Mitten L A, Hinchcliff K W, Pate J L
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Ohio State University, Columbus 43210-1089, USA.
J Appl Physiol (1985). 1996 Jul;81(1):312-7. doi: 10.1152/jappl.1996.81.1.312.
The effect of inhibition of cyclooxygenase activity on the hemodynamic response to exertion was examined in 6 horses. Rates of O2 consumption and CO2 production and carotid, pulmonary arterial, and right atrial pressures were measured while the horses performed a standardized exercise test on a treadmill after treatment with phenylbutazone or a placebo. Phenylbutazone (8.8 mg/kg p.o. for 2 days and 4.4 mg/kg i.v. 60 min before exertion) abolished the exertion-induced increases in plasma 6-ketoprostaglandin F1 alpha and thromboxane B2 concentrations, confirming inhibition of cyclooxygenase activity. Phenylbutazone treatment resulted in significantly (P < 0.05) higher heart rates and right atrial pressures during exertion than did treatment with placebo, which may have been due to increased myocardial sensitivity to sympathetic stimulation and/or decreased venous compliance. There was not a detectable effect of phenylbutazone on carotid or pulmonary arterial pressures, O2 consumption, CO2 production, or blood lactate concentration. Changes in plasma volume during exertion were not influenced by phenylbutazone. These results demonstrate that cyclooxygenase products likely mediate or modulate some of the systemic hemodynamic responses to exertion in horses.
在6匹马中研究了抑制环氧化酶活性对运动时血液动力学反应的影响。在用保泰松或安慰剂治疗后,让马匹在跑步机上进行标准化运动测试,同时测量氧气消耗率、二氧化碳产生率以及颈动脉、肺动脉和右心房压力。保泰松(口服8.8毫克/千克,持续2天,运动前60分钟静脉注射4.4毫克/千克)消除了运动诱导的血浆6-酮前列环素F1α和血栓素B2浓度的升高,证实了环氧化酶活性受到抑制。与安慰剂治疗相比,保泰松治疗导致运动期间心率和右心房压力显著更高(P < 0.05),这可能是由于心肌对交感神经刺激的敏感性增加和/或静脉顺应性降低所致。保泰松对颈动脉或肺动脉压力、氧气消耗、二氧化碳产生或血乳酸浓度没有可检测到的影响。运动期间血浆容量的变化不受保泰松影响。这些结果表明,环氧化酶产物可能介导或调节马匹运动时的一些全身血液动力学反应。