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在使用不同低分子肝素进行血液透析期间,肝细胞生长因子/激活素 A/卵泡抑素系统被激活。

Hepatocyte growth factor/activin A/follistatin system activation during hemodialysis with different low molecular weight heparins.

机构信息

Department of Nephrology and Transplantation, Medical University of Białystok, Białystok, Poland.

出版信息

Ren Fail. 2009;31(9):791-7. doi: 10.3109/08860220903180608.

DOI:10.3109/08860220903180608
PMID:19925286
Abstract

Hepatocyte growth factor (HGF), activin A (Act A), and follistatin (FS) compose an organotrophic system; interestingly it is modified by heparin. To understand if LMWHs (considered distinct drugs) have different clinical profiles regarding the above growth factors, we studied the effects of enoxaparin, nadroparin, and dalteparin on their plasma levels. Seventeen chronic HD patients completed this prospective, crossover trial. They were randomized into six groups: each patient was administered enoxaparin (effective dose of 0.75 mg/kg), nadroparin (70.4 IU/kg) and dalteparin (78.6 IU/kg) in three time periods of two months each. At the end of this period, the cytokine's plasma levels were measured by immunoassays at the start and at 10 min and 180 min of the HD procedure. At 10 min, we observed a striking increase in plasma HGF (32-fold), Act A (4-fold), and FS (53%), all p = 0.0003. The levels of HGF and Act A remained markedly elevated after 180 min (by 295% and 87%, respectively; both p < 0.002), while those of FS returned to baseline. There were no differences in cytokine profile comparing both their peak concentrations and the areas under the curve. Enoxaparin, dalteparin, and nadroparin are seemingly not different considering the release of HGF/Act A/FS during HD procedures; this may reflect their similar profile in other aspects. Moreover, the concentrations of HGF/Act A/FS are close to therapeutic ones, which may partly explain the mechanisms underlying some of the emerging extra-anticoagulant effects of LMWHs.

摘要

肝细胞生长因子(HGF)、激活素 A(Act A)和卵泡抑素(FS)构成了一个器官营养系统;有趣的是,肝素可以对其进行修饰。为了了解低分子肝素(被认为是不同的药物)在上述生长因子方面是否具有不同的临床特征,我们研究了依诺肝素、那屈肝素和达肝素对其血浆水平的影响。17 名慢性血液透析患者完成了这项前瞻性、交叉试验。他们被随机分为六组:每位患者接受依诺肝素(有效剂量为 0.75mg/kg)、那屈肝素(70.4IU/kg)和达肝素(78.6IU/kg),每个时间段为两个月。在这段时间结束时,通过免疫测定法测量细胞因子的血浆水平,在血液透析过程开始时以及 10 分钟和 180 分钟时进行测量。在 10 分钟时,我们观察到血浆 HGF(32 倍)、Act A(4 倍)和 FS(53%)显著增加,所有 p 值均为 0.0003。在 180 分钟后,HGF 和 Act A 的水平仍然明显升高(分别升高 295%和 87%;均 p<0.002),而 FS 的水平恢复到基线。在比较两种峰值浓度和曲线下面积时,细胞因子谱没有差异。依诺肝素、达肝素和那屈肝素在血液透析过程中释放 HGF/Act A/FS 方面似乎没有差异;这可能反映了它们在其他方面的相似特征。此外,HGF/Act A/FS 的浓度接近治疗浓度,这可能部分解释了低分子肝素出现的一些新兴抗凝外作用的机制。

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