Kamegai Jun, Tamura Hideki, Shimizu Takako, Ishii Shinya, Sugihara Hitoshi, Oikawa Shinichi
Department of Medicine, Nippon Medical School, 1-1-5 Sendagi, Bunkyo-Ku, Tokyo 113-8603, Japan.
Regul Pept. 2005 Apr 15;127(1-3):203-6. doi: 10.1016/j.regpep.2004.12.001.
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.
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。