Haem arginate infusion stimulates haem oxygenase-1 expression in healthy subjects

被引:42
作者
Doberer, D. [1 ]
Haschemi, A. [2 ]
Andreas, M. [1 ]
Zapf, T-C [2 ]
Clive, B. [1 ]
Jeitler, M. [2 ]
Heinzl, H. [3 ]
Wagner, O. [2 ]
Wolzt, M. [1 ]
Bilban, M. [2 ]
机构
[1] Med Univ Vienna, Dept Clin Pharmacol, A-1090 Vienna, Austria
[2] Med Univ Vienna, Clin Inst Med & Chem Lab Diagnost, A-1090 Vienna, Austria
[3] Med Univ Vienna, Ctr Med Stat Informat & Intelligent Syst, A-1090 Vienna, Austria
关键词
haem oxygenase; ischaemia-reperfusion injury; healthy volunteers; polymorphism; GENE PROMOTER POLYMORPHISM; CORONARY-ARTERY-DISEASE; MICROSATELLITE POLYMORPHISM; HEMORRHAGIC-SHOCK; DIABETIC-PATIENTS; SERUM BILIRUBIN; RISK-FACTORS; SUSCEPTIBILITY; INDUCTION; CELLS;
D O I
10.1111/j.1476-5381.2010.00990.x
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
BACKGROUND AND PURPOSE Haem oxygenase 1 (HO-1) is an inducible protein that plays a major protective role in conditions such as ischaemia-reperfusion injury and inflammation. In this study, we have investigated the role of haem arginate (HA) in human male subjects in the modulation of HO-1 expression and its correlation with the GT length polymorphism (GT(n)) in the promoter of the HO-1 gene. EXPERIMENTAL APPROACH In a dose-escalation, randomized, placebo-controlled trial, seven healthy male subjects with a homozygous short (S/S) and eight with a long (L/L) GT(n) genotype received intravenous HA. HO-1 protein expression and mRNA levels in peripheral blood monocytes, bilirubin, haptoglobin, haemopexin and haem levels were analysed over a 48 h observation period. KEY RESULTS We found that the baseline mRNA levels of HO-1 were higher in L/L subjects, while protein levels were higher in S/S subjects. HA induced a dose-dependent increase in the baseline corrected area under the curve values of HO-1 mRNA and protein over 48 h. The response of HO-1 mRNA was more pronounced in L/L subjects but the protein level was similar across the groups. CONCLUSIONS AND IMPLICATION HA is an effective inducer of HO-1 in humans irrespective of the GT(n) genotype. The potential therapeutic application of HA needs to be evaluated in clinical trials.
引用
收藏
页码:1751 / 1762
页数:12
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