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催乳素激活蛋白激酶C并刺激大鼠肝脏中与生长相关的基因表达。

Prolactin activates protein kinase C and stimulates growth-related gene expression in rat liver.

作者信息

Crowe P D, Buckley A R, Zorn N E, Rui H

机构信息

Department of Pharmacology and Therapeutics, University of South Florida, Tampa.

出版信息

Mol Cell Endocrinol. 1991 Aug;79(1-3):29-35. doi: 10.1016/0303-7207(91)90092-7.

Abstract

We have examined the effect of prolactin (PRL) on growth-related gene expression, protein kinase C (PKC) activity and diacylglycerol (DAG) mass in rat liver. Hepatic levels of messenger (m)RNA for c-myc, ornithine decarboxylase (ODC) and beta-actin increased in a dose-dependent manner within 1 h after PRL administration. Prolactin also caused a transient elevation of liver DAG levels and particulate-associated PKC activity. The PRL-provoked increases in DAG mass and particulate PKC activity were coincident and maximal at 20 min and began declining toward control levels by 30 min. These results suggest a temporal relationship between PRL-stimulated DAG accumulation and PKC activation. Furthermore, the subsequent rapid induction of growth-related gene expression provides new information on the role of PRL as a hepatic mitogen.

摘要

我们已经研究了催乳素(PRL)对大鼠肝脏中与生长相关的基因表达、蛋白激酶C(PKC)活性和二酰基甘油(DAG)含量的影响。给予PRL后1小时内,肝脏中c-myc、鸟氨酸脱羧酶(ODC)和β-肌动蛋白的信使(m)RNA水平呈剂量依赖性增加。催乳素还导致肝脏DAG水平和颗粒相关PKC活性短暂升高。PRL引起的DAG含量和颗粒PKC活性增加是同时发生的,在20分钟时达到最大值,并在30分钟时开始下降至对照水平。这些结果表明PRL刺激的DAG积累与PKC激活之间存在时间关系。此外,随后迅速诱导的与生长相关的基因表达为PRL作为肝脏有丝分裂原的作用提供了新的信息。

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