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[血管活性肠肽(VIP)和肽组氨酸异亮氨酸(PHI)对豚鼠支气管收缩的抑制作用]

[Inhibitory effect of vasoactive intestinal peptide (VIP) and peptide histidine isoleucine (PHI) on bronchoconstriction in guinea pigs].

作者信息

Aoki S, Kurosawa M, Ishizuka T, Mori M

机构信息

First Department of Internal Medicine, Gunma University School of Medicine, Maebashi, Japan.

出版信息

Nihon Kyobu Shikkan Gakkai Zasshi. 1992 Nov;30(11):1946-50.

PMID:1484433
Abstract

The present studies were conducted to investigate whether or not VIP and PHI have a bronchodilator effect in vivo. VIP or PHI was administered intravenously in guinea pigs, and dynamic respiratory resistance was measured. Intravenous administration of VIP and PHI reduced dynamic respiratory resistance; however, the effect was significantly less than that of isoprenaline. VIP and PHI inhibited the increase in dynamic respiratory resistance by intravenous administration of histamine in a dose-dependent manner, suggesting that VIP and PHI may be involved in the pathogenesis of airway hyperresponsiveness through inhibiting the effect of mediators on the airway.

摘要

进行本研究以调查血管活性肠肽(VIP)和胰高血糖素样肽(PHI)在体内是否具有支气管扩张作用。将VIP或PHI静脉注射给豚鼠,并测量动态呼吸阻力。静脉注射VIP和PHI可降低动态呼吸阻力;然而,其作用明显小于异丙肾上腺素。VIP和PHI以剂量依赖的方式抑制静脉注射组胺引起的动态呼吸阻力增加,表明VIP和PHI可能通过抑制介质对气道的作用而参与气道高反应性的发病机制。

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