Ratnoff O D, Saito H
J Lab Clin Med. 1982 Aug;100(2):248-60.
Ellagic acid (4,4',5,5',6,6'-hexahydroxydiphenic acid 2,6,2',6'-dilactone) can substitute for negatively charged surfaces as a stimulus to reactions of the intrinsic pathway. Incubation of solutions of 4 X 10(-6)M ellagic acid with purified HF (factor XII) induced clot-promoting and amidolytic activity. Clot-promoting activity tested on a substrate of HF-deficient plasma evolved much more rapidly than amidolytic activity. Clot-promoting activity generated in mixtures of HF and ellagic acid alone, but amidolytic activity was observed only if additional proteins such as albumin were also present. Treatment of purified HF with DFP or filtration of HF through columns of SBTI bound to agarose did not prevent its subsequent activation by ellagic acid. Solutions of SBTI, at high concentration, partly inhibited the generation of amidolytic activity,wheras popcorn inhibitor and a crude IgG fraction of anti-HF inhibited the amidolytic activity that had been generated in a mixture of HF and ellagic acid. Generation of clotting and amidolytic properties was accompanied by scission of HF within an internal disulfide loop and by cleavage of HF into fragments with approximate MWs of 50,000 and 30,000; cleavage was completely blocked by popcorn inhibitor and partially blocked by high concentrations of SBTI. These experiments demonstrate that ellagic acid can activate HF in a manner analogous to negatively charged solids such as glass or kaolin.
鞣花酸(4,4',5,5',6,6'-六羟基二苯酸2,6,2',6'-双内酯)可替代带负电荷的表面,作为内源性途径反应的刺激物。将4×10⁻⁶M鞣花酸溶液与纯化的HF(因子XII)一起孵育,可诱导促凝和酰胺水解活性。在缺乏HF的血浆底物上测试的促凝活性比酰胺水解活性发展得快得多。仅在HF和鞣花酸的混合物中产生促凝活性,但仅当还存在诸如白蛋白等其他蛋白质时才观察到酰胺水解活性。用DFP处理纯化的HF或通过与琼脂糖结合的SBTI柱过滤HF并不能阻止其随后被鞣花酸激活。高浓度的SBTI溶液部分抑制酰胺水解活性的产生,而玉米花抑制剂和抗HF的粗IgG组分抑制在HF和鞣花酸混合物中已经产生的酰胺水解活性。凝血和酰胺水解特性的产生伴随着HF在内部二硫键环内的断裂以及HF裂解成分子量约为50,000和30,000的片段;这种裂解被玉米花抑制剂完全阻断,并被高浓度的SBTI部分阻断。这些实验表明,鞣花酸可以以类似于带负电荷的固体如玻璃或高岭土的方式激活HF。