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雄激素可调节生长激素释放因子诱导的牛垂体前叶细胞在静态培养条件下释放生长激素。

Androgens modulate growth hormone-releasing factor-induced GH release from bovine anterior pituitary cells in static culture.

作者信息

Hassan H A, Merkel R A, Enright W J, Tucker H A

机构信息

Department of Animal Science, Michigan State University, East Lansing 48824.

出版信息

Domest Anim Endocrinol. 1992 Jul;9(3):209-17. doi: 10.1016/0739-7240(92)90034-u.

Abstract

Static primary cultures of bovine anterior pituitary (AP) cells were utilized to study the effect of sex steroids on basal growth hormone (GH) and GH-releasing hormone (GRF)-stimulated release of GH. The AP cells (5 x 10(5) cells/well) were allowed to attach for 72 hr and become confluent before treatments were imposed. Cells were incubated for an additional 24, 48 or 72 hr with either estradiol-17 beta (E2, 10(-11) to 10(-8) M), testosterone (T, 10(-8) to 10(-5) M), dihydrotestosterone (DHT, 10(-9) to 10(-6) M) or 5 alpha-androstane-3 alpha, 17 beta-diol (3 alpha-diol, 10(-11) to 10(-8) M). Media were collected every 24 hr and GH concentrations determined by RIA. Incubation of calf AP cells with gonadal steroids did not affect (P > 0.05) basal GH released at 24, 48, or 72 hr. In another experiment, calf AP cells were incubated with the same concentrations of the steroids for 24 hr, media harvested, cells washed and challenged in serum-free media for 1 hr with bovine GRF 1-44-NH2 (10(-8) M). In non-steroid treated wells, GRF increased (P < 0.05) GH from 58 to 134 ng/ml. Incubation with E2 or 3 alpha-diol did not affect (P > 0.05) GRF-induced GH release; however, preincubation with T (10(-5) M) and DHT (10(-9), 10(-8) and 10(-7) M) increased (P < 0.05) GRF-induced GH release above control concentrations (195, 235, 190 and 185 ng/ml, respectively). At the doses tested, sex steroids did not affect basal release of GH, but androgens increased responsiveness of somatotropes to GRF.

摘要

利用牛垂体前叶(AP)细胞的静态原代培养物来研究性类固醇对基础生长激素(GH)以及生长激素释放激素(GRF)刺激的GH释放的影响。在施加处理之前,将AP细胞(5×10⁵个细胞/孔)接种72小时直至汇合。细胞再分别用雌二醇-17β(E2,10⁻¹¹至10⁻⁸M)、睾酮(T,10⁻⁸至10⁻⁵M)、二氢睾酮(DHT,10⁻⁹至10⁻⁶M)或5α-雄甾烷-3α,17β-二醇(3α-二醇,10⁻¹¹至10⁻⁸M)孵育24、48或72小时。每24小时收集培养基,并通过放射免疫分析(RIA)测定GH浓度。用性腺类固醇孵育小牛AP细胞对24、48或72小时释放的基础GH没有影响(P>0.05)。在另一项实验中,将小牛AP细胞用相同浓度的类固醇孵育24小时,收集培养基,洗涤细胞,然后在无血清培养基中用牛GRF 1-44-NH₂(10⁻⁸M)刺激1小时。在未用类固醇处理的孔中,GRF使GH从58 ng/ml增加到134 ng/ml(P<0.05)。用E2或3α-二醇孵育不影响(P>0.05)GRF诱导GH释放;然而,用T(10⁻⁵M)和DHT(10⁻⁹、10⁻⁸和10⁻⁷M)预孵育会使GRF诱导的GH释放高于对照浓度(分别为195、235、190和185 ng/ml,P<0.05)。在所测试的剂量下,性类固醇不影响基础GH释放,但雄激素增加了生长激素细胞对GRF的反应性。

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