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布洛芬和甲泼尼龙对趋化因子诱导的经皮缺氧的保护作用。

Protective effects of ibuprofen and methylprednisolone on chemotactic factor-induced transcutaneous hypoxia.

作者信息

Maderazo E G, Breaux S P, Woronick C L

出版信息

J Pharmacol Exp Ther. 1986 Aug;238(2):453-6.

PMID:3735126
Abstract

We showed previously in vitro that ibuprofen, a nonsteroidal anti-inflammatory agent, at concentrations easily achievable in blood, inhibits polymorphonuclear leukocyte cell swelling and aggregation in response to chemotactic factor stimulation. To confirm this in vivo, we studied the ability of ibuprofen i.v. pretreatment to reverse the transcutaneous hypoxia induced by i.v. infusion of 1 nmol/kg of formyl-methionyl-leucyl-phenylalanine. This effect was compared with that of methylprednisolone. For ibuprofen and methylprednisolone, respectively, the maximum percentage of reversal of hypoxia was 85 and 106%; the dose required to produce 50% of maximum reversal was 2.7 and 4.6 mg/kg; and the serum drug concentration needed to achieve 50% of maximum reversal was 14 and 11 micrograms/ml. We conclude that ibuprofen could be a useful alternative to steroidal antiinflammatory agents for the prevention and treatment of complications of stimulated polymorphonuclear leukocytes.

摘要

我们之前在体外实验中表明,非甾体抗炎药布洛芬在血液中易于达到的浓度下,可抑制多形核白细胞因趋化因子刺激而发生的细胞肿胀和聚集。为了在体内证实这一点,我们研究了静脉注射布洛芬预处理逆转静脉输注1 nmol/kg甲酰甲硫氨酰亮氨酰苯丙氨酸所诱导的经皮缺氧的能力。将此效应与甲泼尼龙的效应进行了比较。对于布洛芬和甲泼尼龙,缺氧逆转的最大百分比分别为85%和106%;产生最大逆转50%所需的剂量分别为2.7和4.6 mg/kg;达到最大逆转50%所需的血清药物浓度分别为14和11 μg/ml。我们得出结论认为,在预防和治疗受刺激多形核白细胞的并发症方面,布洛芬可能是甾体抗炎药的一种有用替代药物。

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