Franks J J, Kirsch R E, Frith L O, Purves L R, Franks W T, Franks J A, Mason P, Saunders S J
J Clin Invest. 1981 Feb;67(2):575-80. doi: 10.1172/JCI110069.
Previous studies are in conflict over the effect of infusing mixed fibrinogen-fibrin degradation products on fibrinogen synthesis, as determined by changes in fibrinogen concentration or by incorporation of labeled amino acids into fibrinogen. We have injected purified homologous fragments D1 and E into rats and measured their fibrinogen and albumin synthetic rates by the [14C]carbonate technique, a method that provides quantitative estimates of hepatic secretory protein synthesis. Fibrinogen fractional synthetic rates were increased 2.5 times in animals injected with fragment D1, compared with saline-injected controls. No increase were observed in fragment E-injected animals. Neither fragment produced changes in albumin synthesis. Fragment D increased plasma fibrinogen concentration, but did not raise plasma haptoglobin levels. These results suggest that fragment D is a regulator of fibrinogen synthesis.
以往的研究在输注混合纤维蛋白原 - 纤维蛋白降解产物对纤维蛋白原合成的影响方面存在冲突,这是通过纤维蛋白原浓度的变化或标记氨基酸掺入纤维蛋白原的情况来确定的。我们已将纯化的同源片段D1和E注入大鼠体内,并通过[14C]碳酸盐技术测量其纤维蛋白原和白蛋白合成率,该方法可对肝脏分泌蛋白合成进行定量估计。与注射生理盐水的对照组相比,注射片段D1的动物纤维蛋白原分数合成率增加了2.5倍。在注射片段E的动物中未观察到增加。两个片段均未引起白蛋白合成的变化。片段D增加了血浆纤维蛋白原浓度,但未提高血浆触珠蛋白水平。这些结果表明片段D是纤维蛋白原合成的调节剂。