Mukaiyama Osamu, Morimoto Kiyoshi, Nosaka Emi, Takahashi Sakiko, Yamashita Makoto
R&D Project Management Department, Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan.
Eur J Pharmacol. 2004 Sep 13;498(1-3):287-94. doi: 10.1016/j.ejphar.2004.07.071.
In this study, we investigated the involvement of neurokinin NK3 receptors in a severe asthma model prepared by administering ovalbumin via inhalation three times to systemically sensitized guinea pigs. [3H]senktide, a neurokinin NK3 receptor ligand, showed significant specific binding to the lungs from the model animals, but not to those from negative control animals. The airway responsiveness to intravenous neurokinin B, a neurokinin NK3 receptor agonist, was increased in the model, indicating an increase in functional NK3 receptors. Furthermore, SB 223956 ((-)-3-methoxy-2-phenyl-N-[(1S)-phenylpropyl]quinoline-4-carboxamide), a selective neurokinin NK3 receptor antagonist, significantly inhibited the ovalbumin-induced airway hyperresponsiveness to inhaled methacholine, but it did not show significant effects on the ovalbumin-induced airway narrowing and eosinophil accumulation. These results suggest that the expressed neurokinin NK3 receptors in the severe asthma model are involved in the development of airway hyperresponsiveness.
在本研究中,我们调查了神经激肽NK3受体在通过对全身致敏的豚鼠进行三次雾化吸入卵清蛋白制备的重度哮喘模型中的作用。神经激肽NK3受体配体[3H]senktide对模型动物的肺显示出显著的特异性结合,但对阴性对照动物的肺则无此现象。模型中,静脉注射神经激肽NK3受体激动剂神经激肽B后气道反应性增加,表明功能性NK3受体增多。此外,选择性神经激肽NK3受体拮抗剂SB 223956((-)-3-甲氧基-2-苯基-N-[(1S)-苯丙基]喹啉-4-甲酰胺)显著抑制了卵清蛋白诱导的对吸入乙酰甲胆碱的气道高反应性,但对卵清蛋白诱导的气道狭窄和嗜酸性粒细胞聚集未显示出显著作用。这些结果表明,重度哮喘模型中表达的神经激肽NK3受体参与了气道高反应性的发展。