Department of Clinical Pharmaceutical Science, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushima-naka, Okayama 700-8530, Japan.
Eur J Pharmacol. 2011 Mar 25;655(1-3):67-73. doi: 10.1016/j.ejphar.2011.01.020. Epub 2011 Jan 25.
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)-α-methylhistamine (α-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 (2μM) and in the presence of guanethidine (5μM), the periarterial nerve stimulation (1, 2Hz)-induced vasodilator response was inhibited by α-methylhistamine (0.1-1μM) perfusion without affecting vasodilation induced by exogenously injected CGRP (5pmol). Clobenpropit (histamine H(3) receptor antagonist, 1μM) canceled the α-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.
大鼠肠系膜动脉被证明受肾上腺素能血管收缩神经和降钙素基因相关肽(CGRP)含量丰富的(CGRP 能)血管舒张神经支配。本研究旨在研究组胺 H(3)受体在血管周围肾上腺素能和 CGRP 能神经递质传递中的作用。从雄性 Wistar 大鼠分离出无内皮的肠系膜血管床,并用 Krebs 溶液灌注,并测量灌注压。在具有静息张力的制剂中,选择性 H(3)受体激动剂(R)-α-甲基组氨酸(α-甲基组氨酸;10-100nM)显著降低了周围神经刺激(2-8Hz)引起的血管收缩和灌流液中去甲肾上腺素的释放,而对外源性注射去甲肾上腺素(0.5、1.0nmol)引起的血管收缩没有影响。在由甲氧胺(2μM)产生的主动张力制剂中,并存在胍乙啶(5μM)的情况下,周围神经刺激(1、2Hz)引起的血管舒张反应被α-甲基组氨酸(0.1-1μM)灌注抑制,而不影响外源性注射 CGRP(5pmol)引起的血管舒张。氯苯丙胺(组胺 H(3)受体拮抗剂,1μM)取消了α-甲基组氨酸引起的周围神经刺激引起的血管收缩和去甲肾上腺素释放以及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,不仅抑制肾上腺素能神经,而且还抑制 CGRP 能神经的神经传递。