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健康志愿者控制性出血时促红细胞生成素的产生:反对腺苷起主要作用的证据

Erythropoietin production in healthy volunteers subjected to controlled haemorrhage: evidence against a major role for adenosine.

作者信息

Gleiter C H, Freudenthaler S, Delabar U, Eckardt K U, Mühlbauer B, Gundert-Remy U, Osswald H

机构信息

Abteilung Klinische Pharmakologie, Universität Göttingen, Germany.

出版信息

Br J Clin Pharmacol. 1996 Dec;42(6):729-35. doi: 10.1046/j.1365-2125.1996.00484.x.

Abstract
  1. This study was carried out to assess the role of adenosine in the regulation of human erythropoietin (EPO) production. To this end we investigated in healthy volunteers whether the nonspecific adenosine antagonist theophylline increases and the adenosine uptake inhibitor dipyridamole decreases EPO production in response to an haemorrhage of 750 ml. 2. Healthy male nonsmokers received i.v. in a parallel, randomized, single-blind trial theophylline (loading dose 5 mg kg-1 over 20 min, followed by 0.5 mg kg-1 min-1), dipyridamole (0.21 mg kg-1 h-1) or placebo (0.9% NaCl) for 6 h following the phlebotomy. EPO concentrations were followed up to 72 h after phlebotomy. 3. Following blood loss EPO concentrations increased during all treatments. The AUCEPO (0,72 h) were not statistically significantly different (theophylline: 398 +/- 30, dipyridamole: 301 +/- 15, placebo: 332 +/- 57 [mu ml-1 h]). Creatinine clearance and urinary cAMP excretion were unaltered by any treatment. Urinary excretion of adenosine was significantly increased during infusion of dipyridamole. Plasma renin activity was significantly increased during theophylline infusion. 4. In our model of controlled, physiological stimulation of EPO production by haemorrhage, adenosine appears unlikely to play a major role as a mediator of renal EPO production.
摘要
  1. 本研究旨在评估腺苷在调节人促红细胞生成素(EPO)产生中的作用。为此,我们在健康志愿者中研究了非特异性腺苷拮抗剂茶碱是否会增加以及腺苷摄取抑制剂双嘧达莫是否会降低因750毫升出血而引起的EPO产生。2. 在一项平行、随机、单盲试验中,健康男性非吸烟者在静脉放血后接受静脉注射茶碱(负荷剂量为5毫克/千克,持续20分钟,随后为0.5毫克/千克·分钟)、双嘧达莫(0.21毫克/千克·小时)或安慰剂(0.9%氯化钠),持续6小时。在静脉放血后对EPO浓度进行长达72小时的随访。3. 失血后,所有治疗期间EPO浓度均升高。EPO的曲线下面积(0,72小时)在统计学上无显著差异(茶碱:398±30,双嘧达莫:301±15,安慰剂:332±57[μ毫升-1·小时])。任何治疗均未改变肌酐清除率和尿cAMP排泄。在输注双嘧达莫期间,腺苷的尿排泄显著增加。在输注茶碱期间,血浆肾素活性显著增加。4. 在我们通过出血对EPO产生进行受控生理刺激的模型中,腺苷似乎不太可能作为肾脏EPO产生的介质发挥主要作用。

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