Wilkinson Katherine A, Huey Kimberly, Dinger Bruce, He Liang, Fidone Salvatore, Powell Frank L
Dept. of Medicine, Univ. of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0623, USA.
J Appl Physiol (1985). 2010 Aug;109(2):424-30. doi: 10.1152/japplphysiol.01311.2009. Epub 2010 May 20.
We studied the effects of the ventilatory stimulant doxapram to test the hypothesis that chronic hypoxia increases the translation of carotid body afferent input into ventilatory motor efferent output by the central nervous system. Chronic hypoxia (inspired Po(2) = 70 Torr, 2 days) significantly increased the ventilatory response to an intravenous infusion of a high dose of doxapram in conscious, unrestrained rats breathing normoxic or hypoxic gas. The in vitro carotid body response to hypoxia increased with chronic hypoxia, but the response was not increased with a high dose of doxapram. Similarly, the phrenic nerve response to doxapram in anesthetized rats with carotid bodies denervated did not change with 7 days of chronic hypoxia. The results support the hypothesis that chronic hypoxia causes plasticity in the central component of the carotid chemoreceptor ventilatory reflex, which increases the hypoxic ventilatory response. We conclude that doxapram provides a promising tool to study the time course of changes in the central gain of the hypoxic ventilatory response during chronic hypoxia in awake animals and humans.
我们研究了呼吸兴奋剂多沙普仑的作用,以验证慢性缺氧会增加中枢神经系统将颈动脉体传入输入转化为呼吸运动传出输出的这一假说。慢性缺氧(吸入氧分压 = 70托,持续2天)显著增强了清醒、不受束缚的大鼠在呼吸常氧或低氧气体时对静脉输注高剂量多沙普仑的呼吸反应。体外实验中,颈动脉体对缺氧的反应随慢性缺氧而增强,但高剂量多沙普仑并不会使其反应增强。同样,在去神经支配颈动脉体的麻醉大鼠中,膈神经对多沙普仑的反应在慢性缺氧7天后并无变化。这些结果支持了慢性缺氧会导致颈动脉化学感受器呼吸反射中枢部分出现可塑性变化从而增强低氧呼吸反应这一假说。我们得出结论,多沙普仑为研究清醒动物和人类在慢性缺氧期间低氧呼吸反应中枢增益变化的时间进程提供了一个有前景的工具。