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胰岛素样生长因子-I下调大鼠垂体中胃饥饿素受体(生长激素促分泌素受体)的表达。

Insulin-like growth factor-I down-regulates ghrelin receptor (growth hormone secretagogue receptor) expression in the rat pituitary.

作者信息

Kamegai Jun, Tamura Hideki, Shimizu Takako, Ishii Shinya, Sugihara Hitoshi, Oikawa Shinichi

机构信息

Department of Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-Ku, Tokyo 113-8603, Japan.

出版信息

Regul Pept. 2005 Apr 15;127(1-3):203-6. doi: 10.1016/j.regpep.2004.12.001.

Abstract

The effects of insulin-like growth factor-I (IGF-I) on the ghrelin receptor [growth hormone secretagogue receptor (GHS-R)] gene expression and on the GH response to GHS in rat pituitary cell cultures were examined. Pituitary GHS-R mRNA levels were decreased in a dose (0.01-10 nM)- and time (4-12 h)-dependent manner by IGF-I as measured with reverse transcriptase (RT)-PCR. The basal GH secretion was not influenced by the pretreatment with IGF-I (1 nM for 8 h); however, the GH response to the receptor ligand, a synthetic GHS, KP-102 (100 nM, 15 min), was significantly reduced by pretreatment with IGF-I. Thus, the present studies indicate that IGF-I could inhibit GH secretion at least in part by regulating the expression of the GHS-R.

摘要

研究了胰岛素样生长因子-I(IGF-I)对大鼠垂体细胞培养物中胃饥饿素受体[生长激素促分泌素受体(GHS-R)]基因表达以及对生长激素(GH)对生长激素促分泌素(GHS)反应的影响。用逆转录酶(RT)-PCR检测发现,IGF-I以剂量(0.01 - 10 nM)和时间(4 - 12小时)依赖性方式降低垂体GHS-R mRNA水平。IGF-I(1 nM,8小时)预处理不影响基础GH分泌;然而,IGF-I预处理显著降低了GH对受体配体(一种合成GHS,KP-102,100 nM,15分钟)的反应。因此,本研究表明IGF-I至少部分通过调节GHS-R的表达来抑制GH分泌。

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