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含非烷基化雌激素成分的口服避孕药。对脂质代谢的影响。

Oral contraception with a nonalkylated estrogen component. Effects on lipid metabolism.

作者信息

Samsioe G, Skryten A, Silfverstolpe G

出版信息

Gynecol Obstet Invest. 1983;15(5):275-82. doi: 10.1159/000299421.

DOI:10.1159/000299421
PMID:6852647
Abstract

All commercially available combined oral contraceptives have 17-C-alkylated estrogens (ethinylestradiol or mestranol) as their estrogen components. In postmenopausal replacement therapy nonalkylated 'natural' estrogens have been shown to induce less adverse effects in lipid metabolism than alkylated estrogens. To see if this difference is valid also when the respective kinds of estrogens are used as components in oral contraceptives, the lipid metabolic effects from two preparations with the same progestogen component (norethisterone acetate) but with nonalkylated (17 beta-estradiol; Netagen) and alkylated (ethinylestradiol) estrogen (Netasyn) have been evaluated. Phospholipids, cholesterol, and triglycerides have been assessed in serum and in ultracentrifugally isolated lipoprotein fractions. The serum lecithin fatty acid composition has been analysed by gas-liquid chromatography. Netasyn increased the triglyceride content of serum and all lipoprotein fractions while Netagen did not. Netasyn caused a redistribution in the 1-position fatty acids of serum lecithin with an increase in palmitic and a concomitant decrease in stearic acid, a pattern associated with the 17-C-alkylation of a steroid and probably its capacity to inhibit liver excretory function. In the present study the preparation with the non-alkylated estrogen component had less adverse lipid metabolic effects than the conventional oral contraceptive.

摘要

所有市售的复方口服避孕药都含有17-C-烷基化雌激素(炔雌醇或炔诺酮)作为其雌激素成分。在绝经后替代疗法中,已证明非烷基化的“天然”雌激素在脂质代谢方面比烷基化雌激素引起的不良反应更少。为了探究当各自种类的雌激素用作口服避孕药的成分时这种差异是否也成立,对两种制剂的脂质代谢作用进行了评估,这两种制剂具有相同的孕激素成分(醋酸炔诺酮),但分别含有非烷基化雌激素(17β-雌二醇;Netagen)和烷基化雌激素(炔雌醇)(Netasyn)。对血清和超速离心分离的脂蛋白组分中的磷脂、胆固醇和甘油三酯进行了评估。通过气液色谱法分析了血清卵磷脂脂肪酸组成。Netasyn增加了血清和所有脂蛋白组分中的甘油三酯含量,而Netagen没有。Netasyn导致血清卵磷脂1位脂肪酸重新分布,棕榈酸增加,硬脂酸相应减少,这种模式与类固醇的17-C-烷基化及其可能抑制肝脏排泄功能的能力有关。在本研究中,含有非烷基化雌激素成分的制剂比传统口服避孕药具有更少的不良脂质代谢作用。

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1
Oral contraception with a nonalkylated estrogen component. Effects on lipid metabolism.含非烷基化雌激素成分的口服避孕药。对脂质代谢的影响。
Gynecol Obstet Invest. 1983;15(5):275-82. doi: 10.1159/000299421.
2
A two-year clinical study of the effects of two triphasic oral contraceptives on plasma lipids.一项关于两种三相口服避孕药对血脂影响的两年临床研究。
Int J Fertil Menopausal Stud. 1994 Sep-Oct;39(5):283-91.
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Oral contraceptive and postmenopausal estrogen effects on lipoprotein triglyceride and cholesterol in an adult female population: relationships to estrogen and progestin potency.口服避孕药和绝经后雌激素对成年女性人群脂蛋白甘油三酯和胆固醇的影响:与雌激素和孕激素效力的关系。
J Clin Endocrinol Metab. 1981 Dec;53(6):1123-32. doi: 10.1210/jcem-53-6-1123.
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Lipid metabolic studies in oophorectomized women: effects induced by two different estrogens on serum lipids and lipoproteins.卵巢切除术后女性的脂质代谢研究:两种不同雌激素对血清脂质和脂蛋白的影响。
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Does progestogen reduction in oral contraception parallel reduced lipid metabolic effects?口服避孕药中孕激素减少是否与脂质代谢影响降低平行?
Acta Obstet Gynecol Scand Suppl. 1982;105:41-4. doi: 10.3109/00016348209155317.
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Effect of estrogen/progestin potency on lipid/lipoprotein cholesterol.雌激素/孕激素效力对脂质/脂蛋白胆固醇的影响。
N Engl J Med. 1983 Apr 14;308(15):862-7. doi: 10.1056/NEJM198304143081502.
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The influence of oral contraceptive steroids on serum lipids.口服避孕类固醇对血脂的影响。
Am J Obstet Gynecol. 1973 Jul 1;116(5):727-49. doi: 10.1016/s0002-9378(15)33144-6.
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Effects of oral contraceptives on lipoprotein triglyceride and cholesterol: relationships to estrogen and progestin potency.口服避孕药对脂蛋白甘油三酯和胆固醇的影响:与雌激素和孕激素效力的关系。
Am J Obstet Gynecol. 1982 Mar 15;142(6 Pt 2):725-31. doi: 10.1016/s0002-9378(16)32478-4.
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[Influence of progestins on adverse effects of oral contraceptives].[孕激素对口服避孕药不良反应的影响]
Contracept Fertil Sex (Paris). 1985 Jan;13(1 Suppl):425-30.
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[Hormonal contraception and lipid metabolism. Prospective and retrospective studies of lipid metabolic parameters during the use of contraceptives].[激素避孕与脂质代谢。避孕药使用期间脂质代谢参数的前瞻性和回顾性研究]
Fortschr Med. 1979 Nov 1;97(41):1858-61.