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人血代用品(贺斯)与纤连蛋白相互作用的体内研究。

In-vivo studies on Haemaccel-fibronectin interaction in man.

作者信息

Damas P, Adam A, Buret J, Renard C, Lamy M, Foidart J B, Mahieu P

出版信息

Eur J Clin Invest. 1987 Apr;17(2):166-73. doi: 10.1111/j.1365-2362.1987.tb02396.x.

DOI:10.1111/j.1365-2362.1987.tb02396.x
PMID:3108005
Abstract

An enzyme-linked immunoassay has been recently set up for direct measurement of the binding capacity of plasma fibronectin to gelatin. This binding capacity could be completely inhibited in vitro by an eight-fold excess of gelatin, of Haemaccel, but not of Geloplasma. On the contrary, the levels of immunoreactive fibronectin measured by laser nephelometry did not change, in presence of 10 to 1000 micrograms ml-1 of gelatin, of Haemaccel or of Geloplasma. When infused into normal volunteers, Haemaccel provoked a strong and immediate inhibition of the plasma fibronectin binding capacity to gelatin. This inhibition was dose-dependent and maximal after infusion of 500 ml of Haemaccel. Twenty-four hours after this infusion, there was a progressive recovery of the gelatin-binding capacity, which was almost completely achieved 96 h later. The formation of complexes between Haemaccel and fibronectin was demonstrated by gel filtration chromatography and by affinity chromatography. Immunoreactive plasma fibronectin levels remained unchanged up to 24 h after infusion of 500 ml of Haemaccel. A transient decline to 50% of its initial value then occurred the second day after the infusion. Therefore, a delay existed between the formation of fibronectin-Haemaccel complexes and their elimination from the bloodstream. This delay decreased when smaller volumes of Haemaccel were infused, which strongly suggests that plasma fibronectin is cleared by means of Haemaccel and does not seem to play a role of opsonin in these conditions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

最近建立了一种酶联免疫测定法,用于直接测量血浆纤连蛋白与明胶的结合能力。这种结合能力在体外可被八倍过量的明胶、贺斯完全抑制,但不能被血浆代用品抑制。相反,在存在10至1000微克/毫升明胶、贺斯或血浆代用品的情况下,通过激光散射比浊法测量的免疫反应性纤连蛋白水平没有变化。当注入正常志愿者体内时,贺斯会立即强烈抑制血浆纤连蛋白与明胶的结合能力。这种抑制是剂量依赖性的,注入500毫升贺斯后达到最大抑制。注入后24小时,明胶结合能力逐渐恢复,96小时后几乎完全恢复。通过凝胶过滤色谱法和亲和色谱法证实了贺斯与纤连蛋白之间形成了复合物。注入500毫升贺斯后24小时内,免疫反应性血浆纤连蛋白水平保持不变。注入后的第二天,其水平短暂下降至初始值的50%。因此,纤连蛋白-贺斯复合物的形成与其从血液中清除之间存在延迟。当注入较小体积的贺斯时,这种延迟会缩短,这强烈表明血浆纤连蛋白是通过贺斯清除的,在这些情况下似乎不发挥调理素的作用。(摘要截短至250字)

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