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生长激素缺乏症小老鼠对生长激素释放肽-2的生长激素反应。

Growth hormone response to growth hormone-releasing peptide-2 in growth hormone-deficient little mice.

机构信息

Biotechnology Department, National Nuclear Energy Commission, Cidade Universitária, São Paulo, SP, Brazil.

出版信息

Clinics (Sao Paulo). 2012;67(3):265-72. doi: 10.6061/clinics/2012(03)11.

DOI:10.6061/clinics/2012(03)11
PMID:22473409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3297037/
Abstract

OBJECTIVE

To investigate a possible direct, growth hormone-releasing, hormone-independent action of a growth hormone secretagogue, GHRP-2, in pituitary somatotroph cells in the presence of inactive growth hormone-releasing hormone receptors.

MATERIALS AND METHODS

The responses of serum growth hormone to acutely injected growth hormone-releasing P-2 in lit/lit mice, which represent a model of GH deficiency arising from mutated growth hormone-releasing hormone-receptors, were compared to those observed in the heterozygous (lit/+) littermates and wild-type (+/+) C57BL/6J mice.

RESULTS

After the administration of 10 mcg of growth hormone-releasing P-2 to lit/lit mice, a growth hormone release of 9.3±1.5 ng/ml was observed compared with 1.04±1.15 ng/ml in controls (p<0.001). In comparison, an intermediate growth hormone release of 34.5±9.7 ng/ml and a higher growth hormone release of 163±46 ng/ml were induced in the lit/+ mice and wild-type mice, respectively. Thus, GHRP-2 stimulated growth hormone in the lit/lit mice, and the release of growth hormone in vivo may be only partially dependent on growth hormone-releasing hormone. Additionally, the plasma leptin and ghrelin levels were evaluated in the lit/lit mice under basal and stimulated conditions.

CONCLUSIONS

Here, we have demonstrated that lit/lit mice, which harbor a germline mutation in the Growth hormone-releasing hormone gene, maintain a limited but statistically significant growth hormone elevation after exogenous stimulation with GHRP-2. The present data probably reflect a direct, growth hormone-independent effect on Growth hormone S (ghrelin) stimulation in the remaining pituitary somatotrophs of little mice that is mediated by growth hormone S-R 1a.

摘要

目的

研究生长激素释放肽-2(GHRP-2)在生长激素释放激素受体失活的情况下,对垂体生长激素细胞是否具有直接的、独立于激素的促生长激素释放作用。

材料与方法

比较了突变型生长激素释放激素受体导致的 GH 缺乏模型(lit/lit 小鼠)和杂合子(lit/+)同窝仔鼠及野生型(+/+)C57BL/6J 小鼠,急性注射 GHRP-2 后血清生长激素的反应。

结果

10μg GHRP-2 给药后,lit/lit 小鼠生长激素释放 9.3±1.5ng/ml,与对照组(p<0.001)的 1.04±1.15ng/ml 相比显著升高。相比之下,lit/+ 鼠和野生型鼠分别诱导出中间水平的 34.5±9.7ng/ml 和更高水平的 163±46ng/ml 生长激素释放。因此,GHRP-2 刺激 lit/lit 小鼠生长激素释放,而体内生长激素的释放可能仅部分依赖于生长激素释放激素。此外,在基础和刺激条件下,还评估了 lit/lit 小鼠的血浆瘦素和 ghrelin 水平。

结论

本研究表明,携带生长激素释放激素基因种系突变的 lit/lit 小鼠,在外源 GHRP-2 刺激下仍能维持有限但具有统计学意义的生长激素升高。这些数据可能反映了 GHRP-2 通过生长激素 S-R1a 对剩余垂体生长激素细胞的直接、独立于激素的作用,刺激生长激素 S(ghrelin)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/167dd59cfd92/cln-67-03-265-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/3db1b7408e6d/cln-67-03-265-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/934b4af54b3f/cln-67-03-265-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/3ec21d9bde81/cln-67-03-265-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/167dd59cfd92/cln-67-03-265-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/3db1b7408e6d/cln-67-03-265-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/934b4af54b3f/cln-67-03-265-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/3ec21d9bde81/cln-67-03-265-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9399/3297037/167dd59cfd92/cln-67-03-265-g004.jpg

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