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猪内毒素血症期间的单羟基二十碳四烯酸。血小板活化因子受体拮抗剂的作用。

Mono-hydroxyeicosatetraenoic acids during porcine endotoxemia. Effect of a platelet-activating factor receptor antagonist.

作者信息

Olson N C, Joyce P B, Fleisher L N

机构信息

Department of Anatomy, Physiological Sciences and Radiology, College of Veterinary Medicine, North Carolina State University, Raleigh.

出版信息

Lab Invest. 1990 Aug;63(2):221-32.

PMID:2116563
Abstract

Infusion of endotoxin into domestic pigs induces an acute respiratory failure that has many similarities with the adult respiratory distress syndrome. We hypothesized that mono-hydroxyeicosatetraenoic acids (HETE) and platelet-activating factor (PAF) might be involved in this model of respiratory failure. Escherichia coli endotoxin (055-B5) was infused intravenously into anesthetized young pigs at 5 micrograms/kg the first hour, followed by 2 micrograms/kg/hour for 3 hours in the presence and absence of SRI 63-675, a specific PAF receptor antagonist. SRI 63-675 (10 mg/kg before endotoxin + 3 mg/kg/hour during endotoxemia) blocked or attenuated endotoxin-induced pulmonary hypertension, bronchoconstriction, hypoxemia, thrombocytopenia, increased permeability of the alveolar-capillary membrane, and the increases in plasma (at 3 and 4 hours) and bronchoalveolar lavage fluid concentrations of 5-, 12-, and 15-HETE. In a separate group of pigs, before treatment with SRI 63-675, ex vivo stimulation of whole blood with calcium ionophore (at -25 min) caused large increases in plasma concentrations of 5-HETE and, to a lesser extent, 12-HETE. At 4 hours, these increases were not significantly modified in blood derived from pigs treated with SRI 63-675 (10 mg/kg + 3 mg/kg/hour from 0 to 4 hours), indicating no direct inhibition of 5- or 12-lipoxygenase and suggesting that the in vivo effects were PAF receptor-mediated. We conclude that PAF contributes to the release of HETEs during endotoxemia and that this phenomenon could be important in the pathophysiology associated with endotoxin-induced lung injury in anesthetized pigs.

摘要

给家猪输注内毒素可诱发急性呼吸衰竭,该病症与成人呼吸窘迫综合征有许多相似之处。我们推测单羟基二十碳四烯酸(HETE)和血小板活化因子(PAF)可能参与了这种呼吸衰竭模型。将大肠杆菌内毒素(055-B5)以5微克/千克的剂量在第一小时静脉注入麻醉的幼猪体内,随后在有或没有特异性PAF受体拮抗剂SRI 63-675的情况下,以2微克/千克/小时的剂量持续输注3小时。SRI 63-675(内毒素注射前10毫克/千克 + 内毒素血症期间3毫克/千克/小时)可阻断或减轻内毒素诱导的肺动脉高压、支气管收缩、低氧血症、血小板减少、肺泡-毛细血管膜通透性增加以及血浆(在3小时和4小时时)和支气管肺泡灌洗液中5-、12-和15-HETE浓度的升高。在另一组猪中,在用SRI 63-675治疗之前,用钙离子载体(在-25分钟时)对全血进行体外刺激会导致血浆中5-HETE浓度大幅升高,12-HETE浓度升高幅度较小。在4小时时,在用SRI 63-675(0至4小时为10毫克/千克 + 3毫克/千克/小时)治疗的猪的血液中,这些升高并未得到显著改变,这表明对5-或12-脂氧合酶没有直接抑制作用,并提示体内效应是由PAF受体介导的。我们得出结论,PAF在内毒素血症期间有助于HETEs的释放,并且这种现象在与麻醉猪内毒素诱导的肺损伤相关的病理生理学中可能很重要。

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