Mooradian A D, Wong N C, Shah G N
St. Louis Veterans Affairs Medical Center, Missouri, USA.
Am J Physiol. 1996 Dec;271(6 Pt 2):R1602-7. doi: 10.1152/ajpregu.1996.271.6.R1602.
To determine the age-related changes in the effect of thyroid hormone on apolipoprotein A1 (ApoA1) gene expression, male Fischer 344 rats at 4 (young) and 26 (aged) mo of age were studied. Hyperthyroidism was induced with daily intraperitoneal injections of 3,5,3'-triiodothyronine (15 micrograms/100 g body wt) for 10 days. Hypothyroidism was induced with 0.025% methimazole in drinking water for 4 wk. Hyperthyroidism was associated with increased serum ApoA1 levels in young rats [7.52 +/- 0.41 vs. 3.67 +/- 0.30 optical density (OD); P < 0.01]. The increase in aged rats (6.5 +/- 0.87 vs. 5.14 +/- 0.09 OD) did not reach statistical significance. Hypothyroidism was not associated with significant changes in serum ApoA1 levels in either young or aged rats. Hyperthyroidism was associated with a 2.5-fold increase in ApoA1 mRNA in young rats and a 1.7-fold increase in aged rats. Hypothyroidism was associated with a 3.6-fold reduction in ApoA1 mRNA in young rats, but there was no significant change in aged hypothyroid rats. Mobility shift assays indicated that the binding of transacting factors to ApoA1 promoter increased in hyperthyroid young rats but not in hyperthyroid aged rats. It is concluded that aging in rats is associated with reduced ApoA1 responsiveness to thyroid hormones. This altered responsiveness could partly be the result of changes in the binding activity of nuclear factors to the ApoA1 promoter.
为了确定甲状腺激素对载脂蛋白A1(ApoA1)基因表达的影响随年龄的变化,研究了4月龄(年轻)和26月龄(老年)的雄性Fischer 344大鼠。通过每天腹腔注射3,5,3'-三碘甲状腺原氨酸(15微克/100克体重)诱导甲状腺功能亢进10天。通过在饮用水中添加0.025%的甲巯咪唑诱导甲状腺功能减退4周。甲状腺功能亢进与年轻大鼠血清ApoA1水平升高有关[7.52±0.41对3.67±0.30光密度(OD);P<0.01]。老年大鼠的升高(6.5±0.87对5.14±0.09 OD)未达到统计学显著性。甲状腺功能减退在年轻或老年大鼠中均与血清ApoA1水平的显著变化无关。甲状腺功能亢进与年轻大鼠ApoA1 mRNA增加2.5倍和老年大鼠增加1.7倍有关。甲状腺功能减退与年轻大鼠ApoA1 mRNA减少3.6倍有关,但老年甲状腺功能减退大鼠无显著变化。凝胶迁移实验表明,甲状腺功能亢进的年轻大鼠中转录因子与ApoA1启动子的结合增加,但甲状腺功能亢进的老年大鼠中未增加。结论是大鼠衰老与ApoA1对甲状腺激素的反应性降低有关。这种反应性改变可能部分是核因子与ApoA1启动子结合活性变化的结果。