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戈那瑞林激动剂类似物地加瑞克对子宫肌瘤和平滑肌层中雌激素、硫酸酯雌激素及孕激素受体的影响。

Effect of Decapeptyl, an agonistic analog of gonadotropin-releasing hormone on estrogens, estrogen sulfates, and progesterone receptors in leiomyoma and myometrium.

作者信息

Pasqualini J R, Cornier E, Grenier J, Vella C, Schatz B, Netter A

机构信息

C.N.R.S. Steroid Hormone Research Unit, Foundation for Hormone Research, Paris, France.

出版信息

Fertil Steril. 1990 Jun;53(6):1012-7.

PMID:2140991
Abstract

Estrogens (estrone [E1] and estradiol [E2]), their sulfates and progesterone receptor (PR) were evaluated in patients with uterine leiomyomata nontreated and treated with Decapeptyl (D-Trp6-gonadotropin-releasing hormone [GnRH]; Ipsen Biotech, Paris, France). Estrogen concentrations are very high in the leiomyoma (secretory phase, pg/g tissue [mean +/- SEM]: n = 10; E1: 147 +/- 24; E2: 850 +/- 116; E1-sulfate: 1,668 +/- 808; E2-sulfate: 718 +/- 126). Decapeptyl treatment provokes a significant decrease in E2 and particularly in E1 and E2 sulfates. Progesterone receptors were higher in the leiomyoma than in the myometrium; after a long treatment (3 to 4 months) a significant decrease in both tissues is observed. The decrease provoked by D-Trp6-GnRH on estrogens (unconjugated and sulfates) and in PR in the leiomyoma after long treatment, supports the hypothesis that estrogens are implicated in the cause of these tumors.

摘要

对未接受治疗及接受曲普瑞林(D-色氨酸6-促性腺激素释放激素[GnRH];法国巴黎益普生生物技术公司生产)治疗的子宫肌瘤患者的雌激素(雌酮[E1]和雌二醇[E2])、其硫酸盐及孕激素受体(PR)进行了评估。子宫肌瘤中的雌激素浓度非常高(分泌期,pg/g组织[均值±标准误]:n = 10;E1:147±24;E2:850±116;E1-硫酸盐:1,668±808;E2-硫酸盐:718±126)。曲普瑞林治疗可使E2,尤其是E1和E2硫酸盐显著降低。子宫肌瘤中的孕激素受体高于子宫肌层;经过长期治疗(3至4个月)后,观察到两种组织中的孕激素受体均显著降低。长期治疗后,D-色氨酸6-GnRH对子宫肌瘤中雌激素(未结合型和硫酸盐型)及PR的降低作用支持了雌激素与这些肿瘤病因有关的假说。

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Effect of Decapeptyl, an agonistic analog of gonadotropin-releasing hormone on estrogens, estrogen sulfates, and progesterone receptors in leiomyoma and myometrium.戈那瑞林激动剂类似物地加瑞克对子宫肌瘤和平滑肌层中雌激素、硫酸酯雌激素及孕激素受体的影响。
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