环孢素A在新生猪体内的药效学和药代动力学。

P. Tsao, S. Ito, P. Wong, I. Radde, S. Bryson, D. Young, J. Caspi, R. J. Diaz, M. Martell, J. Augustine
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引用次数: 4

摘要

新生儿环孢素A的处置动力学以及年龄相关的淋巴细胞对环孢素A反应的差异尚不清楚。新生儿(2.5或5 mg/kg)和成年猪(10 mg/kg)单次静脉输注环孢素A,采用RIA法测定血液环孢素A水平。与成熟动物相比,新生儿的消除半衰期更长,药物清除率更低。淋巴细胞增殖的抑制仅在混合淋巴细胞反应和植物血凝素刺激培养的新生儿2小时样本中观察到,这些样本接受5mg /kg。我们得出结论,新生猪表现出不同的环孢素A药代动力学,对环孢素A的敏感性高于成熟动物。
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Pharmacodynamics and pharmacokinetics of cyclosporin A in the newborn pig.
The disposition kinetics of cyclosporin A in the neonates as well as age-related differences in lymphocyte responses to cyclosporin A are unknown. A single intravenous infusion of cyclosporin A was given to neonatal (2.5 or 5 mg/kg) and mature pigs (10 mg/kg) and blood cyclosporin A levels were measured by RIA. The neonates had longer elimination half-life and lower drug clearance than mature animals. Suppression in lymphocyte proliferation was only observed in mixed lymphocyte reaction and phytohemagglutinin-stimulated cultures of the 2-hour samples from neonates receiving 5 mg/kg. We conclude that neonatal pig exhibit different cyclosporin A pharmacokinetics and show higher sensitivity to cyclosporin A than mature animals.
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