In vivo quantitation of the rat liver's ability to eliminate endotoxin from portal vein blood.

Y Yamaguchi, K Yamaguchi, J L Babb, H Gans
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Abstract

The in vivo uptake of endotoxin by the liver from portal vein blood was assessed during a single passage through the liver. 51Cr labeled and unlabeled endotoxin were infused in different amounts into the femoral vein of three groups of lead-sensitized rats: a nonoperated, a sham-operated, and a surgically created reversed Eck fistula (REF) group. Whereas in the former two the infused endotoxin encounters the lung as the first filter organ, the liver performs this function in the latter experimental model. The mortality rates observed in control and sham-operated, lead-sensitized rats were found to correlate closely and reproducibly to the degree of endotoxemia. This assay was then applied to determine the amount of endotoxin eliminated by the liver by establishing, in the REF rat, the amounts of endotoxin that escaped hepatic clearance. Following infusion of 1 microgram of endotoxin/hr into REF rats, approximately 985 ng is found to be taken up by the liver; following 2 micrograms, 1965 ng is sequestered; following 3 micrograms, 2810 ng; and after 4 micrograms, 3175 ng is retained by the liver. Hence, the capacity of the liver to eliminate endotoxin from portal vein blood during a single passage increases as the portal vein endotoxin level rises; it approaches a maximum, suggesting that endotoxin's interaction with the Kupffer cells conforms to classical saturation kinetics. A Lineweaver-Burk plot prepared from these data indicates that the maximal in vivo capacity of the liver to remove endotoxin from portal vein blood approximates 1.5 micrograms/gm liver/hr. Data obtained with the use of radiolabeled endotoxin corroborate the information obtained with the bioassay technique. Endotoxin eliminated by the Kupffer cells in these quantities is slowly disintegrated; 4 hr after termination of the endotoxin infusion, less than 4% of the radiolabel is found in the urine and none in the bile. These observations indicate that the Kupffer cell's functional capacity to sequester and detoxify endotoxin is extensive and far exceeds the requirements imposed by physiological and most pathological conditions.

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大鼠肝脏清除门静脉内毒素能力的体内定量研究。
通过肝脏的单次通道,评估了肝脏从门静脉血液中摄取内毒素的情况。将51Cr标记内毒素和未标记内毒素按不同量注入三组铅致敏大鼠:未手术组、假手术组和手术造瘘组(REF)。在前两种实验模型中,注入的内毒素作为第一个过滤器官与肺相遇,而在后一种实验模型中,肝脏发挥这一功能。在对照组和假手术的铅致敏大鼠中观察到的死亡率与内毒素血症的程度密切相关,并具有可重复性。然后,通过在REF大鼠中建立逃脱肝脏清除的内毒素的量,应用该试验来确定肝脏消除的内毒素的量。在REF大鼠体内每小时注射1微克内毒素后,发现约985 ng被肝脏吸收;低于2微克,1965纳克被隔离;以下3微克,2810纳克;4微克后,肝脏会保留3175纳克。因此,随着门静脉内毒素水平的升高,肝脏在单次通道中从门静脉血液中清除内毒素的能力增加;它接近最大值,表明内毒素与库普弗细胞的相互作用符合经典的饱和动力学。根据这些数据制作的Lineweaver-Burk图表明,肝脏从门静脉血液中去除内毒素的最大体内能力约为1.5微克/克肝脏/小时。用放射性标记内毒素获得的数据证实了用生物测定技术获得的信息。这些量的内毒素被库普弗细胞消除,然后慢慢分解;终止内毒素输注4小时后,尿中放射性标记物少于4%,胆汁中无放射性标记物。这些观察结果表明,库普弗细胞隔离和解毒内毒素的功能能力是广泛的,远远超过了生理和大多数病理条件所施加的要求。
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