Takahashi Toru, Osanai Shinobu, Nakano Hitoshi, Ohsaki Yoshinobu, Kikuchi Kenjiro
First Department of Medicine, Asahikawa Medical College, 2-1-1-1 Midorigaoka Higash, Asahikawa 078-8510, Japan.
Respir Physiol Neurobiol. 2005 May 12;147(1):1-9. doi: 10.1016/j.resp.2005.01.005.
To determine if doxapram stimulates the carotid body through the same mechanism as hypoxia, we compared the effects of doxapram and hypoxia on isolated-perfused carotid bodies in rabbits. Doxapram stimulated the carotid body in a dose-dependent manner. In Ca(2+)-free solution, neither doxapram nor hypoxia stimulated the carotid body. Although, doxapram had an additive effect on the carotid body chemosensory response to hypercapnia, a synergistic effect was not observed. Also, we investigated the various K(+) channel activators on the response to doxapram and hypoxia: pinacidil and levcromakalim as ATP-sensitive K(+) channel activators; NS-1619 as a Ca(2+)-sensitive K(+) channel activator; and halothane as a TASK-like background K(+) channel activator. The hypoxic response was partially reduced by halothane only, while pinacidil, levcromakalim and NS-1619 had no effect. Interestingly, the effect of doxapram was partially inhibited by NS-1619. Neither pinacidil nor levcromakalim affected the stimulatory effect of doxapram. We conclude that doxapram stimulates the carotid body via a different mechanism than hypoxic chemotransduction.
为了确定多沙普仑是否通过与缺氧相同的机制刺激颈动脉体,我们比较了多沙普仑和缺氧对兔离体灌注颈动脉体的影响。多沙普仑以剂量依赖的方式刺激颈动脉体。在无钙溶液中,多沙普仑和缺氧均未刺激颈动脉体。尽管多沙普仑对颈动脉体对高碳酸血症的化学感受反应有相加作用,但未观察到协同作用。此外,我们研究了各种钾通道激活剂对多沙普仑和缺氧反应的影响:吡那地尔和左旋克罗卡林作为ATP敏感性钾通道激活剂;NS-1619作为钙敏感性钾通道激活剂;氟烷作为类TASK背景钾通道激活剂。仅氟烷部分降低了缺氧反应,而吡那地尔、左旋克罗卡林和NS-1619则无作用。有趣的是,NS-1619部分抑制了多沙普仑的作用。吡那地尔和左旋克罗卡林均未影响多沙普仑的刺激作用。我们得出结论,多沙普仑通过与缺氧化学转导不同的机制刺激颈动脉体。