Mansour E, Abraham W M, Ahmed T
Division of Pulmonary Disease, University of Miami School of Medicine, Mount Sinai Medical Center, Florida 33140.
J Appl Physiol (1985). 1992 Apr;72(4):1529-35. doi: 10.1152/jappl.1992.72.4.1529.
Intratracheal instillation of platelet-activating factor (PAF) in sheep produces bronchoconstriction and airway hyperresponsiveness (AHR) by a two-stage process that involves the initial stimulation of PAF receptors followed by the secondary generation of proinflammatory mediators. Because the biological effects of PAF may be mediated by these proinflammatory metabolites, it is possible that a steroidal anti-inflammatory agent would modify the airway responses of PAF. We measured specific lung resistance (sRL) in sheep (n = 11) before, immediately after, and serially for up to 2 h after intratracheal instillation of PAF (30 micrograms/kg). Airway responsiveness was measured 2 h post-PAF when sRL had returned to baseline and was expressed as the cumulative provocating dose of carbachol that increased sRL to 4 l.cmH2O.l-1.s (PD4). PD4 was determined on a control day and on different experiment days without or after treatment with intravenous methylprednisolone (MPS; 1 mg/kg) administered 3 h before (n = 6), 20 min before PAF (n = 7), or 20 min after PAF challenge (n = 7). PAF increased sRL by 222 +/- 44% (SE) above baseline and decreased PD4 of carbachol by 44 +/- 5% (P less than 0.05). Pretreatment (both 3 h and 20 min) with MPS attenuated the PAF-induced increases in sRL, whereas its administration 20 min post-PAF had no effect. Irrespective of the effects on sRL, MPS administration inhibited the PAF-induced AHR.(ABSTRACT TRUNCATED AT 250 WORDS)
在绵羊气管内注入血小板活化因子(PAF),通过一个两阶段过程产生支气管收缩和气道高反应性(AHR),该过程包括最初对PAF受体的刺激,随后是促炎介质的继发性产生。由于PAF的生物学效应可能由这些促炎代谢产物介导,甾体抗炎药有可能改变PAF引起的气道反应。我们在11只绵羊气管内注入PAF(30微克/千克)之前、之后立即以及连续2小时内测量了比肺顺应性(sRL)。在PAF注入后2小时,当sRL恢复到基线时测量气道反应性,并表示为使sRL增加到4升·厘米水柱·升-1·秒(PD4)的卡巴胆碱累积激发剂量。在对照日以及在不同实验日,在PAF注入前3小时(n = 6)、PAF注入前20分钟(n = 7)或PAF激发后20分钟(n = 7)静脉注射甲泼尼龙(MPS;1毫克/千克),然后测定PD4。PAF使sRL比基线增加222±44%(标准误),并使卡巴胆碱的PD4降低44±5%(P<0.05)。MPS预处理(3小时和20分钟)均减弱了PAF诱导的sRL增加,而在PAF后20分钟给药则无作用。无论对sRL的影响如何,MPS给药均抑制了PAF诱导的AHR。(摘要截短于250字)