Eguchi Shinji, Tezuka Satoko, Hobara Narumi, Akiyama Shinji, Kurosaki Yuji, Kawasaki Hiromu
Department of Clinical Pharmaceutical Science, Graduate School of Natural Science and Technology, Okayama University, 1-1-1 Tsushima-naka, Okayama 700-8530, Japan.
Br J Pharmacol. 2004 Aug;142(7):1137-46. doi: 10.1038/sj.bjp.0705773. Epub 2004 Jul 12.
Previous studies showed that nicotine induces adrenergic nerve-dependent vasodilation that is mediated by endogenous calcitonin gene-related peptide (CGRP) released from CGRP-containing (CGRPergic) nerves. The mechanisms underlying the nicotine-induced vasodilation were further studied. Rat mesenteric vascular beds without endothelium were contracted by perfusion with Krebs solution containing methoxamine, and the perfusion pressure was measured with a pressure transducer. Perfusion of nicotine (1-100 microm) for 1 min caused concentration-dependent vasodilation. Capsazepine (vanilloid receptor-1 antagonist; 1-10 microm) and ruthenium red (inhibitor of vanilloid response; 1-30 microm) concentration-dependently inhibited the nicotine-induced vasodilation without affecting the vasodilator response to exogenous CGRP. Nicotine-induced vasodilation was not inhibited by treatment with 3,4-dihydroxyphenylalanine (DOPA) receptor antagonist (l-DOPA cyclohexyl ester; 0.001-10 microm), dopamine D1 receptor-selective antagonist (SCH23390; 1-10 microm), dopamine D2 receptor antagonist (haloperidol; 0.1-0.5 microm), ATP P2x receptor-desensitizing agonist (alpha,beta-methylene ATP; 1-10 microm), adenosine A2 receptor antagonist (8(p-sulfophenyl)theophylline; 10-50 microm) or neuropeptide Y (NPY)-Y1 receptor antagonist (BIBP3226; 0.1-0.5 microm). Immunohistochemical staining of the mesenteric artery showed dense innervation of CGRP- and vanilloid receptor-1-positive nerves, with both immunostainings appearing in the same neuron. The mesenteric artery was also densely innervated by NPY-positive nerves. Double immunostainings showed that both NPY and CGRP immunoreactivities appeared in the same neuron of the artery. These results suggest that nicotine acts on presynaptic nicotinic receptors to release adrenergic neurotransmitter(s) or related substance(s), which then stimulate vanilloid receptor-1 on CGRPergic nerves, resulting in CGRP release and vasodilation.
先前的研究表明,尼古丁可诱导由含降钙素基因相关肽(CGRP)的神经(CGRP能神经)释放的内源性降钙素基因相关肽介导的肾上腺素能神经依赖性血管舒张。对尼古丁诱导血管舒张的机制进行了进一步研究。用含甲氧明的Krebs溶液灌注使无内皮的大鼠肠系膜血管床收缩,并用压力传感器测量灌注压力。灌注尼古丁(1 - 100微摩尔)1分钟可引起浓度依赖性血管舒张。辣椒素(香草酸受体-1拮抗剂;1 - 10微摩尔)和钌红(香草酸反应抑制剂;1 - 30微摩尔)浓度依赖性地抑制尼古丁诱导的血管舒张,而不影响对外源性CGRP的血管舒张反应。用3,4-二羟基苯丙氨酸(DOPA)受体拮抗剂(L-DOPA环己酯;0.001 - 10微摩尔)、多巴胺D1受体选择性拮抗剂(SCH23390;1 - 10微摩尔)、多巴胺D2受体拮抗剂(氟哌啶醇;0.1 - 0.5微摩尔)、ATP P2x受体脱敏激动剂(α,β-亚甲基ATP;1 - 10微摩尔)、腺苷A2受体拮抗剂(8(对磺苯基)茶碱;10 - 50微摩尔)或神经肽Y(NPY)-Y1受体拮抗剂(BIBP3226;0.1 - 0.5微摩尔)处理均未抑制尼古丁诱导的血管舒张。肠系膜动脉的免疫组织化学染色显示CGRP和香草酸受体-1阳性神经的密集神经支配,两种免疫染色出现在同一神经元中。肠系膜动脉也有密集的NPY阳性神经支配。双重免疫染色显示NPY和CGRP免疫反应性出现在动脉的同一神经元中。这些结果表明,尼古丁作用于突触前烟碱受体以释放肾上腺素能神经递质或相关物质,然后这些物质刺激CGRP能神经上的香草酸受体-1,导致CGRP释放和血管舒张。