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首页> 外文期刊>The Journal of Physiology >Erythropoietin treatment elevates haemoglobin concentration by increasing red cell volume and depressing plasma volume.
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Erythropoietin treatment elevates haemoglobin concentration by increasing red cell volume and depressing plasma volume.

机译:促红细胞生成素治疗通过增加红细胞体积和降低血浆体积来提高血红蛋白浓度。

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Erythropoietin (Epo) has been suggested to affect plasma volume, and would thereby possess a mechanism apart from erythropoiesis to increase arterial oxygen content. This, and potential underlying mechanisms, were tested in eight healthy subjects receiving 5000 IU recombinant human Epo (rHuEpo) for 15 weeks at a dose frequency aimed to increase and maintain haematocrit at approximately 50%. Red blood cell volume was increased from 2933 +/- 402 ml before rHuEpo treatment to 3210 +/- 356 (P < 0.01), 3117 +/- 554 (P < 0.05), and 3172 +/- 561 ml (P < 0.01) after 5, 11 and 13 weeks, respectively. This was accompanied by a decrease in plasma volume from 3645 +/- 538 ml before rHuEpo treatment to 3267 +/- 333 (P < 0.01), 3119 +/- 499 (P < 0.05), and 3323 +/- 521 ml (P < 0.01) after 5, 11 and 13 weeks, respectively. Concomitantly, plasma renin activity and aldosterone concentration were reduced. This maintained blood volume relatively unchanged, with a slight transient decrease at week 11, such that blood volume was 6578 +/- 839 ml before rHuEpo treatment, and 6477 +/- 573 (NS), 6236 +/- 908 (P < 0.05), and 6495 +/- 935 ml (NS), after 5, 11 and 13 weeks of treatment. We conclude that Epo treatment in healthy humans induces an elevation in haemoglobin concentration by two mechanisms: (i) an increase in red cell volume; and (ii) a decrease in plasma volume, which is probably mediated by a downregulation of the rennin-angiotensin-aldosterone axis. Since the relative contribution of plasma volume changes to the increments in arterial oxygen content was between 37.9 and 53.9% during the study period, this mechanism seems as important for increasing arterial oxygen content as the well-known erythropoietic effect of Epo.
机译:促红细胞生成素(Epo)已被建议影响血浆容量,因此除了促红细胞生成外,还具有增加动脉血氧含量的机制。在以增加和维持血细胞比容约为50%的剂量频率接受5000 IU重组人Epo(rHuEpo)的15位健康受试者中,对这和潜在的潜在机制进行了测试。红细胞体积从rHuEpo治疗前的2933 +/- 402 ml增加到3210 +/- 356(P <0.01),3117 +/- 554(P <0.05)和3172 +/- 561 ml(P <0.01) )分别在5、11和13周之后。伴随的是血浆体积从rHuEpo治疗前的3645 +/- 538 ml降至3267 +/- 333(P <0.01),3119 +/- 499(P <0.05)和3323 +/- 521 ml( P <0.01)分别在5、11和13周后出现。同时,血浆肾素活性和醛固酮浓度降低。这样维持的血容量相对不变,在第11周时有短暂的短暂下降,因此在rHuEpo治疗之前血容量为6578 +/- 839 ml,而6477 +/- 573(NS),6236 +/- 908(P <0.05 ),5周,11周和13周后,再注入6495 +/- 935 ml(NS)。我们得出结论,健康人的Epo治疗通过两种机制引起血红蛋白浓度升高:(i)红细胞体积增加; (ii)血浆量减少,这可能是由于肾素-血管紧张素-醛固酮轴的下调所介导的。由于在研究期间血浆体积变化对动脉血氧含量增加的相对贡献在37.9%至53.9%之间,因此这种机制对于增加动脉血氧含量似乎与Epo众所周知的促红细胞生成作用一样重要。

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