Wolfe B M, Huff M W
Department of Medicine, University Hospital, London, Ontario, Canada.
J Clin Invest. 1989 Jan;83(1):40-5. doi: 10.1172/JCI113882.
Treatment of postmenopausal women with low doses of estradiol-17 beta (1 mg/d) and dl-norgestrel (0.075 [corrected] mg/d) significantly reduced fasting serum levels of low density lipoprotein (LDL) cholesterol and lowered very low density lipoprotein (VLDL) triglycerides in four of five subjects. To explain these results, the kinetics of VLDL and LDL apolipoprotein (apo) B turnover were studied by injecting autologous 125I-labeled VLDL and 131I-labeled LDL into subjects before discontinuing long-term (4-yr) treatment with the estradiol-17 beta and dl-norgestrel and again 7 wk after stopping treatment. The 24% mean decrease in VLDL apo B pool size during treatment was associated with a significant increase in VLDL apo B fractional catabolic rate (15 +/- 1 vs. 11 +/- 1 pools/d), whereas production rate was similar to control (24 +/- 3 vs. 21 +/- 2 mg/kg per d). There was a significant 25% mean decrease in LDL apo B pool size (27 +/- 2 vs. 36 +/- 3 mg/kg) due to a significant decrease in total (8.3 +/- 0.3 vs. 11 +/- 1 mg/kg per d) and independent (3.3 +/- 0.5 vs. 6.6 +/- 0.8 mg/kg per d, P less than 0.05) LDL apo B production. Estradiol-17 beta together with dl-norgestrel lowered plasma VLDL by enhancing their clearance and LDL by reducing their production.
用低剂量的17β-雌二醇(1毫克/天)和炔诺孕酮(0.075[校正后]毫克/天)治疗绝经后女性,在五名受试者中有四名显著降低了空腹血清低密度脂蛋白(LDL)胆固醇水平,并降低了极低密度脂蛋白(VLDL)甘油三酯水平。为了解释这些结果,在停止长期(4年)使用17β-雌二醇和炔诺孕酮治疗前,以及停药7周后,通过向受试者注射自体125I标记的VLDL和131I标记的LDL,研究了VLDL和LDL载脂蛋白(apo)B的代谢动力学。治疗期间VLDL apo B池大小平均下降24%,与VLDL apo B分解代谢率显著增加有关(15±1对11±1池/天),而生成率与对照组相似(24±3对21±2毫克/千克每天)。LDL apo B池大小平均显著下降25%(27±2对36±3毫克/千克),这是由于LDL apo B总生成量(8.3±0.3对11±1毫克/千克每天)和独立生成量(3.3±0.5对6.6±0.8毫克/千克每天,P<0.05)显著下降所致。17β-雌二醇与炔诺孕酮一起,通过增强VLDL的清除率降低血浆VLDL水平,并通过减少LDL的生成量降低LDL水平。