Age-related changes in rat hepatic acetyl-coenzyme A carboxylase.

K G Thampy, M J Haas, A D Mooradian
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引用次数: 2

Abstract

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 (M(r) 262,000) on sodium dodecyl sulfate (SDS)-polyacrylamide gels. The specific activity of the purified preparation was 1.5, 1.8, and 1.8 U/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 mols P(i)/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-translational 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.

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大鼠肝乙酰辅酶A羧化酶的年龄相关性变化。
乙酰辅酶a羧化酶(ACC)催化长链脂肪酸合成的限速步骤。由于衰老影响肥胖,我们研究了4月龄、12月龄和24月龄雄性Fischer 344大鼠肝脏中ACC的活性及其mRNA含量。4月龄大鼠肝脏匀浆ACC (mU/mg蛋白)的平均(+/- SEM)活性为1.01 +/- 0.14。12月龄大鼠活性增加80% (1.83 +/- 0.27)(P < 0.01)。然而,24月龄大鼠肝脏的活性明显降低(0.46 +/- 0.06)(P < 0.001)。ACC总活性(每g肝脏)也有相同的变化趋势。通过亲和层析纯化各年龄组的酶。纯化后的产物在十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶上作为一个主要的蛋白带(M(r) 262,000)迁移。纯化后的制剂对4月龄、12月龄和24月龄大鼠的比活性分别为1.5、1.8和1.8 U/mg。4月龄、12月龄和24月龄大鼠的碱活性磷含量分别为5.66 +/- 0.17、5.64 +/- 0.21和6.21 +/- 0.35 mol P(i)/mol亚基。这些与年龄相关的差异并不显著。G3PDH mRNA校正后,24月龄大鼠肝脏ACC mRNA(0.24 +/- 0.03)较12月龄大鼠(0.58 +/- 0.04)或4月龄大鼠(0.43 +/- 0.007)显著降低(P < 0.01)。综上所述:(i)大鼠衰老与ACC活性的显著变化相关;(ii)三个年龄组纯化的ACC制剂具有相似的比活性和相似的磷酸盐含量;(iii) 12月龄大鼠与24月龄大鼠相比,肝脏ACC mRNA含量的变化与总酶活性的变化是平行的,而12月龄大鼠与4月龄大鼠相比,ACC活性的增加不能归因于肝脏mRNA水平的变化。这些结果表明,肝脏ACC的年龄相关变化发生在衰老早期的翻译后水平和衰老晚期的翻译前水平。这些变化可能导致与年龄相关的身体肥胖变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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