Gold E, Stapley S, Goulding A
Department of Medicine, University of Otago, Dunedin, New Zealand.
Horm Metab Res. 1994 Feb;26(2):100-3. doi: 10.1055/s-2007-1000782.
It is important that drugs which are used to protect bone from the osteoporotic effects of estrogen deficiency should not affect plasma lipids adversely. Effects of a) norethisterone acetate and b) tamoxifen citrate on plasma cholesterol and on bone conservation in rats with normal plasma 17B-estradiol and in rats made estrogen-deficient with the LHRH agonist, buserelin are reported. Tamoxifen halved total plasma cholesterol (p < 0.01), whereas norethisterone did not lower plasma cholesterol. Furthermore tamoxifen fully protected bone from estrogen-deficiency osteopenia whereas norethisterone conserved bone less well. Reductions in cholesterol elicited by tamoxifen were similar in estrogen-deficient rats and in rats with normal ovarian function. This is the first report in the rat that tamoxifen has lipid-lowering actions. It is suggested the rat may be useful for future investigations of the lipid-lowering mechanisms of tamoxifen.
用于保护骨骼免受雌激素缺乏导致的骨质疏松影响的药物不应不利地影响血浆脂质,这一点很重要。本文报道了a)醋酸炔诺酮和b)枸橼酸他莫昔芬对血浆17β-雌二醇正常的大鼠以及用促黄体生成素释放激素(LHRH)激动剂布舍瑞林造成雌激素缺乏的大鼠的血浆胆固醇和骨保护作用。他莫昔芬使总血浆胆固醇减半(p < 0.01),而炔诺酮未降低血浆胆固醇。此外,他莫昔芬能充分保护骨骼免受雌激素缺乏导致的骨质减少,而炔诺酮对骨骼的保护作用较差。他莫昔芬引起的胆固醇降低在雌激素缺乏的大鼠和卵巢功能正常的大鼠中相似。这是在大鼠中首次报道他莫昔芬具有降血脂作用。提示大鼠可能对未来研究他莫昔芬的降血脂机制有用。