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Growth hormone-releasing activity of growth hormone-releasing peptide-6 is maintained after short-term oral pretreatment with the hexapeptide in normal aging.

作者信息

Ghigo E, Arvat E, Rizzi G, Goffi S, Grottoli S, Mucci M, Boghen M F, Camanni F

机构信息

Department of Pathophysiology, University of Turin, Italy.

出版信息

Eur J Endocrinol. 1994 Nov;131(5):499-503. doi: 10.1530/eje.0.1310499.

DOI:10.1530/eje.0.1310499
PMID:7952160
Abstract

The reduced activity of the growth hormone (GH)-insulin-like growth factor I (IGF-I) axis in aging may contribute to changes in body composition. As this GH insufficiency is due to hypothalamic pathogenesis, the availability of GH-releasing peptides (GHRPs), such as GHRP-6 (His-D-Trp-Ala-Trp-D-Phe-Lys-NH2) which is active even after oral administration, might be useful to restore it. The aim of our study was to verify the effectiveness of oral administration of GHRP-6 in normal elderly subjects and to investigate whether its GH-releasing activity is maintained or vanishes after short-term oral treatment. Seven normal elderly women (aged 65-82 years) were studied. The effect of oral administration of 300 micrograms/kg GHRP-6 on GH secretion was investigated before and after 4 days of treatment with the hexapeptide given twice daily. The GH response to the maximal effective dose of GHRH (1 microgram/kg i.v.) also was studied. Before treatment, oral administration of 300 micrograms/kg GHRP-6 elicited a clear GH rise (peak 10.7 +/- 3.3 micrograms/l; AUC 353.1 +/- 90.6 micrograms.l-1.h-1), which was significantly higher (p < 0.01) than that induced by intravenous GHRH (peak 5.1 +/- 1.5 micrograms/l; AUC 106.5 +/- 43.9 micrograms.l-1.h-1). After 4 days of treatment with GHRP-6, the GH response to the hexapeptide was maintained, with a trend towards an increase (peak 16.8 +/- 2.9 micrograms/l; AUC 499.8 +/- 107.2 micrograms.l-1.h-1). The IGF-I levels were not increased significantly after treatment (77.1 +/- 8.4 vs 84.1 +/- 12.2 micrograms/l).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

相似文献

1
Growth hormone-releasing activity of growth hormone-releasing peptide-6 is maintained after short-term oral pretreatment with the hexapeptide in normal aging.
Eur J Endocrinol. 1994 Nov;131(5):499-503. doi: 10.1530/eje.0.1310499.
2
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.
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Growth hormone-releasing effect of oral growth hormone-releasing peptide 6 (GHRP-6) administration in children with short stature.口服生长激素释放肽6(GHRP-6)对身材矮小儿童的生长激素释放作用。
Eur J Endocrinol. 1995 Oct;133(4):425-9. doi: 10.1530/eje.0.1330425.
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Short-term administration of intranasal or oral Hexarelin, a synthetic hexapeptide, does not desensitize the growth hormone responsiveness in human aging.短期经鼻或口服六肽生长激素释放肽(一种合成六肽)不会使人体衰老过程中的生长激素反应性脱敏。
Eur J Endocrinol. 1996 Oct;135(4):407-12. doi: 10.1530/eje.0.1350407.
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Influence of endogenous cholinergic tone and alpha-adrenergic pathways on growth hormone responses to His-D-Trp-Ala-Trp-D-Phe-Lys-NH2 in the dog.内源性胆碱能张力和α-肾上腺素能途径对犬生长激素对组氨酸-右旋色氨酸-丙氨酸-右旋色氨酸-右旋苯丙氨酸-赖氨酸-氨基的反应的影响。
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Age-related variations in the neuroendocrine control, more than impaired receptor sensitivity, cause the reduction in the GH-releasing activity of GHRPs in human aging.与年龄相关的神经内分泌控制变化,而非受体敏感性受损,导致了生长激素释放肽(GHRPs)在人类衰老过程中生长激素释放活性的降低。
Pituitary. 1998 Apr;1(1):51-8. doi: 10.1023/a:1009970909015.
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Effects of GHRP-2 and hexarelin, two synthetic GH-releasing peptides, on GH, prolactin, ACTH and cortisol levels in man. Comparison with the effects of GHRH, TRH and hCRH.两种合成的生长激素释放肽GHRP-2和六元瑞林对人体生长激素、催乳素、促肾上腺皮质激素和皮质醇水平的影响。与生长激素释放激素、促甲状腺激素释放激素和人促肾上腺皮质激素释放激素的作用比较。
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Low hexarelin dose and pyridostigmine have additive effect and potentiate to the same extent the GHRH-induced GH response in man.低剂量六氢瑞林和吡啶斯的明具有相加作用,且在同等程度上增强生长激素释放激素诱导的人体生长激素反应。
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Acute growth hormone (GH) response to GH-releasing hexapeptide in humans is independent of endogenous GH-releasing hormone.
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Arginine and growth hormone-releasing hormone restore the blunted growth hormone-releasing activity of hexarelin in elderly subjects.精氨酸和生长激素释放激素可恢复老年受试者中六肽生长激素释放肽减弱的生长激素释放活性。
J Clin Endocrinol Metab. 1994 Nov;79(5):1440-3. doi: 10.1210/jcem.79.5.7962341.

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Age-related variations in the neuroendocrine control, more than impaired receptor sensitivity, cause the reduction in the GH-releasing activity of GHRPs in human aging.
与年龄相关的神经内分泌控制变化,而非受体敏感性受损,导致了生长激素释放肽(GHRPs)在人类衰老过程中生长激素释放活性的降低。
Pituitary. 1998 Apr;1(1):51-8. doi: 10.1023/a:1009970909015.