0.007) P < 0.01. In summary: (i) Aging in rats is associated with significant changes in ACC activity; (ii) the purified ACC preparations from the three age groups had similar specific activity and similar phosphate content; and (iii) the changes in ACC mRNA content of the liver paralleled the changes in total enzyme activity when 12-month-old rats were compared with 24-month-old rats whereas the increase in ACC activity in 12-month-old rats compared with 4-month-old rats could not be ascribed to changes in hepatic mRNA levels. These results indicate that the age-related changes in hepatic ACC occur at a post-translatlonal level during early years of aging and at a pretranslational level at late states of senescence. These changes may contribute to the age-related alterations in body adiposity. |
