• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Parallel studies of His-DTrp-Ala-Trp-DPhe-Lys-NH2 and human pancreatic growth hormone-releasing factor-44-NH2 in rat primary pituitary cell monolayer culture.

作者信息

Sartor O, Bowers C Y, Chang D

出版信息

Endocrinology. 1985 Mar;116(3):952-7. doi: 10.1210/endo-116-3-952.

DOI:10.1210/endo-116-3-952
PMID:3918849
Abstract

His-DTrp-Ala-Trp-DPhe-Lys-NH2 (GH-RP-6) is a synthetic hexapeptide that specifically releases GH both in vivo and in vitro in pituitary incubates. In this study, for the first time, GH-RP-6 was studied in primary pituitary cell monolayer culture. Parallel studies were performed with human pancreatic GH-releasing factor-44 (hpGRF-44). Culture conditions optimal for GH-RP-6 were not optimal for hpGRF-44. Both peptides released GH in a dose- and time-dependent manner. In this assay system, the ED50 for GH-RP-6 was 9 nM, and the ED50 for hp-GRF-44 was 1.6 nM. Calcium-blocking agents inhibited the GH responses of both peptides as well as basal GH release. Pretreatment with GH-RP-6 decreased the subsequent response to both GH-RP-6 and hpGRF-44. hpGRF-44 down regulated itself but not GH-RP-6. Rat sera potentiated the GH response of hpGRF-44 but not that of GH-RP-6. GH-RP-6 and hpGRF-44 GH responses were additive. These results suggest that GH-RP-6 and hpGRF-44 stimulate GH release via different somatotroph receptors.

摘要

相似文献

1
Parallel studies of His-DTrp-Ala-Trp-DPhe-Lys-NH2 and human pancreatic growth hormone-releasing factor-44-NH2 in rat primary pituitary cell monolayer culture.
Endocrinology. 1985 Mar;116(3):952-7. doi: 10.1210/endo-116-3-952.
2
The synergistic effects of His-D-Trp-Ala-Trp-D-Phe-Lys-NH2 on growth hormone (GH)-releasing factor-stimulated GH release and intracellular adenosine 3',5'-monophosphate accumulation in rat primary pituitary cell culture.组氨酸-右旋色氨酸-丙氨酸-色氨酸-右旋苯丙氨酸-赖氨酸-氨基在大鼠原代垂体细胞培养中对生长激素释放因子刺激的生长激素释放及细胞内3',5'-环磷酸腺苷积累的协同作用。
Endocrinology. 1989 Jun;124(6):2791-8. doi: 10.1210/endo-124-6-2791.
3
Differential responsiveness of the somatotroph to growth hormone-releasing factor during early neonatal development in the rat.大鼠出生后早期发育过程中生长激素细胞对生长激素释放因子的反应差异
Endocrinology. 1986 Jan;118(1):69-73. doi: 10.1210/endo-118-1-69.
4
Growth hormone releasing effect of hpGRF-40 in rats at different time intervals following ablation of the mediobasal hypothalamus.下丘脑正中基底部切除术后不同时间间隔下hpGRF-40对大鼠的生长激素释放作用。
Life Sci. 1984 Nov 5;35(19):1989-95. doi: 10.1016/0024-3205(84)90480-6.
5
The effects of growth hormone (GH)-releasing peptides on GH secretion in perifused pituitary cells of adult male rats.生长激素释放肽对成年雄性大鼠垂体细胞灌流中生长激素分泌的影响。
Endocrinology. 1984 Oct;115(4):1432-8. doi: 10.1210/endo-115-4-1432.
6
Effect of intravenous administration of growth hormone-releasing factor (hpGRF-44) and Tyr-D-Trp-Ala-Trp-D-Phe-NH2 on plasma hormones and metabolites in goats.
J Endocrinol. 1984 Nov;103(2):173-8. doi: 10.1677/joe.0.1030173.
7
Evidence for a role of protein kinase-C in His-D-Trp-Ala-Trp-D-Phe-Lys-NH2-induced growth hormone release from rat primary pituitary cells.蛋白激酶-C在组氨酸-右旋色氨酸-丙氨酸-色氨酸-右旋苯丙氨酸-赖氨酸-氨基诱导大鼠原代垂体细胞释放生长激素中作用的证据。
Endocrinology. 1991 Dec;129(6):3337-42. doi: 10.1210/endo-129-6-3337.
8
The effects of thyroid hormone deprivation in vivo and in vitro on growth hormone (GH) responses to human pancreatic (tumor) GH-releasing factor (1-40) by dispersed rat anterior pituitary cells.体内和体外甲状腺激素缺乏对大鼠分散垂体前叶细胞对人胰腺(肿瘤)生长激素释放因子(1-40)的生长激素(GH)反应的影响。
Endocrinology. 1985 Mar;116(3):1066-70. doi: 10.1210/endo-116-3-1066.
9
Pituitary growth hormone response in rats during a 24-hour infusion of growth hormone-releasing factor.
Endocrinology. 1984 May;114(5):1613-6. doi: 10.1210/endo-114-5-1613.
10
Variables determining the growth hormone response of His-D-Trp-Ala-Trp-D-Phe-Lys-NH2 in the rat.决定大鼠体内His-D-Trp-Ala-Trp-D-Phe-Lys-NH2生长激素反应的变量。
Endocrinology. 1985 Oct;117(4):1441-7. doi: 10.1210/endo-117-4-1441.

引用本文的文献

1
Functional Pituitary Networks in Vertebrates.脊椎动物的功能性垂体网络。
Front Endocrinol (Lausanne). 2021 Jan 27;11:619352. doi: 10.3389/fendo.2020.619352. eCollection 2020.
2
Differential regulation of GHRH-receptor and GHS-receptor expression by long-term in vitro treatment of ovine pituitary cells with GHRP-2 and GHRH.用生长激素释放肽-2(GHRP-2)和生长激素释放激素(GHRH)对绵羊垂体细胞进行长期体外处理后,生长激素释放激素受体(GHRH-receptor)和生长激素促分泌素受体(GHS-receptor)表达的差异调节
Endocrine. 2006 Aug;30(1):55-62. doi: 10.1385/ENDO:30:1:55.
3
Revealing the large-scale network organization of growth hormone-secreting cells.
揭示生长激素分泌细胞的大规模网络组织。
Proc Natl Acad Sci U S A. 2005 Nov 15;102(46):16880-5. doi: 10.1073/pnas.0508202102. Epub 2005 Nov 4.
4
The effects of a continuous infusion of hexarelin on pulsatile growth hormone release, growth axis and galanin gene expression and on the response of the growth axis to growth hormone-releasing hormone.持续输注六肽生长激素释放肽对脉冲式生长激素释放、生长轴和甘丙肽基因表达以及生长轴对生长激素释放激素反应的影响。
Pituitary. 2000 May;2(4):253-60. doi: 10.1023/a:1009957015563.
5
Influence of beta-adrenergic agonists and antagonists on the GH-releasing effect of Hexarelin in man.β-肾上腺素能激动剂和拮抗剂对海沙瑞林在人体中促生长激素释放作用的影响。
J Endocrinol Invest. 1996 Jan;19(1):25-9. doi: 10.1007/BF03347854.
6
GH responsiveness to repeated GHRH or hexarelin administration in normal adults.正常成年人中生长激素(GH)对重复给予生长激素释放激素(GHRH)或司坦雷肽的反应性。
J Endocrinol Invest. 1995 Oct;18(9):718-22. doi: 10.1007/BF03349794.
7
Arginine enhances the growth hormone-releasing activity of a synthetic hexapeptide (GHRP-6) in elderly but not in young subjects after oral administration.口服后,精氨酸可增强合成六肽(GHRP - 6)在老年受试者中的生长激素释放活性,但在年轻受试者中则不然。
J Endocrinol Invest. 1994 Mar;17(3):157-62. doi: 10.1007/BF03347707.
8
Thyroid hormones and growth hormone secretion.甲状腺激素与生长激素分泌
J Endocrinol Invest. 1992 Apr;15(4):313-30. doi: 10.1007/BF03348744.