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去势和雄激素治疗对大鼠前列腺腹叶中前列腺结合蛋白合成及其mRNA浓度的影响。

Influence of castration and androgen treatment on the synthesis of prostatic binding protein and the concentration of its mRNA in the rat ventral prostate.

作者信息

Bossyns D, Delaey B, Rombauts W, Heyns W

出版信息

J Steroid Biochem. 1986 Mar;24(3):661-8. doi: 10.1016/0022-4731(86)90840-x.

Abstract

The regulation by androgens of the synthesis of prostatic binding protein (PBP), an abundant secretory protein of the rat ventral prostate, was studied by measuring the rate of incorporation of [3H]leucine into total protein and into PBP by prostatic tissue in vitro. PBP-specific synthesis dropped to 30% of the intact level after 3 days and to 5.5% after 7 days. Administration of androgens to 7 day-castrated rats reversed these changes: 36% of the control value was reached after 3 days of treatment and 70% after 5 days. The mRNAs of PBP were measured under similar conditions by means of dot hybridization, using C1-, C2- and C3-specific cDNA-clones. The 3 mRNAs followed a parallel course. They decreased to about 18% on the third day after castration and to about 2% after 7 days. Androgen treatment of 7-day castrated rats produced a small increase of these levels after 1 day. After 3 days 15% of the intact level was reached. The general similarity of the time course of PBP synthesis and PBP mRNA levels in castrated and androgen treated rats supports a transcriptional regulation mechanism, although there also is some evidence for an influence on protein synthesis in general.

摘要

通过体外测定前列腺组织将[3H]亮氨酸掺入总蛋白和前列腺结合蛋白(PBP)中的速率,研究了雄激素对大鼠腹侧前列腺丰富分泌蛋白PBP合成的调节作用。PBP特异性合成在3天后降至完整水平的30%,7天后降至5.5%。给7天去势大鼠注射雄激素可逆转这些变化:治疗3天后达到对照值的36%,5天后达到70%。在类似条件下,使用C1、C2和C3特异性cDNA克隆,通过点杂交法测定PBP的mRNA。这三种mRNA遵循平行变化过程。去势后第三天它们降至约18%,7天后降至约2%。对7天去势大鼠进行雄激素治疗1天后,这些水平略有升高。3天后达到完整水平的15%。去势和雄激素处理大鼠中PBP合成和PBP mRNA水平的时间进程总体相似,这支持了转录调节机制,尽管也有一些证据表明雄激素对一般蛋白质合成有影响。

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