Hydrocortisone administration increases pulmonary artery pressure in asphyxiated newborn piglets reoxygenated with 100% oxygen

被引:7
作者
Chapados, Isabelle [1 ]
Lee, Tze-Fun [1 ]
Chik, Constance L. [2 ]
Cheung, Po-Yin [1 ]
机构
[1] Univ Alberta, Dept Paediat, Edmonton, AB T6G 2M7, Canada
[2] Univ Alberta, Dept Med, Edmonton, AB T6G 2M7, Canada
基金
加拿大健康研究院;
关键词
Hydrocortisone; Hypoxia-reoxygenation; Piglets; Oxygen; Pulmonary hypertension; Haemodynamics; SEPTIC SHOCK; NITRIC-OXIDE; REFRACTORY HYPOTENSION; ADRENAL INSUFFICIENCY; TRANSITIONAL PERIOD; HEMODYNAMIC-CHANGES; CORTISOL RESPONSE; DIAGNOSIS; PRETERM; HYPERTENSION;
D O I
10.1016/j.ejphar.2010.10.089
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In severely asphyxiated neonates developing vasopressor-resistant shock, hydrocortisone is commonly used to improve perfusion. However, its acute haemodynamic effects in asphyxiated neonates are largely unknown. In a swine model of neonatal asphyxia, effects of hydrocortisone on systemic and pulmonary circulations were examined. Piglets (1-3 d, 1.5-2.4 kg) were acutely instrumented to measure heart rate, systemic and pulmonary artery pressures, and pulmonary artery flow. After 2 h of normocapnic hypoxia, animals were resuscitated with 100% oxygen for 1 h followed by 21% oxygen for 3 h. Intravenous hydrocortisone (1 mg/kg) or saline was given in a blinded, randomized fashion 2 h after reoxygenation (n = 6/group). Haemodynamic parameters, blood gases, plasma cortisol, as well as levels of endothelin-1, nitrite/nitrate, nitrotyrosine, matrix metalloproteinases-2 and -9 in the lung were analysed. Severe hypoxia caused metabolic acidosis (mean pH: 6.91-6.97, mean plasma lactate: 17.2-18.3 mM), tachycardia and shock. Hydrocortisone did not affect systemic haemodynamics which recovered with reoxygenation, but it increased pulmonary artery pressure at 90-120 min after administration (36 +/- 3 vs. 27 +/- 2 and 26 +/- 1 mm Hg for hypoxia-reoxygenation control and sham-operated piglets, respectively, P<0.05). In the lung tissue, hydrocortisone significantly increased endothelin-1 and nitrite/nitrate levels, but had no effect on nitrotyrosine. Further, it decreased lung matrix metalloproteinase-9, but not matrix metalloproteinase-2, activity, which were both elevated with hypoxia-reoxygenation. It is most likely that the increase in pulmonary artery pressure observed after hydrocortisone treatment was associated with increased endothelin-1 level in the lung. Our findings caution the use of hydrocortisone as a first-intention treatment of shock in asphyxiated neonates. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:111 / 116
页数:6
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