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血小板活化因子介导甘油诱导的大鼠急性肾衰竭。

Platelet-activating factor mediates glycerol-induced acute renal failure in rats.

作者信息

López-Farré A, Gómez-Garre D, Bernabeu F, Ramón y Cajal S, Perez-Rodrigo P, Braquet P, López-Novoa J M

机构信息

Medical Research Institute, Fundación Jiménez Diaz-CSIC, Madrid, Spain.

出版信息

Clin Sci (Lond). 1990 Dec;79(6):551-8. doi: 10.1042/cs0790551.

Abstract
  1. We have studied the effect of inhibiting the interaction of platelet-activating factor with its receptor by using two structurally different antagonists BN-52021 (1 mg/kg, intraperitoneally) and alprazolam (1 and 5 mg/kg, intraperitoneally) on the evolution of glomerular filtration and renal blood flow, in the experimental model of acute renal failure induced by the intramuscular injection of glycerol in rats. 2. We have also measured arteriovenous differences in platelet-activating factor concentration, as well as platelet-activating factor content in glomeruli from rats with glycerol-induced acute renal failure. 3. After glycerol injection, untreated rats showed a marked reduction in inulin clearance which reached 77% in the first 30 min. The reduction was only 27% in the rats treated with BN-52021 and 38% in the rats treated with alprazolam (5 mg/kg), with statistically significant differences between treated and untreated groups. 4. Clearance of p-aminohippuric acid was also improved with BN-52021 or alprazolam treatment. 5. This protective effect of BN-52021 was observed in a more prolonged follow-up (3 days). 6. Glomeruli from rats with acute renal failure, treated or untreated with BN-52021, showed similar amounts of platelet-activating factor, whereas it was undetectable in glomeruli from normal rats. Furthermore, rats with glycerol-induced acute renal failure released greater amounts of platelet-activating factor. 7. These results provide evidence of a role for platelet-activating factor in the genesis of this model of experimental acute renal failure.
摘要
  1. 我们使用两种结构不同的拮抗剂BN - 52021(1毫克/千克,腹腔注射)和阿普唑仑(1毫克/千克和5毫克/千克,腹腔注射),在大鼠肌肉注射甘油诱导的急性肾衰竭实验模型中,研究了抑制血小板活化因子与其受体相互作用对肾小球滤过和肾血流变化的影响。2. 我们还测量了甘油诱导的急性肾衰竭大鼠的血小板活化因子浓度动静脉差异以及肾小球中血小板活化因子的含量。3. 注射甘油后,未治疗的大鼠菊粉清除率显著降低,在最初30分钟内降至77%。用BN - 52021治疗的大鼠降低幅度仅为27%,用阿普唑仑(5毫克/千克)治疗的大鼠降低幅度为38%,治疗组和未治疗组之间存在统计学显著差异。4. 用BN - 52021或阿普唑仑治疗也改善了对氨基马尿酸的清除率。5. 在更长时间的随访(3天)中观察到了BN - 52021的这种保护作用。6. 用或未用BN - 52021治疗的急性肾衰竭大鼠的肾小球显示出相似数量的血小板活化因子,而在正常大鼠的肾小球中未检测到。此外,甘油诱导的急性肾衰竭大鼠释放出更多的血小板活化因子。7. 这些结果提供了证据,证明血小板活化因子在这种实验性急性肾衰竭模型的发生中起作用。

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