首页> 外文期刊>European Journal of Pharmacology: An International Journal >Histamine H(3) receptor-mediated modulation of perivascular nerve transmission in rat mesenteric arteries.
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Histamine H(3) receptor-mediated modulation of perivascular nerve transmission in rat mesenteric arteries.

机译:组胺H(3)受体介导的大鼠肠系膜动脉血管周围神经传递的调节。

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The rat mesenteric artery has been shown to be innervated by adrenergic vasoconstrictor nerves and calcitonin gene-related peptide (CGRP)-containing (CGRPergic) vasodilator nerves. The present study was designed to investigate the involvement of histamine H(3) receptors in the neurotransmission of perivascular adrenergic and CGRPergic nerves. The mesenteric vascular beds without an endothelium isolated from male Wistar rats were perfused with Krebs solution and perfusion pressure was measured. In preparations with resting tension, the selective H(3) receptor agonist (R)-alpha-methylhistamine (alpha-methylhistamine; 10-100nM) significantly reduced periarterial nerve stimulation (2-8Hz)-induced vasoconstriction and noradrenaline release in the perfusate without an effect on the vasoconstriction induced by exogenously injected noradrenaline (0.5, 1.0nmol). In preparations with active tone produced by methoxamine (2muM) and in the presence of guanethidine (5muM), the periarterial nerve stimulation (1, 2Hz)-induced vasodilator response was inhibited by alpha-methylhistamine (0.1-1muM) perfusion without affecting vasodilation induced by exogenously injected CGRP (5pmol). Clobenpropit (histamine H(3) receptor antagonist, 1muM) canceled the alpha-methylhistamine-induced decrease in the periarterial nerve stimulation-induced vasoconstriction and noradrenaline release and periarterial nerve stimulation-induced vasodilation. These results suggest that the stimulation of H(3) receptors located in rat perivascular nerves inhibits presynaptically the neurotransmission of not only adrenergic nerves, but also CGRP nerves, by decreasing neurotransmitters.
机译:已显示大鼠肠系膜动脉被肾上腺素能血管收缩神经和降钙素基因相关肽(CGRP)所含(CGRPergic)血管扩张神经所支配。本研究旨在调查组胺H(3)受体参与血管周围肾上腺素能和CGRPergic神经的神经传递。用克雷布斯溶液灌注不分离自雄性Wistar大鼠的内皮的肠系膜血管床,并测量灌注压力。在具有静息张力的制剂中,选择性H(3)受体激动剂(R)-α-甲基组胺(α-甲基组胺; 10-100nM)显着降低了动脉周围神经刺激(2-8Hz)诱导的血管收缩和去甲肾上腺素在灌注液中的释放,而无对外源性去甲肾上腺素(0.5、1.0nmol)注射引起的血管收缩的影响。在由甲氧胺(2μM)产生活性调且在胍乙啶(5μM)存在的情况下,α-甲基组胺(0.1-1μM)灌注抑制动脉周围神经刺激(1、2Hz)诱导的血管舒张反应,而不影响诱导的血管舒张通过外源注射CGRP(5pmol)。 Clobenpropit(组胺H(3)受体拮抗剂,1μM)取消了α-甲基组胺引起的动脉周围神经刺激引起的血管收缩和降肾上腺素释放以及动脉周围神经刺激引起的血管舒张的减少。这些结果表明,位于大鼠血管周围神经中的H(3)受体的刺激通过减少神经递质来抑制突触前神经递质,不仅是肾上腺素能神经,而且是CGRP神经。

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