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阿片肽通过胆碱能机制调控人体生长激素。

Opiate peptides control growth hormone through a cholinergic mechanism in man.

作者信息

Delitala G, Grossman A, Besser G M

出版信息

Clin Endocrinol (Oxf). 1983 Apr;18(4):401-5. doi: 10.1111/j.1365-2265.1983.tb00585.x.

DOI:10.1111/j.1365-2265.1983.tb00585.x
PMID:6409456
Abstract

Opiate peptides are known to elevate circulating GH in man, and data in other animals suggest that acetylcholine may be involved. We have administered the long-acting met-enkephalin analogue DAMME to 6 normal males, and have shown that the resulting elevation in GH is blocked by the specific cholinergic antagonist, pirenzepine. It seems likely that a cholinergic mechanism may interact with opiate-induced changes in GH in man.

摘要

已知阿片肽可提高人体循环中的生长激素水平,其他动物的数据表明乙酰胆碱可能与之有关。我们给6名正常男性注射了长效甲硫氨酸脑啡肽类似物DAMME,并发现生长激素的升高被特异性胆碱能拮抗剂哌仑西平所阻断。胆碱能机制似乎可能与人中阿片类药物诱导的生长激素变化相互作用。

相似文献

1
Opiate peptides control growth hormone through a cholinergic mechanism in man.阿片肽通过胆碱能机制调控人体生长激素。
Clin Endocrinol (Oxf). 1983 Apr;18(4):401-5. doi: 10.1111/j.1365-2265.1983.tb00585.x.
2
Growth hormone-releasing effect of an enkephalin analog in the dog: evidence for cholinergic mediation.
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Blockade of hp-GRF-40-induced GH release in normal men by a cholinergic muscarinic antagonist.
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Changes in pituitary hormone levels induced by met-enkephalin in man--the role of dopamine.
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Opioids stimulate growth hormone (GH) release in man independently of GH-releasing hormone.阿片类药物可独立于生长激素释放激素刺激人体释放生长激素。
J Clin Endocrinol Metab. 1989 Aug;69(2):356-8. doi: 10.1210/jcem-69-2-356.
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Effects of a Met-enkephalin analogue and naloxone infusion on anterior pituitary hormone secretion in acromegaly.一种甲硫氨酸脑啡肽类似物和纳洛酮输注对肢端肥大症患者垂体前叶激素分泌的影响。
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Inhibition of vasopressin release in man by an opiate peptide.一种阿片肽对人体血管加压素释放的抑制作用。
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Studies off the opiate control of prolactin, GH and TSH.关于阿片类物质对催乳素、生长激素和促甲状腺激素控制的研究。
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引用本文的文献

1
Neuroendocrine regulation of human growth hormone secretion. Diagnostic and clinical applications.人类生长激素分泌的神经内分泌调节。诊断及临床应用。
J Endocrinol Invest. 1988 Jun;11(6):441-62. doi: 10.1007/BF03349081.