Roh Sang-Gun, Doconto Maria, Feng Dan Dan, Chen Chen
Department of Food Production Science, Faculty of Agriculture, Shinshu University, Nagano-ken 5399-4598, Japan.
Endocrine. 2006 Aug;30(1):55-62. doi: 10.1385/ENDO:30:1:55.
GH secretion is regulated by GHRH and somatostatin via actions on their specific receptors in pituitary somatotropes. Ghrelin and synthetic analogs, GHRPs, also stimulate GH release via GHS-receptors (GHS-R). To examine the long-term effect of GHRH and/or GHRP on somatotropes, primary cultured ovine somatotropes were treated with GHRH (10(-9) and 10(-8) M) and GHRP-2 (10(-8) and 10(-7) M) for up to 2 d. After treatment, culture medium was collected for GH assay, and total RNA was extracted for RT-PCR analysis. To evaluate cell cultures used in this report, somatotrope-enriched pituitary cells were challenged by 6 h GHRH and dexamethasone (DEX) treatment. As expected, GHRH significantly decreased, whereas DEX increased, the levels of GHRHR mRNA. Combined low doses of GHRH (10(-9) M) and GHRP-2 (10(-8) M) treatment for 24 h increased accumulated GH secretion, significantly more than that induced by high doses of GHRH (10(-8) M) and GHRP-2 (10(-7) M). While levels of GHRH-R mRNA increased, GHS-R mRNA levels were decreased by low doses of GHRH and GHRP-2 for 24 h. High doses of GHRH and/or GHRP-2 for 2 d did not increase GH secretion in the second day of treatment and reduced the level of GHRH-R mRNA. High doses of GHRP-2 treatment decreased the levels of both GHRH-R and GHS-R mRNA. Low doses of GHRH and/or GHRP-2 for 2 d increased the level of GHS-R mRNA without changing GHRH-R mRNA levels. Such treatment also increased ghrelin- (10(-9) M) or ghrelin/GHRH (10(-9) M)-induced GH secretion. These results suggest that low doses of GHRP-2 and GHRH prime somatotropes for stimulation by GHRH and ghrelin.
生长激素(GH)的分泌受生长激素释放激素(GHRH)和生长抑素调节,它们通过作用于垂体生长激素细胞上的特定受体发挥作用。胃饥饿素及其合成类似物生长激素释放肽(GHRPs)也通过生长激素促分泌素受体(GHS-R)刺激GH释放。为了研究GHRH和/或GHRP对生长激素细胞的长期影响,将原代培养的绵羊生长激素细胞用GHRH(10⁻⁹和10⁻⁸M)和GHRP-2(10⁻⁸和10⁻⁷M)处理长达2天。处理后,收集培养基进行GH测定,并提取总RNA进行逆转录聚合酶链反应(RT-PCR)分析。为了评估本报告中使用的细胞培养物,用GHRH和地塞米松(DEX)处理富含生长激素细胞的垂体细胞6小时。正如预期的那样,GHRH显著降低,而DEX增加了生长激素释放激素受体(GHRHR)mRNA的水平。联合低剂量的GHRH(10⁻⁹M)和GHRP-2(10⁻⁸M)处理24小时增加了累积的GH分泌,显著多于高剂量的GHRH(10⁻⁸M)和GHRP-2(10⁻⁷M)诱导的分泌。虽然GHRH受体(GHRH-R)mRNA水平增加,但低剂量的GHRH和GHRP-2处理24小时会降低GHS-R mRNA水平。高剂量的GHRH和/或GHRP-2处理2天在处理的第二天并没有增加GH分泌,反而降低了GHRH-R mRNA的水平。高剂量的GHRP-2处理降低了GHRH-R和GHS-R mRNA的水平。低剂量的GHRH和/或GHRP-2处理2天增加了GHS-R mRNA的水平,而没有改变GHRH-R mRNA的水平。这种处理还增加了胃饥饿素(10⁻⁹M)或胃饥饿素/GHRH(10⁻⁹M)诱导的GH分泌。这些结果表明,低剂量的GHRP-2和GHRH使生长激素细胞对GHRH和胃饥饿素的刺激产生预适应。