Knigge U, Willems E, Kjaer A, Jørgensen H, Warberg J
Department of Medical Physiology, The Panum Institute, Copenhagen N, Denmark.
Endocrinology. 1999 Aug;140(8):3713-9. doi: 10.1210/endo.140.8.6891.
Activation of histaminergic and noradrenergic/adrenergic neurons in the brain stimulates the release of the neurohypophysial hormones arginine vasopressin (AVP) and oxytocin (OT) and are involved the mediation of the hormone responses to physiological stimuli such as dehydration and suckling. We therefore investigated whether the two neuronal systems interact in their regulation of AVP and OT secretion in conscious male rats. When administered intracerebroventricularly (i.c.v.), histamine (HA) as well as the H1 receptor agonist 2-thiazolylethylamine or the H2 receptor agonist 4-methylHA stimulated AVP and OT secretion. Prior i.c.v. infusion of antagonists specific to alpha or beta adrenergic receptors or their subtypes did not significantly affect the hormone response to HA or the histaminergic agonists. Infused i.c.v. norepinephrine (NE) or epinephrine (E) increased AVP and OT secretion. Prior i.c.v. infusion of the H1 receptor antagonist mepyramine or the H2 receptor antagonist cimetidine significantly inhibited the AVP and OT responses to NE and the AVP response to E, whereas only cimetidine inhibited the OT response to E significantly. Systemic pretreatment with imetit, which by activation of presynaptic H3 receptors inhibits neuronal synthesis and release of HA, decreased the AVP and OT responses to NE and E significantly. In the doses used, HA and E had no significant effect on mean arterial blood pressure. NE increased mean arterial blood pressure 10% at 1 and 2.5 min, whereafter the blood pressure returned to basal level within 10 min. The results indicate that noradrenergic and adrenergic neurons stimulate AVP and OT secretion via an involvement of histaminergic neurons, which may occur at magnocellular neurons in the supraoptic and paraventricular nuclei of the hypothalamus. The stimulatory effect of the amines on neurohypophysial hormone secretion seems to be independent of a central action on blood pressure. In contrast, a functionally intact noradrenergic and adrenergic neuronal system seems not to be a prerequisite for a HA-induced release of AVP and OT. The present findings further substantiate the role of histaminergic neurons in the central regulation of neurohypophysial hormone secretion.
脑内组胺能和去甲肾上腺素能/肾上腺素能神经元的激活会刺激神经垂体激素精氨酸加压素(AVP)和催产素(OT)的释放,并参与对脱水和哺乳等生理刺激的激素反应调节。因此,我们研究了这两个神经元系统在清醒雄性大鼠中对AVP和OT分泌的调节是否相互作用。当脑室内注射(i.c.v.)组胺(HA)以及H1受体激动剂2-噻唑基乙胺或H2受体激动剂4-甲基HA时,会刺激AVP和OT的分泌。事先脑室内注射α或β肾上腺素能受体或其亚型的特异性拮抗剂,对激素对HA或组胺能激动剂的反应没有显著影响。脑室内注射去甲肾上腺素(NE)或肾上腺素(E)会增加AVP和OT的分泌。事先脑室内注射H1受体拮抗剂美吡拉敏或H2受体拮抗剂西咪替丁,会显著抑制AVP和OT对NE的反应以及AVP对E的反应,而只有西咪替丁能显著抑制OT对E的反应。用伊美替进行全身预处理,通过激活突触前H3受体抑制神经元HA的合成和释放,会显著降低AVP和OT对NE和E的反应。在所使用的剂量下,HA和E对平均动脉血压没有显著影响。NE在1分钟和2.5分钟时使平均动脉血压升高10%,此后血压在10分钟内恢复到基础水平。结果表明,去甲肾上腺素能和肾上腺素能神经元通过组胺能神经元的参与来刺激AVP和OT的分泌,这可能发生在下丘脑视上核和室旁核的大细胞神经元处。胺类对神经垂体激素分泌的刺激作用似乎与对血压的中枢作用无关。相反,功能完整的去甲肾上腺素能和肾上腺素能神经元系统似乎不是HA诱导AVP和OT释放的先决条件。本研究结果进一步证实了组胺能神经元在神经垂体激素分泌中枢调节中的作用。