Dekker Douwe, Dorresteijn Mirrin J, Peters Wilbert Hm, Bilos Albert, Pennings Sebastiaan W C, Wagener Frank A D T G, Smits Paul
Department of Pharmacology and Toxicology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands.
Department of Pharmacology and Toxicology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands Department of Intensive Care Medicine, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands.
Diab Vasc Dis Res. 2016 Jan;13(1):41-8. doi: 10.1177/1479164115605047. Epub 2015 Oct 14.
This translational randomized and vehicle-controlled cross-over study was performed to assess the impact of haem arginate treatment on haem oxygenase-1 induction, endothelial function and insulin sensitivity in subjects with the metabolic syndrome (n = 14). Both treatment periods consisted of 5 days. Haem arginate or vehicle (l-arginine) was administered intravenously on Days 1 and 3. Forearm blood flow in response to acetylcholine and nitroglycerine was measured by venous occlusion plethysmography (Day 3), insulin sensitivity by a hyperinsulinaemic clamp procedure (Day 5). Haem arginate did not improve endothelial function or insulin sensitivity but significantly reduced the vasodilator response to nitroglycerine (p < 0.01). These negative findings are in contrast to the preclinical data, which may be due to short duration of therapy and limited haem oxygenase-1 induction as well as interference by markedly elevated plasma haem levels observed after haem arginate treatment (p < 0.01). Future studies should pay attention to the delicate balance between sufficient dosing and timely normalization of plasma haem levels.
本转化性随机、安慰剂对照交叉研究旨在评估精氨酸血红素治疗对代谢综合征患者(n = 14)血红素加氧酶-1诱导、内皮功能和胰岛素敏感性的影响。两个治疗期均为5天。在第1天和第3天静脉注射精氨酸血红素或安慰剂(L-精氨酸)。通过静脉阻塞体积描记法测量乙酰胆碱和硝酸甘油刺激后的前臂血流量(第3天),通过高胰岛素钳夹术测量胰岛素敏感性(第5天)。精氨酸血红素并未改善内皮功能或胰岛素敏感性,但显著降低了对硝酸甘油的血管舒张反应(p < 0.01)。这些负面结果与临床前数据相反,这可能是由于治疗持续时间短、血红素加氧酶-1诱导有限以及精氨酸血红素治疗后观察到的血浆血红素水平显著升高的干扰(p < 0.01)。未来的研究应关注足够剂量与血浆血红素水平及时正常化之间的微妙平衡。