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内毒素注射后绵羊体内淋巴源性因子对淋巴泵功能的调节作用。

Modulation of lymphatic pumping by lymph-borne factors after endotoxin administration in sheep.

作者信息

Elias R M, Johnston M G

机构信息

Department of Pathology, University of Toronto, Ontario, Canada.

出版信息

J Appl Physiol (1985). 1990 Jan;68(1):199-208. doi: 10.1152/jappl.1990.68.1.199.

DOI:10.1152/jappl.1990.68.1.199
PMID:2312460
Abstract

The purpose of this study was to test the hypothesis that endotoxin administration to sheep results in host-derived lymph-borne factors that modulate lymphatic pumping activity. To achieve this, two sheep were used for each experiment. In the test animal, a segment of intestinal lymphatic was isolated from all lymph input and provided with lymph from a reservoir. Pumping activity was initiated with a fixed transmural pressure applied to the test vessel, and the only input to this duct was provided by lymph from an indwelling catheter in a second donor sheep. The intravenous administration of endotoxin to the donor animals (33 micrograms/kg) generally resulted in increased pumping in the test vessels over the 1st h, but this was followed by reductions in pumping until flow stopped in all preparations. In control experiments (no endotoxin administered) pumping was unaffected. Further investigation revealed that these activities were relatively unstable and, in the case of the inhibitory material, appeared to act by decreasing the sensitivity of the vessel to changes in transmural pressure, because flow could be reestablished in the test vessels by elevating transmural pressures above the level originally chosen for the experiment. Endotoxin itself had no direct effect on sheep lymphatics in vivo or on bovine lymphatic vessels in vitro. However, the appearance of erythrocyte hemolysate (erythrolysate) in lymph was regularly observed after endotoxin infusion, and we demonstrated that erythrolysate (diluted to contain 10(-5) M hemoglobin) was a potent inhibitor of lymphatic pumping in vivo and in vitro.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是验证以下假设

给绵羊注射内毒素会导致宿主来源的淋巴源性因子,这些因子可调节淋巴泵血活动。为实现这一目标,每次实验使用两只绵羊。在受试动物中,一段肠淋巴管与所有淋巴输入隔离,并从储液器中获取淋巴。通过对受试血管施加固定的跨壁压力来启动泵血活动,该管道的唯一输入是来自第二只供体绵羊体内留置导管的淋巴。给供体动物静脉注射内毒素(33微克/千克)通常会导致受试血管在第1小时内泵血增加,但随后泵血减少,直至所有制剂中的血流停止。在对照实验(未注射内毒素)中,泵血不受影响。进一步研究表明,这些活性相对不稳定,就抑制性物质而言,似乎是通过降低血管对跨壁压力变化的敏感性来起作用的,因为通过将跨壁压力提高到高于实验最初选择的水平,可以在受试血管中重新建立血流。内毒素本身对绵羊体内淋巴管或体外牛淋巴管没有直接影响。然而,在内毒素输注后,经常观察到淋巴中出现红细胞溶血产物(红细胞溶解产物),并且我们证明红细胞溶解产物(稀释至含有10^(-5) M血红蛋白)在体内和体外都是淋巴泵血的有效抑制剂。(摘要截短于250字)

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