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类固醇对大鼠内毒素诱导的肺水肿及前列腺素E2药代动力学的影响

Modification by steroids of pulmonary oedema and prostaglandin E2 pharmacokinetics induced by endotoxin in rats.

作者信息

Izumi T, Bakhle Y S

机构信息

Department of Pharmacology, Hunterian Institute, Royal College of Surgeons, London.

出版信息

Br J Pharmacol. 1988 Apr;93(4):955-63. doi: 10.1111/j.1476-5381.1988.tb11485.x.

Abstract
  1. A single i.p. injection of bacterial endotoxin in rats (3.5 mg kg-1) caused lung injury assessed as changes in lung dry:wet weight ratio and leukopaenia over the subsequent 28 h. 2. This treatment also slowed the efflux of 14C from [14C]-prostaglandin E2 (PGE2), i.e., increased t1/2 and increased the survival of PGE2 in isolated perfused lungs over the same period. 3. These effects of endotoxin were reversed by methylprednisolone (30 mg kg-1), given 30 min after the endotoxin. 4. Another synthetic corticosteroid, budesonide (1.2 mg kg-1) given 1 h before endotoxin partially prevented the lung injury and leukopaenia but did not affect the increased t1/2 for PGE2 nor its survival. 5. The reversal by methylprednisolone of both the physical signs of lung injury and the changes in PGE2 pharmacokinetics caused by endotoxin suggests that changes in PGE2 pharmacokinetics could serve as an index of acute lung injury following sepsis.
摘要
  1. 给大鼠腹腔注射一次细菌内毒素(3.5毫克/千克)会导致肺损伤,在随后的28小时内,通过肺干湿重比和白细胞减少来评估。2. 这种处理还减缓了[14C] - 前列腺素E2(PGE2)中14C的流出,即增加了半衰期,并在同一时期增加了PGE2在离体灌注肺中的存留时间。3. 内毒素给药30分钟后给予甲基强的松龙(30毫克/千克)可逆转内毒素的这些作用。4. 另一种合成皮质类固醇布地奈德(1.2毫克/千克)在内毒素给药前1小时给予,可部分预防肺损伤和白细胞减少,但不影响PGE2半衰期的增加及其存留时间。5. 甲基强的松龙对内毒素引起的肺损伤体征和PGE2药代动力学变化的逆转表明,PGE2药代动力学变化可作为脓毒症后急性肺损伤的一个指标。

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