Burgaud J L, Oudart N
Laboratoire de Pharmacologie, UFR de Pharmacie, Limoges, France.
J Pharm Pharmacol. 1993 Nov;45(11):955-8. doi: 10.1111/j.2042-7158.1993.tb05634.x.
From the bronchioles of guinea-pigs, preparations were isolated for registration of perfused pressure on electrical field stimulation (EFS) and by application of drugs. The perfused bronchioles contracted when EFS was applied in the presence of atropine and phentolamine suggesting a non-adrenergic non-cholinergic (NANC) response. (R)-alpha-Methylhistamine (methylhistamine), a selective H3 agonist, reduced the NANC bronchoconstrictor response in a concentration-dependent manner. beta-Adrenoceptors, muscarinic and histamine (H1 and H2 receptor) antagonists, epithelial removal and cyclooxygenase inhibition had no effect on this inhibitory action of methylhistamine whereas the H3 antagonist, thioperamide, reduced the inhibitory effect of methylhistamine with a Ki value of 2.98 x 10(-9) M. Methylhistamine had no effect on the concentration-dependent contraction induced by exogenous substance P and neurokinin A, demonstrating that an H3 receptor might inhibit the release of transmitter from NANC nerves on guinea-pig perfused bronchioles in-vitro.
从豚鼠细支气管中分离出标本,用于记录电场刺激(EFS)和应用药物时的灌注压力。在阿托品和酚妥拉明存在的情况下施加EFS时,灌注的细支气管收缩,提示非肾上腺素能非胆碱能(NANC)反应。选择性H3激动剂(R)-α-甲基组胺(甲基组胺)以浓度依赖性方式降低NANC支气管收缩反应。β-肾上腺素能受体、毒蕈碱和组胺(H1和H2受体)拮抗剂、去除上皮和抑制环氧化酶对甲基组胺的这种抑制作用没有影响,而H3拮抗剂硫代哌啶以2.98×10⁻⁹ M的Ki值降低了甲基组胺的抑制作用。甲基组胺对外源性P物质和神经激肽A诱导的浓度依赖性收缩没有影响,表明H3受体可能在体外抑制豚鼠灌注细支气管中NANC神经递质的释放。