Silver P J, Broughton R, Bouthillier J, Quinn T A, Wallace A M, Weishaar R E
IBEX Technologies Inc., Malvern, Pennsylvania 19355, USA.
Thromb Res. 1998 Aug 1;91(3):143-50. doi: 10.1016/s0049-3848(98)00093-0.
Neutralase (heparinase I; E.C. 4.2.2.7) is a heparin-degrading enzyme undergoing clinical evaluation as an alternative to protamine for reversing the anticoagulant effects of heparin in coronary bypass surgery. The objective of this study was to assess the relative effects of Neutralase and protamine on reversal of heparin-dependent elevations in coagulation parameters and inhibition of clot formation in a rabbit vena caval stasis model. Rabbits were treated with saline or heparin (300 U/kg) for 10 minutes, followed by saline, protamine (2.6 mg/kg), or Neutralase (10 or 30 microg/kg, representing 1.23 IU/kg and 3.69 IU/kg, respectively). Twenty minutes later, venous stasis was induced, and vena caval clots were excised, weighed, and characterized. Coagulation parameters [activated partial thromboplastin time (aPTT) and thrombin clotting time (TCT)] and antiFactor IIa and Xa levels were measured throughout the protocol. Both protamine and Neutralase reversed heparin-mediated increases in aPTT (>300 seconds to 26-35 seconds) and TCT (>300 seconds to 29-56 seconds) to values that were not different from saline-treated, nonheparinized animals. Thrombus weight in the nonheparinized saline group was 62+/-7 mg; heparin-treated animals had no detectable clots. Protamine reversal of heparin was associated with clot formation (89+/-20 mg) while Neutralase reversal was not (no clots). Heparin-induced increases in antiFactor IIa activity were reversed similarly by protamine and Neutralase (from 4.3-8.8 U/ml to 0.2-0.3 U/ml) while antiFactor Xa activity was differentially reversed (from 3.9-5.9 U/ml to 0.7-1.3 U/ml Neutralase; 5.5 U/ml to 0.02 U/ml protamine). These results are consistent with a hypothesis that Neutralase cleaves heparin into fragments, which are devoid of antiFactor IIa activity that retain modest antiFactor Xa activity, resulting in reversal of anticoagulant, but not antithrombotic, heparin activity. This property of Neutralase may be beneficial in reducing post-surgical thrombotic events after reversal of heparin.
中性酶(肝素酶I;E.C. 4.2.2.7)是一种正在进行临床评估的肝素降解酶,可作为鱼精蛋白的替代物,用于在冠状动脉搭桥手术中逆转肝素的抗凝作用。本研究的目的是在兔腔静脉淤滞模型中评估中性酶和鱼精蛋白对逆转肝素依赖性凝血参数升高及抑制血栓形成的相对作用。用生理盐水或肝素(300 U/kg)处理兔子10分钟,随后分别给予生理盐水、鱼精蛋白(2.6 mg/kg)或中性酶(10或30 μg/kg,分别相当于1.23 IU/kg和3.69 IU/kg)。20分钟后,诱导静脉淤滞,切除腔静脉血栓,称重并进行特性分析。在整个实验过程中测量凝血参数[活化部分凝血活酶时间(aPTT)和凝血酶凝血时间(TCT)]以及抗因子IIa和Xa水平。鱼精蛋白和中性酶均可将肝素介导的aPTT升高(>300秒至26 - 35秒)和TCT升高(>300秒至29 - 56秒)逆转至与生理盐水处理的未肝素化动物无差异的值。未肝素化生理盐水组的血栓重量为62±7 mg;肝素处理的动物未检测到血栓。鱼精蛋白逆转肝素与血栓形成相关(89±20 mg),而中性酶逆转则无血栓形成。肝素诱导的抗因子IIa活性增加被鱼精蛋白和中性酶类似地逆转(从4.3 - 8.8 U/ml降至0.2 - 0.3 U/ml),而抗因子Xa活性的逆转则存在差异(从3.9 - 5.9 U/ml降至0.7 - 1.3 U/ml中性酶;从5.5 U/ml降至0.02 U/ml鱼精蛋白)。这些结果与以下假设一致:中性酶将肝素切割成片段,这些片段缺乏抗因子IIa活性,但保留适度的抗因子Xa活性,从而导致肝素的抗凝活性而非抗血栓活性被逆转。中性酶的这一特性可能有助于减少肝素逆转后手术后的血栓形成事件。