[Study of principles in pathogenesis and therapy of fat embolism. IV. In vivo studies of drug-induced mobilization of embolized lung fat].

R Gottlob, R Kokoschka, K Porschinski, H Bergmann, T Sogukoglu, F Saghir
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Abstract

Pluronic F 108 added to serum in a concentration of 1 g/dl proved as the optimal means to increase the fat emulgatory capacity. Similar concentrations were achieved in living rabbits by infusing 4.5 g per kg body weight. In spite of this higher dosage we failed to mobilize 131 J labelled fat, embolized into the lungs of the animals. It is concluded that also in humans there exists no possibility to mobilize fat emboli from the lungs by the application of tensides (non-ionic detergents, lecithin-preparations, bile salts) or of organic solvents (alcohol, ether). All these agents are capable to emulsify fat in vitro, however, only under vigorous shaking.--Because of the side effects of those agents their application on patients, suffering from posttraumatic fat embolism seems not to be justified.

脂肪栓塞的发病机理及治疗原理研究。IV.药物诱导栓塞肺脂肪动员的体内研究[j]。
在血清中添加1 g/dl的Pluronic f108被证明是提高脂肪乳化能力的最佳方法。在活兔中,每公斤体重注射4.5 g,也能达到类似的浓度。尽管使用了更高的剂量,我们仍未能动员131 J标记的脂肪,使其栓塞到动物的肺部。结论是,在人类中,也不可能通过使用张力剂(非离子洗涤剂、卵磷脂制剂、胆汁盐)或有机溶剂(酒精、乙醚)来清除肺部的脂肪栓塞。所有这些试剂都能在体外乳化脂肪,但是,只有在剧烈摇动下。由于这些药物在患者身上的副作用,创伤后脂肪栓塞似乎是不合理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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