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组胺刺激和H2受体抑制对男性垂体催乳素和促肾上腺皮质激素释放以及皮质醇分泌的影响。

The effect of histamine stimulation and H2 -receptor inhibition on the pituitary prolactin and ACTH release and on cortisol secretion in human males.

作者信息

Knigge U, Wollesen F, Dejgaard A, Larsen K, Christiansen P M

出版信息

Horm Metab Res. 1983;15(2):89-91. doi: 10.1055/s-2007-1018637.

DOI:10.1055/s-2007-1018637
PMID:6131028
Abstract

The effects of histamine (HA) on prolactin (PRL), ACTH, and cortisol secretion in human males were investigated. Specific H2 -receptor blockade caused an immediate and significant PRL release, while specific H2 -receptor stimulation (HA and mepyramine) was without effect on PRL secretion. HA significantly stimulated both ACTH and cortisol secretion, and this stimulation was probably mediated through H2 -receptors, H2 -receptor blockade caused a late, but significant ACTH release. This release was not accompanied by a release of cortisol, and might therefore be due to a spontaneous oscillation in ACTH secretion. The results support the theory that HA acts as a modulator of human ACTH secretion. A similar effect on PRL secretion as postulated by others could not be confirmed in this study.

摘要

研究了组胺(HA)对男性催乳素(PRL)、促肾上腺皮质激素(ACTH)和皮质醇分泌的影响。特异性H2受体阻断导致PRL立即且显著释放,而特异性H2受体刺激(HA和甲氧苄胺)对PRL分泌无影响。HA显著刺激ACTH和皮质醇分泌,这种刺激可能通过H2受体介导,H2受体阻断导致ACTH延迟但显著释放。这种释放未伴随皮质醇释放,因此可能是由于ACTH分泌的自发振荡。结果支持HA作为人类ACTH分泌调节剂的理论。本研究未证实其他人所假设的对PRL分泌的类似影响。

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1
The effect of histamine stimulation and H2 -receptor inhibition on the pituitary prolactin and ACTH release and on cortisol secretion in human males.组胺刺激和H2受体抑制对男性垂体催乳素和促肾上腺皮质激素释放以及皮质醇分泌的影响。
Horm Metab Res. 1983;15(2):89-91. doi: 10.1055/s-2007-1018637.
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Effects of intracerebroventricular injection of histamine and related compounds on corticosterone release in rats.脑室内注射组胺及相关化合物对大鼠皮质酮释放的影响。
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Safety of acid-suppressing drugs.
抑酸药物的安全性。
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Drug-induced changes in prolactin secretion. Clinical implications.药物引起的催乳素分泌变化。临床意义。
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Adverse reactions and interactions with H2-receptor antagonists.H2受体拮抗剂的不良反应及相互作用。
Med Toxicol. 1986 May-Jun;1(3):192-216. doi: 10.1007/BF03259837.