Tatsumi K, Pickett C K, Weil J V
Cardiovascular Pulmonary Research Laboratory, University of Colorado Health Sciences Center, Denver 80262.
J Appl Physiol (1985). 1992 May;72(5):1945-52. doi: 10.1152/jappl.1992.72.5.1945.
In a previous work, we showed that the adult cat demonstrates a ventilatory decline during sustained hypoxia (the "roll off" phenomenon) and that the mechanism responsible for this secondary decrease in ventilation lies within the central nervous system (J. Appl. Physiol. 63: 1658-1664, 1987). In this study, we sought to determine whether central dopaminergic mechanisms could have a role in the roll off. We studied the effects of haloperidol, a peripheral and centrally acting dopamine receptor antagonist, on the ventilatory response to sustained isocapnic hypoxia (end-tidal PO2 40-50 Torr, 20-25 min) in awake cats. In vehicle control cats (n = 5), sustained hypoxia elicited a biphasic respiratory response, during which an initial ventilatory stimulation is followed by a 24 +/- 6% (P less than 0.01) reduction. In contrast, in haloperidol- (0.1 mg/kg) treated cats (n = 5) the ventilatory roll off was virtually abolished (-1 +/- 1%; P = NS). We also measured ventilatory, carotid sinus nerve (CSN) and phrenic nerve (PhN) responses to sustained isocapnic hypoxia in anesthetized animals (n = 6) to explore the influence of haloperidol on peripheral and central response during the roll off. Control responses to hypoxia showed an initial increase in ventilation, PhN, and CSN activity, followed by a subsequent decline in ventilation and PhN activity of 17 +/- 3 and 17 +/- 5%, respectively (P less than 0.05). In contrast, CSN activity remained unchanged during the roll off. Administration of haloperidol (1 mg/kg) reduced the initial increment in ventilation, while the initial increase in CSN activity was augmented.(ABSTRACT TRUNCATED AT 250 WORDS)
在之前的一项研究中,我们发现成年猫在持续性低氧期间会出现通气量下降(“衰减”现象),且这种通气量继发性下降的机制存在于中枢神经系统中(《应用生理学杂志》63: 1658 - 1664, 1987)。在本研究中,我们试图确定中枢多巴胺能机制是否在这种衰减中起作用。我们研究了外周及中枢多巴胺受体拮抗剂氟哌啶醇对清醒猫持续性等碳酸血症性低氧(呼气末PO₂ 40 - 50 Torr,20 - 25分钟)通气反应的影响。在给予赋形剂的对照猫(n = 5)中,持续性低氧引发双相呼吸反应,在此期间,最初的通气刺激之后是通气量降低24±6%(P < 0.01)。相比之下,在接受氟哌啶醇(0.1 mg/kg)治疗的猫(n = 5)中,通气量衰减几乎被消除(-1±1%;P = 无显著性差异)。我们还测量了麻醉动物(n = 6)对持续性等碳酸血症性低氧的通气、颈动脉窦神经(CSN)和膈神经(PhN)反应,以探讨氟哌啶醇在衰减期间对外周和中枢反应的影响。对低氧的对照反应显示,通气、PhN和CSN活动最初增加,随后通气和PhN活动分别下降17±3%和17±5%(P < 0.05)。相比之下,在衰减期间CSN活动保持不变。给予氟哌啶醇(1 mg/kg)可降低通气的初始增量,而CSN活动的初始增加则增强。(摘要截短于250字)