Decreased synthesis of tissue plasminogen activator antigen in users of oral contraceptives

K.R. Petersen , M. Jørgensen , N. Vinberg , J. Gram , S.O. Skouby , K.H. Tønnesen , J. Jespersen
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Abstract

Objective: To study why the plasma antigen concentrations of tissue-plasminogen activator (t-PA) and plasminogen activator inhibitor type 1 (PAI-1) are reduced in users of oral contraceptives (OCs).

Design:Open, non-randomized study.

Setting: University departments in Copenhagen and Esbjerg, Denmark.

Subjects: Sixteen healthy female volunteers between 21 and 32 years of age. Eight women used an OC containing ethinyl estradiol and gestodene (OC group) and eight women used non-hormonal contraception (control group).

Intervention: Determination of splanchnic plasma flow and total plasma volume; measurement of t-PA and PAI-1 antigen as well as active t-PA and PAI-1 in plasma from an artery and a liver vein

Main outcome measures:Extraction, clearance, net rate of catabolism and mean transit time of t-PA and PAI-1 in the splanchnic circulation.

Results: Arterial plasma concentrations of t-PA and PAI-1 antigen were reduced in the OC group whereas the concentrations of active t-PA and active PAI-I were similar. The arterio-venous (A-V) difference for t-PA antigen and active t-PA was positive in both groups. The net splanchnic catabolism of t-PA antigen was reduced in the OC group, while the extraction, clearance and mean transit time were similar. The extraction, clearance, net rate of catabolism and mean transit time of active t-PA did not differ between the two groups. For PAI-1, differences in the main outcome measures between the two groups could not be determined, as there was no statistically significant A-V difference for PAI-1 antigen in any of the groups and a significant A-V difference for active PAI-1 in the control group only.

Conclusion: The reduced net splanchnic catabolism of t-PA antigen in the OC users probably reflects a decreased peripheral synthesis of t-PA, which may explain the low plasma concentration in these women. The mechanism underlying the reduced concentration of PAI-1 antigen in the OC users could not be determined by the present methodology.

口服避孕药使用者组织纤溶酶原激活物抗原合成降低
目的:研究口服避孕药使用者血浆组织型纤溶酶原激活剂(t-PA)和纤溶酶原激活物抑制物1型(PAI-1)抗原浓度降低的原因。设计:开放、非随机研究。背景:哥本哈根和丹麦埃斯比约格的大学系。受试者:16名年龄在21-32岁之间的健康女性志愿者。8名妇女使用含有炔雌醇和孕甾烯的OC(OC组),8名妇女采用非激素避孕(对照组)。干预:测定内脏血流量和总血容量;动脉和肝静脉血浆中t-PA和PAI-1抗原以及活性t-PA和PA I-1的测量主要结果测量:内脏循环中t-PA、PAI-1的提取、清除、净分解代谢率和平均转运时间。结果:OC组动脉血浆t-PA和PAI-1抗原浓度降低,而活性t-PA和活性PAI-1的浓度相似。两组t-PA抗原和活性t-PA的动静脉(A-V)差异均为阳性。OC组t-PA抗原的净内脏分解代谢减少,而提取、清除和平均转运时间相似。活性t-PA的提取、清除率、净分解代谢率和平均转运时间在两组之间没有差异。对于PAI-1,两组之间主要结果指标的差异无法确定,因为任何一组的PAI-1抗原没有统计学上显著的A-V差异,只有对照组的活性PAI-1有显著的A-V差异。结论:OC使用者内脏内t-PA抗原净分解代谢的减少可能反映了外周t-PA合成的减少,这可能解释了这些女性血浆浓度低的原因。OC使用者体内PAI-1抗原浓度降低的机制无法通过本方法确定。
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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