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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。

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.

作者信息

Muruais J, Peñalva A, Dieguez C, Casanueva F F

机构信息

Department of Medicine, Faculty of Medicine, University of Santiago de Compostela, Spain.

出版信息

J Endocrinol. 1993 Aug;138(2):211-8. doi: 10.1677/joe.0.1380211.

DOI:10.1677/joe.0.1380211
PMID:8228729
Abstract

His-D-Trp-Ala-Trp-D-Phe-Lys-NH2 (GHRP-6) is a synthetic peptide unrelated to any known hypothalamic-releasing hormone including growth hormone-releasing hormone (GHRH). Interestingly, this peptide induces a dose-related increase in plasma GH levels in all species tested so far. The aim of this study was to investigate the action of GHRP-6 alone or in combination with GHRH on GH release in dogs. In addition, the activation or blockade of endogenous cholinergic tone and alpha-1 adrenoceptors on GHRP-6-stimulated GH secretion was assessed. In adult Beagle dogs (n = 10), GHRP-6 (90 micrograms i.v.) increased basal GH levels from 2.6 +/- 1.5 to 14.4 +/- 3.1 micrograms/l (mean +/- S.E.M.) after 15 min. GHRH (50 micrograms i.v.) induced a GH peak of 9.7 +/- 2.2 micrograms/l at 15 min. The combined administration of GHRP-6 and GHRH strikingly potentiated canine GH release with a peak of 54 +/- 9.0 micrograms/l (P < 0.01). Pretreatment with the cholinergic agonist pyridostigmine (30 mg per os) increased GHRP-6-stimulated GH secretion (37.9 +/- 10.1 micrograms/l P < 0.05), while the muscarinic blocker atropine (100 micrograms i.v.) completely abolished (GH peak lower than 2 micrograms/l) the stimulatory action of GHRP-6. On the other hand, administration of the alpha-2 adrenergic agonist clonidine (4 micrograms/kg i.v.) increased basal plasma GH levels without affecting GH responses to GHRP-6.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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(GHRP-6)是一种合成肽,与任何已知的下丘脑释放激素无关,包括生长激素释放激素(GHRH)。有趣的是,到目前为止,在所有测试物种中,这种肽都会引起血浆生长激素水平呈剂量相关的升高。本研究的目的是调查GHRP-6单独或与GHRH联合对犬生长激素释放的作用。此外,还评估了内源性胆碱能张力和α-1肾上腺素能受体的激活或阻断对GHRP-6刺激的生长激素分泌的影响。在成年比格犬(n = 10)中,静脉注射90微克GHRP-6后15分钟,基础生长激素水平从2.6±1.5微克/升升高至14.4±3.1微克/升(平均值±标准误)。静脉注射50微克GHRH在15分钟时诱导生长激素峰值达到9.7±2.2微克/升。GHRP-6和GHRH联合给药显著增强犬生长激素释放,峰值达到54±9.0微克/升(P < 0.01)。胆碱能激动剂新斯的明(口服30毫克)预处理可增加GHRP-6刺激的生长激素分泌(37.9±10.1微克/升,P < 0.05),而毒蕈碱阻断剂阿托品(静脉注射100微克)则完全消除了GHRP-6的刺激作用(生长激素峰值低于 < 2微克/升)。另一方面,静脉注射α-2肾上腺素能激动剂可乐定(4微克/千克)可提高基础血浆生长激素水平,但不影响生长激素对GHRP-6的反应。(摘要截断于250字)

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